GENERAL SURGERY

Neck Masses
Breast Disease
Skin and Soft Tissue
Esophagus, Stomach and Duodenum
Abdominal Pain
Biliary Tract Disease
Colon and Rectal Disease
Benign Perianal Disease
Hernias
Vascular


NECK MASSES

Learning Objectives:

  • DDX of anterior cervical triangle, midline, and low neck masses presenting in children.

    1. Thyroglossal duct cyst (midline), branchial cleft cyst (lateral), lymphadenopathy, abscess, cystic hygroma, hamangioma, teratoma/dermoid cyst, thyroid nodule, lymphoma/leukemia, (also, parathyroid tumors, neuroblastoma, histiocytosis X, rhabdomydosarcoma, salivary gland tumors, neurofibroma) branchiogenic anomalies (cysts, fistulas), granulomatous lymphadenitis (cat-scratch dz),lymphangiomas.

    2. Infants: congenital (branchial cleft cysts, thyroglossal duct cysts

    3. Adolescents: Inflammatory (cervical adenitis #1) with congenital also possible

    4. Adults: Malignancy (squamous #1), esp. if painless and immobile.

    5. 80% rule: In general, 80% of neck masses are benign in children; 80% are malignant in adults > 40.

    Appropriate measures for evaluation and management of anterior cervical triangle, midline,and low neck masses.

    1. Full head + neck exam, indirect laryngoscopy, CT and MRI to search for hidden primary; FNA for tissue Dx; biopsy contraindicated as it has an adverse effect on survival if malignant

    2. Seven cardinal symptoms: dysphagia, odynophagia, hoarseness, stridor (upper airway obstruction), globus, speech disorder, referred ear pain (via V, IX, or X). Hxof CA in the region. Medical, social, occupational and family Hx. Tobacco and EtOH use. Exposure to ionizing radiation and chemical carcinogens. Nutritional Hx including diet and weight loss.

    3. PE starts with inspection of skin and palpation. Neurologic exam. Lymph nodes along jugular chain although PE not accurate (30% with clinically nodes negative have metastases, 20% suspicious are free of metastases).

    4. Additional studies include CXR (routine), CT scanning is imaging study of choice for advanced head and neck lesions. Barium swallow, and endoscopic viewing may be appropriate. MRI use is equivocal with most use in skull base, parapharyngeal space and orbits.

    5. Treatment: surgical excision for congenital or neoplastic; two most important procedures for CA Tx are radical and modified neck dissection.

    Discuss the role of cervical lymph node biopsy in the evaluation of neck masses.

    1. Biopsy contraindicated as it has an adverse effect on survival if malignant.

    2. Since the majority of head and neck tumors are squamous cell carcinomas, metastases most often involve regional lymph nodes. Salivary gland tumors, papillary carcinoma of the thyroid, and melanoma also spread principally via lymphatics. An accurate prediction of the origin of a metastasis can often be made just by knowing the site of the involved node.

    Adult DDx

    1. Inflammatory: cervical lymphadenitiss, cat-scratch dz, infectious mono, infection in neck spaces

    2. Congenital: thyroglossal duct cyst (midline, elevates with tongue protrusion), branchial cleft cysts (lateral), dermoid cysts (midline submental), hemangioma, cystic higroma

    3. Neoplastic: primary or metastatic

    Case Histories

    #1: 51-YO W male, firm nontender, 2cm mass below angle of the mandible; 3 weeks, non-painful; Shx--long history of smoking and EtOH. Ddx, plan for work-up.

    #2: 3-YO W female, firm, anterior midline neck mass; no complaints, no drainage; 1.5cm cystic mass at midline below hyoid. Ddx, plan for work-up.

    #3 11-YO female, 1cm mass in anterior cervical triangle; 4 months, noted after pharyngitis.

    #4 58 YO male, 1.5cm hard mass at left parotid gland; intraoral exam WNL, no neck adenopathy palpable. Evaluation and treatment.

    #5 44-YO male, lump on left side of neck; non-painful, denies hypo- or hyperthyroidism s/s; 2cm nodule in left lobe of thyroid; no palpable nodes. Diagnostic work-up.

    #6 24-YO W female, 3cm nodule in right lobe of thyroid; Phx: radiation to neck for recurrent tonsillitis and tonsilar hypertrophy at age 4. Proceed?

    #7 52-YO W male, 3cm thyroid nodule; Fhx--mother and 4 relatives deceased d/t thyroid carcinoma. Work-up, appropriate Tx plan. Family screening.

    #8 37-YO W female, s/s of hyperthyroidism with enlarged thyroid gland; Dx of Graves made by you. Tx options, rationale for Tx choice.


    BREAST DISEASE

    Learning Objectives

    Is a breast lump benign or malignant? History-taking and risk factors predictive.

    1. Breast CA RF: White, older age, breast CA in mother or sister (especially bilateral or pre-menopause), previous Hx (endometrial CA, some forms of mammary dysplasia--fibrocystic dz or proliferative changes or papillomatosis or atypical epithelial hyperplasia, CA in other breast), early menarche (before 12), late menopause (after 50), late first pregnancy.

    Breast lump benign or malignant? Predict likelihood based on PE findings.

    1. Fibroadenomas: benign breast mass. Easiest to recognize; common; younger women (teens to 30s), discovered at 1-3cm size; may be multiple or bilateral. Firm, smooth, roungd, well defined, and easily movable ("breast mouse"). Rapid growth with estrogen exposure.

    2. Fibrocystic disease: Most common lesion affecting female breast. Cycle with menstrual cycle. Fibrous elements and cysts that may be in close proximity or distant;single area or multiple, unilateral or bilateral; monthly cyclic tenderness is common with most of tenderness 1 week before the menstrual period and subsides one week later; irregular fibrous rubbery tissue of some areas and cystic feeling of other areas; some areas of fibrosis may form a hard, well-demaracated mass with ill-defined margins that may feel suspiciously like cancer; 30-50 years old, most demonstrable in post-menopausal women.

    3. Rare benign masses: Lipomas, palillomas, galactoceles, fat necrosis, breast abscesses, and cystosarcoma phyllodes; rare and may be confused with fibroadenomas on physical exam (called "giant fibroadenomas"); any age but often young girls.

    4. Breast CA: Irregular mass with ill-defined margins that invades adjacent tissues. The mass usually is not movable and is inseparable from adjacent tissues. Specific signs include: asymmetry, skin discoloration, skin edea or thickening, skin dimpling or retraction, skin redness, skin ulceration, nipple discharge, nipple crusting or ulceration, nipple retraction, prominent or palpable veins, breast mass without tenderness, breast mass with tenderness, pain and tenderness without mass, lymph nodes, are edema.

    Mammogram. Differentiate between normal anatomy vs. breast cyst vs. fibroadenoma vs. breast carcinoma.

    1. Mammography more helpful in older women because breast tissue undergoes fatty replacement with age and masses are more easily visible; young women have more fibrous tissue making mammogram harder to interpret.

    2. Mammograms are radiologic images that only increase or decrease the suspicion of CA. They are not conclusive diagnostic tools and have a high false-negative rate in young women.

    Diagnostic modalities and sequence in work-up for palpable breast mass vs. bloody/non-bloody discharge vs. mammogram suspicious for carcinoma without palpable mass.

    1. Most common cause of bloody d/c = intraductal papilloma.

    2. Diagnostic tests: all suspicious masses should be bx! Needle bx has 15% false-negative rate (negative bx always followed by open bx). Open bx--preffered method; small lesions should be completely excised

    3. Non-palpable mass on mammogram: needle localization by radiologist, followed by bx; removed breast tissue must be checked by mammogram to ensure all of suspicious lesion has been excised.

    4. Breast mass: First requires Hx, PE, and mammogram (optional). Round, well-circumscribed mass should be excised and pathology done. Cystic mass should be aspirated, if clear fluid and mass disappears without recurrence then follow-up. If no fluid, bloody fluid, cyst recurs, particulate matter, or residual mass then excise with pathology done. Firm irregular mass requires open bx with frozen sections and estrogen and progesterone receptors done. Options for CA become different forms of mastectomy and lumpectomy with post-surgical radiation.

    Evaluation and Tx plan for fibroadenoma vs. asymptomatic and symptomatic fibrocystic disease.

    1. Fibroadenoma most common breast tumor in pt <30

    2. Fibroadenoma Tx is complete surgical excision because they do not resolve spontaneously, may harbor a sarcoma, and diagnosis needs histologic confirmation.

    3. Fibrocystic disease can have aspiration and excision performed with histology done. If aspiration is benign then no treatment is necessary; nothing is consistently effective. Analgesics may be administered, may try limiting caffeine. Severe fibrocystic dz may require mastectomy.

    Breast cancer types and staging.

    1. Types of breast CA in order of prognosis:
      • In situ intraductal or lobular cancer,
      • comedo carcinoma or papillary carcinoma confined to ducts
      • Paget's dz of nipple along with intraductal carcinoma
      • well-differentiated adenocarcinoma
      • medullary carcinoma
      • colloid or mucinous carcinoma
      • tubular carcinoma
      • infiltrating ductal (scirrhous) carcinoma and infiltrating lobular carcinoma
      • undifferntiated carcinoma with obvious blood vessel invasion
      • unflammatory carcinoma
        MOST COMMON IS INFILTRATING DUCTAL CARCINOMA

    2. Classification of Tumors

      Staging:

      • Stage I: <2cm tumor without metastases, no nodes, T1
      • Stage II: Tumor 2-5 cm diameter with + mobile nodes, no mets, T2
      • Stage III:
        • 1. Tumor >5cm, T3, N2
        • 2. Also any of the following: Peau d'Orange, Chest wall invasion / fixation, Inflammatory CA, breast skin ulceration, breast skin satellite mets, fixed axillary nodes
      • Stage IV: Any size tumor, any # of nodes, with distant metastases, T4

      T = tumor itself

      • T1 Tumor < 2 cm
        • a = not fixed to pectoralis fascia
        • b = fixed to pectoralis fascia
      • T2 Tumor < 2cm, < 5cm
        • a and b as above
      • T3 Tumor > 5cm
        • a and b as above
      • T4 Tumor invading chest wall (beyond pectoralis major)
        • a = fixation to chest wall
        • b = edema (peau d'orange) or skin ulceration, satellite nodule of cancer on skin of same breast
        • c = both of above
        • d = inflammatory CA

      N = Node involvement

      • N0 = no palpable axillary nodes
      • N1 = movable palpable nodes
        • a = not suspicious for metastases
        • b = suspicious for metastases
      • N2 = nodes containing metastases are fixed to one another
      • N3 = supra- or infraclavicular nodes with mets or arm edema

      M = Metastases

      • M0 = no evidence of distant metastases
      • M1 = distant mets or skin recurrence beyond breast area

      Local, regional, and systemic breast CA: treatment options (surgical, non-surgical, combination)

      1. The terms local, regional, and systemic dz are often used in describing the extent of breast CA. Tx depends on the clinical extent of the disease. Treatment of local-regional dz (stages I and II or A and B) is essentially surgical. Options of treatment are:
        • A. Radical mastectomy; almost completely abandoned d/t significant morbidity without significant improvement in survival.
        • B. Modified radical mastectomy; now the most common modality
        • C. Simple mastectomy in special circumstances
        • D. Segmental mastectomy ("lumpectomy") with axillary dissection and radiation of residual breast tissue
        • E. Lumpectomy, simple mastectomy, modified radical, radical, chemotherapy, radiation, tamoxifen

      Breast CA Tx: rationale for adjuvant chemotherapy, radiation, and hormone therapy.

      1. In the vast majority of cases, surgical Tx is indicated for earlier clinical stages (I and II or A and B), where there is potential for cure. When the potential for cure is small or nonexistent (stage III and IV or C and D), surgical Tx alone is not recommended and mastectomy is performed in addition to other modalities for palliation only.
      2. Adjuvant therapy in breast CA treated by surgery depends on three factors:
        • the evidence supporting the early systemic nature of breast CA
        • the high recurrence rate despite apparent adequate local surgical therapy at the time of diagnosis
        • the hypothesis that a small tumor load may respond better to chemotherapy, radiation, or hormonal therapy.
      3. Adjuvant combination chemotherapy should become standard care in premenopausal women with positive axillary nodes, regardless of hormone receptor status. Adjuvant therapy with tamoxifen should be given to postmenopausal women with positive nodes and positive receptor levels. There is little justification for the routine use in other pts.

      Treated breast CA: survival and results according to clinical stage

      1. Axillary nodes10-year Survival (%)
        • Nodes negative: 72-76%
        • Nodes positive (overall): 25-48%
        • 1-3 nodes involved: 34-68%
        • 4 or more nodes involved: 14-27%
        • Metastatic disease: 0%

      Breast CA: Tx plan for local recurrence and metastatic forms

      1. Local chest wall recurrence can be treated by radiation therapy or by hormonal manipulation (if receptor positive). Bony mets may not be amenable to extensive radiation and can be treated by hormonal manipulation or chemotherapy.
      2. For almost all mets except liver mets, hormonal therapy should probably be tried before chemotherapy is used if receptor positive; this is not due to increased effectiveness but as first line because of low side effects and toxicity. If no response then go to chemo.

        Treated breast carcinoma: program for follow-up and management

        1. Women with a personal history of breast CA should consult their physicians about the need for more frequent examinations or about beginning periodic mammography before age 50.

        Case Histories

        #1 63-YO W female, lump in R breast post-self exam; RF= family Hx with mother died at 41 d/t breast CA; PE=2.5cm firm mobile mss in UOQ with negative axillary exam. Work-up and options for therapy.

        #2 41-YO premenopausal female 10 days post modified radical for infiltrating intraductal carcinoma; path shows 2/21 nodes positive with positive estrogen receptors. Plans for adjuvant therapy.

        #3 55-YO female with mammogram showing stipling and calcifications in R breast with PE WNL. Manage?

        #4 18-YO student with small, smooth, moveable, nontender, well-circumscribed breast mass. Plan for work-up and Tx.

        #5 32-YO lactating female, painful breast mass and temp of 101. Most likely diagnosis? Treatment?


        SKIN AND SOFT TISSUE

        Learning Objectives:

        Abscess vs. Cellulitis

        1. Abscess = localized collection of pus anywhere in the body, surrounded and walled offby damaged and inflammed tissues.
        2. Cellulitis = diffuse nonblancing erythema and tenderness extending from a break in the skin barrier.

        Differentiate subungual hematoma vs. paronychia vs. felon, based on PE

        1. Subungual hematoma: accumulation of blood within the tissues (beneath nail), which clot to form a solid swelling
        2. Paronychia: Infection on side of finger nail: Tx by drainage and hot soaks; staphylococcal infection of the proximal fingernail
        3. Felon: Infection in tip of finger pad (felon = fingerprint); drain; deep infections of the pulp space of ther terminal phalanx; usually occur after penetrating injuries of the distal phalanx.

        Procedure for wound closure using interrupted and running suture techniques

        1. The most common stitch for skin closure is the simple or over-and-over suture. The suture may be interrupted (each stitch placed and tied independently) or run in a continuous fashion. The running simple suture has the advantage of saving time but also has the disadvantage of total wound disruption if the suture breaks or is cut.

        Indications, dose and use of LA for simple surgical wounds, abrasions and regional blocks in the hand and elsewhere.

        1. Local anesthesia is for a small confined area of the body where regional blocks a region of the body. Lidocaine and bupivicaine are used for both. Epinephrine is CI for fingers, toes, penis, lips, areola where end arterioles are present.
        2. Local anesthesia is generally adequate for smaller wounds. Xylocaine 1% or 0.5% is usually sufficient. Marcaine may be used for longer duration anesthesia. Epinephrine for vasoconstriction is helpful for areas with a rich blood supply. Difference between good and bad anesthetic is 5 minutes. Toxic dose is 7mg/kg.

        Technique for removal of small skin or SQ lesions.

        1. The most common skin lesions are skin tags, papillomas, which are treatd by cauterizing; large lesions may require LA then sharp dissection. Warts can be treated with cautery or liquid nitrogen. Sebaceous cysts should be excised.
        2. Majority of SQ lesions are lipomas and should be incised.

        Management of ingrown toenails

        1. Digital block. Remove the offending portion, the entire nail if very thick and deeply embedded, then curretage if the nail bed.

        Pigmented skin lesions, benign vs. malignant: pertinent distinguishing characteristics.

        LESIONS
        CHARACTERISTICS
        Junctional nevi early years of life, particulary adolescence, few mm to several cm; light to dark brown in color with a flat, smooth survace and irregular edges
        Compound nevi brown or black with a raised nodular surface frequently containing hair; usually < 1cm; all age groups
        Intradermal nevi can be very large, usually < 1cm; color from light to dark brown, raised warty or smooth surface; presence of coarse hairs distinghishes them
        Blue nevi smooth blue or blue-black lesions < 1cm with well-defined regular margins; face, dorsum of feet and hands, and buttocks; rarely associated with melanoma
        Basal cell carcinoma most common in middle-aged; pigmented bcc has a blue-black coloration with raised edges and capillary neovascularization; intially smooth but may ulcerate
        Sehorrheic keratoses occasionally black in color; usually 1cm or larger, typically raised, warty, greasy, with appearance of being "stuck" onto skin
        Dermatofibroma dark brown, usually smooth, slightly raised, y sin pelo; grows slowly and never malignant
        Subungual hemorrhage sudden in onset and sharply defined beneath the nail bed; melanoma slow onset and poor borders with streaks along nail; confimed by puncturing nail

        Sebaceous cyst vs. lipoma: differentiate based on PE.

        1. Lipomas are freely movable, deep to the skin, and therefore will not move when the skin is moved over them. If the lesion moves when the skin is moved then they are either a sebaceous cyst or a dermatofibroma. A sebaceous cyst can be identified by the pore where the cyst started.

        Ddx of lymphadenopathy in the neck vs. supraclavicular area vs. axilla vs. groin.

        Melanoma: therapy

        1. Melanomas are initially assessed by either excisional or incisional biopsy. Local therapy considers two questions: the width and depth of the excision. Current recommendations are 2-cm lateral margins and to the depth of the fascia. Clinically palpable lymph nodes should be excised, also if the primary lesion is >0.75-mm thick. Distant dz is managed either by radiation therapy or chemotherapy (DTIC).

        Basal and squamous cell carcinoma: Tx

        1. Two principles involved in Tx both: confirmation of the diagnosis histologically and complete removal or destruction of the tumor. Small lesions receive cryotherapy or curettage. Surgical excision involves taking a 1cm margin in most, 0.5 if around criical structures, and 1..5 for morphea-like or fibrosing tumors. Multiple frozen sections to determine if complete border is excised. The only major difference with SCC is consideration of lymph node removal. Close follow-up is needed in both cases.

        Tetanus prophylaxis: indications and administration.

        1. Tetanus is caused by Clostridium tetani with s/s of lockjaw, muscle spasm, laryngospasm, convulsions, and respiratory failure. If pt has a a tetanus-prone injury and previous immunization x 3 then tetanus toxoid only; if no previous immunization, or unknown, then requires tetanus immunoglobulin IM and tetanus toxoid IM at different sites.
        2. Tetanus prone are > 6 hours old, type (crush, avulsion, extensive abrasion, burn/frostbite), and contaminants (soil, saliva) are present. If last booster was > 5 years then should administer toxoid. The only contraindication is a neurologic or sever hypersensitivity reaction from a previous dose of tetanus toxoid.

        Wound infection: clinical signs, management

        1. S/S: Pain at incision site, erythema, drainage. Tx by removing skin sutures / staples, digital examination to rule out fascial dehiscence, pack wound open
        2. Spanish signs: rubor, calor, turgor, dolor, laessa functionale. NEC manifests by nonblanching erythema with blisters and frank necrosis of the skin.

        Infection
        Physical Findings
        Treatment
        Cellulitis Diffuse nonblanching erythema tenderness Systemic abx, local wound cleansing
        Furuncle, carbuncle localized induration, erythema, tenderness, swelling, creamy pus formation I&D, systemic abx for carbuncle
        Hidradenitis suppurativa Multiple abscesses; drainage; thick pus from axilla, groin regions I&D small lesions; wide debridement; excision and grafting, large areas
        Lymphangitis Swelling and erythema distal extremity, inflamed streaks along involved lymphatic channels Local wound cleansing, removal of any foreign body, systemic abx
        Gangrene Necrotic skin/fascia, extremity swelling, grayish liquid discharge, crepitation /gas fromation within tissue planes Radical debridement of all involved tissues, parenteral abx


        ESOPHAGUS, STOMACH AND DUODENUM

        Learning Objectives:

        Esophago-gastro-duodenoscopy: indications

        1. The mucosa can be examined in detail and if an ulcer is present it can usually be seen. In pts who are bleeding, the exact size of hemorrhage can be determined. Endoscopy can also identify concomitant disease or reveal alternative diagnoses in certain pts. Biopsies can be performed.

        Esophago-gastro-duodenoscopy: complications

        Esophagoscopy: technique; findings in reflux esophagitis vs. esophageal CA vs. paraesophageal hernia

        1. Reflux esophagitis: endoscopy plus bx;
        2. Esophageal CA:
        3. Paraesophageal hernia: reveals herniation of the fundus

        Esophagoscopy: risks, benefits

        Gastric ulcers: fidings in pt with benign vs. malignant

        1. Gastric ulcer pain usually occurs in the epigastrium and may radiate through to the back. It is produced by the ingestion of food, while duodenal ulcer pain is relieved by eating.
        2. Because hydrochloric acid is necessary for a true gastric ulcer, if the pt is found to have achorhydria, the chances of malignancy are substantially increased.
        3. Endoscopy with multiple biopsies will help to establish the presence or absence of carcinoma. Cytology and brushings are also helpful as an adjunct to bx.
        4. If the ulcer is refractory to medical Tx after 6 weeks then suspicion is heightened for malignancy.

        PUD: evaluation and management

        1. 10% of all Americans will suffer from PUD during their lifetime. S/s pain, hemorrhage, perforation, obstruction. Associated with Helicobacter pylori.
        2. Evaluation: Hx of burning epigastric abdominal pain accentuated by fasting, awakens pt from sleep and is relieved by antacids or food. Weight gain is not uncommon. Pain characterized as "boring in nature" and may radiate to back with posterior-penetrating ulcers. Massive UGI hemorrhage may occur giving s/s of syncope, tachycardia, hypotension, nausea and hematemesis. Perforation may give acute abd. s/s of tachyrardia, severe abd. tenderness and pain, guarding, and rigidity. Scarred duodenal bulb will give gastric outlet obstruction with s/s of weight loss, persistent vomiting immediately postprandial, and chronic gastric dilatation.
        3. Management is surgical with hemorrhage, perforation, obstruction, or failure of non-operative management. Perforation without contraindications to surgery should result in exploratory laparotomy. Surgical abdomen less than 6 hours old should result in plication and acid-reducing procedure; if > 6 hours then plication alone.
        4. UGI hemorrhage should have NG decompression, gastric lavage, and antacid therapy. Evaluate coagulation status and prep blood; if > 6 units in 12 hours then operate. Older people tolerate hypotension more poorly than younger folks and should be candidates for earlier intervention.
        5. Gastric outlet obstruction should have NG decompression and NPO for 5-6 days. Should have acid-reducing operation and pyloroplasty.

        Case Histories

        #1 69-YO B male, 2-month Hx of inreasing swallowing difficulty; 12-pound weight loss over 6 weeks; UGE shows obstructing mass in distal 1/3 of esophagus; Bx reveals adenocarcinoma of esophagus; CT shows 4cm esophageal mass without evidence of lymph node spread or metastatic dz. Tx plan.

        #2 49-YO W male in ER with sudden severe epigastric pain; diagnosed with duodenal ulcer via UGE post two year, on cimetidine for one year; Shx= moderate drinker, 1PPD; PE=hypertensive, tachycardiac, with rigid abdomen, no bowel sounds. Plan for further eval and Tx.

        #3 57-YO W male post UGE for abdominal pain and early satiety, shows 2cm gastric ulcer. How is pathogenesis different case #2? Plan for further eval and Tx.

        #4 61-YO W female with long Hx of PUD in ER with N/V; UGE shows J-shaped stomach and gastric outlet obstruction. Plan for further eval and Tx.


        ABDOMINAL PAIN

        Learning Objectives:

        Acute abdominal pain: DDX and plan for work-up

        1. Peritoneal signs: extreme tenderness, rebound tenderness, voluntary guarding, pain with movement such as rocking the pts pelvis or by striking heel of the pt, decreased or absent bowel sounds, and involuntary guarding / rigidity late.
        2. RUQ: cholecystitis, hepatitis, PUD, perforated ulcer, pancreatitis, liver tumors, gastritis, hepatic abscess, choledocholithiasis, cholangitis, pyelonephritis, nephrolithiasis, appendicitis (pregnancy); thoracic causes--pleurisy / pneumonia, PE, pericarditis, MI (esp. inferior MI)
        3. LUQ: PUD, perforated ulcer, gastritis, splenic dz or rupture, abscess, reflux, dissecting aortic aneurysm, thoracic causes per above, pyelonephritis, nephrolihiasis, hiatal hernia (strangulated paraesophageal hernia), Boerhaave's syndrome, Mallory-Weiss tear
        4. LLQ: Diverticulitis, sigmoid volvulus, perforated colon, colon CA, UTI, SBO, IBD, nephrolithiasis, pyelonephritis, fluid accumulation from aneurysm or perforation, referred hip pain; GYN causes--ectopic pregnancy, PID, mittelschmerz, ovarian cyst, fibroid degeneration, endometriosis, GYN tumor, torsion of cyst or fallopian tube
        5. RLQ: Same as LLQ, especially appendicitis, also mesenteric lymphadenitis, cecal diverticulitis, Meckel's diverticulum, intussusception
        6. Work-up includes a focus on history, especially the pain characterization and changes, abdominal exam, rectal, exam, pelvic exam, CBC, UA, and PA and lateral decubitus abd films.

        2. Chronic abdominal pain: DDX and plan for work-up.


        BILIARY TRACT DISEASE

        Learning Objectives:

        1. Cholelithiasis: management decisions if dx known

        1. Initially, gallstones do not cause clinical symptoms. Most data indicated that asymptomatic gallstones should be followed until such time that they become symptomatic (20% lifetime risk) making a cholecystectomy justifiable. However, select pts should undergo elective cholecystectomy if their course would be complicated by infection (diabetics).
        2. IVFs, abx, NG tube decompression, Cholecystectomy, or if poor operative candidate: cholecystostomy

        Case Histories

        #1 46-YO W female in ER with epigastric and RUQ pain; pain post one hour eating fried chicken followed by N/Vj and fever to 101; Phx unremarkable except diet-controlled DM; PE=BP WNL, pulse=94, temp=101.8, exquisitely tender 4cm mass below the right liver edge and tenderness in the subscapular region on the right, no peritoneal signs; WBC=14.3 58p 17b, bili=2.2 amy=134, LFTs WNL. DDX. Risk factors and suggest plan for further eval and Tx.

        #2 44-YO female, healthy, gallstones in US, no s/s of biliary tract dz. Advise pt.

        #3 58-YO female 5 days post elective lap chole d/t multiple stones; pain and tenderness in RUQ and fever to 101.5. DDX and Tx recommendations for each Dx.

        #4 40-YO female 8 weeks post lap chole with RUQ pain and nausea= same s/s prior to surgery. DDX. Further investigation.


        COLON AND RECTAL DISEASE

        Learning Objectives:

        1. Work-up: occult lower GI bleed, hematochezia, massive lower GI bleed

        1. Begin on IVFs: LR, PRBC as needed (through at least 16G peripheral IVs x2), Foley to follow UO. Hx, PE, NG tube aspirate (r/o UGI bleed must see bile or blood, if not do EGD), then do proctosigmoidoscopy / colonoscopy; proctoscopic exam in ER. If too much blood to visualize with scope then do radiolabeled RBC scan (need 0.1 ml/min) or arteriography (need >0.5 ml/min).
        2. Most common cause = diverticulosis, #2 = angiodysplasia; DDx: diverticular dz, angiodysplasia, colon CA, hemorrhoids, trauma, hereditary hemorrhagic telangiectasia, intussusception, volvulus, ischemic colitis, IBD (espec. UC), anticoagulation, rectal CA, Meckel's diverticulum (w/ ectopic gastric mucosa), colonic ulcer, chemotherapy, irradiation injury, infarcted bowel, strangulated hernia

        Colonoscopy: indications

        1. Primary diagnostic modality to evaluate lower GI bleeding of unknown etiology, IBD, polyps, equivocal BE findings, posttumor removal, pseudoobstruction, and stricture.

        Colonoscopy: complications

        Sigmoidoscoopy: indications for flexible and rigid

        1. Rigid sigmoidoscopy was the standard method of visualizing the distal colon and rectum; it has largely been replaced by fiberoptic flexible sigmoidoscopy which provides an higher diagnostic yield and is much less uncomfortable for the patient. This examination allows visulaization of the last 30-65cm of the colorectal complex and detects 60% of colorectal neoplasms.

        Sigmoidoscopy: complications

        Colorectal CA: screening plan

        1. Annual digital rectal exam starting at age 40 (10% of tumors palpable)
        2. Annual test for fecal occult blood starting at age 40
        3. Sigmoidoscopy at ages 50 &51, then every 3-5 years
        4. More aggressive monitoring for pts with FHx of familial polyposis

        Colonoscopy vs. BE: C and C for pt comfort, cost and relative usefulness

        Radiographic appearance: diverticulosis, diverticulitis, inflammatory bowel disease, colon and rectal polyps and CA

        1. Diverticuolsis: segmental spasm and luminal narrowing have been reported.
        2. Diverticulitis: x-ray = ileus, partially obstructed colon, air fluid levels, free air if perfed; abdominal/pelvic CT = swollen, edematous bowel wall, this test is particularly helpful to show an abscess that may be a complicating factor
        3. IBD: UC has lead pipe appearance on BE, Crohn's shows cobblestoning and string sign
        4. Polyps show up as clear circular patches (islands) on BE.
        5. CA shows up as a mass on BE

        Colorectal CA: rational follow-up protocol post surgery

        1. High rate of recurrence (30-40%) prompts post-operative therapy with radiation combined with 5-FU. To most efficiently detect recurrence, the pt should be seen for Hx, CEA, and physical every 3 months for 2 years, then every 6 months for 2 years. A pt without recurrence at 5 years is most likely clear of dz. Further surveillance should be via screening colonscopy every 3 years thereafter.

        Ostomy: common problems and management options

        Case Histories

        #1 64-YO male with guaiac positive stool and anemia. Plan for diagnostic work-up.

        #2 69-YO W male in ER with 3 hours Hx of passing large amounts of dark wine-colored stool; Hx-diverticular disease from BE post 4 years; Orthostatic on admission, received adequate fluid resuscitation; DDX for massive lower GI bleed in this age group, how to proceed with eval? Bleed localized to ascending colon, continues to bleed and receives total of 10 units PRBCs. Recommendation for eval and Tx?

        #3 61-YO male with 4 month Hx of blood streaking the stoosl with a decrease in caliber of stools; 10 pound weight loss; rectal exam reveals no masses and guiac positive stool; LFTs are normal but CEA is 27. Plan for further eval and Tx?

        #4 67-YO male with guaiac positive stool; air-contrast BE reveals 3cm polyp at splenic flexure. Appropriate management? Association between polyp size and risk of carcinoma?

        #5 41-YO with 6 year Hx of UC for f/u colonoscopy; Bx reveals a focus of adenocarcinoma in left colon. Tx recommendation?

        #6 64-YO W male with no Hx of intraabdominal problems with cc of passing air in urine over last several days. DDX? Evaluation of problem?


        BENIGN PERIANAL DISEASE

        Learning Objectives:

        External and internal hemmorhoids: differentiate on PE and describe anatomical differences.

        1. External hemmorhoids are below the dentate line and are painful d/t presence of pain nerve fibers, converse is true for internal hemorrhoids.
        2. Inferior / external hemorrhoids connect directly to systemic circulation, superior /internal hemorrhoids return to portal system.
        Hemorrhoids: 4 clinical stages.
        1. First degree: hemorrhoids that do not prolapse
        2. Second degree: prolapse with defecation but return on their own
        3. Third degree: prolapse with defecation or any type of Valsalva maneuver and require active manual reduction (eat fiber)
        4. Fourth degree: Prolapsed hemorrhoids that cannot be reduced

        Hemorrhoidal disease: etiology and predisposing conditions.

        1. Engorgement of the venous plexi of the rectum and/ or anus, with protrusion of mucosa and / or of the anal margin. Predisposed by constipation/straining, portal HTN, pregnancy.
        2. Other factors include low-residue diet, excessive exercise, increased anal sphincter tone, musculoskeletal dz, and systemic abnormalities such as portal HTN. Not simply varicose veins, but a complex of the vascular cushion that contains venous and arterial components.

        External and internal hemorrhoids: s/s

        1. Anal mass/prolapse, bleeding, itching, pain.
        2. External hemorrhoids present with severe pain when they undergo thrombosis. Internal hemorrhoids often present with discomfort, bleeding, and prolapse.
        3. Must undergo examination to r/o other concomitant disease such as rectal prolapse, pruritus, anorectal inflammation, CA, IBD, and STD. Look for fissures, masses, perianal dz, protruding external hemorrhoids, skin irritation, lichenification, or hyperemia of the skin. Note sphincter spasm, ulceration, fistulas, draining sinuses, cysts, warts, or discharges. Digital exam checking for polyps, stenosis, tumors, Blumer's shelf, and fluctuant masses. Instrumentation with proctoscope, rigid sigmoidoscope, or flexible sigmoidoscope.
        4. Questions must be asked about: bleeding, constipation, diarrhea, discharge, itching, mucus, pain of the anorectal area, protrusion, stools, and tenesmus.

        External and internal hemorrhoids: management (operative and nonoperative)

        1. High-fiber diet, anal hygiene, topical steroids, sitz baths rubber band ligation of most (no LA for internal) and surgical resection for large refractory roids.
        2. Treatment modalities include sclerotherapy, cryosurgery, dietary manipulation, banding, and surgical hemorrhoidectomy. First-, second-, and third-degree hemorrhoids do best with banding, while refractory hemorrhoids and fourth-degree require surgical excision.

        Role of anal crypts in perineal (perianal?) abscess formation and describe the various types of perianal infections.

        1. Most abscesses develop from the anal crypts that are present at the dentate line and become infected. The infecting organisms burrow into the anal glands, producing circumscribed area of microabscesses in teh subcutaneous, submucosal, and intramuscular perirectal regions of the rectum.
        2. Two classifications of abscesses:
          • infralevator (common) including perianal, ischiorectal, and postanal
          • supralevator (rare) including postrectal and pelvirectal.

        Perianal infections: s/s, physical findings.

        1. Rectal pain, drainage of pus, fever, perianal mass
        2. Two categories: infralevator (common) and supralevator (rare). Most are abscesses that develop at teh dentate line and become infected. They present with perianal cellulitis and diffuse inflammation, characterized by generallized edema, swelling, and redness that is not yet localized. Abscesses begin at sites other than the crypts in Crohn's dz and TB. Pain is the most common presenting symptom. Some present with systemic symptoms of fever, chills, generalized malaise, nausea, and vomiting. Supralevator abscess should be considered in pt with rectal pain and systemic symptoms. Digital examination may reveal an abscess higher in the anal canal. Confirmation comes by needle aspiration of pus under LA.

        Perianal infections: management (abx, incision and drainage, fistulectomy)

        1. As with all abscesses, drainage and abx against colonic flora. Anorectal fistulas require marsupialization of fistula tract and wound care.
        2. External abscesses are excised under LA with adequate I&D including excision of a portion of the skin, preferably closing with a drain in place.
        3. Infections with subsequent fistula formation require marsupialization of the tract with complete excision.

        Pilonidal cyst: s/s, physical findings, management

        Anal fissure: s/s, physical findings, Tx

        1. Painful linear ulcer at the margin of the anus. Constipation or diarrhea is the most likely historical antecedent with anal abrasions and acute ulcers at the anal verge. Associated with infections in the crypts, an enlarged papilla, skin tags, and a narrow anal canal. May develop secondary to proctitis, anal surgery, or basal cell carcinoma. Dx is by inspection with a clear, punched lesion, neither large nor indolent, rarely multiple.
        2. Tx for lesion of < 2 weeks involves non-operative therapy with good anal hygiene, stool softeners, cleansing with sponges, and the application of hydrocortisone foam or suppositories, high-residue diet, and anesthetic ointment. Conditions longer than two weeks generally require surgery. Associated conditions such as skin tags and papillae need to be excised and any hemorrhoids removed. Many surgeons employ a partial internal sphincterotomy.

        Case Histories

        #1 52-YO W male with long Hx of constipation and hemorrhoids with brbpr; blood on TP post BM; Hemorrhoidal prolapse during BM requiring manual reduction. Plan for eval and management?

        #2 69-YO W male with Hx or perirectal abscess post 7 yars now with mild periregal pain and purulent discharge; exam reveals external opening at 2 o'clock. Pathophysiology of this condition? Treatment?

        #3 43-YO W male with severe R-sided perirectal pain; exam reveals temp 101; tender, fluctuant mass in R perirectal area with overlying edema. How to proceed?

        #4 3-YO W female with brbpr on TP with BM; serious problem with constipation over the last three weeks, cries loudly with each BM; exam reveals 1cm tear in perianal skin in post. midline. Conservative Tx plan? Recommendation if conservative Tx fails?

        #5 39-YO W female with severe perianal itching; itching worse at night and disturbs sleep; scrkupulous personal hygiene; Exam reveals erythema and oxcoriation of perianal area; work-up inlcuding BE and sigmoidoscopy fails to reveal colorectal pathology. Tx?

        #6 51-YO male truck driver with pain and tenderness in midline just above anus; purulent drainage from this area; Exam reveals an opening in midline draining pus with surrounding arythema and fluctuance. Tx plan? Most common complication of surgical managenet?


        HERNIAS

        Learning Objectives:

        Hernia repair: postoperative instructions

        1. No lifting or abdominal straining

        Indirect and direct inguinal hernias: anatomic and developmental differences.

        1. Direct: within floor of Hesselbach's triangle, acquired defect from mechanical breakdown over the years, 1% of all males, increased frequency with advancing age, no hernia sac.
        2. Indirect: through the internal ring of the inguinal canal, traveling down toward the external ring, may enter the scrotum; patent processus vaginalis (i.e., congenital) which gives an hernia sac; approx. 5% of all males, most common hernia in both males and females

        Inguinal hernias: 3 predisposing clinical conditions

        1. Increased intraabdominal pressure: straining at defecation or urination (rectal CA, colon CA, prostatic enlargement, constipation), obesity, pregnancy, ascites, valsavagenic (coughing), COPD
        2. Presence of an abnormal congenital anatomical route (i.e., patent processus vaginalis)

        4. Indirect, direct, and femoral hernias: relative frequency by age and gender

        1. 5-10% lifetime incidence overall; 50% are indirect inguinal, 25% are direct inguinal, and about 15% are femoral. Direct increase in frequency with advancing age being rare in childhood but 40% of males, indirect always more common. Indirect most common in both males and females. Femoral more common in females than males (assoc. with women, pregnancy, exertion), but indirect still most common in females.

        "Sliding" hernia, incarcerated hernia, strangulated hernia: define

        1. Sliding: herina sac is partially formed by the wall of a viscus (i.e., bladder, cecum); type of hiatal hernia with displacement of GE junction = type I hiatal hernia; > 90% of hiatal hernia
        2. Incarcerated: bowel swollen and fixed within the hernia sac, may or may not cause intestinal obstruction (imprisoned); irreducible
        3. Strangulated: incarcerated hernia with resulting ischemia; will result in s/s of ischemia and intestinal obstruction (pain and vomiting; = choked

        6. Femoral hernia: clinical presentation

        1. Hernia traveling beneath the inguinal ligament down the femoral canal medial to the femoral vessels; about 1/3 incarcerate, much higher rate than others.

        Groin hernia: management and treatment

        1. On first encounter, manual reduction is warranted as 60-70% reduce in this manner. The overall management is by repair: a) reduce any abdominal viscus to the abdominal cavity; b) obliterate the processus vaginalis (indirect) at a point high against the abdominal wall; c)reform a snug abdominal ring around the spermatic cord.

        Umbilical hernia in infant and adult: etiology, natural Hx, complications

        1. Three types:
          • small, insignificant incomplete closure of umbilicus, covered by all layers of skin, common in infants with protusion of omentum, bowel, or intraabdominal organs, usually resolve spontaneously by preschool, may be some threat if remain in adulthood as stiffness of linea alba may incarcerate and strangulate
          • omphalocele from incomplete closure of abdominal wall by birth with a portion of abdominal contents herniating into the base of the umbilical cord, only covered by thin membrane of peritoneum and the amnion
          • gastroschisis is an even more severe defect with a full-thickness abdominal wall defect lateral to the umbilicus, no sac covers abdominal contents which protrude out of the abdomen.
        2. Tx is by reducing the abdominal contents and establishing abdominal wall continuity. Surgical therapy for omphalocele and gastroschisis is more intricate and complex, requiring bowel resections and formation of extraanatomic compartments fashioned of prosthetic materials. Mortality rates remain high.

        Umbilical hernia in infant and adult: Tx

        1. Hernia is through the umbilical ring, associated with ascites, pregnancy, and obesity. See Tx above in question #8.

        Incisional hernia: 4 factors contributing to development

        1. Hernia through an incisional site; most common cause is a wound infection. Other implications include orientation of incision, suture materials chosen, and various technical details


        VASCULAR

        Learning Objectives:

        Asymptomatic aortic aneurysms of various sizes (3cm, 5cm, 7cm): plan for f/u and management

        1. No medical therapy for an aneurysm
        2. 3cm: Watchful waiting, US and/or CT not aortography
        3. 5cm: Surgical repair, 1/3 of all AAA > 5cm will rupture in 3 years; grow 2-4cm/year on average (larger ones grow faster)
        4. 7cm: Surgical repair

        Extracranial cerebrovascular disease: current noninvasive tests, indications for use indetermining the need for arteriography and surgical intervention

        1. Stethescope= carotid bruits, angle of the jaw, high-pitched
        2. Noninvasive methods of evaluating:
          • Carotid ultrasound/doppler gives general location and degree and character of stenosis; enhanced accuracy with duplex scan
          • Oculoplethysmography measures indirectly the flow through the ophthalmic artery, first branch off carotid
          • Supraorbital Doppler detects reversal of flow in the supraorbital arteries seen with occlusion of the internal carotid
        3. Definitive study is arteriography. Arteriography is appropriate in all symptomatic patients and in asymtomatic patients with high-grade stenoses or ulcers identified by noninvasive tests.

        Venous ulcers and varicose veins: diagnostic, operative and nonoperative management.

        1. Venous ulcers: locaed in"gaiter"distribtion around the ankle, especially medial and lateral malleoli, diffuse, shallow with some granulation, treated with elastic support and elevation; ligation may be appropriate if an isolated incompetent perforator can be demonstrated venographically, otherwise support and debridement.
        2. Varicose veins: In general, varicose veins should be treated nonoperatively. Primary varicose veins due to valvular incompetence in greater saphenous vein=familial, discomfort, no ankle edema or ulcers and no abnormality of deep venous system, may Tx selected pts with ligation and stripping. Secondary varicose veins d/t abnormalities in deep venous system from DVT and valvular destruction and incompetent perforating veins, should only undergo stripping if deep venous system is patent and venous ulcers refractory to nonoperative Tx.

        Claudication: justify choice for conservative or surgical management

        1. Natural Hx of untrated claudication is generally benign; Framingham study: 5% risk of major amputation in 5 years if Tx conservatively compare to 20% who die from other causes
        2. Conservative: vast majority get conservative Tx, including exercise, stop smoking, Tx HTN and hyperlipidemia, diet
        3. Surgical:
          • rest pain
          • tissue necrosis or threatened limb
          • severe claudication refractory to conservative Tx and that affects quality of life / livelihood.

        Swollen leg: DDX and evaluation process.

        1. DDx of acute edema with leg pain: DVT, CHF, trauma, ruptured plantaris tendon, acute or chronic arterial insufficiency, infection, lymphangitis, lumbosacral strain and sciatica, muscle hematoma, renal failure
        2. Physical findings with DVT: calf tenderness, swelling of the leg or ankle, and Homans' sign.
        3. Noninvasive diagnosis is very accurate. Most common is Doppler US with duplex scanning to assess venous flow; indirect tests including ipedance plethysmography and phleborheography can supplement Doppler exam. Invasive techniques inclufe 125I fibrinogen scanning for calf vein thrombosis; venography is the gold standard.

        Venous valvular incompetence and DVT: noninvasive and invasive testing procedures.

        1. Noninvasive: clinical manifestation of postphlebitis syndrome including chronically swollen legs with hyperpigmentation and venous stasis ulcerations; see #5 above noninvasive techniques
        2. Invasive: venography

        Varicose veins: management

        1. See #3 above. In general, varicose veins should be treated non-operatively.

        Chronic venous insufficiency with and without ulceration: management

        1. Treatment is geared toward reduction of edema and pressure by elevation of the legs and the use of external support such as elastic stockings or medicinal boots (UNNA boot).

        Acute extremity ischemia: evaluation and management steps

        1. Evaluation: Hx
          • in situ thrombosis of preexistent occlusive dz
          • arterial emboli,
          • vascular trauma
          • thrombosis of an aneurysm.
          • In situ thrombosis pt may describe claudication or rest pain that has recently and suddenly accelerated. Sudden occlusion gives more sever symptoms. S/S include 6Ps: pallor, pain, paresthesia, poikilothermia, paralysis, and pulselessness. Venous occlusion also gives pain but darker color, venous distension, and swelling. Other Hx include rheumatic mitral stenosis, a-fib, radiation exposure, neoplastic dz. Common sites include axillary, popliteal, iliac arteries, aortic bifurcation, and SMA.
        2. Management: immediate anticoagulation with IV heparin unless new neurologic defect or active bleed. Evaluate base deficits, pharmacologic support of severe cardiac dz. May administer dextran and mannitol. Question of viability of limb would lead o immediate embolectomy or thrombectomy. Arteriography is not essential in Dx and Tx. Anticoagulation alone may be sufficient and may cosider thrombolytics in others.
        3. Surgical approach is considered for bypass grafting or endarterectomy of preexisting thrombosis. In embolic occlusion thrombectomies can be performed both proximally and distally. Beware of compartment syndrome which would necessitate a fasciotomy. Continue anticoagulation as recurrence is 30% in 30 days without post-op anticoaluation which reduces to 10% recurrence.

        Case Histories

        #1 72-YO male with Hx of episodic loss of vision in OS for 5-15 minutes; vision is lost "from top down, like a shade being pulled over the eye;" four episodes in past two weeks; no motor or sensory deficits during said episodes; PE=BP 118/78 with regular pulse, ocular exam reveals Hollenhorst plaque in OS; carotid bruit noted on R side but none on L; chest and heart exam WNL. Plan for further eval and management?

        #2 59-YO W male with palpable 5 cm aneurysm on PE; meds for HTN and mild-mod COPD; MI post 4 years with no current angina; Tx plan? Risks associated with both observation and surgical management?

        #3 54-YO male with worsening cramping pain in L calf after one block of walking, pain relieved with sitting, no pain at night, Hx of CABG post 3 years and MI post 4 years, angina only with extreve exertion; PE of extremities reveals no dependent rubor or elevation pallor, pulses normal in R leg but posterior tib and dorsalis pedis pulse absent on L, ABI is 0.85 on R and 0.52 on L. Management of pt? Indications for peripheral vascular bypass?

        #4 49-YO female with 2 day Hx of R calf and thigh swelling and pain; PE consistent with DVT. How to proceed with eval? If DVT confirmed, plan for management?

        #5 51-YO male with sudden onset of a cold, painful R leg; long Gx of cardiac problems with two previous Mis and current A-fib. Plan for eval and management?

        #6 52-YO female with venous stasis ulcers over medial melleoli for 4 years; vein stripping and local wound care have not yielded healing; Trendelenburg test, lower leg veins fill immediately upon standing with tourniquet in place. Primary or secondary venous insufficiency? Tx recommendations?