Ischemic Colitis
Epidemiology, Clinical Features, High-Risk Factors, and Outcome of Acute Large Bowel Ischemia
Ischemic Colitis
Epidemiology, Clinical Features, High-Risk Factors, and Outcome of Acute Large Bowel Ischemia
Pneumoperitoneum
Chest x-ray, pneumoperitonuem, air under diaphragms
Pneumoperitoneum – Radiology & Imaging
Rectus Sheath Hematoma
link: http://emedicine.medscape.com/article/776871-overview
Updated: Jul 1, 2009
Rectus sheath hematoma (RSH) is an uncommon and often clinically misdiagnosed cause of abdominal pain. It is the result of bleeding into the rectus sheath from damage to the superior or inferior epigastric arteries or their branches or from a direct tear of the rectus muscle. The emergency physician should be familiar with rectus sheath hematoma because it can mimic almost any abdominal condition. While usually a self-limiting entity, rectus sheath hematoma can cause hypovolemic shock following sufficient expansion, with associated mortality.
Rectus sheath hematoma is an ancient disorder first being accurately described by Hippocrates and mentioned by Galen. The first reported case in the United States was by Richardson in 1857.
Anatomic features
The best aid to understanding the pathogenesis and making the diagnosis of rectus sheath hematoma is knowledge of the relevant anatomy. The rectus sheath consists of the rectus abdominis muscles, an enveloping fascial sheath, and their blood supply via the epigastric arteries and veins.
The rectus abdominis muscles are two parallel vertically aligned muscles. The rectus abdominis muscles arise from the superior ramus of the pubis and insert into the ventral aspect of the fifth, sixth, and seventh costal cartilages and the xiphoid process. The rectus muscles are separated in the midline by the linea alba. The lateral boundary of the rectus sheath is the linea semilunaris.
The arcuate line is located about 5 cm below the umbilicus and functionally separates the rectus sheath into superior and inferior portions. Above the arcuate line, the aponeuroses of the external oblique, the internal oblique, and the transversalis muscles invest the rectus muscle. Three to four transverse tendinous inscriptions attach the rectus muscle to the enveloping fascia, usually above the arcuate line. The tendinous inscriptions form the typical segmental pattern of the rectus abdominis muscle.
Below the arcuate line, the aponeuroses remain intact anteriorly, but only the weak transversalis fascia and peritoneum separate the muscle mass from the abdominal viscera posteriorly. The inferior retrorectus space communicates with the prevesicular space of Retzius. This communication creates a natural dissection plane between the posterior rectus sheath and the bladder.
The arterial supply to the rectus sheath is derived from the superior and inferior epigastric arteries. The inferior epigastric artery originates from the external iliac artery. It rises from the inguinal ligament to enter the posterior rectus sheath inferiorly. The inferior epigastric artery then ascends loosely between the rectus abdominis muscle and the posterior rectus sheath. During contractions of the rectus abdominis muscle, the length of the muscle changes, and the artery must glide with the muscle to avoid tearing. The combination of the loose attachment of the inferior epigastric artery with the stabilization of its perforating branches fixed to the muscle belly makes the artery prone to shearing stresses at branching sites during strong muscular contraction.The superior epigastric artery originates from the external thoracic artery. The superior epigastric artery enters the sheath from behind the seventh costal cartilage and descends between the rectus abdominis muscle and the posterior rectus sheath. The superior and inferior epigastric arteries form rich anastomoses near the level of the umbilicus. The anastomoses are microscopic, helping to diminish the likelihood of trauma to the vessels during muscular contraction.
Rectus sheath hematomas (RSHs) are generally caused either by rupture of one of the epigastric arteries or by a muscular tear with shearing of a small vessel. The immediate cause of the rupture may be external trauma to the abdominal wall, iatrogenic trauma from surgery, or excessively vigorous contractions of the rectus muscle. These vigorous contractions are often seen in strenuous exercise or repeated Valsalva maneuvers with severe coughing, vomiting, or straining at the stool. Because the arteries supply the recti posteriorly, most hematomas are posterior to the muscle, making diagnosis by means of palpation more difficult.
Teske’s 1946 case series of 100 patients with rectus sheath hematoma showed 60% to be on the right side and more than 80% to be in the lower quadrants.[1 ]Right-sided hematomas are presumably more common because more people are right handed and, thus, are more prone to right-sided strain of the rectus muscle during strenuous activity. The lower quadrants are more frequently involved because of the long vascular branches that are present and because muscle excursion during contraction with the absence of the tendinous inscriptions is greater.
Hematomas above the arcuate line are generally caused by damage to the superior epigastric artery or its perforating branches. Patients usually present with unilateral, small, spindle-shaped masses because these hematomas are isolated by the rectus sheath and the tendinous inscriptions, causing tamponade of the bleeding.
Hematomas below the arcuate line are caused by damage to the inferior epigastric artery or its perforating branches. They protrude posteriorly and appear spherical because the rectus abdominis muscle is only supported posteriorly by the transversalis fascia and the parietal peritoneum. Below the arcuate line, hematomas bleed more and may dissect extensively because no posterior sheath wall or tendinous inscriptions are present to tamponade the bleeding. Rectus sheath hematomas below the arcuate line are more likely to cross the midline and become bilobar.
Hematomas near the umbilicus are rare. They are small when they do occur because the microscopic anastomoses of the superior and inferior epigastric arteries near the umbilicus do not allow for significant bleeding.
Hematomas near the peritoneum can result in peritoneal irritation, subsequent abdominal rigidity, and gastrointestinal symptoms. Dissection of the hematoma inferiorly into the prevesicular space of Retzius can masquerade as a pelvic tumor or irritate the bladder, resulting in urinary complications.
In 1996, Berna et al used the appearance of rectus sheath hematomas on CT scans to differentiate 3 levels of severity with disposition and therapeutic implications.[2 ]
After resolution, rectus sheath hematomas usually do not recur and typically do not cause long-term sequelae.
Rectus sheath hematoma is an uncommon, but not rare, cause of abdominal pain. In 1999, Klingler et al found an incidence of 1.8% among 1257 patients admitted to the hospital with abdominal pain and undergoing ultrasonography for diagnosis.[3 ]Anticoagulation is a well-known risk factor. The incidence is thought to be on the rise, with the increased use of oral anticoagulation drugs and low molecular weight heparins (LMWH).
Although usually a benign self-limiting condition, rectus sheath hematoma (RSH) may be fatal. Mortality figures are prone to error because of the uncommon incidence of rectus sheath hematoma and the paucity of recent mortality data. Overall, the mortality rate is reported to be 4%. The mortality rate for iatrogenic rectus sheath hematoma is reported to be 18%, whereas the mortality rate for patients with rectus sheath hematoma who are undergoing anticoagulation therapy is reported to be 25%. Pregnant patients have a reported mortality rate of 13%, with a 50% mortality rate for the fetus.
These mortality rates were reported prior to the widespread use of ultrasonography and CT scanning to aid in the early diagnosis of rectus sheath hematoma. Early diagnosis likely reduces the mortality rate, but no studies to date are available to demonstrate this.
The high mortality rate in patients undergoing anticoagulant therapy is related to the larger hematomas as well as the increased age and significant comorbidities of these patients.
The morbidity of rectus sheath hematoma is primarily the result of incorrect diagnosis leading to unnecessary exploratory laparotomy, delay in cessation of anticoagulant therapy, or delay in fluid resuscitation and blood transfusion.
As with other abdominal pathology in the older patient, extra care should be devoted to an expedient and accurate diagnosis in elderly patients. Elderly patients are more likely than younger patients to require aggressive resuscitation, anticoagulation reversal, and admission. For these reasons, elderly patients also experience an increased mortality rate.
Rectus sheath hematoma is reported to occur less often in African Americans, with only 4% of rectus sheath hematomas occurring in people of this race. Whether this low rate is physiologic, a result of sample reporting, or diagnostic bias is unknown.
Rectus sheath hematoma is 2-3 times more common in females than in males. The higher incidence in women has been attributed to their decreased muscle mass. The sex distribution seems to be equal in younger age groups, although the predisposing factors differ. Pregnancy is a risk factor in younger females, whereas males more commonly develop rectus sheath hematoma after trauma or muscular exertion.
In a 1946 review of 100 cases, Teske reported the occurrence of rectus sheath hematoma in patients aged 4-83 years, with an average age of 47 years.[1 ]The peak age of incidence is in the fifth decade of life. Incidence increases with age as the protection provided by the rectus sheath becomes compromised by decreased muscle mass. The effects of arteriosclerosis and hypertension also render vessels more susceptible to injury.
Common historical features of rectus sheath hematoma (RSH) include acute abdominal pain, fever, nausea, and vomiting. The nonspecific nature of these symptoms combined with the low incidence of the disorder lead to difficulty in considering this diagnosis. Rectus sheath hematoma should be included in the differential diagnosis of every patient who presents with abdominal pain.
This patient complains of pain and the medical man finds the swelling. The trouble is that he seldom knows how long the swelling has been present…The main point is the recognition that these swellings are part and parcel of the abdominal wall. This is generally made by noting that they can still be felt when the recti are in action, and that they become fixed as the muscles contract
Several risk factors of rectus sheath hematoma (RSH) can be obtained in the history. In most cases of rectus sheath hematoma, one or more precipitating factors can be found. Reports of spontaneous rectus sheath hematoma exist, but more likely, in these cases, the precipitating factor was not appreciated. Anticoagulation is the most frequent predisposing factor, and severe coughing is the most important inciting factor.
| Abdominal Pain in Elderly Persons | Ovarian Cysts |
| Abdominal Trauma, Blunt | Ovarian Torsion |
| Abruptio Placentae | Pancreatitis |
| Aneurysm, Abdominal | Pediatrics, Appendicitis |
| Appendicitis, Acute | Pediatrics, Gastroenteritis |
| Cholecystitis and Biliary Colic | Pediatrics, Intussusception |
| Cholelithiasis | Pregnancy, Ectopic |
| Diverticular Disease | Pregnancy, Trauma |
| Gastritis and Peptic Ulcer Disease | Pregnancy, Urinary Tract Infections |
| Gastroenteritis | Shock, Hemorrhagic |
| Hernias | Shock, Hypovolemic |
| Mesenteric Ischemia | Urinary Obstruction |
| Obstruction, Large Bowel | Urinary Tract Infection, Female |
| Obstruction, Small Bowel | Urinary Tract Infection, Male |
Intra-abdominal neoplasms
Abdominal wall neoplasms
Tubo-ovarian abscess
Abdominal wall abscess
Peptic ulcer disease
Perforations
Once rectus sheath hematoma (RSH) is diagnosed, the patient’s clinical condition determines appropriate treatment and disposition. Treatment may be either conservative or invasive.
All patients who are admitted for rectus sheath hematoma (RSH) should have a surgical consultation, either general or vascular, depending on the institution. The diagnosing clinician should also consider surgical or primary care consultation for discharged patients and provide follow-up evaluation and long-term pain control.
The goals of pharmacotherapy are to reduce morbidity and to prevent complications.
Patients on warfarin can have their anticoagulation reversed with phytonadione.
Vitamin K is a necessary cofactor for gamma carboxylation in the synthesis of factors II, VII, IX, and X in the liver. Used therapeutically in RSH to treat warfarin-induced hypoprothrombinemia.
1-10 mg IV slow (<1 mg/min); IM and SC routes are not recommended because response is unpredictable and may be delayed; a dose of 10 mg IV is associated with prolonged warfarin resistance but is the recommended dose by the American College of Chest Physicians for major or life-threatening bleeding in the anticoagulated patient on warfarin
Not established
Broad-spectrum antibiotics, quinidine, quinine, and salicylates may increase phytonadione requirements
Documented hypersensitivity
C – Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
IV form has been associated with rare anaphylactoid reactions and death, even when care has been taken to administer the drug slowly; transient flushing sensations and peculiarities of taste have been reported following vitamin K injection
Protamine forms a complex with heparin to create a nonreactive salt. Heparin is neutralized within 5 min of protamine administration. The duration of effect is 2 h. The half-life of protamine is less than heparin; therefore, multiple dosing may be required. LMWHs can be partially reversed with protamine.
The half-life of heparin is 60 min. Therefore, enough protamine should be administered to reverse all of the heparin administered in the last 30 min, one half of the heparin administered the previous hour, and one fourth of the heparin administered the hour before that, assuming no recent bolus.
1 mg IV per 100 U of heparin to be neutralized; not to exceed 50 mg with a maximum rate of 5 mg/min
Not established
None reported
Documented hypersensitivity
C – Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Upon metabolism, the salt complex may liberate heparin, causing heparin rebound and requiring multiple dosing of protamine; protamine sulfate has its own anticoagulant effect, which may become apparent if administered in doses larger than necessary to inactivate heparin
RSHs are very painful conditions that often mimic or present as an acute abdomen. The clinician should have a low threshold for narcotic analgesia. The clinician should also recognize the theoretic complication of platelet inhibition with nonsteroidal anti-inflammatory analgesics.
Drug combination indicated for moderate to severe pain.
1-2 tab or cap PO q4-6h prn pain
<12 years: 10-15 mg/kg/dose acetaminophen PO q4-6h prn; not to exceed 2.6 g/d acetaminophen
>12 years: 750 mg acetaminophen PO q4h; not to exceed 10 mg hydrocodone bitartrate per dose or 5 doses/24 h
Coadministration with phenothiazines may decrease analgesic effects; toxicity increases with CNS depressants or tricyclic antidepressants
Documented hypersensitivity; high altitude cerebral edema (HACE) or elevated intracranial pressure (ICP)
C – Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Tab contain metabisulfite, which may cause hypersensitivity; caution in patients dependent on opiates since this substitution may result in acute opiate-withdrawal symptoms; caution in severe renal or hepatic dysfunction
Drug combination indicated for the relief of moderate to severe pain.
1-2 tab or cap PO q4-6h prn pain
0.05-0.15 mg/kg/dose oxycodone PO; not to exceed 5 mg/dose of oxycodone q4-6h prn
Phenothiazines may decrease analgesic effects of this medication; toxicity increases with coadministration of either CNS depressants or tricyclic antidepressants
Documented hypersensitivity
C – Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Duration of action may increase in elderly patients; be aware of total daily dose of acetaminophen patient is receiving (do not exceed 4,000 mg/24 h of acetaminophen; higher doses may cause liver toxicity)
rectus sheath hematoma, abdominal wall hematoma, epigastric artery rupture, rectus muscle, rectus muscle tear, rectus sheath hematoma symptoms, rectus sheath hematoma treatment, rectus sheath hematoma, causes, pelvic pseudotumor, RSH, abdominal pain, hypovolemic shock, hematoma, anticoagulation
Wan-Tsu Chang, MD, Staff Physician, Department of Emergency Medicine, University of Cincinnati
Wan-Tsu Chang, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, Emergency Medicine Residents Association, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
William A Knight IV, MD, Assistant Professor, Department of Emergency Medicine, University of Cincinnati School of Medicine
William A Knight IV, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Emergency Physicians, Emergency Medicine Residents Association, Society for Academic Emergency Medicine, and Society of Critical Care Medicine
Disclosure: Nothing to disclose.
Steven G Werdehoff, MD, Consulting Staff, Department of Emergency Medicine, Huntsville Emergency Physicians Group
Steven G Werdehoff, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Emergency Physicians, Emergency Medicine Residents Association, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Andra L Blomkalns, MD, Associate Professor, Vice Chair – Academic Affairs, Department of Emergency Medicine, University of Cincinnati School of Medicine
Andra L Blomkalns, MD is a member of the following medical societies: American College of Emergency Physicians, American Heart Association, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Jerry Balentine, DO, Professor of Emergency Medicine, New York College of Osteopathic Medicine; Executive Vice President, Chief Medical Officer, Attending Physician in Department of Emergency Medicine, St. Barnabas Hospital
Jerry Balentine, DO is a member of the following medical societies: American College of Emergency Physicians, American College of Osteopathic Emergency Physicians, American College of Physician Executives, American Osteopathic Association, and New York Academy of Medicine
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment
Fred Harchelroad, MD, FACMT, FAAEM, FACEP, Chair, Department of Emergency Medicine, Director of Medical Toxicology – Allegheny General Hospital, Associate Professor, Department of Emergency Medicine, Drexel University College of Medicine
Disclosure: Nothing to disclose.
John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Steven C Dronen, MD, FAAEM, Director of Emergency Services, Director of Chest Pain Center, Department of Emergency Medicine, Ft Sanders Sevier Medical Center
Steven C Dronen, MD, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Appendicitis Images
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Short Bowel Syndrome
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Cholecystostomy
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Hemobilia
http://rad.usuhs.edu/medpix/master.php3?mode=print_case&pt_id=7153&showall=yes
Content below:
![]() Case of the Week – Patient Summary 7153Peer Reviewed and Certified – |
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| Contributed by: Michael Anthony Riel | |
| Approved by: James G. Smirniotopoulos, M.D. – | |
| Demographics: 50 y.o. woman | |
| History & Chief complaint: | |
| 8 days post liver biopsy. Anticoagulation started for central line thrombus. |
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| Physical exam: Not Available | |
| Summary of Findings: | |
| Differential Diagnosis: | |
| Diagnosis: | |
Hemobilia |
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| Disease Discussion – Â Hemobilia | |
| Hemobilia means blood in the bile | |
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Copyrighted materials are reproduced here with their Permission. The MedPix® Classification Schema copyright © 1999-2010 by J.G.Smirniotopoulos,M.D.
Inguinal anatomy
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Anal Cancer Flashcards
Content of flashcards
| Term | Definition |
| Anal Cancer: Background | Anal Cancer: Background
Malignancies of the anal cancer are relatively uncommon and represent only 2-3% of all anorectal carcinomas. The position of the tumor in the anal canal relative to the dentate line is important with regard to the biologic behavior of the tumor. This is based on the lymphatic drainage in these two areas. Most tumors spread by direct extension and lymphatic drainage. Hematologic spread is less common. Anal tumors are classified into two groups based on location: 1) anal cana tumors 2) anal margin tumors mnt reid p.452 |
| Anal Cancer: Epidermoid carcinoma | Anal Cancer: Epidermoid carcinoma
- Epidermoid carcinoma (1-2% of all colorectal carcinomas) are referred to as squamous, basaloid, cloacogenic, or transitional carcinomas. - Although each has different histologic features, they exhiit similar biologic behavior and are thus grouped together. - typically seen in patients 50-70 years of age - seen more frequently in women - two cell types – squamous cell (keratinizing) and transitional cell (nonkeratinizing) - rectal pain, bleeding, or mass are common presenting symptoms - 40-50% have pelvic lymph node involvement at diagnosis, whereas 15-36% have inguinal nodal involvement and 10% have distant metastasis - excellent prognosis when discovered prior to nodal involvement and invasion to adjacent structures. - 80% of tumors are cured by chemotherapy/radiation therapy alone - chemotherapy with mitomycin C and 5-fluorouracil combined with radiation is the treatment of choice. - this may be followed by surgical rsection - abdominoperineal resection is indicated for residual disease or recurrence mont reid p.453 |
| Anal Cancer: Malignant melanoma | Anal Cancer: Malignant melanoma
- 0.5-1% of malignant anal tumors - anal canal is the 3rd most common site after skin and eyes - typically occurs adjacent to the dentate line - rectal bleeding is the most frequent complaint - most are not highly pigmented, and diagnosis is difficult - tumor is aggressive and often widely metastatic. abdominoperineal resection is indicated in selected patients. - tumors often radioresistant and unresponsive to chemotherapy - 5-yaer survival is <15% mont reid p.453 |
| Anal Cancer: Tumors of the anal margin
squamous cell carcinoma, basal cell carcinoma, bowen’s disease, paget’s disease of bone |
Anal Cancer: Tumors of the anal margin
squamous cell carcinoma, basal cell carcinoma, bowen’s disease, paget’s disease of bone - these tumors are similar to skin tumors elsewhere and are treated likewise - include squamous cell and basal cell carcinomas, Bowen’s disease, and Paget’s disease of bone mont reid p.453 |
| Anal Cancer / Bowen: surgery resident handbook | Anal Cancer / Bowen: surgery resident handbook
ANAL CANCER and BOWEN DISEASE Anatomy-loosely speaking, above dentate line is columnar, below is squamous. A 1cm transition zone (cloacogenic zone) is present which can contain columnar, cuboidal, or transitional epithelium. Anal canal = 4cm tube from anal verge (what you see looking from outside) to anorectal ring (about 2cm above dentate line) Anal margin = skin from anal verge to point 5cm away circumferentially. Is the intersphincteric space. Dentate line = transition point, located about 2cm above anal verge. Term “anal cancer” comprises 2 entities: anal canal cancer (anal verge to 2cm above dentate line) and anal margin (anal verge out to 5cm skin) cancer. Overlapping behavior and treatment. Typically well-differentiated and slow growing. Epidemiology: F:M 5:1, mean age 60s. Associated with HPV genotypes 16 and 18, anal receptive intercourse, immunosuppressed states (HIV, organ transplant) SSx: change in bowel habits, hematochezia, pain, urgency, tenesmus, pruritis. Workup: punch or wedge biopsy diagnostic. Stage with EUS, exam of inguinal nodes with FNA for suspicious nodes, CT abdomen/pelvis, CXR. ANAL CANAL LESIONS EPIDERMOID (SQUAMOUS) CARCINOMA Arises from the cloacogenic zone. Includes squamous cell carcinoma basaloid carcinoma cloacogenic mucoepidermoid carcinoma. generally spread to inguinal LNs. higher incidence of superior rectal LN metastasis. Staging of anal canal cancers T1 Tumor <2cm T2 Tumor 2-5cm T3 Tumor >5cm T4 Tumor of any size with invasion into adjacent organ N1 Perirectal nodes N2 Unilateral internal iliac or inguinal lymph nodes N3 N1 and N2, or bilateral N2. M1 diatant metastases Stage I T1N0M0 Stage II T2-3 N0M0 Stage IIIa T1-3N1M0, T40M0 Stage IIIb T4N1M0, anyT N2-3 M0 Stage IV M1 Treatment is wide local excision for small, well-differentiated, localized tumors confined to submucosa. All others receive Nigro protocol. Historically, anal canal cancers were treated with APR but results were poor: 50% recurrence rates, 5-yr survival 24-62%.  In 1970s, sensitivity to chemoXRT established. NIGRO protocol: chemoradiation of 30Gy XRT of tumor, pelvic, and inguinal nodes from day 1 to 21, plus 5FU 1000mg/m^2 days 1-4 and 28-31 plus mitomycin C 15mg/m^2 on day1 If grossly disease disappears, no further treatment is necessary. LNs treated as well regardless of status, outcomes as good as formal LAN. Repeat Biopsy at 6wks. If pos, perform APR 4-6weeks after completion of radiation therapy OR repeat chemo (first line choice). Complete response >90%. 5yr sur 85%. Surveillance: Most recurrences are locoregionally. If nodal recurrence, treat with chemoXRT. anoscopy q3mos x 2years, then q6mos PE          q3mos x 2years, then q6mos CT, LFTs, EUS: surveillance debatable. ANAL MARGIN LESIONS BASAL CELL CARCINOMA Rare. Local excision. BOWEN DISEASE SSx: discrete scaly, crusty, or moist plaques surrounding the anus. Diagnose with skin biopsy. Treat with wide local excsion. PERIANAL PAGET’S DISEASE Rare intraepidermal neoplasm of apocrine glands. Long preinvasive phase. PE reveals scaly or red plaque. Dx with biopsy. Workup with full colonoscopy because 50% incidence of synchronous adenocarcinoma. Rx with wide local excision. Negative margins a must. If underlying carcinoma, APR is required. SQUAMOUS CELL CARCINOMA Rare. Less aggressive than SCCs of the anal canal. Treat with local excision, not Nigro protocol. Metastasizes to inguinal LNs. BUSCHKE-LOWENSTEIN TUMOR – giant condyloma acuminatum. Tend to erode into adjacent sturctures. Local excision. Consider chemoXRT for larger lesions. |
| Anal cancer: Multiple choice question [copy and paste] |
Multiple choice question
A 57 year old woman sees blood on the toilet paper. Her doctor notes the presence of an excoriated bleeding 2.8cm mass at the anus. Boipsy confirms the clinical suspicoin of anal cancer. In planning the management of a 2.8cm epidermoid carcinoma of the anus, which of the following is the best initial mangement strategy? a. Abdominoperineal resection b. Wide local resection with bilateral inguinal node dissection c. Local radiation therapy d. Systemic chemotherapy e. Combined radiation therapy and chemotherapy The aswer is e. (Greenfield, pp1131-1136) Epidermoid cancers of the anal canal metastasize to inguinal nodes as well as to the perirectal and mesenteric nodes. The results for local radical surgery have been disappointing. Combined external radiation with synchronous chemotherapy (fluorouracil and mitomycin), also known as the Nigro protocol, has been used as the standard treatment of the disease, whereas radical surgical approaches are now generally reserved for treatment failures and recurrences. pretest usrgery p.220;338 questoin 338 |
Colectomy flashcards
Content of flashcards:
| Term | Definition |
March 4, 2010Anatomy ImagesAnatomy Images http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHF1600R.html Identify the following regions in the image above: Rectus abdominus – External oblique – Serratus posterior inferior – Latissimus dorsi – Sacrospinalis – Multifidus – Psoas major – Right lobe of liver – Left lobe of liver – Gallbladder – Body of stomach – Right kidney – Left kidney – Descending aorta – Inferior vena cava – Vertebral body – Spinal cord ———————————— http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHF1650R.html Identify the following regions in the image above: Rectus abdominus – External oblique – Internal oblique – Latissimus dorsi – Psoas major – Sacrospinalis – Multifidus – Right kidney – Left kidney – Ascending colon – Transverse colon – Descending colon – Jejunum – Descending aorta – Inferior vena cava – Left adrenal gland – Vertebral body – Apophyseal joint – Spinal cord ————————– http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHF1700R.html Identify the following regions in the image above: Rectus abdominus – External oblique – Sacrospinalis – Multifidus – Psoas major – Ascending colon – Transverse colon – Descending colon – Descending aorta – Jejunum – Mesentery – Inferior vena cava – Vertebral body – Spinal canal ———————————— Upper abdomen, male L1 level http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHM1550R.html Identify the following regions in the image above: Rectus abdominus – External oblique – Latissimus dorsi – Serratus posterior inferior – Sacrospinalis – Multifidus – Body of stomach – Colonic splenic flexure – Jejunum – Pancreas – Spleen – Diaphragm – Descending aorta – Inferior vena cava – Gallbladder – Liver – Vertebral body – Spinal cord —————– Upper abdomen, male L1 level http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHM1560R.html Identify the following regions in the image above: Rectus abdominus – External oblique – Latissimus dorsi – Serratus posterior inferior – Sacrospinalis – Multifidus – Body of stomach – Pylorus – Duodenal bulb – Colonic splenic flexure – Colonic hepatic flexure – Jejunum – Pancreas – Spleen – Diaphragm – Descending aorta – Inferior vena cava – Left adrenal gland – Right adrenal gland – Gallbladder – Liver – Vertebral body – Spinal cord ————————– Upper abdomen, male L1-L2 level http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHM1580R.html Identify the following regions in the image above: Rectus abdominus – External oblique – Latissimus dorsi – Sacrospinalis – Multifidus – Pyloric antrum – Colonic splenic flexure – Colonic hepatic flexure – Jejunum – Pancreas – Splenic vein – Spleen – Diaphragm – Descending aorta, celiac axis branch – Inferior vena cava – Left adrenal gland – Right adrenal gland – Left kidney – Right kidney – Gallbladder – Liver – Intervertebral disc – Spinal cord —————————————– Abdomen, male L2 level http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHM1600R.html Identify the following regions in the image above: Rectus abdominus – Transversus abdominis – Intercostal m. – External oblique – Internal oblique – Latissimus dorsi – Sacrospinalis – Multifidus – Erector spinae m. – Psoas major – Uncinate process of pancreas – Transverse colon – Jejunum – Descending colon – Spleen tip – Left kidney – Right kidney – Crus of diaphragm – Liver – Descending aorta, superior mesenteric branch – Inferior vena cava – Superior mesenteric vein – Vertebral body – Conus medullaris Abdomen, male L3-L4 level http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHM1650R.html Identify the following regions in the image above: Rectus abdominus – External oblique – Internal oblique – Latissimus dorsi – Sacrospinalis – Multifidus – Psoas major – Quadratus lumborum – Iliocostalis – Longissimus dorsi – Spinalis dorsi – Ascending colon – Descending colon – Transverse colon – Jejunum – Left kidney – Right kidney – Left ureter – Right ureter – Descending aorta – Inferior vena cava – Superior mesenteric vein – Intervertebral disc – Cauda equina Lower abdomen, male L4 level http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHM1700R.html Identify the following regions in the image above: Linea alba – Rectus abdominus – External oblique – Internal oblique – Transversus abdominis – Sacrospinalis – Multifidus – Erector spinae muscle group (iliocostalis, longissimus dorsi, spinalis dorsi) – Psoas major – Quadratus lumborum – Ascending colon – Descending colon – Ileum – Descending aorta – Inferior vena cava – Vertebral body – Superior articular process – Inferior articular process – Apophyseal joint – Spinal canal with cauda equina – Thoracolumbar fascia Anatomy ImagesAnatomy Images http://library.med.utah.edu/WebPath/HISTHTML/ANATOMY/VHF1550R.html Identify the following regions in the image above: Rectus abdominus – External oblique – Serratus posterior inferior – Latissimus dorsi – Sacrospinalis – Multifidus – Right lobe of liver – Left lobe of liver – Body of stomach – Spleen – Diaphragm – Descending aorta – Inferior vena cava – Left adrenal gland – Right adrenal gland – Vertebral body – Spinal cord Anatomy ImagesAnatomy Images Identify the following regions in the image above: Latissimus dorsi – Serratus anterior – External oblique – Rectus abdominis – Sacrospinalis – Sternum – Breast – Liver, right lobe – Left lower lobe – Right lower lobe – Esophagus – Descending aorta – Vertebral body – Spinal cord Liver PathologyLiver Pathology Normal
Steatosis
Cirrhosis
Pigmentary Disorders
Neoplasms
Viral Hepatitis
Miscellaneous Parenchymal Diseases
Hepatocellular CarcinomaHepatic AdenomaHepatic Adenoma
IMAGING OF HEPATITIC AENOMA HemochromatosisHemochromatosis
source: http://library.med.utah.edu/WebPath/TUTORIAL/IRON/IRON.html Portal HypertensionLiver CirrhosisLiver Cirrhosis
Fatty Liver or SteatosisLiver AnatomyMarch 3, 2010DiverticulosisColon PolypsColon Polyps
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