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Small Bowel Tumors Keith D. Lillemoe M.D. Dept. of Surgery
Indiana University School of Medicine
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Small Bowel Tumors Epidemiology
Exceedingly rare - < 5500 new cases,1200 deaths/year Explanations lack of bacteria rapid transit role of pancreatic and mucosal enzymes secretory Ig A / intramural lymphoid tissue
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Predisposing Conditions
Small Bowel Tumors Predisposing Conditions Adenocarcinoma HNPCC Familial Adenomatous Polyposis Crohn’s Disease Lymphoma Celiac Disease Crohn’s Disease Immunologic Dysfunction
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Small Bowel Tumors Pathology - Benign Adenomas (20 – 30%)
simple tubular adenomas villous adenomas Brunner’s gland adenomas Leiomyomas (30 – 40%) Lipomas (15 – 20%) Hemangiomas (<10%) Hamartomas (<5%)
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Small Bowel Tumors Pathology - Malignant Distribution (%)
Type of Tumor Duodenum Jejunum Ileum % of Total Adenocarcinoma Carcinoid Tumor Lymphoma Gastrointestinal Stromal Tumors
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Small Bowel Tumors Clinical Presentation Benign Malignant Symptom %
Pain Obstruction Bleeding Asymptomatic <50 Malignant Symptom % Weight Loss Abdominal Pain Obstruction Abdominal Mass Perforation Bleeding Jaundice
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Small Bowel Tumors Diagnosis Radiology Endoscopy Plain films Upper
Contrast Studies CT Laparotomy/Laparoscopy Endoscopy Upper Lower Enteroscopy Capsule endoscopy
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Small Bowel Tumors Management – Benign Neoplasms Adenomas:
Duodenum : Endoscopic polypectomy Transduodenal excision Duodenectomy Jejunum/Ileum : Local excision
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Small Bowel Tumors Management – Benign Tumors
Hamartomas – Limited resection of responsible lesion (s) Hemangiomas – Resection Electrocautery
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Small Bowel Tumors Management - Adenocarcinoma
Duodenum – Pancreaticoduodenectomy 5 year – survival : % Jejunum-ileum – En bloc resection of bowel/mesentery 5 year survival : overall % node 15% node Θ 50-70% ? role for adjuvant therapy
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Small Bowel Tumors Gastrointestinal Stomal Tumors
formerly leiomyoma / leiomyosarcoma arise from mesenchymal tissue interstital (cell of Cajal) grow extrinsically, often to large size present with palpable mass, hemorrhage associated with mutation of C-kit
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Small Bowel Tumors Management – Gastrointestinal Stromal Tumors
Limited surgical resection Imatnib Mesylate (gleevac) 5 year survival %
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Small Bowel Tumors Lymphomas
vague symptoms – fatigue, malaise, weight loss, pain perforation, obstruction – 25% palpable mass – 33%
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Small Bowel Tumors Lympoma – Pathology/Staging
Non-Hodgkin’s, B-cell Usually intermediate/high grade with large cell features Ann Arbor classification IE – Tumor continued to SI without lymph nodes IIE – Regional lymph node involvement IIIE – Nonresectable lymph nodes IVE – Spread to nonlymphatic organs
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Small Bowel Tumors Management - Lymphoma
I-E / II-E – Limited resection, ?CTX 5-year survival : 60% III-E / IV-E – Limited resection + CTX / Radiation 5-year survival : rare
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Small Bowel Tumors Carcinoid Tumors arise from enterochromatin cells
often present late with nodal/hepatic metastasis obstruction due to desmoplastic reaction of mesentery carcinoid syndrome
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Small Bowel Tumors Management – Carcinoid Tumors
segmental resection with en bloc mesenteric resection aggressive treatment of metastatic disease treatment of carcinoid syndrome : octreotide 5 year survival : localized 100% regional 65% distant %
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Small Bowel Tumors Metastatic Neoplasms
direct extension, carcinomatosis Hematogenous metastasis (melanoma, hypernephroma, breast, lung)
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