Pancreatic adenocarcinoma in a patient with Peutz-Jeghers syndrome: Report of a case and literature review

Hepato-Gastroenterology

Volumn 47, Issue 34, 2000, Pages 1159-1161

  Hirao, S ^a   Sho, M ^a   Kanehiro, H ^a   Hisanaga, M ^a   Ikeda, N ^a   Tsurui, H ^a   Nakajima, Y ^a   Nakano, H ^a  

^a NARA MEDICAL UNIVERSITY   (Japan)

Author keywords

Pancreatic cancer; Peutz Jeghers Syndrome

Indexed keywords

ADULT; ARTICLE; CANCER DIAGNOSIS; CANCER SCREENING; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; HUMAN; MALE; PANCREAS ADENOCARCINOMA; PANCREATICODUODENECTOMY; PEUTZ JEGHERS SYNDROME; PRIORITY JOURNAL; PROGNOSIS;

ADENOCARCINOMA; CARCINOMA, PANCREATIC DUCTAL; CASE REPORT; HUMAN; MALE; MIDDLE AGE; PANCREATIC NEOPLASMS; PANCREATICODUODENECTOMY; PEUTZ-JEGHERS SYNDROME;

EID: 0033803556     PISSN: 01726390     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (19)

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2. Generalized intestinal polyposis and melanin spots of the oral mucosa, lips, and digits: A syndrome of diagnostic significance
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5. Increased risk of cancer in the Peutz-Jehgers syndrome
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8. Peutz-Jeghers syndrome: A clinicopathologic survey of the 'Harrisburg family' with a 49-year follow-up
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14. Ovarian sex cord tumor with annular tubules
15. Gastrointestinal Polyposis with mucocutaneous pigmentation (Peutz-Jeghers syndrome)
16. Peutz-Jeghers sydrome is caused by mutations in a novel serine threonine kinase
17. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
18. Most human carcinomas of the exocrine pancreas contain mutant c-K-ras genes
19. K-ras and p53 gene mutations in pancreatic cancer: Ductal and nonductal tumors progress through different genetic lesions