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2011 | 83 | 11 | 627-629
Tytuł artykułu

Neuroendocrine Tumor in Choledochal Cyst - Case Report and Review of Literature

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The report presents a rare case of carcinoid tumor in a 17 year female who presented with epigastric pain of one week duration. She was diagnosed to have type I choledochal cyst on abdominal ultrasound and MRI. She underwent total excision of choledochal cyst with roux-en-Y hepaticojejunostomy. His-topathological examination revealed a neuroendocrine tumor within choledochal cyst which was immunoreactive for Chromogranin A. Patient is well at 6 months of follow up. These tumors are characteristically slow-growing, therefore awareness of its presence preoperatively can facilitate optimal management by performing surgical resection with negative margins which offers the best chance of long-term survival.
Wydawca

Rocznik
Tom
83
Numer
11
Strony
627-629
Opis fizyczny
Daty
wydano
2011-11-01
online
2012-01-13
Twórcy
autor
  • Department of HPB Surgery, Hospital Selayang, Batu Caves, Selangor, Malaysia
  • Department of HPB Surgery, Hospital Selayang, Batu Caves, Selangor, Malaysia
autor
  • Department of HPB Surgery, Hospital Selayang, Batu Caves, Selangor, Malaysia
Bibliografia
  • Capella C, Solcia E, Sobin LH et al.: Endocrine tumors of the gall-bladder and extrahepatic bile ducts. WHO Classification of Tumors. Hamilton R, Aaltonen LA (eds) Pathology and Genetics of Tumors of the Digestive System. 2000 Oct. IARC Press, Lyon, pp 214-66.
  • Christie AC: Three cases illustrating presence of Argentaffin (Kulchitsky) cells in human gall-bladder. J Clin Pathol 1954; 7: 318-21.
  • Chamberlain RS, Blumgart LH: Carcinoid tumors of the extrahepatic bile duct. A rare cause of malignant biliary obstruction. Cancer 1999; 86: 1959-65.[PubMed]
  • Albores-Saavedra J, Henson D, Klimstra D: Tumors of the Gall-bladder, Exrahepatic Biliary Ducts and Ampulla of Vater. AFIP Atlas of Tumor Pathology, 3rd ser. Washington, DC: Armed Forces Institute of Pathology, 2000.
  • Carriaga MT, Henson DE: Liver, gall bladder, extrahepatic bile ducts, and pancreas. Cancer 1995; 75 (Suppl): 171-90.[PubMed]
  • Modilin IM, Lye KD, Kidd M: A 5-decade analysis of 13,715 carcinoid tumors. Cancer 2003; 97: 934-59.
  • Davies AJ: Carcinoid tumors (Argentaffinomata). Ann R Coll Surg Engl 1959; 25: 277-97.
  • Barron-Rodriguez LP, Manivel JC, Mendez-Sanchez N et al.: Carcinoid tumor of the common bile duct: Evidence for its origin in metaplastic endocrine cells. Am J Gastroenterol 1991; 86: 1073-76.
  • Ueyama T, Ding J, Tsuneyoshi M et al.: Carcinoid tumor arising in the wall of a congenital bile duct cyst. Arch Pathol Lab Med 1992; 116 (3): 291-93.
  • Tonnhofer U, Balassy C, Reck CA et al.: Neuroendocrine tumor of the common hepatic duct, mimicking a choledochal cyst in a six-year-old child. J Paed Surg 2009; 44: E23-E25.[WoS]
  • Fellows IW, Leach IH, Smith PG et al.: Carcinoid tumor of the common bile duct-a novel complication of von-Hippel-Lindau syndrome. Gut 1990; 31: 728-29.
  • Kim DH, Song MH, Kim DH: Malignant carcinoid tumor of the common bile duct: report of a case. Surg Today 2006; 36: 485-89.[PubMed][WoS]
  • Marita A, Krueger JE, Tascilar M et al.: Carcinoid tumors of the extrahepatic bile ducts. A study of seven cases. The Am J Surg Pathol 2000; 24 (11): 1501-10.
  • Nesi G, Lombardi A, Batignani G et al.: Well-differentiated endocrine tumor of the distal bile duct: A case study and literature review. Virchows Arch 2006; 449: 104-11.
  • Podnos YD, Jimenez JC, Zainabadi K et al.: Carcinoid tumors of the bile duct: report of two cases. Surg Today 2003; 33: 553-55.
  • Hubert C, Sempoux C, Berquin A et al.: Bile duct carcinoid tumors: an uncommon disease with a good prognosis? Hepatogastroenterology 2005; 52: 1042-47.
  • Gusani NJ, Marsh JW, Nalesnik MA et al.: Carcinoid of the extra-hepatic bile duct: a case report with long-term follow-up and review of literature. The American Surgeon 2008; 74 (1): 87-90
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_v10035-011-0099-0
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