학술논문

“Ampullary gangliocytic paraganglioma:” A rare neuroendocrine tumor can be safely treated with ampullectomy.
Document Type
Article
Source
Journal of Digestive Endoscopy. Apr-Jun2018, Vol. 9 Issue 2, p82-84. 3p.
Subject
*PARAGANGLIOMA
*NEUROENDOCRINE tumors
*AMPULLA of Vater
*METASTASIS
*NEUROFIBROMATOSIS
*SURGERY
Language
ISSN
0976-5042
Abstract
Ampullary Gangliocytic paraganglioma is a rare gastro-entero-pancreatic neuroendocrine tumor with a characteristic histologic appearance involving epitheliod, spindle and ganglion cells. Endoscopic ultrasound is useful to determine depth of invasion and regional metastasis. Endoscopic resection, Ampullectomy and pancreato-duodenenectomy have been described as management options in literature but no consensus has been established. The index case describes an asymptomatic 42 y/o lady with a background of plexiform neurofibromatosis referred for cholestatic derangement of liver function. She was found to have a dilated biliary system with a periampullary mass which proved to be a Gangliocytic Paraganglioma without local lymph node metastasis. She underwent successful endoscopic ampullectomy with complete normalization of LFT and decompression of the biliary system with no clinical or endoscopic recurrence at 2 years follow up. We advocate that Partial Ampullectomy could be done safely as a treatment of localized Ampullary GP allowing long term resolution of symptoms. [ABSTRACT FROM AUTHOR]