A case of gangliocytic paraganglioma in the ampulla of Vater
نویسندگان
چکیده
BACKGROUND Duodenal gangliocytic paraganglioma is an extremely rare tumor and few cases have been reported to date. CASE PRESENTATION The authors report a case of gangliocytic paraganglioma verified by post-op pathology after pancreaticoduodenectomy for a tumor in the ampulla of Vater. The 56-year-old male patient concerned visited our emergency room with melena that started one week prior to hospitalization. The patient was diagnosed to have a tumor in the ampulla of Vater with bleeding on its surface. However post-op, he was diagnosed as having gangliocytic paraganglioma by immunohistochemistry. CONCLUSION This tumor has precise clinical implications, and if continuous follow up is conducted after careful diagnosis and surgical treatment, invasive major operations, such as, radical pancreaticoduodenectomy can be avoided.
منابع مشابه
Gangliocytic paraganglioma in the ampulla of Vater: Case report and review of the literature
Gangliocytic paraganglioma (GP) is a rare tumor. Until today, only few cases have been reported. Usually GPs are encountered in the second portion of the duodenum, commonly occurring as small submucosal lesions. Histologically, they are characterized by the presence of three different types of cells: epithelioid cells with endocrine growth pattern, resembling paraganglioma or carcinoid tumor ce...
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Gangliocytic paraganglioma (GP) is a rare gastrointestinal tumor and 90% of the cases are found in the duodenum, with a predilection for the region of the ampulla of Vater.1--3 The most common clinical presentation includes melena and abdominal pain and it typically follows a benign course.1--3 Surgical resection is the most common treatment and only around 20 cases managed with endoscopic rese...
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عنوان ژورنال:
دوره 8 شماره
صفحات -
تاریخ انتشار 2010