Intra Abdominal Fibromatosis Mimicking GIST; A Case Report and Review of the Literature
نویسندگان
چکیده
منابع مشابه
Subsequent leiomyoma and intra-abdominal fibromatosis mimicking recurrent gastrointestinal stromal tumor: a case report
Gastrointestinal stromal tumor (GIST) is the most common mesenchymal tumors of the gastrointestinal tract. In this report, we present a case of GIST patient who had been treated with imatinib, but developed leiomyoma and intra-abdominal fibromatosis (IAF) at the site of GIST resection beds mimicking recurrent GIST. To our knowledge, no patient with the 3 gastrointestinal tumor types we encounte...
متن کاملRenal Capillary Hemangioma Mimicking Urothelial Carcinoma, A Case Report and Review of the Literature
Renal hemangioma is a rare tumor which can be capillary or cavernous. There have been less than 30 renal capillary hemangioma cases reported in the English literature. Herein we will report a case of renal hemangioma which was detected in a 74-year-old man operated with the impression of urothelial carcinoma of hilum.
متن کاملA Fibromatosis Case Mimicking Abdominal Aorta Aneurysm
Retroperitoneal fibrosis is a rare fibrosing reactive process that may be confused with mesenteric fibromatosis. Abdominal aorta aneurysm is rare too and mostly develops secondary to Behcet's disease, trauma, and infection or connective tissue diseases. Incidence of aneurysms occurring as a result of atherosclerotic changes increases in postmenopausal period. Diagnosis can be established with a...
متن کاملIsolated giant mesenteric fibromatosis (intra-abdominal desmoid tumors). Case report.
A rare case of isolated giant mesenteric fibromatosis is presented. The tumor originated from the fibrous mesenteric tissue. The patient underwent laparotomy because of abdominal discomfort and sub-occlusive symptoms due to the giant mass. Differential diagnosis of mesenteric masses is discussed and the Authors also review the literature concerning this rare disease.
متن کاملAdrenocortical Carcinoma Mimicking Pheochromocytoma: A case Report and Review of Literature
Adrenocortical carcinoma (ACC) is an uncommon malignancy originating from cortex of adrenal gland. The most common pitfall in diagnosis of ACC is to distinguish it from pheochromocytoma. Here we report a 62-year-old hypertensive man with presentation of dyspnea. The laboratory data showed an increase in urine cortisol and renin with a mild increase in aldosterone, but decrease in adrenocorticot...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of Tumor Medicine & Prevention
سال: 2017
ISSN: 2575-890X
DOI: 10.19080/jtmp.2017.01.555567