Angiomyolipoma of stomach is extremely rare. Only 1 case has been reported earlier. We report a case of 40-year-old female who presented with gastrointestinal bleeding. Upper gastrointestinal endoscopy suggested a polypoidal growth in the stomach. Biopsy from the growth was suggestive of mesenchymal tumor. The contrast-enhanced computed tomography of abdomen revealed a pedunculated 4×3 cm, intramural lesion at the junction of first and second parts of duodenum, likely lipoma. The stalk seemed to be arising from distal stomach. At laparoscopy, a highly mobile lesion was observed arising from the posterior wall of stomach. Wedge resection of the lesion was performed laparoscopically after doing an anterior gastrotomy. The final diagnosis on histopathology was a gastric angiomyolipoma.
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http://dx.doi.org/10.1097/SLE.0b013e31823cd1f5 | DOI Listing |
Front Surg
December 2023
Department of Hepatobiliary Surgery, Mianyang Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Mianyang, China.
Hepatic angiomyolipoma is a rare and possibly cancerous mesenchymal tumor that consists of three components: blood vessels, smooth muscle cells, and adipose tissue. In this paper, we reported a case of a 36-year-old man who had a giant hepatic angiomyolipoma with spontaneous rupture and hemorrhage. The patient was admitted to our hospital with sudden upper abdominal pain for 3 h.
View Article and Find Full Text PDFBMC Med Genet
March 2020
Section of General Surgery and Gastrointestinal Surgery, Department of Surgery I, Faculdade de Medicina do ABC, Avenida Lauro Gomes, 2000, Santo André/São Paulo, CEP 09060-870, Brazil.
Background: Birt-Hogg-Dubé syndrome (BHDS) is a rare autosomal dominant genodermatosis characterized by benign growth of the hair follicles, the presence of pulmonary cysts, spontaneous pneumothorax, and bilateral renal tumors that are usually hybrid oncocytic or multifocal chromophobe renal cell carcinoma. The diagnosis is confirmed by the presence of a pathogenic variant in the tumor suppressor folliculin (FLCN) gene mapped at 17p11.2.
View Article and Find Full Text PDFACG Case Rep J
December 2018
Department of Pathology, Amrita Institute of Medical Sciences, Kochi, Kerala, India.
Gastric angiomyolipoma (AML) is extremely rare, with only 3 cases reported in English literature, all of which presented with upper gastrointestinal bleed, either in the form of hematemesis or melena. A 42-year-old man presented with upper gastrointestinal bleed, the source of which was found to be a large mass in the stomach, which was shown histologically to be gastric AML. This is the fourth but largest tumor (9 × 6 × 5 cm) to be reported to date.
View Article and Find Full Text PDFFam Cancer
April 2018
The University of New Mexico Comprehensive Cancer Center, 1201 Camino de Salud, MSC07 4025, Albuquerque, NM, 87131, USA.
The majority of pancreatic neuroendocrine tumors (PNETs) are sporadic while 10-15% are attributable to one of several familial cancer syndromes. Hereditary forms are more commonly associated with Multiple Endocrine Neoplasia Type I and von Hippel Lindau Syndrome. However, patients with Tuberous sclerosis complex also have an increased incidence of PNETs.
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