OJPathology  Vol.2 No.4 , October 2012
Plexiform Angiomyxoid Myofibroblastic Tumor of the Stomach
ABSTRACT
Plexiform angiomyxoid myofibroblastic tumor (PAMT) is a recently described gastric tumor with a peculiar plexiform pattern, bland spindle cells and a myxoid stroma rich in arborizing blood vessels. PAMT of the stomach is a very rare tumor without distinctive clinical manifestations. In this study, we report a new case of PAMT which is the first Chinese case in English literature. A 47-year-old Chinese woman was admitted with a 6-month history of intermittent epigastric discomfort, and abdominal pain for 2 months. Gastroscopy showed an elevated mass in the anterior wall of the gastric antrum. Endoscopic ultrasound revealed a focal hypoechoic lesion protruding into the lumen. A laparoscopic distal gastrectomy was performed, and the patient made an uneventful recovery and remains well 1.5 years later. A diagnosis of PAMT was made by histopathology and immunochemistry.

Cite this paper
P. Li, Q. Zhang, X. Jia, Q. Li, Z. Li and Z. Wang, "Plexiform Angiomyxoid Myofibroblastic Tumor of the Stomach," Open Journal of Pathology, Vol. 2 No. 4, 2012, pp. 147-149. doi: 10.4236/ojpathology.2012.24027.
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