Well differentiated papillary mesothelioma of abdomen- a rare case with diagnostic dilemma

Author:

Saha Aniruddha1,Mandal Palash Kumar2,Manna Anupam1,Khan Kalyan3,Pal Subrata2

Affiliation:

1. Anandaloke Sonoscan Centre, Siliguri, West Bengal, India

2. Department of Pathology, College of Medicine and Sagore Dutta Hospital, Kolkata, West Bengal, India

3. Department of Pathology, North Bengal Medical College, Siliguri, West Bengal, India

Abstract

AbstractWell-differentiated papillary mesothelioma is a rare tumor occurring predominantly in the peritoneum of young women, a few with history of asbestos exposure. A 28-year-old woman presented with ascites and pain abdomen. Ultrasonography and computed tomography scan of the abdomen revealed a mass in the retroperitoneum measuring 15 cm × 12 cm. Histopathological examination along with immunohistochemistry (IHC) confirmed it to be a papillary mesothelioma in the peritoneum. It is difficult to differentiate from more common malignant mesothelioma and papillary adenocarcinoma, which also have poorer prognosis. The difficulty can be resolved by clinico-radiological correlation along with histopathological examination and IHC.

Publisher

Georg Thieme Verlag KG

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