CC BY-NC-ND 4.0 · J Lab Physicians 2018; 10(02): 248-250
DOI: 10.4103/JLP.JLP_167_16
Case Report

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

Aniruddha Saha
Anandaloke Sonoscan Centre, Siliguri, West Bengal, India
,
Palash Kumar Mandal
Department of Pathology, College of Medicine and Sagore Dutta Hospital, Kolkata, West Bengal, India
,
Anupam Manna
Anandaloke Sonoscan Centre, Siliguri, West Bengal, India
,
Kalyan Khan
Department of Pathology, North Bengal Medical College, Siliguri, West Bengal, India
,
Subrata Pal
Department of Pathology, College of Medicine and Sagore Dutta Hospital, Kolkata, West Bengal, India
› Author Affiliations
Financial support and sponsorship Nil
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Abstract

Well-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.



Publication History

Received: 19 December 2016

Accepted: 13 November 2017

Article published online:
19 February 2020

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