Epithelioid Mesothelioma of Peritoneum Masquerading as Peritoneal Carcinomatosis

Jyotsna Naresh Bharti1

  • 1Department of Pathology, All India Institute of Medical Science, Mangalagiri, Guntur, India.

PubMed
Abstract

Insights

This case study presents a rare instance of epithelioid mesothelioma in a 45-year-old female, diagnosed through omentectomy and histopathology. The findings highlight the importance of thorough diagnostic evaluation for unexplained abdominal symptoms.

Area of Science:

  • Oncology
  • Pathology
  • Gastroenterology

Background:

  • Mesothelioma is a rare cancer originating from mesothelial cells, typically affecting the pleura but occasionally other cavities like the peritoneum.
  • Epithelioid mesothelioma is the most common subtype, characterized by distinct cellular morphology and immunohistochemical markers.

Observation:

  • A 45-year-old female presented with significant abdominal distension, pain, and rapid weight loss.
  • Physical examination revealed ascites, muscle wasting, and bilateral lower limb edema.
  • Atypical cells in ascitic fluid prompted an omentectomy for histopathological examination.

Findings:

  • Histopathology confirmed epithelioid mesothelioma with a 15% Ki67 labeling index.
  • Immunohistochemistry showed tumor cell reactivity for EMA, cytokeratin, vimentin, calretinin, WT-1, and D2-40.
  • The tumor cells were negative for markers such as desmin, inhibin, BerEP4, and TTF-1, aiding in differential diagnosis.

Implications:

  • This case underscores the importance of considering mesothelioma in the differential diagnosis of unexplained ascites and abdominal masses, even in the absence of typical risk factors like asbestos exposure.
  • Accurate diagnosis through immunohistochemistry is crucial for appropriate patient management and treatment planning for peritoneal mesothelioma.