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Epithelioid Mesothelioma of Peritoneum Masquerading as Peritoneal Carcinomatosis
1Department of Pathology, All India Institute of Medical Science, Mangalagiri, Guntur, India.
Introduction:
Mesothelioma is an insidious neoplasm that develops from mesothelial cells. About 80% of mesotheliomas originate in the pleural cavity. Other sites where it has been reported are the peritoneal cavity, tunica vaginalis, and the pericardium.
Case Presentation:
A 45-year-old female complained of abdominal distention and pain for three months. There was a significant weight loss of approximately 15 kg in the past three months, and there was no family history of any malignancy, tuberculosis, substance abuse, or asbestosis exposure. Physical examination revealed signs of muscle wasting, loss of subcutaneous fat, and hollowing of the eye sockets. There was pitting edema in the bilateral lower limbs; per abdomen examination revealed abdominal distension with umbilicus in the midline. No visible peristalsis or dilated veins were seen all over the abdomen. Hernial sites were normal. Gross ascites were present, and no organomegaly, definitive mass, or lump was palpable. The dull note was heard all over the abdomen, and fluid thrill was noted on percussion. Bowel sounds were normal on auscultation. The ascitic fluid examination revealed the presence of atypical cells. An omentectomy was done and it was sent for histopathological examination.
Conclusion:
The specimen of omentectomy was in multiple fragments and measured 17x16x3cm; a few of the fragments were nodular, soft to firm on palpation. The cut section of mass was gray and white with areas of necrosis. Microscopic examination showed sheets of malignant cells. These tumor cells were immunoreactive to EMA, cytokeratin, vimentin, calretinin, WT-1, and D2-40 and immune negative to desmin (highlighting only the entrapped reactive mesothelial cells), inhibin, BerEP4, TTF-1, CD 68, napsin, ER, CEA, CDX2, PR, PAX-8, and SALL4. Ki67 labelling index was 15%. The features were of epithelioid mesothelioma.
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.
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