Malignant peritoneal mesothelioma presenting as a complex omental lesion.

OA: gold CC-BY-NC-ND-4.0
AI-generated summary by claude@2026-07, 2026-07-14

This case report describes a rare, aggressive malignant peritoneal mesothelioma in a young female that presented as a complex, diffuse abdominal lesion mimicking ovarian malignancy.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-07, 2026-07-14 · read from full text

This paper describes a case of malignant peritoneal mesothelioma in a 28-year-old woman presenting with abdominal pain, distension, and a large heterogeneous abdominopelvic mass, evaluated with ultrasound and CT that showed multinodular peritoneal lesions, ascites, and pleuropericardial effusions. Surgery included complete omentectomy with cytoreductive surgery and total abdominal hysterectomy with bilateral salpingo-ovariectomy due to clinical suspicion of ovarian malignancy; histopathology showed spindle-cell tumor features and immunohistochemistry was positive for CD10, WT1, and C-Kit with negative ER/PR, confirming malignant peritoneal mesothelioma, and the patient was asymptomatic after chemotherapy at two months. The paper also reviews imaging patterns (dry, wet, mixed) and key differential diagnoses, noting that the diagnosis can be simulated by several conditions including intraperitoneal endometriosis, while emphasizing the rarity and aggressive nature of the tumor. Relevance to endometriosis: intraperitoneal endometriosis is explicitly listed as a differential diagnosis that can simulate malignant peritoneal mesothelioma, though the paper’s main focus is a single mesothelioma case and diagnostic context.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Malignant peritoneal mesothelioma is a rare, aggressive neoplasm with a poor prognosis. It simulates a spectrum of conditions and thus poses great difficulty in diagnosis and management. We report a case of malignant peritoneal mesotheolima in a young female whose abdominal CT showed a complex lesion occupying the entire abdominal cavity. This lesion mimicked an ovarian malignancy with peritoneal carcinomatosis.
Full text 6,116 characters · extracted from pmc-nxml · 3 sections · click to expand

Case

A 28-year-old female patient presented with abdominal pain, abdominal distension, and loss of appetite for one month. On examination, she was pale and had a large, palpable, abdominopelvic mass. Pervaginal examination revealed a palpable mass in the posterior fornix. Baseline investigations were within normal limit except for hemoglobin, which was 7.3 gm/ml. An ultrasonogram showed a large heterogeneous mass with predominantly cystic components and a few solid components occupying the entire abdominal cavity. The endometrium was thickened and measured 2.3 cm. CT of the abdomen showed large, nonenhancing, multinodular lesions of attenuation 27-35 HU distributed around the periphery of the abdominal cavity, with a centrally displaced small bowel and mesentery ( Fig. 1 ). Another cystic lesion was seen in the left adnexa ( Fig. 2 ). Ascites was also seen around the liver ( Fig. 3 ). CT of the thorax showed moderate left pleural and pericardial effusion. Serum alpha-fetoprotein, CA–125, and CA-19.9 were found to be within normal limits. Intraoperatively, multiple nodular lesions were seen infliltrating the omentum with centrally encased bowel loops ( Fig. 4 ). The patient underwent complete omentectomy with cytoreductive surgery, and total abdominal hysterectomy with bilateral salphingo-ovariectomy. Histopathological examination of the resected specimen showed a highly cellular tumor consisting of spindle cells arranged in interlacing bundles and sheets. The cells had hyperchromatic nuclei with mild anisocytosis ( Fig. 5 ). Immunohistochemical analysis was positive for CD 10, WT1, and C-Kit, and negative for ER and PR, confiming the histological diagnosis of malignant peritoneal mesothelioma ( Figs. 6A and 6B ). The abdominal hysterectomy with salpingo-ovariectomy was based on the clinical suspicion of ovarian maligancy, but subsequent histology showed a hyperplastic endometrium and a benign physiological left ovarian cyst. The patient was followed up with chemotherapy and was asymptomatic two months after the surgery.

Discussion

Malignant peritoneal mesothelioma is the second most common type of mesothelioma; it accounts for about 30% of all malignant mesotheliomas, with an overall incidence of 2 to 2.6 cases per million annually. A causal relationship between malignant peritoneal mesothelioma and asbestos exposure is implicated (especially the cridolite variety). However, half of these patients do not have any history of asbestos exposure. Exposure to mica, talc, and thorium and infection with Simian Virus 40 (SV 40) have also been reported as risk factors for mesotheliomas. There are three different presentations of malignant peritoneal mesothelioma ( 2 ): • Dry painful type: The commonest form of presentation, it presents with abdominal pain with little or no ascites. • Wet type: It presents with abdominal distension and ascites. • Mixed type: It presents with abdominal pain and distension. Dry painful type: The commonest form of presentation, it presents with abdominal pain with little or no ascites. Wet type: It presents with abdominal distension and ascites. Mixed type: It presents with abdominal pain and distension. Weight loss, bowel obstruction, and anemia are the other common clinical features. Paraneoplastic syndromes associated with peritoneal mesothelioma are thrombocytosis, hypoglycemia, hypoalbuminemia, venous thrombosis, paraneoplastic hepatopathy, and a wasting syndrome. Abdominal radiography may show features of abdominal distension. Ultrasonography demonstrates ascites, the amount depending on the pattern of presentation ( 3 ). It may present as small masses that may have either a sheetlike appearance or be irregularly shaped. The small nodules progress to form confluent plaque-like masses, resulting in “omental caking”. Peritoneal mesotheliomas can appear three different ways on CT: • Dry painful type: A large peritoneal mass or multiple, diffuse, small peritoneal nodules with little or no ascites. • Wet type: Ascites with or without multiple small nodules or plaques. • Mixed type: Combination of the dry and wet types. Dry painful type: A large peritoneal mass or multiple, diffuse, small peritoneal nodules with little or no ascites. Wet type: Ascites with or without multiple small nodules or plaques. Mixed type: Combination of the dry and wet types. CT also demonstrates thickening of the peritoneum, mesenteric infiltration, and omental caking. Mesenteric infiltration produces the characteristic stellate and fixed appearance. Calcification is rare. Scalloping of the adjacent viscera, especially the liver and colon due to mass effect, can be observed. About half of these patients show evidence of pleural plaques, pleural calcification, and parenchymal lung disease. MRI aids in planning of radiotherapy for localized disease and in assessment of the tumor extent and invasion. Positron-emission tomography (PET) can assess the likelihood of a tumor, and its extent and invasion. It also helps in staging the disease by identifying the tumor at other sites. A combination of cytoreductive surgery, intraperitoneal chemotherapy, and radiotherapy is reported to have a better prognosis and to increase the survival rate of patients with mesothelioma. Palliative chemotherapy is offered in inoperable cases. Younger age (under 60 years), female gender, epithelioid subtype of mesothelioma, combination of cytoreductive surgery, chemotherapy and radiotherapy, and absence of tumor invasion to the deeper structures are associated with better prognosis ( 4 ). Peritoneal carcinomatosis, lymphoma, pseudomyxoma peritonei, and tuberculous peritonitis commonly simulate malignant peritoneal mesothelioma ( 5 ). Other, less common differential diagnoses include retractile mesenteritis, intraperitoneal endometriosis, desmoid tumor, carcinoid tumor, and atypical mesothelial hyperplasia.

Introduction

Malignant peritoneal mesothelioma is a rare but aggressive neoplasm arising from the mesothelial lining of the peritoneum. It can occur in the mesothelial cells of the pleura, peritoneum, pericardium, and tunica vaginalis of the testis ( 1 ).

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: pmc-nxml

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.

Source provenance

europepmc
last seen: 2026-07-26T06:08:39.051465+00:00
unpaywall
last seen: 2026-05-21T02:00:01.467718+00:00
License: CC-BY-NC-ND-4.0