Primary Malignant Deciduoid Mesothelioma: A Challenging Diagnosis

Primary malignant deciduoid mesothelioma is a rare subtype of epithelioid mesothelioma that was first described in the peritoneum in young women without a history of asbestos exposure. It was thought to be a distinct clinicopathologic entity with ominous prognosis; recent studies have better charact...

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Veröffentlicht in:Archives of pathology & laboratory medicine (1976) 2019-04, Vol.143 (4), p.531-533
Hauptverfasser: Regragui, Meriem, Guebessi, Nisrine Bennani
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Guebessi, Nisrine Bennani
description Primary malignant deciduoid mesothelioma is a rare subtype of epithelioid mesothelioma that was first described in the peritoneum in young women without a history of asbestos exposure. It was thought to be a distinct clinicopathologic entity with ominous prognosis; recent studies have better characterized this entity. On morphology, primary malignant deciduoid mesothelioma is characterized by cytomorphologic features resembling decidualized tissue. Pleomorphism is variable. The immunoprofile is similar to other epithelioid mesotheliomas. The prognosis is the same as other epithelioid mesotheliomas and seems to depend on histological grade.
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subjects Abdomen
Anaplastic large-cell lymphoma
Antigens
Asbestos
Carcinoembryonic antigen
CD30 antigen
CD45 antigen
Clear cell-type renal cell carcinoma
Cytokeratin
Cytoplasm
Decidua - pathology
Diagnosis
Electron microscopy
Female
Humans
Kidney cancer
Leukocytes (eosinophilic)
Lung Neoplasms - pathology
Lymphoma
Medical diagnosis
Medical prognosis
Melanoma
Mesothelioma
Mesothelioma - pathology
Mesothelioma, Malignant
Metastases
Metastasis
Microscopy
Morphology
Non-Hodgkin's lymphoma
Nucleoli
Pemetrexed
Peritoneal Neoplasms - pathology
Peritoneum
Pregnancy
Protein-tyrosine kinase
Rhabdomyosarcoma
Thyroid transcription factor 1
Tumors
Womens health
Young women
title Primary Malignant Deciduoid Mesothelioma: A Challenging Diagnosis
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