| Literature DB >> 30506035 |
Riki Okita1, Yuji Nojima1, Shinsuke Saisho1, Katsuhiko Shimizu1, Ryo Shirai2, Naoki Kanomata3, Mikio Oka2, Masao Nakata1.
Abstract
Here, we report a patient with deciduoid type malignant pleural mesothelioma (MPM), which rapidly progressed. A 55-year-old man who might have been exposed to asbestos a few decades ago had severe back pain. The chest X-ray scanning and computed tomography (CT) revealed pleural thickness on his right thoracic space, without the presence of a lung mass. A pleural biopsy was performed and the patient was histologically diagnosed with deciduoid type MPM. Although he received two cycles of chemotherapy, his disease rapidly progressed and he died within two months of the diagnosis of deciduoid type MPM.Entities:
Keywords: Deciduoid type malignant pleural mesothelioma (MPM); chemotherapy; pleomorphic malignant mesothelioma (pleomorphic MM)
Year: 2018 PMID: 30506035 PMCID: PMC6232047 DOI: 10.21037/acr.2018.09.02
Source DB: PubMed Journal: AME Case Rep ISSN: 2523-1995