血小板增多症作为一种副肿瘤综合征在形态学双相性转移性恶性腹膜间皮瘤中模仿卵巢腺癌：一例报告。
Thrombocytosis as a paraneoplastic syndrome in metastatic malignant peritoneal mesothelioma of biphasic morphology mimicking ovarian adenocarcinoma: A case report.
作者信息
Alhamadh Moustafa S, Alanazi Rakan B, Wadaan Osama Mohaamad, Alhabeeb Abdulrahman Yousef, Alkaiyat Mohammad, Aljarbou Ohoud Zaid, Sabatin Fouad
机构信息
College of Medicine King Saud bin Abdulaziz University for Health Sciences, Ministry of the National Guard-Health Affairs Riyadh Saudi Arabia.
King Abdullah International Medical Research Center Ministry of the National Guard-Health Affairs Riyadh Saudi Arabia.
出版信息
Clin Case Rep. 2023 Mar 2;11(3):e6974. doi: 10.1002/ccr3.6974. eCollection 2023 Mar.
Malignant peritoneal mesothelioma (MPM) is a rare malignancy, presenting with non-specific and potentially-misleading manifestations. It represents a diagnostic pitfall as it mimics ovarian carcinoma. Maintaining a low diagnostic threshold, obtaining a detailed history, and utilizing immunohistochemical markers to diagnose MPM is crucial as early diagnosis and treatment might improve survival.
恶性腹膜间皮瘤（MPM）是一种罕见的恶性肿瘤，表现为非特异性且可能具有误导性的症状。由于它可模仿卵巢癌，因此是诊断上的一个陷阱。保持较低的诊断阈值、获取详细病史并利用免疫组化标志物来诊断MPM至关重要，因为早期诊断和治疗可能会提高生存率。
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