A Case Report on Plasma Cell Leukemia Presenting as a Chest Wall Mass

N. Zaghba, Z. Benmerzouq, H. Benjelloun, K. Chaanoun, N. Yassine
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Abstract

Plasma cell leukemia (PCL) is an uncommon neoplasm of plasma cells with an aggressive clinical course and a poor outcome, even with the current standard of care. It can occur either de novo (primary PCL) or as a progression of multiple myeloma (MM). This disease has unique diagnostic criteria, but certain genetic markers and clinical features may overlap with multiple myeloma (MM). Due to the low prevalence of PCL, guidelines on its management are extrapolated from the management of MM and are based on small retrospective studies and case reports/series. We report the case of a sixty-nine-year-old man referred to the hematology department for the diagnosis of pPCL, revealed by thoracic plasmacytomas mimicking a thoracic neoplasm. The diagnostic approach, management, and outcomes of PCL are discussed.
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以胸壁肿块为表现的浆细胞白血病病例报告
浆细胞白血病(PCL)是一种不常见的浆细胞肿瘤,临床病程凶险,即使采用目前的标准治疗方法,预后也很差。它既可从新发病(原发性 PCL),也可由多发性骨髓瘤(MM)发展而来。这种疾病有独特的诊断标准,但某些遗传标记和临床特征可能与多发性骨髓瘤(MM)重叠。由于PCL的发病率较低,其治疗指南是根据MM的治疗方法推断出来的,并以小型回顾性研究和病例报告/系列病例为基础。我们报告了一例因胸部浆细胞瘤模仿胸部肿瘤而转诊至血液科诊断为 pPCL 的 69 岁男性病例。文中讨论了 PCL 的诊断方法、管理和结果。
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