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Bilateral pleural effusion as an initial manifestation of multiple myeloma: A case report and literature review

机译:双侧胸腔积液为多发性骨髓瘤的初步表现:一例病例报告并文献复习

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摘要

Multiple myeloma (MM) is a rare type of malignant hematological neoplasm. Although primarily involving the bone marrow, MM has a significant risk of metastasizing to other organs and may present with various clinical symptoms. However, the involvement of the respiratory system in the course of MM is extremely uncommon, particularly presenting with bilateral pleural effusion as the sole initial manifestation, which may result in a delayed diagnosis of MM. The present study describes the extremely rare case of a patient with MM presenting with myelomatous pleural effusion (MPE). The 78-year-old patient was admitted to the Department of Respiratory Medicine, Taizhou People’s Hospital (Taizhou, China) in March 2014, complaining of persistent dyspnea. Following admission, chest computed tomography scans revealed bilateral pleural effusion and a small amount of pericardial effusion, but no evident mass lesion. Thoracentesis was performed and the resulting pleural effusion was exudative and slightly bloody. In the following cytological examination, myeloma cells were identified in the pleural effusion. The patient was diagnosed definitively with MM following a histopathological study of the bone marrow aspiration. Therefore, the observations of the present case report may promote the consideration of MM in the differential diagnosis of patients with unexplained and refractory pleural effusion. The present study also reviewed the literature with regard to the association between MM and pleural effusion.
机译:多发性骨髓瘤(MM)是一种罕见的恶性血液肿瘤。尽管主要累及骨髓,但MM有转移至其他器官的巨大风险,并可能表现出各种临床症状。然而,在MM的过程中呼吸系统受累极少见,特别是表现为双侧胸腔积液为唯一的最初表现,这可能导致MM的诊断延迟。本研究描述了伴有骨髓瘤性胸腔积液(MPE)的MM患者的极少数情况。这位78岁的患者因持续性呼吸困难,于2014年3月被泰州人民医院呼吸内科收治。入院后,胸部CT检查显示双侧胸腔积液和少量心包积液,但未见明显肿块病变。进行胸腔穿刺术,导致的胸腔积液渗出且略带血。在随后的细胞学检查中,在胸腔积液中发现了骨髓瘤细胞。经过对骨髓抽吸的组织病理学研究,该患者被明确诊断为MM。因此,本病例报告的观察结果可能会促进在原因不明和难治性胸腔积液患者的鉴别诊断中考虑MM。本研究还回顾了有关MM与胸腔积液之间关系的文献。

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