特发性骨髓纤维化患者对胸膜减压和羟基脲反应的继发于髓外造血的胸腔积液。

S N Jowitt, D K Burke, H M Leggat, P S Lewis, R J Cryer
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引用次数: 17

摘要

特发性骨髓纤维化的情况下,表现为继发髓外造血的胸腔积液被描述。在诊断出骨髓增生性疾病大约2年后,患者出现呼吸困难。体征符合胸膜积液,放射学证实。渗出液细胞学显示髓系前体,包括巨核细胞。积液需要反复引流,并进行胸膜清扫,以防止积液重新积聚。手术很成功,5个月的随访表明,该侧胸腔没有再发生胸腔积液。后来另一侧发生积液,但经引流保守处理。在这个阶段引入了羟基脲,但不久之后患者死于一个无关的原因。我们回顾了这种罕见的骨髓纤维化并发症的文献,并讨论了治疗这种疾病的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pleural effusion secondary to extramedullary haemopoiesis in a patient with idiopathic myelofibrosis responding to pleurodesis and hydroxyurea.

A case of idiopathic myelofibrosis presenting with a pleural effusion secondary to extramedullary haemopoeisis is described. Approximately 2 years following the diagnosis of his myeloprolioferative disorder the patient presented with dyspnoea. Physical signs were consistent with a pleural effusion which was confirmed radiologically. Cytology of the effusion fluid demonstrated myeloid precursors, including megakaryocytes. The effusion required repeated draining and a pleurodesis was undertaken in an attempt to prevent reaccumulation of the fluid. The procedure was successful and follow up over a period of 5 months demonstrated no recurrence of the pleural effusion on that side of the chest. An effusion later occurred on the other side but was managed conservatively by drainage. Hydroxyurea was introduced at that stage, but shortly afterwards the patient died from an unrelated cause. We review the literature on this uncommon complication of myelofibrosis and discuss the options available to treat the disorder.

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