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Primary systemic amyloidosis and persistent pleural effusions.

机译:原发性系统性淀粉样变性和持续性胸腔积液。

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摘要

Persistent pleural effusions are not common in patients with primary systemic amyloidosis (AL). A recent review of this complication of the disease hypothesized that the pathophysiology of these effusions is pleural amyloid deposition, disrupting lymphatic drainage. We report the case of a 73-year-old woman with primary systemic AL and persistent bilateral pleural effusions, refractory to diuresis and repeated thoracenteses. The patient's cardiac and renal dysfunction was not severe enough to explain these persistent effusions. Thus, despite a lack of biopsy-proven amyloid deposition, we suggest that these effusions may be secondary to pleural amyloid deposition.
机译:持续性胸腔积液在原发性系统性淀粉样变性(AL)患者中并不常见。最近对该病并发症的回顾认为,这些积液的病理生理是胸膜淀粉样蛋白沉积,破坏了淋巴引流。我们报道一例73岁女性,原发性全身性AL和持续性双侧胸腔积液,利尿难治,反复胸腔穿刺。患者的心脏和肾功能不全不足以解释这些持续的积液。因此,尽管缺乏经活检证实的淀粉样蛋白沉积,我们建议这些积液可能继发于胸膜淀粉样蛋白沉积。

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