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Plexogenic pulmonary hypertension associated with POEMS syndrome

机译:致血管性肺动脉高压合并POEMS综合征

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摘要

Pulmonary hypertension is one of the well-known clinical manifestations of polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome, occurring in approximately 25–30% of the affected individuals. However, the histopathologic spectrum of pulmonary hypertension associated with POEMS syndrome has not been fully documented in the literature. Herein, we report an autopsy case of POEMS syndrome in a patient whose lung tissues showed histopathology indistinguishable from that of idiopathic pulmonary arterial hypertension with abundant plexiform lesions in the small pulmonary arteries.
机译:肺动脉高压是多发性神经病,器质性肿大,内分泌病,单克隆丙种球蛋白病和皮肤变化(POEMS)综合征的著名临床表现之一,约有25%至30%的患病个体发生。但是,与POEMS综合征相关的肺动脉高压的组织病理学光谱尚未在文献中得到充分记录。在本文中,我们报告了一名患者的POEMS综合征的尸检病例,该患者的肺组织显示出的组织病理学与特发性肺动脉高压的组织病理学难以区分,在小肺动脉中有丰富的丛状病变。

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