Czeczok Thomas, Lin Peter, Yi Eunhee
Mayo Clinic, Rochester MN, United States.
Respir Med Case Rep. 2017 Aug 12;22:168-170. doi: 10.1016/j.rmcr.2017.08.011. eCollection 2017.
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.
肺动脉高压是多神经病、器官肿大、内分泌病、单克隆丙种球蛋白病和皮肤改变(POEMS)综合征的常见临床表现之一,约25%-30%的患者会出现。然而,与POEMS综合征相关的肺动脉高压的组织病理学谱在文献中尚未得到充分记载。在此,我们报告一例POEMS综合征尸检病例,该患者肺组织的组织病理学表现与特发性肺动脉高压难以区分,小肺动脉出现大量丛状病变。