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[淋巴管平滑肌瘤病(LAM)——双侧自发性气胸的罕见病因]

[Lymphangioleiomyomatosis (LAM)--an uncommon cause of bilateral spontaneous pneumothorax].

作者信息

Grigorescu Cristina, Bosânceanu M, Boişteanu Daniela, Aldea A, Chiseliţă Irina, Cozma Laurette Graziella

机构信息

Clinica de Chirurgie Toracică, Facultatea de Medicină, Universitatea de Medicină si Farmacie "Gr. T. Popa", Iaşi.

出版信息

Rev Med Chir Soc Med Nat Iasi. 2007 Jan-Mar;111(1):125-8.

Abstract

LAM, a rare lung disease typically affecting women of reproductive age, is characterized by abnormal proliferation of smooth--muscle cells and progressive loss of pulmonary function due to destruction of lung parenchyma. Two cases of bilateral successive recurrent spontaneous pneumothorax and haemoptysis are presented. Repeated conventional and video-assisted surgery was required in both cases, for drainage of the recurrent pneumothorax and resection of subpleural bulla, with good immediate postoperative evolution. Immunohistochemical studies of resected specimens revealed LAM cells in the lung parenchyma with receptors for oestrogen and progesterone. HMB45 monoclonal antibodies in the LAM cells were identified in one case. The follow-up of the patients revealed no signs of recurrence at 84 and 18 months respectively, although pulmonary transplantation should be considered in case of further deterioration of respiratory function.

摘要

淋巴管平滑肌瘤病(LAM)是一种罕见的肺部疾病,通常影响育龄女性,其特征是平滑肌细胞异常增殖,并因肺实质破坏导致肺功能进行性丧失。本文报告两例双侧相继复发性自发性气胸和咯血的病例。两例均需要反复进行传统手术和电视辅助手术,以引流复发性气胸和切除胸膜下肺大疱,术后即刻恢复良好。对切除标本进行免疫组织化学研究,结果显示肺实质中有LAM细胞,这些细胞具有雌激素和孕激素受体。在其中一例中,LAM细胞中鉴定出HMB45单克隆抗体。对患者的随访显示,分别在84个月和18个月时未发现复发迹象,不过如果呼吸功能进一步恶化,应考虑进行肺移植。

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