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结节性硬化症中的肺淋巴管平滑肌瘤病。病例报告。

Pulmonary lymphangioleiomyomatosis in tuberous sclerosis. A case report.

作者信息

De Rosa N

机构信息

U.O.C. di Anatomia Patologica, A.O.R.N. Monaldi, Naples, Italy.

出版信息

Pathologica. 2009 Oct;101(5):186-9.

Abstract

Pulmonary lymphangioleiomyomatosis (PLAM) is a rare disease that exclusively affects young women of reproductive age. It is characterized by widespread pulmonary proliferation of abnormal, "immature smooth muscle cells (lam cells) leading to cystic destruction of the lung parenchyma. Lam occurs frequently in the thoracic duct and in axial lymph nodes, mediastinal or retroperitoneal. It can occur either in association with tuberous sclerosis complex (TSC-LAM) or without TSC (sporadic LAM). A case of TSC-LAM is reported, and the histogenesis and the role of lymphangiogenesis in the progression of disease is discussed.

摘要

肺淋巴管平滑肌瘤病(PLAM)是一种罕见疾病,仅影响育龄期年轻女性。其特征是肺部广泛出现异常的“未成熟平滑肌细胞(LAM细胞)”增殖,导致肺实质的囊性破坏。LAM常见于胸导管以及纵隔或腹膜后的轴向淋巴结。它可与结节性硬化症(TSC-LAM)相关联出现,也可无TSC(散发性LAM)单独出现。本文报告了一例TSC-LAM病例,并讨论了疾病进展中的组织发生及淋巴管生成的作用。

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