肺lymphangiomyomatosis。报告1例免疫组织化学及超微结构表现。

Applied pathology Pub Date : 1989-01-01
E Schiaffino, E Tavani, L Dellafiore, C Schmid
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引用次数: 0

摘要

肺淋巴管肌瘤病是一种罕见的疾病,其特征是淋巴管和血管周围、小气道和间质中平滑肌细胞的广泛增生。受影响的几乎只有处于生育状态的年轻妇女。自发性复发性气胸是最重要的症状。乳糜积液占37.5%。我们的观察对象是一位43岁的女性。描述了光镜和电子显微镜的发现。平滑肌细胞上检测到雌激素受体。双侧卵巢切除及黄体酮治疗均成功。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulmonary lymphangiomyomatosis. Report of a case with immunohistochemical and ultrastructural findings.

Pulmonary lymphangiomyomatosis is a rare disease characterized by wide-spread proliferation of smooth muscle cells around lymphatic and blood vessels, smaller airways and in the interstitium. Young women in the fertile status are almost exclusively affected. Spontaneous recurrent pneumothorax is the most important symptom. Chylous effusions are reported in 37.5% of cases. Our observation deals with a woman aged 43. Light- and electron-microscopic findings are described. Estrogen receptors have been detected on smooth muscle cells. Bilateral oophorectomy and treatment with progesterone were successful.

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