Pulmonary Lymphangioleiomyomatosis: A Case Report
摘要
Lymphangioleiomyomatosis (LAM) is a progressive disease occuring exclusively in women of child-bearing age. It is a rare disease, possessing distinctive clinical, pathological and radiological findings. A case is reported of surgically- proved lymphangioleiomyomatosis in a 29-year-old woman with recurrent pneumothorax. Chest plain film showed bilateral reticular and honeycomb patterns with a normal lung volume. High resolution computed tomography (HRCT) revealed characteristic diffuse cystic changes of the lungs. Recognition of this characteristic radiological feature is helpful in suggesting the diagnosis of LAM.
引用本文（GB/T 7714）
Pao-Sheng Yen, Yung‐Liang Wan, Shu‐Hang Ng, 等. Pulmonary Lymphangioleiomyomatosis: A Case Report[J]. 未知来源, 1995.
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