LYMPHANGIOLEIOMYOMATOSIS - PHYSIOLOGIC-PATHOLOGIC-RADIOLOGIC CORRELATIONS
- 1 January 1977
- journal article
- research article
- Published by Elsevier
- Vol. 116 (6), 977-995
- https://doi.org/10.1164/arrd.1977.116.6.977
Abstract
Lymphangioleiomyomatosis (LAM) is a rare disease of women of child-bearing age in which there is hyperplasia of atypical smooth muscle along lymphatics in the lung, thorax and abdomen. Among 6 patients, 2 had recurrent pneumothorax, lymphangioleiomyomatosis being discovered during parietal pleurectomy. The other 4 underwent biopsy because of progressive dyspnea. Subsequent manifestations included 25 pneumothoraces in 4, hemoptysis in 3 and chylothorax and a retroperitoneal hemorrhage in 1 each. Corticosteroid and immunosuppressive therapy were ineffective. Four died after 2-11 yr, and 2 are living 1 and 8 yr later. Although roentgenograms of the chest initially were normal in 4, lung biopsy of 2 showed advanced disease. Eventually all showed a paradoxic picture of an enlarging lung volume with a reticulonodular pattern and cystlike spaces. Physiologic alterations were unique. Spirometrically determined lung volumes were normal or decreased; radiographically and plethysmographically determined total lung capacity were greatly enlarged, suggesting severe air trapping. Obstructive disease was confirmed by mean of forced expiratory flow in the middle half of the forced vital capacity of 24%. In lymphangioleiomyomatosis the mean single-breath diffusing capacity was only 33.2% and the mean total lung capacity, 96.3%; in 229 patients with intestinal disease there was a good correlation between the single-breath diffusing capacity and total lung capacity (r = 0.57, P < 0.01). Histologic findings of uneven obstruction by lymphangioleiomyomatosis of bronchioles, lymphatics and small pulmonary veins explained the unusual radiologic findings. Progressive dyspnea, chylous effusions, repeated pneumothoraces and hemoptysis in women of child-bearing age should suggest lymphangioleiomyomatosis. Airflow obstruction, disproportionately poor gas exchange and radiographically enlarged lung despite increasingly prominent interstitial markings are virtually diagnostic.This publication has 2 references indexed in Scilit:
- Clinical and Physiological Considerations in Pulmonary Muscular HyperplasiaAnnals of Internal Medicine, 1962
- AN ANALYSIS OF FACTORS AFFECTING THE MEASUREMENT OF PULMONARY DIFFUSING CAPACITY BY THE SINGLE BREATH METHOD*Journal of Clinical Investigation, 1961