Early Detection of Pulmonary Lymphangioleiomyomatosis by Spontaneous Pneumothorax A Case Report
A 31-year-old female was admitted because of dyspnea. A chest X-ray showed pneumothorax. A computed tomography (CT) scan of the chest revealed scattered thin-walled cystic lesions in both lung fields. Pulmonary lymphangioleiomyomatosis (LAM) was confirmed by a thoracoscopic lung biopsy, which reveal...
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Published in | Kita Kantō igaku (The Kitakanto Medical Journal) Vol. 53; no. 3; pp. 303 - 307 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English Japanese |
Published |
The Kitakanto Medical Society
2003
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Subjects | |
Online Access | Get full text |
ISSN | 1343-2826 1881-1191 |
DOI | 10.2974/kmj.53.303 |
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Summary: | A 31-year-old female was admitted because of dyspnea. A chest X-ray showed pneumothorax. A computed tomography (CT) scan of the chest revealed scattered thin-walled cystic lesions in both lung fields. Pulmonary lymphangioleiomyomatosis (LAM) was confirmed by a thoracoscopic lung biopsy, which revealed the nodular proliferation of immature smooth muscle cells that stained positive for HMB-45, desmin, α-smooth muscle actin, progesterone receptor and estrogen receptor when examined using immunostaining techniques. Medroxyprogesterone was prescribed. This report describes the early detection of LAM using chest CT scans and a thoracoscopic lung biopsy in a patient that experienced a spontaneous pneumothorax. |
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ISSN: | 1343-2826 1881-1191 |
DOI: | 10.2974/kmj.53.303 |