Pulmonary lymphangiomyomatosis (LAM) developing chylothorax

10Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

We describe a case of pulmonary lymphangiomyomatosis (LAM) with chylothorax that developed in a 46-year-old Japanese woman. This patient exhibited clinical symptoms of dyspnea and chest X-ray showed right pleural effusion. Thoracocentesis demonstrated chylous effusion. Chest computed tomography (CT) scan revealed multiple cystic lesions. Subsequent thoracoscopy revealed the chylorrhea from swelled vessels on the diaphragm. The clinical diagnosis, based on histological examinations with biopsy specimens obtained by thoracoscopy, was pulmonary LAM. Although the hormone therapy was not effective, chylous effusion was improved by the pleurodesis. Pulmonary LAM developing chylothorax is rare in Japan.

Cite

CITATION STYLE

APA

Morimoto, N., Hirasaki, S., Kamei, T., Horiike, A., Miyatake, H., Ogita, Y., & Nakano, H. (2000). Pulmonary lymphangiomyomatosis (LAM) developing chylothorax. Internal Medicine, 39(9), 738–741. https://doi.org/10.2169/internalmedicine.39.738

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free