1.
Article
| IMSEAR
| ID: sea-196139
Résumé
Lymphangioleiomyomatosis (LAM) is a rare, genetically determined, progressive interstitial lung disease, which almost exclusively affects women, especially at the childbearing age. The initial symptoms and radiographic changes in a patient with LAM are always associated with the respiratory system. Here, we present a case of mediastinal and abdominal LAM of a 22-year-old male, where LAM cells are negative for human melanoma black-45 ( HMB-45). The report of this uncharacterized LAM case will make a significant contribution to the realization of LAM associated clinical features, diagnostic approaches, and its afterward treatments.
2.
Southeast Asian J Trop Med Public Health
;
1994 Mar; 25(1): 19-24
Article
Dans Anglais
| IMSEAR
| ID: sea-32341