PULMONARY LYMPHANGIOLEIOMYOMATOSIS: A RARE CAUSE OF CYSTIC LUNG DISEASE - A CASE REPORT
- Department of Respiratory Diseases, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University, Oujda, Morocco.
- Research and Medical Sciences Laboratory, Faculty of Medicine and Pharmacy of Oujda, Mohammed First University, Oujda, Morocco.
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Lymphangioleomyomatosis in sporadic form is a rare and progressive lung disease that primarily affects women, especially during the reproductive phase. We report a case of a 66-year-old patient who consulted for exertional dyspnea. The thoracoabdominopelvic CT scan revealed several pulmonary cystic lesions and renal angiomyolipomas, allowing the diagnosis of lymphangioleimyomatosis. The diagnosis of lymphangioleimyomatosis should be considered in young women presenting with spontaneous pneumothorax, unexplained dyspnea, or angiomyolipoma. While a definitive diagnosis can be confirmed through a lung biopsy, current guidelines allow for non-invasive methods based on characteristic imaging findings and clinical features.
[Ouiame Nabou, Oumayma Haloui, Meriem Rhazari, Afaf Thouil and Hatim Kouismi (2025); PULMONARY LYMPHANGIOLEIOMYOMATOSIS: A RARE CAUSE OF CYSTIC LUNG DISEASE - A CASE REPORT Int. J. of Adv. Res. (Jun). 465-470] (ISSN 2320-5407). www.journalijar.com
Department of Respiratory Diseases, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy of Oujda, Mohammed first University, Oujda, Morocco
Morocco