Title of article
Sporadic Lymphangioleiomyomatosis Disease: A Case Report
Author/Authors
Nikmanesh ، Yousef Gastroenterohepatology Research Center - Shiraz University of Medical Sciences , Shokripour ، Mansoureh Department of Pathology - School of Medicine - Shiraz University of Medical Sciences , Mokhtari ، Maral Department of Pathology - School of Medicine - Shiraz University of Medical Sciences , Khazayi ، Mahdi Department of Internal Medicine - School of Medicine - Bushehr University of Medical Sciences , Monabati ، Ahmad Department of Pathology - School of Medicine - Shiraz University of Medical Sciences , Rezayi ، Ramin Department of Internal Medicine - School of Medicine - Bushehr University of Medical Sciences , Bahtouee ، Mehrzad Department of Internal Medicine - School of Medicine - Bushehr University of Medical Sciences
From page
516
To page
521
Abstract
Pulmonary Lymphangioleiomyomatosis (LAM) is a rare disease of the lung and lymphatic system that primarily affects women of childbearing age. LAM is a progressive disease with a terrible prognosis, which worsens over time and is extremely difficult to treat. In this study, we discuss the case of a 31-year-old woman with LAM who was initially misdiagnosed with leiomyoma and the way that led to a true diagnosis and effective treatment. Following a precise diagnosis based on comprehensive clinical data and particular immunohistochemical tests, sirolimus treatment was initiated, and the patient entirely responded to the treatment. This case report demonstrated that LAM is an uncommon condition that is challenging to diagnose, which causes its treatment to be delayed.
Keywords
Lymphangioleiomyomatosis , Lung , Rare diseases , Pneumothorax
Journal title
Iranian Journal of Medical Sciences (IJMS)
Journal title
Iranian Journal of Medical Sciences (IJMS)
Record number
2751710
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