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A Case of Pulmonary Lymphangioleiomyomatosis Associated with Tuberous Sclerosis and Renal Angiomyolipoma / 대한내과학회지
Korean Journal of Medicine ; : 775-779, 2011.
Article in Korean | WPRIM | ID: wpr-143830
ABSTRACT
Tuberous sclerosis is an autosomal dominant disorder characterized by facial skin lesions, epilepsy, and mental retardation. Pulmonary involvement in tuberous sclerosis is rare and shows characteristic reticulonodular infiltration and cystic changes. Lymphangioleiomyomatosis is characterized by the progressive proliferation of smooth muscle cells and occurs in 0.1-1% of patients with tuberous sclerosis. We encountered a case of pulmonary lymphangioleiomyomatosis associated with tuberous sclerosis and bilateral renal angiomyolipoma in a 31-year-old female patient. This case is reported here along with a brief review of the literature.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Tuberous Sclerosis / Lymphangioleiomyomatosis / Angiomyolipoma / Myocytes, Smooth Muscle / Epilepsy / Intellectual Disability Limits: Adult / Female / Humans Language: Korean Journal: Korean Journal of Medicine Year: 2011 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Skin / Tuberous Sclerosis / Lymphangioleiomyomatosis / Angiomyolipoma / Myocytes, Smooth Muscle / Epilepsy / Intellectual Disability Limits: Adult / Female / Humans Language: Korean Journal: Korean Journal of Medicine Year: 2011 Type: Article