A Case of Pulmonary Lymphangioleiomyomatosjs Associated with Thberous Sclerosis and Renal Angiomyolipoma / 결핵
Tuberculosis and Respiratory Diseases
;
: 1184-1193, 1997.
Artigo
em Coreano
| WPRIM
| ID: wpr-158856
ABSTRACT
Lymphangioleiomyomatosis(LAM) is rare and essentially limited to women in the reproductive ages. A 39-year-old female was admitted due to progressive exerUional dyspnea and intermittent productive cough. Chest PA showed marked hyperinflation of the lung associated with a diffuse reticulo-nodular pattern. High resolution CT scan of the thorax demonstrated that diffusely scattered thin-walled cysts were distributed throughout the bilateral lung fields. Abdominal CT scan showed variable sized multiple angiomyolipoma of both kidney. By open lung biopsy, she was diagnosed as pulmonary LAM associated with Tuberous sclerosis and renal Angiomyolipoma. We present the case and discuss the connection between pulmonary LAM and Tuberous sclerosis.
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DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Esclerose
/
Tórax
/
Esclerose Tuberosa
/
Biópsia
/
Tomografia Computadorizada por Raios X
/
Angiomiolipoma
/
Tosse
/
Dispneia
/
Rim
/
Pulmão
Limite:
Adulto
/
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Tuberculosis and Respiratory Diseases
Ano de publicação:
1997
Tipo de documento:
Artigo
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