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Tuberous sclerosis and polycystic kidney disease. A case report.

Polycystic kidney disease is a relatively uncommon finding of tuberous sclerosis. Furthermore, the renal insufficiency by the severe polycystic kidney disease is extremely rare in tuberous sclerosis. The patient was a 27-year-old man, complaining of generalized seizure and progressive abdominal dist...

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Detalles Bibliográficos
Autores principales: Choi, K. C., Kim, S. W., Kim, N. H., Kang, Y. J.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054259/
https://www.ncbi.nlm.nih.gov/pubmed/9008103
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author Choi, K. C.
Kim, S. W.
Kim, N. H.
Kang, Y. J.
author_facet Choi, K. C.
Kim, S. W.
Kim, N. H.
Kang, Y. J.
author_sort Choi, K. C.
collection PubMed
description Polycystic kidney disease is a relatively uncommon finding of tuberous sclerosis. Furthermore, the renal insufficiency by the severe polycystic kidney disease is extremely rare in tuberous sclerosis. The patient was a 27-year-old man, complaining of generalized seizure and progressive abdominal distension. His clinical features were chracterized by epilepsy, mental retardation, skin abnormalities including adenoma sebaceum, shagreen patch and ash-leaf spots. Abdominal computed tomography demonstrated numerous variable sized cysts throughout both kidneys. Clinical and laboratory findings revealed chronic renal failure due to severe polycystic kidneys. On reviewing the literature, the present case is the first report of polycystic kidneys associated with tuberous sclerosis in Korea.
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spelling pubmed-30542592011-03-15 Tuberous sclerosis and polycystic kidney disease. A case report. Choi, K. C. Kim, S. W. Kim, N. H. Kang, Y. J. J Korean Med Sci Research Article Polycystic kidney disease is a relatively uncommon finding of tuberous sclerosis. Furthermore, the renal insufficiency by the severe polycystic kidney disease is extremely rare in tuberous sclerosis. The patient was a 27-year-old man, complaining of generalized seizure and progressive abdominal distension. His clinical features were chracterized by epilepsy, mental retardation, skin abnormalities including adenoma sebaceum, shagreen patch and ash-leaf spots. Abdominal computed tomography demonstrated numerous variable sized cysts throughout both kidneys. Clinical and laboratory findings revealed chronic renal failure due to severe polycystic kidneys. On reviewing the literature, the present case is the first report of polycystic kidneys associated with tuberous sclerosis in Korea. Korean Academy of Medical Sciences 1996-12 /pmc/articles/PMC3054259/ /pubmed/9008103 Text en
spellingShingle Research Article
Choi, K. C.
Kim, S. W.
Kim, N. H.
Kang, Y. J.
Tuberous sclerosis and polycystic kidney disease. A case report.
title Tuberous sclerosis and polycystic kidney disease. A case report.
title_full Tuberous sclerosis and polycystic kidney disease. A case report.
title_fullStr Tuberous sclerosis and polycystic kidney disease. A case report.
title_full_unstemmed Tuberous sclerosis and polycystic kidney disease. A case report.
title_short Tuberous sclerosis and polycystic kidney disease. A case report.
title_sort tuberous sclerosis and polycystic kidney disease. a case report.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054259/
https://www.ncbi.nlm.nih.gov/pubmed/9008103
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