Renal angiomyolipoma; polycystic kidney, and renal cell carcinoma in patient with tuberous sclerosis

Charles M. Lynne; Hernan M. Carrion; Kiumuras Bakshandeh; M. Nadji; E. Russel; Victor A. Politano

doi:10.1016/0090-4295(79)90153-5

Renal angiomyolipoma; polycystic kidney, and renal cell carcinoma in patient with tuberous sclerosis

Charles M. Lynne, Hernan M. Carrion, Kiumuras Bakshandeh, M. Nadji, E. Russel, Victor A. Politano

Research output: Contribution to journal › Article › peer-review

31 Scopus citations

Abstract

A patient with tuberous sclerosis presented with renal failure secondary to bilateral angiomyolipoma. The angiomyolipoma was associated with polycystic disease and a foci of renal cell carcinoma. This unusual combination has not been reported previously, although each entity has been described separately in tuberous sclerosis.

Original language	English (US)
Pages (from-to)	174-176
Number of pages	3
Journal	Urology
Volume	14
Issue number	2
DOIs	https://doi.org/10.1016/0090-4295(79)90153-5
State	Published - Aug 1979

ASJC Scopus subject areas

Urology

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title = "Renal angiomyolipoma; polycystic kidney, and renal cell carcinoma in patient with tuberous sclerosis",

abstract = "A patient with tuberous sclerosis presented with renal failure secondary to bilateral angiomyolipoma. The angiomyolipoma was associated with polycystic disease and a foci of renal cell carcinoma. This unusual combination has not been reported previously, although each entity has been described separately in tuberous sclerosis.",

author = "Lynne, {Charles M.} and Carrion, {Hernan M.} and Kiumuras Bakshandeh and M. Nadji and E. Russel and Politano, {Victor A.}",

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AU - Lynne, Charles M.

AU - Carrion, Hernan M.

AU - Bakshandeh, Kiumuras

AU - Nadji, M.

AU - Russel, E.

AU - Politano, Victor A.

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AB - A patient with tuberous sclerosis presented with renal failure secondary to bilateral angiomyolipoma. The angiomyolipoma was associated with polycystic disease and a foci of renal cell carcinoma. This unusual combination has not been reported previously, although each entity has been described separately in tuberous sclerosis.

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