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Ovarian sex cord tumor with annular tubules in a patient with Turner syndrome.

A case of ovarian sex cord tumor with annular tubules (SCTAT) in a 24-year old woman with Turner syndrome is presented. Close association of dysgenetic gonads and gonadoblastoma has been clearly documented, and there have been sporadic reports of patients with other gonadal tumors. To our knowledge,...

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Detalles Bibliográficos
Autores principales: Moon, W. S., Lee, D. G.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054339/
https://www.ncbi.nlm.nih.gov/pubmed/9539327
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author Moon, W. S.
Lee, D. G.
author_facet Moon, W. S.
Lee, D. G.
author_sort Moon, W. S.
collection PubMed
description A case of ovarian sex cord tumor with annular tubules (SCTAT) in a 24-year old woman with Turner syndrome is presented. Close association of dysgenetic gonads and gonadoblastoma has been clearly documented, and there have been sporadic reports of patients with other gonadal tumors. To our knowledge, a case of SCTAT in a patient with 45,X/46,XX Turner syndrome has not been reported. On the basis of histopathologic, immunohistochemical, and ultrastructural findings, we suggest that the SCTAT originated from pluripotential stem cells of the gonads and differentiated into either granulosa cells or Sertoli cells. We postulate a possible relationship between the SCTAT and gonadoblastoma based on the morphologic resemblance and occurrence in dysgenetic gonads.
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spelling pubmed-30543392011-03-15 Ovarian sex cord tumor with annular tubules in a patient with Turner syndrome. Moon, W. S. Lee, D. G. J Korean Med Sci Research Article A case of ovarian sex cord tumor with annular tubules (SCTAT) in a 24-year old woman with Turner syndrome is presented. Close association of dysgenetic gonads and gonadoblastoma has been clearly documented, and there have been sporadic reports of patients with other gonadal tumors. To our knowledge, a case of SCTAT in a patient with 45,X/46,XX Turner syndrome has not been reported. On the basis of histopathologic, immunohistochemical, and ultrastructural findings, we suggest that the SCTAT originated from pluripotential stem cells of the gonads and differentiated into either granulosa cells or Sertoli cells. We postulate a possible relationship between the SCTAT and gonadoblastoma based on the morphologic resemblance and occurrence in dysgenetic gonads. Korean Academy of Medical Sciences 1998-02 /pmc/articles/PMC3054339/ /pubmed/9539327 Text en
spellingShingle Research Article
Moon, W. S.
Lee, D. G.
Ovarian sex cord tumor with annular tubules in a patient with Turner syndrome.
title Ovarian sex cord tumor with annular tubules in a patient with Turner syndrome.
title_full Ovarian sex cord tumor with annular tubules in a patient with Turner syndrome.
title_fullStr Ovarian sex cord tumor with annular tubules in a patient with Turner syndrome.
title_full_unstemmed Ovarian sex cord tumor with annular tubules in a patient with Turner syndrome.
title_short Ovarian sex cord tumor with annular tubules in a patient with Turner syndrome.
title_sort ovarian sex cord tumor with annular tubules in a patient with turner syndrome.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054339/
https://www.ncbi.nlm.nih.gov/pubmed/9539327
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