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Pulmonary lymphangioleiomyomatosis in a male.

Pulmonary lymphangioleiomyomatosis has been observed almost exclusively in women, usually in their reproductive years. Exacerbations with pregnancy and after hormonal manipulation have been documented, and it has been suggested that its pathogenesis is due to the influence of hormonal(estrogenic) st...

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Detalles Bibliográficos
Autores principales: Kang, H. W., Kim, C. J., Kang, S. K., Lee, K. S., Lee, C. S., Kim, Y. H.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1991
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049679/
https://www.ncbi.nlm.nih.gov/pubmed/1888454
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author Kang, H. W.
Kim, C. J.
Kang, S. K.
Lee, K. S.
Lee, C. S.
Kim, Y. H.
author_facet Kang, H. W.
Kim, C. J.
Kang, S. K.
Lee, K. S.
Lee, C. S.
Kim, Y. H.
author_sort Kang, H. W.
collection PubMed
description Pulmonary lymphangioleiomyomatosis has been observed almost exclusively in women, usually in their reproductive years. Exacerbations with pregnancy and after hormonal manipulation have been documented, and it has been suggested that its pathogenesis is due to the influence of hormonal(estrogenic) stimulus. The clinical, roentgenographic, and histopathologic features of this case of pulmonary lymphangioleiomyomatosis in a 22-year-old male are all characteristic of those described in prior reports, except for the patient's sex. With the following case of pulmonary lymphangioleiomyomatosis in a male, we suggest the possibility of the existence of an additional pathogenetic mechanism.
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spelling pubmed-30496792011-03-09 Pulmonary lymphangioleiomyomatosis in a male. Kang, H. W. Kim, C. J. Kang, S. K. Lee, K. S. Lee, C. S. Kim, Y. H. J Korean Med Sci Research Article Pulmonary lymphangioleiomyomatosis has been observed almost exclusively in women, usually in their reproductive years. Exacerbations with pregnancy and after hormonal manipulation have been documented, and it has been suggested that its pathogenesis is due to the influence of hormonal(estrogenic) stimulus. The clinical, roentgenographic, and histopathologic features of this case of pulmonary lymphangioleiomyomatosis in a 22-year-old male are all characteristic of those described in prior reports, except for the patient's sex. With the following case of pulmonary lymphangioleiomyomatosis in a male, we suggest the possibility of the existence of an additional pathogenetic mechanism. Korean Academy of Medical Sciences 1991-03 /pmc/articles/PMC3049679/ /pubmed/1888454 Text en
spellingShingle Research Article
Kang, H. W.
Kim, C. J.
Kang, S. K.
Lee, K. S.
Lee, C. S.
Kim, Y. H.
Pulmonary lymphangioleiomyomatosis in a male.
title Pulmonary lymphangioleiomyomatosis in a male.
title_full Pulmonary lymphangioleiomyomatosis in a male.
title_fullStr Pulmonary lymphangioleiomyomatosis in a male.
title_full_unstemmed Pulmonary lymphangioleiomyomatosis in a male.
title_short Pulmonary lymphangioleiomyomatosis in a male.
title_sort pulmonary lymphangioleiomyomatosis in a male.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049679/
https://www.ncbi.nlm.nih.gov/pubmed/1888454
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