Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report

Lymphangioleiomyomatosis is a rare disorder of unknown origin that usually presents pulmonary symptoms. Retroperitoneal lymphangioleiomyomatosis without lung involvement has rarely been reported. We present a 38-year-old woman, the fourth case reported of retroperitoneal lymphangioleiomyomatosis wit...

Descripción completa

Detalles Bibliográficos
Autores principales: Herce, José Manuel Lorente, Luque, Virgilio Ruiz, Luque, José Aguilar, García, Pablo Martínez, Gómez, Daniel Díaz
Formato: Texto
Lenguaje:English
Publicado: Cases Network Ltd 2009
Materias:
Case report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2769287/
https://www.ncbi.nlm.nih.gov/pubmed/19918577
http://dx.doi.org/10.4076/1757-1626-2-6331
_version_ 1782173562794147840
author Herce, José Manuel Lorente
Luque, Virgilio Ruiz
Luque, José Aguilar
García, Pablo Martínez
Gómez, Daniel Díaz
author_facet Herce, José Manuel Lorente
Luque, Virgilio Ruiz
Luque, José Aguilar
García, Pablo Martínez
Gómez, Daniel Díaz
author_sort Herce, José Manuel Lorente
collection PubMed
description Lymphangioleiomyomatosis is a rare disorder of unknown origin that usually presents pulmonary symptoms. Retroperitoneal lymphangioleiomyomatosis without lung involvement has rarely been reported. We present a 38-year-old woman, the fourth case reported of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis in the literature.
format Text
id pubmed-2769287
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Cases Network Ltd
record_format MEDLINE/PubMed
spelling pubmed-27692872009-11-16 Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report Herce, José Manuel Lorente Luque, Virgilio Ruiz Luque, José Aguilar García, Pablo Martínez Gómez, Daniel Díaz Cases J Case report Lymphangioleiomyomatosis is a rare disorder of unknown origin that usually presents pulmonary symptoms. Retroperitoneal lymphangioleiomyomatosis without lung involvement has rarely been reported. We present a 38-year-old woman, the fourth case reported of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis in the literature. Cases Network Ltd 2009-08-07 /pmc/articles/PMC2769287/ /pubmed/19918577 http://dx.doi.org/10.4076/1757-1626-2-6331 Text en © 2009 Herce et al.; licensee Cases Network Ltd. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case report
Herce, José Manuel Lorente
Luque, Virgilio Ruiz
Luque, José Aguilar
García, Pablo Martínez
Gómez, Daniel Díaz
Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report
title Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report
title_full Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report
title_fullStr Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report
title_full_unstemmed Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report
title_short Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report
title_sort association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2769287/
https://www.ncbi.nlm.nih.gov/pubmed/19918577
http://dx.doi.org/10.4076/1757-1626-2-6331
work_keys_str_mv AT hercejosemanuellorente associationofretroperitoneallymphangioleiomyomatosiswithendosalpingiosisacasereport
AT luquevirgilioruiz associationofretroperitoneallymphangioleiomyomatosiswithendosalpingiosisacasereport
AT luquejoseaguilar associationofretroperitoneallymphangioleiomyomatosiswithendosalpingiosisacasereport
AT garciapablomartinez associationofretroperitoneallymphangioleiomyomatosiswithendosalpingiosisacasereport
AT gomezdanieldiaz associationofretroperitoneallymphangioleiomyomatosiswithendosalpingiosisacasereport

Ejemplares similares