Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report

Abstract

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.

DOI: 10.4076/1757-1626-2-6331

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@inproceedings{Herce2009AssociationOR, title={Association of retroperitoneal lymphangioleiomyomatosis with endosalpingiosis: a case report}, author={Jos{\'e} Manuel Lorente Herce and Virgilio Ruiz Luque and Jos{\'e} Aguilar Luque and Pablo Mart{\'i}nez Garc{\'i}a and Daniel D{\'i}az G{\'o}mez}, booktitle={Cases journal}, year={2009} }