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Lymphangioleiomyomatosis: an explosive presentation of a rare disease

Lymphangioleiomyomatosis (LAM) is a rare cystic lung disease, commonly affecting women in the reproductive age group. Exacerbation of pre-existing disease is common during pregnancy likely due to the up-regulation of estrogen and progesterone receptors present within the proliferating smooth muscle...

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Autores principales: Pais, Faye, Fayed, Mohamed, Evans, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461433/
https://www.ncbi.nlm.nih.gov/pubmed/28616248
http://dx.doi.org/10.1093/omcr/omx023
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author Pais, Faye
Fayed, Mohamed
Evans, Timothy
author_facet Pais, Faye
Fayed, Mohamed
Evans, Timothy
author_sort Pais, Faye
collection PubMed
description Lymphangioleiomyomatosis (LAM) is a rare cystic lung disease, commonly affecting women in the reproductive age group. Exacerbation of pre-existing disease is common during pregnancy likely due to the up-regulation of estrogen and progesterone receptors present within the proliferating smooth muscle cells. This case highlights a dramatic presentation of LAM for the first time in pregnancy, its rapid progression during gestation, and a partial resolution with delivery. The unusual radiographic imaging in this patient, lacked the characteristic cystic lesions commonly associated with LAM, but instead demonstrated a dense interstitial pattern with micronodular expansion of the interlobular septa suggesting severe lymphatic obstruction.
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spelling pubmed-54614332017-06-14 Lymphangioleiomyomatosis: an explosive presentation of a rare disease Pais, Faye Fayed, Mohamed Evans, Timothy Oxf Med Case Reports Case Report Lymphangioleiomyomatosis (LAM) is a rare cystic lung disease, commonly affecting women in the reproductive age group. Exacerbation of pre-existing disease is common during pregnancy likely due to the up-regulation of estrogen and progesterone receptors present within the proliferating smooth muscle cells. This case highlights a dramatic presentation of LAM for the first time in pregnancy, its rapid progression during gestation, and a partial resolution with delivery. The unusual radiographic imaging in this patient, lacked the characteristic cystic lesions commonly associated with LAM, but instead demonstrated a dense interstitial pattern with micronodular expansion of the interlobular septa suggesting severe lymphatic obstruction. Oxford University Press 2017-06-07 /pmc/articles/PMC5461433/ /pubmed/28616248 http://dx.doi.org/10.1093/omcr/omx023 Text en © The Author 2017. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Pais, Faye
Fayed, Mohamed
Evans, Timothy
Lymphangioleiomyomatosis: an explosive presentation of a rare disease
title Lymphangioleiomyomatosis: an explosive presentation of a rare disease
title_full Lymphangioleiomyomatosis: an explosive presentation of a rare disease
title_fullStr Lymphangioleiomyomatosis: an explosive presentation of a rare disease
title_full_unstemmed Lymphangioleiomyomatosis: an explosive presentation of a rare disease
title_short Lymphangioleiomyomatosis: an explosive presentation of a rare disease
title_sort lymphangioleiomyomatosis: an explosive presentation of a rare disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461433/
https://www.ncbi.nlm.nih.gov/pubmed/28616248
http://dx.doi.org/10.1093/omcr/omx023
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