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Spontaneous Pneumothorax in a Young Female With Lymphangioleiomyomatosis

Lymphangioleiomyomatosis (LAM) is a rare disorder of abnormal proliferation of smooth muscle-like cells which results in the formation of thin-walled cysts and progressive lung destruction. It commonly presents with progressive dyspnea that is often associated with a history of pneumothorax or chylo...

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Autores principales: Ukponmwan, Osato, Gorantla, Asher, Patel, Krunal H, Gabutan, Elmer, Zhonghua, Li, McFarlane, Samy I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581502/
https://www.ncbi.nlm.nih.gov/pubmed/37854755
http://dx.doi.org/10.7759/cureus.45413
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author Ukponmwan, Osato
Gorantla, Asher
Patel, Krunal H
Gabutan, Elmer
Zhonghua, Li
McFarlane, Samy I
author_facet Ukponmwan, Osato
Gorantla, Asher
Patel, Krunal H
Gabutan, Elmer
Zhonghua, Li
McFarlane, Samy I
author_sort Ukponmwan, Osato
collection PubMed
description Lymphangioleiomyomatosis (LAM) is a rare disorder of abnormal proliferation of smooth muscle-like cells which results in the formation of thin-walled cysts and progressive lung destruction. It commonly presents with progressive dyspnea that is often associated with a history of pneumothorax or chylothorax particularly among females of reproductive age. In this report, we present a case of hydropneumothorax as the initial presentation of LAM in a 33-year-old woman, a rather rare presentation. We also discuss the pathogenetic mechanisms, the diagnosis, and treatment strategies using mTOR inhibitors like sirolimus.
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spelling pubmed-105815022023-10-18 Spontaneous Pneumothorax in a Young Female With Lymphangioleiomyomatosis Ukponmwan, Osato Gorantla, Asher Patel, Krunal H Gabutan, Elmer Zhonghua, Li McFarlane, Samy I Cureus Pathology Lymphangioleiomyomatosis (LAM) is a rare disorder of abnormal proliferation of smooth muscle-like cells which results in the formation of thin-walled cysts and progressive lung destruction. It commonly presents with progressive dyspnea that is often associated with a history of pneumothorax or chylothorax particularly among females of reproductive age. In this report, we present a case of hydropneumothorax as the initial presentation of LAM in a 33-year-old woman, a rather rare presentation. We also discuss the pathogenetic mechanisms, the diagnosis, and treatment strategies using mTOR inhibitors like sirolimus. Cureus 2023-09-17 /pmc/articles/PMC10581502/ /pubmed/37854755 http://dx.doi.org/10.7759/cureus.45413 Text en Copyright © 2023, Ukponmwan et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pathology
Ukponmwan, Osato
Gorantla, Asher
Patel, Krunal H
Gabutan, Elmer
Zhonghua, Li
McFarlane, Samy I
Spontaneous Pneumothorax in a Young Female With Lymphangioleiomyomatosis
title Spontaneous Pneumothorax in a Young Female With Lymphangioleiomyomatosis
title_full Spontaneous Pneumothorax in a Young Female With Lymphangioleiomyomatosis
title_fullStr Spontaneous Pneumothorax in a Young Female With Lymphangioleiomyomatosis
title_full_unstemmed Spontaneous Pneumothorax in a Young Female With Lymphangioleiomyomatosis
title_short Spontaneous Pneumothorax in a Young Female With Lymphangioleiomyomatosis
title_sort spontaneous pneumothorax in a young female with lymphangioleiomyomatosis
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581502/
https://www.ncbi.nlm.nih.gov/pubmed/37854755
http://dx.doi.org/10.7759/cureus.45413
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