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La microlithiase alvéolaire: à propos d’une nouvelle observation

Alveolar microlithiasis (AM) is a rare disease, characterized by the accumulation of calcium concretions in the pulmonary alveolar lumen. We report a new case of AM suspected on chest X-ray and confirmed by chest CT scan, whose appearance was pathognomonic, and by transbronchial pulmonary biopsy. AM...

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Autores principales: Zaghba, Nahid, Hachimi, Kawtar El, Benjelloun, Hanane, Yassine, Najiba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989273/
https://www.ncbi.nlm.nih.gov/pubmed/29881486
http://dx.doi.org/10.11604/pamj.2017.28.241.13876
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author Zaghba, Nahid
Hachimi, Kawtar El
Benjelloun, Hanane
Yassine, Najiba
author_facet Zaghba, Nahid
Hachimi, Kawtar El
Benjelloun, Hanane
Yassine, Najiba
author_sort Zaghba, Nahid
collection PubMed
description Alveolar microlithiasis (AM) is a rare disease, characterized by the accumulation of calcium concretions in the pulmonary alveolar lumen. We report a new case of AM suspected on chest X-ray and confirmed by chest CT scan, whose appearance was pathognomonic, and by transbronchial pulmonary biopsy. AM is often asymptomatic, contrasting with the importance of lesions on X-ray which are characteristics of this disease. The cause of this disease is unknown. However autosomal recessive inheritance with mutation in the SLC34A2 gene is suspected.
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spelling pubmed-59892732018-06-07 La microlithiase alvéolaire: à propos d’une nouvelle observation Zaghba, Nahid Hachimi, Kawtar El Benjelloun, Hanane Yassine, Najiba Pan Afr Med J Case Report Alveolar microlithiasis (AM) is a rare disease, characterized by the accumulation of calcium concretions in the pulmonary alveolar lumen. We report a new case of AM suspected on chest X-ray and confirmed by chest CT scan, whose appearance was pathognomonic, and by transbronchial pulmonary biopsy. AM is often asymptomatic, contrasting with the importance of lesions on X-ray which are characteristics of this disease. The cause of this disease is unknown. However autosomal recessive inheritance with mutation in the SLC34A2 gene is suspected. The African Field Epidemiology Network 2017-11-17 /pmc/articles/PMC5989273/ /pubmed/29881486 http://dx.doi.org/10.11604/pamj.2017.28.241.13876 Text en © Nahid Zaghba et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. 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 work is properly cited.
spellingShingle Case Report
Zaghba, Nahid
Hachimi, Kawtar El
Benjelloun, Hanane
Yassine, Najiba
La microlithiase alvéolaire: à propos d’une nouvelle observation
title La microlithiase alvéolaire: à propos d’une nouvelle observation
title_full La microlithiase alvéolaire: à propos d’une nouvelle observation
title_fullStr La microlithiase alvéolaire: à propos d’une nouvelle observation
title_full_unstemmed La microlithiase alvéolaire: à propos d’une nouvelle observation
title_short La microlithiase alvéolaire: à propos d’une nouvelle observation
title_sort la microlithiase alvéolaire: à propos d’une nouvelle observation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989273/
https://www.ncbi.nlm.nih.gov/pubmed/29881486
http://dx.doi.org/10.11604/pamj.2017.28.241.13876
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