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Acute pulmonary embolism in a child with ANCA-negative idiopathic pulmonary capillaritis

Diffuse alveolar hemorrhage is an uncommon and often fatal condition in children that is characterized by distinct histopathological etiologies. Herein, we discuss the case of an 11-year-old girl who presented with acute worsening of hypoxia and left-sided chest pain. The patient had lung biopsy-pro...

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Autores principales: Asseri, Ali A., Zeng, Yi, Daines, Cori L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Saudi Medical Journal 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778752/
https://www.ncbi.nlm.nih.gov/pubmed/31219497
http://dx.doi.org/10.15537/smj.2019.6.24210
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author Asseri, Ali A.
Zeng, Yi
Daines, Cori L.
author_facet Asseri, Ali A.
Zeng, Yi
Daines, Cori L.
author_sort Asseri, Ali A.
collection PubMed
description Diffuse alveolar hemorrhage is an uncommon and often fatal condition in children that is characterized by distinct histopathological etiologies. Herein, we discuss the case of an 11-year-old girl who presented with acute worsening of hypoxia and left-sided chest pain. The patient had lung biopsy-proven idiopathic pulmonary capillaritis and was being treated with prednisolone every alternate day, azathioprine, and hydroxychloroquine. A contrast-computed tomography (CT) scan of the chest showed an acute left lower-lobe pulmonary embolism. Negative results were obtained on a test for thrombophilia. In children, pulmonary embolism with anti-neutrophil cytoplasmic antibody-negative idiopathic pulmonary capillaritis is a rare clinical condition. The exact cause of thrombus formation in this case is unknown; however, obesity, immobility, and chronic systemic corticosteroid therapy probably played a role.
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spelling pubmed-67787522021-02-04 Acute pulmonary embolism in a child with ANCA-negative idiopathic pulmonary capillaritis Asseri, Ali A. Zeng, Yi Daines, Cori L. Saudi Med J Case Report Diffuse alveolar hemorrhage is an uncommon and often fatal condition in children that is characterized by distinct histopathological etiologies. Herein, we discuss the case of an 11-year-old girl who presented with acute worsening of hypoxia and left-sided chest pain. The patient had lung biopsy-proven idiopathic pulmonary capillaritis and was being treated with prednisolone every alternate day, azathioprine, and hydroxychloroquine. A contrast-computed tomography (CT) scan of the chest showed an acute left lower-lobe pulmonary embolism. Negative results were obtained on a test for thrombophilia. In children, pulmonary embolism with anti-neutrophil cytoplasmic antibody-negative idiopathic pulmonary capillaritis is a rare clinical condition. The exact cause of thrombus formation in this case is unknown; however, obesity, immobility, and chronic systemic corticosteroid therapy probably played a role. Saudi Medical Journal 2019 /pmc/articles/PMC6778752/ /pubmed/31219497 http://dx.doi.org/10.15537/smj.2019.6.24210 Text en Copyright: © Saudi Medical Journal http://creativecommons.org/licenses/by-nc This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial License (CC BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Asseri, Ali A.
Zeng, Yi
Daines, Cori L.
Acute pulmonary embolism in a child with ANCA-negative idiopathic pulmonary capillaritis
title Acute pulmonary embolism in a child with ANCA-negative idiopathic pulmonary capillaritis
title_full Acute pulmonary embolism in a child with ANCA-negative idiopathic pulmonary capillaritis
title_fullStr Acute pulmonary embolism in a child with ANCA-negative idiopathic pulmonary capillaritis
title_full_unstemmed Acute pulmonary embolism in a child with ANCA-negative idiopathic pulmonary capillaritis
title_short Acute pulmonary embolism in a child with ANCA-negative idiopathic pulmonary capillaritis
title_sort acute pulmonary embolism in a child with anca-negative idiopathic pulmonary capillaritis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6778752/
https://www.ncbi.nlm.nih.gov/pubmed/31219497
http://dx.doi.org/10.15537/smj.2019.6.24210
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