Idiopathic Pulmonary Hemosiderosis: An Unexplored Cause of Treatment Refractory Pediatric Iron Deficiency Anemia

Idiopathic pulmonary hemosiderosis (IPH) is an unusual cause of pediatric iron deficiency anemia (IDA) characterized by alveolar hemorrhage leading to hemosiderin deposition and fibrosis in the lungs. Though the typical triad of presentation is hemoptysis, IDA, and lung opacities on thoracic radiogr...

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Autores principales: Reghunath, Anjuna, Biswas, Joyutpal, Mittal, Mahesh Kumar, Kanaujiya, Reeta, Khanna, Geetika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical and Scientific Publishers Private Ltd. 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448246/
https://www.ncbi.nlm.nih.gov/pubmed/34556935
http://dx.doi.org/10.1055/s-0041-1734334
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author Reghunath, Anjuna
Biswas, Joyutpal
Mittal, Mahesh Kumar
Kanaujiya, Reeta
Khanna, Geetika
author_facet Reghunath, Anjuna
Biswas, Joyutpal
Mittal, Mahesh Kumar
Kanaujiya, Reeta
Khanna, Geetika
author_sort Reghunath, Anjuna
collection PubMed
description Idiopathic pulmonary hemosiderosis (IPH) is an unusual cause of pediatric iron deficiency anemia (IDA) characterized by alveolar hemorrhage leading to hemosiderin deposition and fibrosis in the lungs. Though the typical triad of presentation is hemoptysis, IDA, and lung opacities on thoracic radiographs, often the sole manifestation of IPH may be severe IDA in children.
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spelling pubmed-84482462021-09-22 Idiopathic Pulmonary Hemosiderosis: An Unexplored Cause of Treatment Refractory Pediatric Iron Deficiency Anemia Reghunath, Anjuna Biswas, Joyutpal Mittal, Mahesh Kumar Kanaujiya, Reeta Khanna, Geetika Indian J Radiol Imaging Idiopathic pulmonary hemosiderosis (IPH) is an unusual cause of pediatric iron deficiency anemia (IDA) characterized by alveolar hemorrhage leading to hemosiderin deposition and fibrosis in the lungs. Though the typical triad of presentation is hemoptysis, IDA, and lung opacities on thoracic radiographs, often the sole manifestation of IPH may be severe IDA in children. Thieme Medical and Scientific Publishers Private Ltd. 2021-04 2021-07-28 /pmc/articles/PMC8448246/ /pubmed/34556935 http://dx.doi.org/10.1055/s-0041-1734334 Text en Indian Radiological Association. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Reghunath, Anjuna
Biswas, Joyutpal
Mittal, Mahesh Kumar
Kanaujiya, Reeta
Khanna, Geetika
Idiopathic Pulmonary Hemosiderosis: An Unexplored Cause of Treatment Refractory Pediatric Iron Deficiency Anemia
title Idiopathic Pulmonary Hemosiderosis: An Unexplored Cause of Treatment Refractory Pediatric Iron Deficiency Anemia
title_full Idiopathic Pulmonary Hemosiderosis: An Unexplored Cause of Treatment Refractory Pediatric Iron Deficiency Anemia
title_fullStr Idiopathic Pulmonary Hemosiderosis: An Unexplored Cause of Treatment Refractory Pediatric Iron Deficiency Anemia
title_full_unstemmed Idiopathic Pulmonary Hemosiderosis: An Unexplored Cause of Treatment Refractory Pediatric Iron Deficiency Anemia
title_short Idiopathic Pulmonary Hemosiderosis: An Unexplored Cause of Treatment Refractory Pediatric Iron Deficiency Anemia
title_sort idiopathic pulmonary hemosiderosis: an unexplored cause of treatment refractory pediatric iron deficiency anemia
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448246/
https://www.ncbi.nlm.nih.gov/pubmed/34556935
http://dx.doi.org/10.1055/s-0041-1734334
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