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Extensive Idiopathic Calcinosis in a Child – A Diagnostic and Therapeutic Imbroglio

Idiopathic calcinosis is a disorder characterized by diffuse calcium deposits at various sites of the body. Etiopathogenic associations are described with inherited disorders, connective tissue disorders, infections, tumors, trauma, and endocrine disturbances. No diagnostic tests or standard therape...

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Autores principales: Bhattarai, Dharmagat, Banday, Aaqib Z., Patra, Pratap K., Risal, Ujjwol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650747/
https://www.ncbi.nlm.nih.gov/pubmed/36386760
http://dx.doi.org/10.4103/idoj.idoj_184_22
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author Bhattarai, Dharmagat
Banday, Aaqib Z.
Patra, Pratap K.
Risal, Ujjwol
author_facet Bhattarai, Dharmagat
Banday, Aaqib Z.
Patra, Pratap K.
Risal, Ujjwol
author_sort Bhattarai, Dharmagat
collection PubMed
description Idiopathic calcinosis is a disorder characterized by diffuse calcium deposits at various sites of the body. Etiopathogenic associations are described with inherited disorders, connective tissue disorders, infections, tumors, trauma, and endocrine disturbances. No diagnostic tests or standard therapeutic guidelines are established for this entity. There is paucity of literature on idiopathic calcinosis. We describe a girl child with extensive calcinosis in the skin and around muscle bundles without any clinical and laboratory evidence for etiological associations. Aggressive treatment modalities resulted a notable improvement in lesions in index child. Growing evidence will help to establish the ground for understanding and developing standard therapy.
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spelling pubmed-96507472022-11-15 Extensive Idiopathic Calcinosis in a Child – A Diagnostic and Therapeutic Imbroglio Bhattarai, Dharmagat Banday, Aaqib Z. Patra, Pratap K. Risal, Ujjwol Indian Dermatol Online J Case Report Idiopathic calcinosis is a disorder characterized by diffuse calcium deposits at various sites of the body. Etiopathogenic associations are described with inherited disorders, connective tissue disorders, infections, tumors, trauma, and endocrine disturbances. No diagnostic tests or standard therapeutic guidelines are established for this entity. There is paucity of literature on idiopathic calcinosis. We describe a girl child with extensive calcinosis in the skin and around muscle bundles without any clinical and laboratory evidence for etiological associations. Aggressive treatment modalities resulted a notable improvement in lesions in index child. Growing evidence will help to establish the ground for understanding and developing standard therapy. Wolters Kluwer - Medknow 2022-09-21 /pmc/articles/PMC9650747/ /pubmed/36386760 http://dx.doi.org/10.4103/idoj.idoj_184_22 Text en Copyright: © 2022 Indian Dermatology Online Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Bhattarai, Dharmagat
Banday, Aaqib Z.
Patra, Pratap K.
Risal, Ujjwol
Extensive Idiopathic Calcinosis in a Child – A Diagnostic and Therapeutic Imbroglio
title Extensive Idiopathic Calcinosis in a Child – A Diagnostic and Therapeutic Imbroglio
title_full Extensive Idiopathic Calcinosis in a Child – A Diagnostic and Therapeutic Imbroglio
title_fullStr Extensive Idiopathic Calcinosis in a Child – A Diagnostic and Therapeutic Imbroglio
title_full_unstemmed Extensive Idiopathic Calcinosis in a Child – A Diagnostic and Therapeutic Imbroglio
title_short Extensive Idiopathic Calcinosis in a Child – A Diagnostic and Therapeutic Imbroglio
title_sort extensive idiopathic calcinosis in a child – a diagnostic and therapeutic imbroglio
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650747/
https://www.ncbi.nlm.nih.gov/pubmed/36386760
http://dx.doi.org/10.4103/idoj.idoj_184_22
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