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Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease
Engelmann-Camurati disease (ECD) is a rare bone disorder characterized by autosomal dominant inheritance. It usually presents in early childhood and is associated with symmetrical diaphyseal sclerosis. We report a 20-year-old female with scintigraphic findings characteristic of ECD. She was treated...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180724/ https://www.ncbi.nlm.nih.gov/pubmed/21969782 http://dx.doi.org/10.4103/0972-3919.84615 |
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author | Harisankar, Chidambaram Natrajan Balasubramanian Kamleshwaran, Koramadai Karuppuswamy Bhattacharya, Anish Singh, Baljinder Bhadada, Sanjay Mittal, Bhagwant Rai |
author_facet | Harisankar, Chidambaram Natrajan Balasubramanian Kamleshwaran, Koramadai Karuppuswamy Bhattacharya, Anish Singh, Baljinder Bhadada, Sanjay Mittal, Bhagwant Rai |
author_sort | Harisankar, Chidambaram Natrajan Balasubramanian |
collection | PubMed |
description | Engelmann-Camurati disease (ECD) is a rare bone disorder characterized by autosomal dominant inheritance. It usually presents in early childhood and is associated with symmetrical diaphyseal sclerosis. We report a 20-year-old female with scintigraphic findings characteristic of ECD. She was treated with corticosteroids and showed marked clinical improvement. |
format | Online Article Text |
id | pubmed-3180724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-31807242011-10-03 Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease Harisankar, Chidambaram Natrajan Balasubramanian Kamleshwaran, Koramadai Karuppuswamy Bhattacharya, Anish Singh, Baljinder Bhadada, Sanjay Mittal, Bhagwant Rai Indian J Nucl Med Case Report Engelmann-Camurati disease (ECD) is a rare bone disorder characterized by autosomal dominant inheritance. It usually presents in early childhood and is associated with symmetrical diaphyseal sclerosis. We report a 20-year-old female with scintigraphic findings characteristic of ECD. She was treated with corticosteroids and showed marked clinical improvement. Medknow Publications 2011 /pmc/articles/PMC3180724/ /pubmed/21969782 http://dx.doi.org/10.4103/0972-3919.84615 Text en Copyright: © Indian Journal of Nuclear Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Harisankar, Chidambaram Natrajan Balasubramanian Kamleshwaran, Koramadai Karuppuswamy Bhattacharya, Anish Singh, Baljinder Bhadada, Sanjay Mittal, Bhagwant Rai Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease |
title | Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease |
title_full | Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease |
title_fullStr | Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease |
title_full_unstemmed | Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease |
title_short | Tc99m-MDP bone scintigraphy in Engelmann-Camurati disease |
title_sort | tc99m-mdp bone scintigraphy in engelmann-camurati disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180724/ https://www.ncbi.nlm.nih.gov/pubmed/21969782 http://dx.doi.org/10.4103/0972-3919.84615 |
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