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Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation

Juvenile Dermatomyositis (JDM) is a rare autoimmune disease in children and adolescents. In these patients calcinosis might be the most characteristic symptom. However there are only few reported cases of intramuscular calcinosis in Dermatomyositis. We report a case of calcinosis universalis (CU) of...

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Autores principales: Boelch, Sebastian Philipp, Barthel, Thomas, Goebel, Sascha, Rudert, Maximilian, Plumhoff, Piet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633560/
https://www.ncbi.nlm.nih.gov/pubmed/26579322
http://dx.doi.org/10.1155/2015/505420
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author Boelch, Sebastian Philipp
Barthel, Thomas
Goebel, Sascha
Rudert, Maximilian
Plumhoff, Piet
author_facet Boelch, Sebastian Philipp
Barthel, Thomas
Goebel, Sascha
Rudert, Maximilian
Plumhoff, Piet
author_sort Boelch, Sebastian Philipp
collection PubMed
description Juvenile Dermatomyositis (JDM) is a rare autoimmune disease in children and adolescents. In these patients calcinosis might be the most characteristic symptom. However there are only few reported cases of intramuscular calcinosis in Dermatomyositis. We report a case of calcinosis universalis (CU) of the elbow in JDM successfully treated with broaching. The patient, a 24-year-old woman, suffered from a long history of JDM. On examination she presented with a fistula lateral to the olecranon and pain of the right elbow joint. Plain X-rays displayed a diffuse pattern of multiple periarticular, subcutaneous, and intramuscular calcifications. The patient underwent surgery for histological and microbiological sampling as well as broaching. Intraoperatively sinus formation and subfascial hard calcium deposition were found. Due to the risk of collateral tissue damage, incomplete broaching was performed. A local infection with Staphylococcus was diagnosed and treated with antibiotics. On six-week and 30-month follow-up the patient was free of pain and had very good function. Calcifications on standard radiographs had almost resolved entirely. This case report gives a summary on calcinosis in Dermatomyositis and adds a new case of recalcitrant CU to the literature. Broaching surgery proved to be a reliable treatment option in symptomatic calcinosis.
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spelling pubmed-46335602015-11-17 Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation Boelch, Sebastian Philipp Barthel, Thomas Goebel, Sascha Rudert, Maximilian Plumhoff, Piet Case Rep Orthop Case Report Juvenile Dermatomyositis (JDM) is a rare autoimmune disease in children and adolescents. In these patients calcinosis might be the most characteristic symptom. However there are only few reported cases of intramuscular calcinosis in Dermatomyositis. We report a case of calcinosis universalis (CU) of the elbow in JDM successfully treated with broaching. The patient, a 24-year-old woman, suffered from a long history of JDM. On examination she presented with a fistula lateral to the olecranon and pain of the right elbow joint. Plain X-rays displayed a diffuse pattern of multiple periarticular, subcutaneous, and intramuscular calcifications. The patient underwent surgery for histological and microbiological sampling as well as broaching. Intraoperatively sinus formation and subfascial hard calcium deposition were found. Due to the risk of collateral tissue damage, incomplete broaching was performed. A local infection with Staphylococcus was diagnosed and treated with antibiotics. On six-week and 30-month follow-up the patient was free of pain and had very good function. Calcifications on standard radiographs had almost resolved entirely. This case report gives a summary on calcinosis in Dermatomyositis and adds a new case of recalcitrant CU to the literature. Broaching surgery proved to be a reliable treatment option in symptomatic calcinosis. Hindawi Publishing Corporation 2015 2015-10-22 /pmc/articles/PMC4633560/ /pubmed/26579322 http://dx.doi.org/10.1155/2015/505420 Text en Copyright © 2015 Sebastian Philipp Boelch et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under 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
Boelch, Sebastian Philipp
Barthel, Thomas
Goebel, Sascha
Rudert, Maximilian
Plumhoff, Piet
Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation
title Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation
title_full Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation
title_fullStr Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation
title_full_unstemmed Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation
title_short Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation
title_sort calcinosis universalis of the elbow: a rare case with classical presentation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633560/
https://www.ncbi.nlm.nih.gov/pubmed/26579322
http://dx.doi.org/10.1155/2015/505420
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