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Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease

Camurati-Engelmann disease (CED) is an extremely rare, sclerosing bone disorder of intramedullary ossification with only 300 reported cases worldwide. The pathogenesis is related to activating mutations in transforming growth factor beta 1, which results in bilateral, symmetric hyperostosis affectin...

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Detalles Bibliográficos
Autores principales: Taylor, Adam J., Runner, Robert P., Longjohn, Donald B., Najibi, Soheil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076616/
https://www.ncbi.nlm.nih.gov/pubmed/33937459
http://dx.doi.org/10.1016/j.artd.2021.03.011
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author Taylor, Adam J.
Runner, Robert P.
Longjohn, Donald B.
Najibi, Soheil
author_facet Taylor, Adam J.
Runner, Robert P.
Longjohn, Donald B.
Najibi, Soheil
author_sort Taylor, Adam J.
collection PubMed
description Camurati-Engelmann disease (CED) is an extremely rare, sclerosing bone disorder of intramedullary ossification with only 300 reported cases worldwide. The pathogenesis is related to activating mutations in transforming growth factor beta 1, which results in bilateral, symmetric hyperostosis affecting primarily the diaphysis of long bones. Despite effective pharmacological treatment options, the diagnosis of CED is problematic owning to its rarity and variability of clinical presentation. We present a patient with known CED with advanced early hip osteoarthritis, secondary to underlying hip dysplasia, for which she underwent a successful total hip arthroplasty via a direct anterior approach with the use of bulk femoral head autograft to reconstruct her native acetabulum.
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spelling pubmed-80766162021-04-29 Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease Taylor, Adam J. Runner, Robert P. Longjohn, Donald B. Najibi, Soheil Arthroplast Today Case Report Camurati-Engelmann disease (CED) is an extremely rare, sclerosing bone disorder of intramedullary ossification with only 300 reported cases worldwide. The pathogenesis is related to activating mutations in transforming growth factor beta 1, which results in bilateral, symmetric hyperostosis affecting primarily the diaphysis of long bones. Despite effective pharmacological treatment options, the diagnosis of CED is problematic owning to its rarity and variability of clinical presentation. We present a patient with known CED with advanced early hip osteoarthritis, secondary to underlying hip dysplasia, for which she underwent a successful total hip arthroplasty via a direct anterior approach with the use of bulk femoral head autograft to reconstruct her native acetabulum. Elsevier 2021-04-14 /pmc/articles/PMC8076616/ /pubmed/33937459 http://dx.doi.org/10.1016/j.artd.2021.03.011 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Taylor, Adam J.
Runner, Robert P.
Longjohn, Donald B.
Najibi, Soheil
Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease
title Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease
title_full Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease
title_fullStr Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease
title_full_unstemmed Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease
title_short Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease
title_sort anterior total hip arthroplasty with bulk femoral head autograft in a patient with camurati-engelmann disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076616/
https://www.ncbi.nlm.nih.gov/pubmed/33937459
http://dx.doi.org/10.1016/j.artd.2021.03.011
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