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Staged Bilateral Total Hip Arthroplasty in a 17-Year-Old With Type VI Mucopolysaccharidosis

Mucopolysaccharidosis encompasses multiple lysosomal storage disorders that are relevant to the orthopedic surgeon as they lead to disruption in bone and cartilage development. These patients may present with early-onset joint pain, including end-stage hip arthritis warranting total hip replacement....

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Detalles Bibliográficos
Autores principales: Robin, Joseph X., Brash, Andrew I., Schwarzkopf, Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729915/
https://www.ncbi.nlm.nih.gov/pubmed/36507284
http://dx.doi.org/10.1016/j.artd.2022.10.008
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author Robin, Joseph X.
Brash, Andrew I.
Schwarzkopf, Ran
author_facet Robin, Joseph X.
Brash, Andrew I.
Schwarzkopf, Ran
author_sort Robin, Joseph X.
collection PubMed
description Mucopolysaccharidosis encompasses multiple lysosomal storage disorders that are relevant to the orthopedic surgeon as they lead to disruption in bone and cartilage development. These patients may present with early-onset joint pain, including end-stage hip arthritis warranting total hip replacement. The altered hip anatomy in this disorder is of specific importance to the arthroplasty surgeon as it presents challenges when reconstructing the proximal femur and acetabulum and informs implant choice. We present a 17-year-old patient with end-stage bilateral hip arthritis who underwent staged bilateral total hip arthroplasty. We discuss technical considerations in surgical technique and the consequences of acetabular and femoral deformity on implant selection.
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spelling pubmed-97299152022-12-09 Staged Bilateral Total Hip Arthroplasty in a 17-Year-Old With Type VI Mucopolysaccharidosis Robin, Joseph X. Brash, Andrew I. Schwarzkopf, Ran Arthroplast Today Arthroplasty in Patients with Rare Conditions Mucopolysaccharidosis encompasses multiple lysosomal storage disorders that are relevant to the orthopedic surgeon as they lead to disruption in bone and cartilage development. These patients may present with early-onset joint pain, including end-stage hip arthritis warranting total hip replacement. The altered hip anatomy in this disorder is of specific importance to the arthroplasty surgeon as it presents challenges when reconstructing the proximal femur and acetabulum and informs implant choice. We present a 17-year-old patient with end-stage bilateral hip arthritis who underwent staged bilateral total hip arthroplasty. We discuss technical considerations in surgical technique and the consequences of acetabular and femoral deformity on implant selection. Elsevier 2022-12-06 /pmc/articles/PMC9729915/ /pubmed/36507284 http://dx.doi.org/10.1016/j.artd.2022.10.008 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Arthroplasty in Patients with Rare Conditions
Robin, Joseph X.
Brash, Andrew I.
Schwarzkopf, Ran
Staged Bilateral Total Hip Arthroplasty in a 17-Year-Old With Type VI Mucopolysaccharidosis
title Staged Bilateral Total Hip Arthroplasty in a 17-Year-Old With Type VI Mucopolysaccharidosis
title_full Staged Bilateral Total Hip Arthroplasty in a 17-Year-Old With Type VI Mucopolysaccharidosis
title_fullStr Staged Bilateral Total Hip Arthroplasty in a 17-Year-Old With Type VI Mucopolysaccharidosis
title_full_unstemmed Staged Bilateral Total Hip Arthroplasty in a 17-Year-Old With Type VI Mucopolysaccharidosis
title_short Staged Bilateral Total Hip Arthroplasty in a 17-Year-Old With Type VI Mucopolysaccharidosis
title_sort staged bilateral total hip arthroplasty in a 17-year-old with type vi mucopolysaccharidosis
topic Arthroplasty in Patients with Rare Conditions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729915/
https://www.ncbi.nlm.nih.gov/pubmed/36507284
http://dx.doi.org/10.1016/j.artd.2022.10.008
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