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The Surgical Management of the Rare Neurogenic Myositis Ossificans of the Hip: A Report of 3 Cases

INTRODUCTION: Myositis ossificans (MO) is a benign non-neoplastic condition in which heterotopic bone formation occurs in soft tissues. Neurogenic MO is one variant of MO where the lesion is a result of neurological disorders, including brain and spinal cord injuries, especially when followed by imm...

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Autores principales: Hammad, Yazan, Akiely, Reem, Hajjaj, Nada, Tahboub, Farah, Al-Ajlouni, Jihad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241266/
https://www.ncbi.nlm.nih.gov/pubmed/34239827
http://dx.doi.org/10.13107/jocr.2021.v11.i03.2082
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author Hammad, Yazan
Akiely, Reem
Hajjaj, Nada
Tahboub, Farah
Al-Ajlouni, Jihad
author_facet Hammad, Yazan
Akiely, Reem
Hajjaj, Nada
Tahboub, Farah
Al-Ajlouni, Jihad
author_sort Hammad, Yazan
collection PubMed
description INTRODUCTION: Myositis ossificans (MO) is a benign non-neoplastic condition in which heterotopic bone formation occurs in soft tissues. Neurogenic MO is one variant of MO where the lesion is a result of neurological disorders, including brain and spinal cord injuries, especially when followed by immobility and spasticity. MO can also be a result of direct trauma or even genetic mutations. CASE REPORT: We present three cases of young men (16, 37, and 22-year-old) who developed MO of the hip joint following brain or spinal cord injuries. One of them had also sustained a direct trauma to the affected hip joint at the time of the accident. All three patients presented with inability to walk independently due to diminished range of motion at the affected joint. X-rays and computerized tomography (CT) scans with 3-dimentional (3D) reconstruction suggested the diagnosis of MO, but the serum alkaline phosphatase was within normal limits at the time of presentation. The first case had bilateral involvement with unmistakable separation between the heterotopic bone formation and the frank hip joints on CT. This patient underwent successful staged excision of the ossifications. The second patient had unilateral hip joint involvement with the absence of clear separation between the heterotopic bone formation and the hip joint, thus, underwent total hip replacement for the affected side as excision was not possible. The third patienthad unilateral hip joint involvement and underwent excision of the ossification with dynamic hip screw insertion after sustaining a stable intertrochanteric fracture intraoperatively. Postoperatively, all three patients received physiotherapy and oral indomethacin. Upon recovery, they were able to walk independently with a near-normal range of motion at the hip joint. There was no evidence of recurrence upon follow-up visits, and CT scans in patients I and II. Follow-ups for patient III were not possible as the patient died 1 month after surgery due to pulmonary embolism. CONCLUSION: The surgical management of MO is indicated when non-operative methods fail to provide an adequate range of motion around the hip joint. Pre-operative assessment utilizing 3D-CT scans proved to be essential in dictating the appropriate surgical approach. During post-operative follow-ups, the physiotherapy and oral indomethacin provided additional improvement in outcome and patients’ satisfaction.
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spelling pubmed-82412662021-07-07 The Surgical Management of the Rare Neurogenic Myositis Ossificans of the Hip: A Report of 3 Cases Hammad, Yazan Akiely, Reem Hajjaj, Nada Tahboub, Farah Al-Ajlouni, Jihad J Orthop Case Rep Case Report INTRODUCTION: Myositis ossificans (MO) is a benign non-neoplastic condition in which heterotopic bone formation occurs in soft tissues. Neurogenic MO is one variant of MO where the lesion is a result of neurological disorders, including brain and spinal cord injuries, especially when followed by immobility and spasticity. MO can also be a result of direct trauma or even genetic mutations. CASE REPORT: We present three cases of young men (16, 37, and 22-year-old) who developed MO of the hip joint following brain or spinal cord injuries. One of them had also sustained a direct trauma to the affected hip joint at the time of the accident. All three patients presented with inability to walk independently due to diminished range of motion at the affected joint. X-rays and computerized tomography (CT) scans with 3-dimentional (3D) reconstruction suggested the diagnosis of MO, but the serum alkaline phosphatase was within normal limits at the time of presentation. The first case had bilateral involvement with unmistakable separation between the heterotopic bone formation and the frank hip joints on CT. This patient underwent successful staged excision of the ossifications. The second patient had unilateral hip joint involvement with the absence of clear separation between the heterotopic bone formation and the hip joint, thus, underwent total hip replacement for the affected side as excision was not possible. The third patienthad unilateral hip joint involvement and underwent excision of the ossification with dynamic hip screw insertion after sustaining a stable intertrochanteric fracture intraoperatively. Postoperatively, all three patients received physiotherapy and oral indomethacin. Upon recovery, they were able to walk independently with a near-normal range of motion at the hip joint. There was no evidence of recurrence upon follow-up visits, and CT scans in patients I and II. Follow-ups for patient III were not possible as the patient died 1 month after surgery due to pulmonary embolism. CONCLUSION: The surgical management of MO is indicated when non-operative methods fail to provide an adequate range of motion around the hip joint. Pre-operative assessment utilizing 3D-CT scans proved to be essential in dictating the appropriate surgical approach. During post-operative follow-ups, the physiotherapy and oral indomethacin provided additional improvement in outcome and patients’ satisfaction. Indian Orthopaedic Research Group 2021-03 /pmc/articles/PMC8241266/ /pubmed/34239827 http://dx.doi.org/10.13107/jocr.2021.v11.i03.2082 Text en Copyright: © Indian Orthopaedic Research Group https://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
Hammad, Yazan
Akiely, Reem
Hajjaj, Nada
Tahboub, Farah
Al-Ajlouni, Jihad
The Surgical Management of the Rare Neurogenic Myositis Ossificans of the Hip: A Report of 3 Cases
title The Surgical Management of the Rare Neurogenic Myositis Ossificans of the Hip: A Report of 3 Cases
title_full The Surgical Management of the Rare Neurogenic Myositis Ossificans of the Hip: A Report of 3 Cases
title_fullStr The Surgical Management of the Rare Neurogenic Myositis Ossificans of the Hip: A Report of 3 Cases
title_full_unstemmed The Surgical Management of the Rare Neurogenic Myositis Ossificans of the Hip: A Report of 3 Cases
title_short The Surgical Management of the Rare Neurogenic Myositis Ossificans of the Hip: A Report of 3 Cases
title_sort surgical management of the rare neurogenic myositis ossificans of the hip: a report of 3 cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241266/
https://www.ncbi.nlm.nih.gov/pubmed/34239827
http://dx.doi.org/10.13107/jocr.2021.v11.i03.2082
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