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

[box type=”bio”] Learning Point of the Article: [/box]

Careful radiographic and metabolic evaluation are needed in the MO before the surgical intervention.

Authors: Yazan Hammad[1], Reem Akiely2, Nada Hajjaj[2], Farah Tahboub[2], Jihad Al-Ajlouni[1]

[1]Department of Orthopaedic Surgery, Jordan University Hospitals, Amman, Jordan,
[2]Department of Orthopedic surgery School of Medicine, The University of Jordan, Amman, Jordan.

Address of Correspondence:
Dr. Yazan Hammad,
Department of Orthopaedic Surgery, Jordan University Hospital, Aljubeiha, Amman.
E-mail: yazanshammad@yahoo.com

Abstract

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.
Keywords: Myositis ossificans, total hip replacement, arthrolysis.

Introduction
Myositis ossificans (MO), often referred to as heterotopic ossification (HO), is a rare benign non-neoplastic condition in which heterotopic bone formation occurs in soft tissues, with muscles being mostly involved[1, 2, 3]. One variant of MO, termed MO circumscriptaor traumatica, can occur as a result of a direct blow or repeated minor trauma and is estimated to account for the majority of cases of MO[1,4]. MO, without a history of direct trauma to the involved region, can be seen with burns, hemophilia, and neurological disorders [1]. Prolonged immobility and spasticity increase the risk of developing neurogenic HO following traumatic brain or spinal cord injuries[5]. A genetic variant of MO, termed MO progressiva, is associated with the condition fibrodysplasia ossificans progressiva, a rare autosomal dominant disorder caused by a mutation in AVCR1 gene resulting in congenital skeletal malformations and progressive HOs [6]. MO can present with a variety of clinical symptoms, ranging from minor swelling to severe pain and joint stiffness [7]. For the diagnosis, radiographic findings are often sufficient; however, computerized tomography (CT) scanning, magnetic resonance imaging (MRI), or bone scintigraphy may be necessary in certain instances such as in early disease process; before any calcifications have settled, or when another soft tissue pathology is suspected [7, 8, 9, 10, 11]. Moreover, it is important to acknowledge the important role that biopsy plays in the diagnostic process of MO, specifically, whenever any indeterminate lesion is encountered and imaging is non-diagnostic [7]. Given the benign and self-limiting natural course of the disease process, conservative nonsurgical management focusing on symptomatology control is often the preferred choice when it comes to the management of MO [12]. Surgical excision is generally reserved for lesions that fail to be controlled with conservative management and/or introduce severe limitations to the activities of daily living [7, 13]. In this report, we present three cases of MO of the hip joint from Jordan University Hospital that was managed by the Orthopedic Surgery Department between the years 2016 and 2020.

Case Report
Case I
A 16-year-old boy who was involved in a quarrel sustained a stab wound in the back at the level of D10 that resulted in internal bleeding and vascular injury to the spinal cord with immediate paraplegia and urinary incontinence. He received physical therapy that led to partial recovery. The patient regained continence and became able to move from bed to wheelchair. During one physiotherapy session, the patient sustained a left femur shaft fracture and was treated by flexible nails. He presented to us 1 year after the initial injury with severe bilateral hip ankylosis (Fig. 1).On physical examination, the patient could move from bed to chair and walk only a few steps with flexed hips and adduction, neutral rotation, and extension of both lower limbs. Power was 4/5 all over the lower extremities bilaterally, with hypoesthesia below D10 level (i.e., the level of stab injury). The rest of the physical examination was unremarkable.
Radiographs of the hip joints revealed evident ossification that suggested the diagnosis of MO (Fig. 1). Moreover, 3-dimentional (3D)-CT scan(Fig. 2)revealed anterior and posterior ossification around the hip joint bilaterally. Importantly, however, the HO was separated from the actual femur bone and hip joint by soft tissue. Serum alkaline phosphatase (SAP) level was within normal limits and bone scan was normal. The patient underwent successful staged excision of the ossifications; the right side followed by the leftside after 1 month (Fig. 3). Upon recovery from the operation, the patient was able to walk independently with residual hip flexion. Postoperatively, he received physiotherapy and indomethacin (75 mg PO for 6 weeks) to prevent a recurrence. Follow-ups over 5 years demonstrated achievement of community ambulation without assistance and no signs of recurrence of MO (Fig. 4).

Case II
A 37-year-old man who was involved in a car accident sustained a head injury and a left acetabular fracture. The head injury yielded intracerebral hemorrhage and the patient was in a coma for several months. After regaining his full consciousness, he was bed-bound with the inability to walk independently or mobilize from bed to chair, with evident left-sided hemiparesis. The patient received physical therapy that led to restoring his ability to walk only with the aid of a walker. He presented to us 1.5 years after the initial accident with severe left hip ankylosis(Fig. 5). On physical examination, the patient was continent; the left hip joint was absolutely stiff with flexion deformity. The right hip had a completely normal range of motion. The rest of the physical examination was unremarkable.
Radiographs of the hip joints revealed evident ossification(Fig. 5) and 3D-CT(Fig. 6) revealed anterior and posterior ossification around the left hip joint that suggested the diagnosis of MO. No soft tissue was visualized between the ossification and the actual femur bone around the hip. At the presentation, the level of SAP was within normal limits. The patient was consented for arthrolysis versus left total hip replacement but eventually underwent total hip replacement as excision was not possible intraoperatively (Fig. 7). Upon recovery from the operation, the patient was able to walk independently with residual hip flexion. Postoperatively, the patient received physiotherapy and indomethacin (75 mg PO for 6 weeks) to prevent a recurrence. Follow-ups over 4 years demonstrated the full function of the affected limb and no signs of recurrence (Fig. 8).

Case III
A 22-year-old man who was involved in a car accident sustained a hemorrhagic cerebrovascular accident. His hospital stay extended for several months and was remarkable for prolonged intubation (2.5 months),tracheostomy tube placement, jejunostomy tube placement, and recurrent chest infections. During his hospital stay, the patient did not receive any lower limb physical therapy. Upon discharge, he had right-sided spastic hemiparesis with aphasia and was started on private physiotherapy and rehabilitation. He presented to our outpatient clinic after 1.5 years of physiotherapy with significant resistance and progressive limitation in the range of movement around the right hip joint. At this stage, the patient was bed ridden with the inability to ambulate independently. On physical examination, the patient was continent, the right hip joint was absolutely stiff with flexion deformity and fixed external rotation, and power was 4/5 all over the right lower extremity with intact sensation. His left hip joint had a completely normal range of motion and the rest of the physical examination was unremarkable.Radiographs of the right hip joint revealed evident ossification (Fig. 9). On 3D-CT, HO surrounding the right hip joint was seen associated with atrophied muscles and partial fusion of the proximal femur and dorsal acetabulum/ischium, causing fixed external rotation of the right femur (Fig. 10). SAP level at presentation was within normal limit. The bone scan initially demonstrated increased blood flow and hyperemia at the involved region, suggesting that the observed HO was immature; however, when repeated after 6 months, the bone scan was normal. The patient was consented for excision and arthrolysis. Intraoperatively, the patient sustained a stable intertrochanteric fracture and a dynamic hip screw (DHS) was inserted (Fig. 11). Postoperatively, there was a significant improvement in the range of motion with physiotherapy and oral indomethacin as the first two cases. Sadly, however, the follow-up was only for 1 month as the patient died from a pulmonary embolism.

Discussion
MO, often referred to as HO, is a rare benign non-neoplastic condition in which heterotopic bone formation occurs in soft tissues, with muscles being mostly involved [1, 2, 3]. Even though MO is relatively an uncommon condition, it has been well described in the literature possessing distinct clinical, radiological, and pathological properties [7]. It is suggested that the pathogenesis of MO formation is dependent on dysregulation of local stem cells in response to injury-induced inflammation with resultant endothelial-mesenchymal transition; a process in which certain cytokines released as part of the inflammatory cascade drive endothelial cells of skeletal muscles to undergo endothelial-mesenchymal transition [14, 15]. These endothelial-derived mesenchymal stem cells are described as the key players in the pathogenesis of MO, as they are the source of heterotopic bone formation in extra-skeletal tissues [15]. Conventionally, MO was linked to antecedent trauma, especially sport-related injuries. However, the attention toward non-traumatic cases has grown over the past few years [7]. The literature lacks accurate data about the prevalence of distinct variants of MO; however, neurogenic MO is often described as being a rare condition [16, 17]. In our report, we described three cases of MO of the hip joint that was managed at our institute between the years 2016 and 2020. All three patients had an antecedent history of brain or spinal cord injury. The patient in Case II had also sustained a direct injury to the left hip joint that resulted in an acetabular fracture, which may have contributed to the pathophysiology of HO in this particular case. The involved site in our 3 cases is consistent with previous reports, suggesting that MO ossificans around the hip joint is more often seen with neurogenic causes such as spinal cord injuries and cerebral palsy [16, 18]. This is in contrast to traumatic cases of MO that often involve the flexor muscles of the arm and extensor muscles of the thigh [7, 19]. MO can present with a wide variety of symptoms, with pain and joint stiffness being the classic ones [7]. The site of the lesion and proximity to joints as well as the stage of the disease process are the key factors dictating symptomatology [7]. Pain often subsides as the lesion matures, while a limited range of motion of the adjacent joint often progresses and a subset of patients develop frank ankylosis resulting in the significant functional limitation of the affected joint [7, 20]. None of our patients complained of pain or evident swelling at the time of presentation; they all presented merely with a limited range of motion at the hip joint. Imaging studies constitute a fundamental part in the diagnostic process of MO [7]. Radiographic findings in many cases are sufficient to establish the diagnosis; however, more sophisticated imaging modalities, such as CT scan, MRI, or bone scintigraphy, may be necessary to reach a final diagnosis [7, 8, 9, 10, 11]. CT scans are superior to radiographs as they allow an accurate assessment of the lesion pre-operatively and they best delineate the pattern of calcification[6,21].For our patients, we ordered CT scan of the pelvis with 3D reconstruction to check the site and distribution of the HO as well as determine its relationship to the joint as either attached or separated by soft tissue. A bone scan can reveal increased uptake in the involved area and is considered very sensitive if ordered early enough in the disease course; however, literature lacks clear evidence regarding the practical value that bone scintigraphy offers in determining the appropriate timing for surgical intervention [7, 11]. Historically, it has been suggested that SAP in the setting of traumatic MO may start to increase 3 weeks after the initial injury and levels peak, and can reach values that exceed 10 times the normal limit, at approximately 10 weeks and then return to normal levels by 18 weeks [7, 20, 22]. However, SAP level merely cannot determine the maturity or activity of a lesion as it can remain normal even in active lesions [22]. Thus, SAP levels need to be interpreted within both the clinical and radiographic contexts. Upon presentation, all our cases had SAP levels within normal limits. Since MO ossificans is generally a self-limiting pathology, surgical excision is not the primary choice of treatment in most cases [3, 23]. Failure of non-surgical approach in controlling the symptoms, the presence of intractable pain, neurovascular compromise caused by compression effect, or decreased range of motion affecting the quality of life is all valid indications for surgical management of MO [7,13,17]. When surgery is indicated, excision of the lesion is performed after the lesion has matured; a decision best made with input from the clinical, laboratory (i.e., SAP level), and radiological aspects [17, 19]. In the three cases presented here, the indication for surgical management was the significant reduction in the range of motion around the affected hip joint(s),causing severe limitation of activities of daily living. Based on the findings of the different modalities of imaging that were ordered and the SAP levels, all the cases were considered to be mature MO before surgery. Patients were consented for arthrolysis versus total hip replacement. In the first case, the patient was young and had bilateral hip involvement. In addition, his CT scan revealed the presence of soft tissue separating the ossification from the actual femur bone around the hip joint. This patient successfully underwent staged surgical excision of the ossifications, one side at a time. In the second case, arthrolysis was not possible intraoperatively due to the extensive connection between the HO and the hip joint. The patient thus had a total hip replacement. The third patient underwent excision of the ossification but sustained a stable intertrochanteric fracture intraoperatively, for which a DHS was inserted. Previous reports suggest that post-operative physiotherapy and short-term indomethacin can both contribute to improved outcomes and decreased risk of recurrence [24, 25]. Some researchers also suggest that delivery of radiation locally, whether postoperatively following excision or as part of non-surgical approaches, was associated with positive outcomes [17, 19, 25]. Unfortunately, this modality is not available at our institute. Our three patients all received physiotherapy and oral indomethacin following. At most recent follow-up visits, all three patients demonstrated substantial improvement in the range of motion around the affected hip joint. Patients I and II became able to walk independently and perform all activities of daily living with no limitations. Moreover, they did not demonstrate any signs of recurrence of HOs, whether clinically or radiographically. Unfortunately, our last patient died 1 month after surgery due to pulmonary embolism, making follow-ups for post-operative outcome assessment not possible.

Conclusion
Although MO without a history of direct trauma is considered to be rare, this condition needs to be addressed in more detail in future studies as incidence seems to be increasing with correlation to road traffic accidents yielding brain/spinal cord injuries. Neurogenic MO of the hip joint introduces significant limitation in the activities of daily living, and thus, the quality of life. This condition must be addressed aggressively and managed surgically when indicated. The exact operative approach and timing of surgery are best determined by clinical, laboratory, and radiological inputs. CT scans with 3D reconstruction provide valuable data in determining the best surgical approach. Bone scans and SAP levels can provide useful input regarding the maturity of the lesion. For MO of the hip joint, surgical management by arthrolysis or total hip replacement, followed by post-operative physiotherapy and oral indomethacin, seems to provide satisfactory results.

Clinical Message
Although rare, the neurogenic MO of the hip needs clinical evaluation of its maturity through bone scan and alkaline phosphatase, followed by CT-3D evaluation and surgical planning. Arthrolysis or hip replacement showed significant improvement in range of motion and daily activity when associated with physiotherapy and indomethacin.

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Dr. Yazan Hammad	Dr. Reem Akiely	Dr. Nada Hajjaj	Dr. Farah Tahboub	Dr. Jihad Al-Ajlouni

How to Cite This Article: Hammad Y, Akiely R, Hajjaj N, Tahboub F, Al-Ajlouni J. The surgical management of the rare neurogenic myositis ossificans of the hip: A report of 3 cases. Journal of Orthopaedic Case Reports 2021 March;11(3): 45-51.

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