Unusual complication following revised total hip arthroplasty

Clinical Cases 10.06.2022
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Section: Musculoskeletal system
Case Type: Clinical Cases
Patient: 79 years, female
Authors: Deng Jia1, Cynthia Assimta Peter1, Farah Gillan Irani1,2
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AI Report

Clinical History

A 79-year-old underwent right total hip arthroplasty (THA) for congenital dislocation with avascular necrosis. Revision surgery a decade later for loosening was complicated by torrential bleeding requiring embolization. Multiple admissions over the following decade for recurrent hemorrhage required embolization leading to hind-quarter amputation due to aggressive osteolysis.

Imaging Findings

Frontal pelvic radiograph (2013) (Figure 1) showed THA with cortical irregularity and sclerosis of right iliac bone at the acetabular cup with adjacent hematoma.

Axial computed tomography (CT) (2017) (Figure 2) showed a hematoma with bony erosion at the right iliac wing.

Contrast CT femur (2020) (Figure 3) demonstrated active arterial sub-capsular haemorrhage with bone erosion and remodelling. Digital subtraction angiography of the right internal iliac artery (2020) (Figure 4) showed extravasation into the hematoma.

Magnetic resonance imaging (MRI), axial T2-weighted image (Figure 5) showed susceptibility artefacts within an expanding aggressive hematoma.

Frontal pelvic radiograph (2021) (Figure 6) showed explantation of right acetabular cup with deformity of right ilium, acetabulum, and pubic rami and calcified rim of hematoma near the medial aspect of the proximal femur.

Coronal and Axial CT (2021) (Figure 7) demonstrated the presence of a pedicled musculocutaneous anterolateral thigh flap in the region of the right ilium.

Discussion

Background

Post-surgical hematoma that persists and enlarges over time is referred to as chronic expanding hematoma (CEH) [1]. Patients with bleeding diathesis and anticoagulant therapy have a higher risk of developing hematomas. Although not completely understood, it is hypothesized that the pathogenesis of CEH is due to fibroblastic reaction in response to the development of the fibrin matrix and cellular breakdown products of haemoglobin and platelets within the hematoma. This activates the inflammatory process, increases vascular permeability, and instigates bleeding from the fragile and dilated capillaries lining the internal cavity of the hematoma [2, 3]. Over time this results in hematoma expansion and in our case, eventual adjacent iliac wing osteolysis.

Clinical perspective

CEH may manifest as anaemia due to continuing blood loss, compressive mass effect over adjacent structures such as neurovascular bundle and ureter, and aggressive behavior such as osteolysis and bone remodelling.  Our patient presented with severe pain and flexion deformity at the hip with inability to ambulate owing to aggressive osteolysis and bone destruction.

Imaging perspective

The usual CT appearance of an acute/ subacute hematoma is a hyperdense lesion (attenuation value 40-75 HU) with a smooth margin. Chronic hematoma is hypodense on CT due to old blood products and may demonstrate a pseudocapsule or a fibrous capsule that demonstrates peripheral enhancement related to new capillaries and granulation tissue [4].

MRI demonstrates internal low, intermediate, and high signals on T1 and T2-weighted imaging related to blood products of varying ages. Enhancement of the irregular pseudocapsule, granulation tissue, and new capillaries can make it challenging to differentiate CEH from a soft tissue sarcoma [5, 6]. Pseudocapsule with low signal intensity on T1- and T2-weighted imaging is also characteristic of CEH [7].

DSA shows active arterial blush in multiple feeding vessels as seen in our patient.

Histologically, CEH appears as a pseudocystic blood-filled lesion with a pseudocapsule composed of fibrous tissue with hemosiderin deposits and iron-laden macrophages [1, 3].

Outcome

The primary treatment of CEH is embolization. Prophylactic fixations are performed in areas of bone erosion and weakening. Complete surgical excision, including resection of the pseudocapsule is considered the gold standard treatment as it allows obtainment of the definitive histologic diagnosis. Incomplete removal may lead to recurrence [8].

Teaching point

CEH is a rare diagnosis with refractory bleeding. Differentiating from malignant tumours can be challenging.

Written informed patient consent for publication has been obtained.

Differential Diagnosis List

Aggressive osteolysis by chronic expanding hematoma
Hemangioma
Soft tissue sarcoma
Inflammatory pseudotumor
Hemangiopericytoma

Final Diagnosis

Aggressive osteolysis by chronic expanding hematoma

Figures

Pelvic Radiograph

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Frontal pelvic radiograph shows right THR with cortical irregularity and sclerosis of right iliac bone related to the acetabu

CT Pelvis

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Axial CT pelvis shows high-density hematoma (white arrow) with erosion of the adjacent right iliac bone margins (black arrow

CT Femur

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CT femur shows hematoma at the fracture site with bone erosion and bone remodeling

DSA angiography of the right internal iliac artery

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DSA angiography of the right internal iliac artery demonstrates significant extravasation into the superior and inferior port

MRI Pelvis

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Axial T2w TRM image shows susceptibility artefacts owing to blood products within an expanding hematoma

Pelvic Radiograph

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Frontal pelvic radiograph shows explantation of right acetabular cup with deformity of right ilium, acetabulum and pubic rami

CT Pelvis

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Cor and Ax CT scan demonstrates presence of pedicled musculocutaneous anterolateral thigh flap in the region of right ilium,