1.Three Level Thoracolumbar Spondylectomy for Recurrent Giant Cell Tumour of the Spine: A Case Report
Faruk NA ; Mohd-Amin MZ ; Awang-Ojep DN ; Teo YY ; Wong CC
Malaysian Orthopaedic Journal 2018;12(3):50-52
Giant cell tumour (GCT) is a benign tumour but can be locally aggressive and with the potential to metastasise especially to the lungs. Successful treatments have been reported for long bone lesions; however, optimal surgical and medical treatment for spinal and sacral lesions are not well established. In treating spinal GCTs, the aim is to achieve complete tumour excision, restore spinal stability and decompress the neural tissues. The ideal surgical procedure is an en bloc spondylectomy or vertebrectomy, where all tumour cells are removed as recurrence is closely related to the extent of initial surgical excision. However, such a surgery has a high complication rate, such as dura tear and massive blood loss. We report a patient with a missed pathological fracture of T12 treated initially with a posterior subtraction osteotomy, who had recurrence three years after the index surgery and subsequently underwent a three level vertebrectomy and posterior spinal fusion.
2.Pigmented Villonodular Synovitis (PVNS) of the Knee mimicking Septic Arthritis in a Paediatric Patient: A Case Report
Indra F ; Anuar-Ramdhan IM ; Vick-Duin E ; Awang-Ojep DN
Malaysian Orthopaedic Journal 2021;15(No.3):122-126
Pigmented villonodular synovitis (PVNS) is a benign but
rare proliferative disorder of the synovium. It commonly
occurs in the adult population and usually presents as a
monoarticular disease. There are two types of PVNS, namely
the localised and diffused type. The disease is often
misdiagnosed due to its rarity especially in paediatric
patients. Knee involvement in PVNS is the commonest form
in children although other joints such as hip, foot, ankle, hip,
sacroiliac joint and concurrent multiple joint involvements
have also been reported. PVNS in paediatric patients is often
misdiagnosed as septic arthritis, juvenile rheumatoid arthritis
and bone sarcoma, and the diagnosis is usually often made
late due to its vague presentation. The majority of PVNS
cases are managed by surgery either via open or arthroscopic
synovectomy except in a few paediatric patients as described
in the literature. This case report of PVNS is of a knee in 11-
year-old boy who was initially treated as septic arthritis. The
synovium appearance mimicked the features of PVNS
during a knee arthrotomy washout, and histopathological
examination confirmed the diagnosis. The knee symptoms
had significantly improved without additional surgery, and
good functional knee motion was achieved, with no sign of
recurrence, after two years of follow-up.