Kaneko Hiroshi, Kitoh Hiroshi, Wasa Junji, Nishida Yoshihiro, Ishiguro Naoki
Department of Orthopaedic Surgery, Nagoya University, School of Medicine, Nagoya, Aichi, Japan.
J Pediatr Orthop B. 2012 Mar;21(2):179-82. doi: 10.1097/BPB.0b013e3283484c31.
Chondroblastoma is a rare benign chondroid bone tumor, which typically arises from the epiphysis of a long tubular bone. We present a 13-year-old girl with persistent hip synovitis caused by a chondroblastoma that arose from the femoral neck (metaphysis) and uniquely extended extraosseously into the hip joint. Computed tomography scan clearly demonstrated a tumoral lesion of the left femoral neck and a periosteal reaction along the anterior cortex of the femur, distal to the legion. Magnetic resonance imaging showed reactive synovitis with marked joint effusion of the hip and an extensive edema in the proximal femur and the surrounding soft tissues. Aneurysmal bone cysts formation secondary to chondroblastoma was confirmed by histologic examinations of the excised specimens. Complete relief of pain and an improvement in the range of movement of the hip joint was obtained after surgical resection of the tumor.
软骨母细胞瘤是一种罕见的良性软骨样骨肿瘤,通常起源于长管状骨的骨骺。我们报告一名13岁女孩,患有由起源于股骨颈(干骺端)并独特地向骨外延伸至髋关节的软骨母细胞瘤引起的持续性髋关节滑膜炎。计算机断层扫描清楚地显示了左股骨颈的肿瘤性病变以及沿股骨前皮质在病变远端的骨膜反应。磁共振成像显示反应性滑膜炎伴髋关节明显关节积液以及股骨近端和周围软组织广泛水肿。切除标本的组织学检查证实了软骨母细胞瘤继发的骨囊肿形成。肿瘤手术切除后疼痛完全缓解,髋关节活动范围得到改善。