Oe Kenichi, Sasai Kunihiko, Yoshida Yugo, Ohnari Hiroyuki, Iida Hirokazu, Sakaida Noriko, Uemura Yoshiko
Department of Orthopaedic Surgery, Kansai Medical University, 2-3-1 Shinmachi, Hirakata City, Osaka, 573-1191, Japan.
Eur Spine J. 2007 Dec;16 Suppl 3(Suppl 3):301-5. doi: 10.1007/s00586-007-0403-1. Epub 2007 Jun 14.
The authors successfully treated a rare case of pigmented villonodular synovitis (PVNS) that originated from the lumbar facet joint (L4-5). A 43-year-old man presented with a complaint of left severe sciatica causing difficulty in walking. Magnetic resonance imaging (MRI) demonstrated an extradural mass on the left side at L4 and the mass compressed the dural tube and was continuous with the left L4-5 facet joint. A computed tomography myelogram revealed an extradural defect of contrast medium at the L4 level and an erosion of the L4 lamina. A total synovectomy with unilateral osteoplastic laminectomy was performed. The histological findings were a diagnosis of PVNS. The patient's symptoms resolved completely and the MRI at postoperative 3 years demonstrated no recurrence of PVNS. It is important to totally remove the synovium, which is the origin of PVNS in order to prevent the recurrence. We think that our procedure is reasonable and adequate for lumbar PVNS.
作者成功治疗了一例罕见的起源于腰小关节(L4-5)的色素沉着绒毛结节性滑膜炎(PVNS)。一名43岁男性因左侧严重坐骨神经痛导致行走困难前来就诊。磁共振成像(MRI)显示L4左侧硬膜外肿块,该肿块压迫硬膜囊并与左侧L4-5小关节相连。计算机断层扫描脊髓造影显示L4水平硬膜外造影剂缺损及L4椎板侵蚀。行全滑膜切除联合单侧骨成形性椎板切除术。组织学检查结果诊断为PVNS。患者症状完全缓解,术后3年的MRI显示PVNS无复发。为防止复发,彻底切除作为PVNS起源的滑膜很重要。我们认为我们的手术方法对于腰椎PVNS是合理且充分的。