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进行性假类风湿性发育不良:一个家族中的三例病例

Progressive pseudorheumatoid dysplasia: three cases in one family.

作者信息

Bennani Loubna, Amine Bouchra, Ichchou Linda, Lazrak Noufissa, Hajjaj-Hassouni Najia

机构信息

Rheumatology Department, El-Ayachi Hospital, Rabat-Salé Teaching Hospital, Rabat-Salé, Morocco.

出版信息

Joint Bone Spine. 2007 Jul;74(4):393-5. doi: 10.1016/j.jbspin.2006.11.014. Epub 2007 May 25.

Abstract

UNLABELLED

Progressive pseudorheumatoid dysplasia is an inherited skeletal dysplasia with autosomal recessive transmission. Radiographs of the spine show abnormalities similar to those seen in spondyloepiphyseal dysplasia tarda. The clinical presentation, but not the imaging study findings, suggest juvenile idiopathic arthritis. We report 3 cases of progressive pseudorheumatoid dysplasia in the same family.

CASE-REPORTS: A 4-year-old girl had been receiving follow-up for 3 years for seronegative, polyarticular juvenile idiopathic arthritis progressing by flares and remissions. The disease was unresponsive to anti-inflammatory medications. Findings at admission included inflammatory joint pain, joint swelling, range-of-motion limitation, and joint deformities in the hands, wrists, ankles, and knees. The hips were normal. Normal values were found for the erythrocyte sedimentation rate and C-reactive protein level. Synovial fluid removed from one of the knees exhibited mechanical properties. Plain radiographs of the hands and forefeet showed no evidence of joint destruction. Bilateral hip dysplasia was noted on a radiograph of the pelvis. The diagnosis of juvenile idiopathic arthritis was reconsidered. A study of the family identified two similar cases, in a brother and paternal uncle. The brother, who was 14 years old, had similar manifestations without laboratory evidence of inflammation; radiographs disclosed dysplasia of the hips and metacarpophalangeal epiphyses. Manifestations in a paternal uncle consisted of spinal stiffness, thoracic kyphosis, and motion-range limitation at the hips; radiographs showed normal sacroiliac joints and bilateral hip dysplasia. A diagnosis of progressive pseudorheumatoid dysplasia with polyarticular involvement was given.

DISCUSSION

Progressive pseudorheumatoid dysplasia is an autosomal recessive disease characterized by abnormal cartilage homeostasis. It should be included among the differential diagnoses of juvenile idiopathic arthritis.

摘要

未标注

进行性假类风湿性发育不良是一种常染色体隐性遗传的骨骼发育不良疾病。脊柱X线片显示的异常与迟发性脊椎骨骺发育不良所见相似。临床表现提示幼年特发性关节炎,但影像学检查结果并非如此。我们报告了同一家庭中的3例进行性假类风湿性发育不良病例。

病例报告

一名4岁女孩因血清阴性、多关节幼年特发性关节炎呈发作与缓解交替进展,已接受3年随访。该疾病对抗炎药物无反应。入院时的表现包括炎症性关节疼痛、关节肿胀、活动范围受限以及手部、腕部、踝部和膝部的关节畸形。髋部正常。红细胞沉降率和C反应蛋白水平正常。从一侧膝关节抽取的滑液显示出机械性能。手部和前足的X线平片未显示关节破坏迹象。骨盆X线片显示双侧髋关节发育不良。重新考虑幼年特发性关节炎的诊断。对该家庭进行的一项研究发现,在一名兄弟和其父亲的叔叔身上有两例类似病例。该兄弟14岁,有类似表现,但无炎症的实验室证据;X线片显示髋关节和掌指骨骺发育不良。其父亲的叔叔的表现为脊柱僵硬、胸椎后凸以及髋部活动范围受限;X线片显示骶髂关节正常,双侧髋关节发育不良。诊断为多关节受累的进行性假类风湿性发育不良。

讨论

进行性假类风湿性发育不良是一种常染色体隐性疾病,其特征为软骨内环境稳定异常。它应列入幼年特发性关节炎的鉴别诊断之中。

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