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遗传性感觉和自主神经病变III型和IV型中的周围关节病

Peripheral arthropathy in hereditary sensory and autonomic neuropathy types III and IV.

作者信息

Feldman David S, Ruchelsman David E, Spencer Daniel B, Straight Joseph J, Schweitzer Mark E, Axelrod Felicia B

机构信息

Division of Pediatric Orthopaedic Surgery, New York University Hospital for Joint Diseases, New York, NY 10003, USA.

出版信息

J Pediatr Orthop. 2009 Jan-Feb;29(1):91-7. doi: 10.1097/BPO.0b013e31818f9cc4.

Abstract

BACKGROUND

To determine the features of the underlying destructive arthropathy in the peripheral joints of children with hereditary sensory and autonomic neuropathy (HSAN) type III and to compare and contrast this to the arthropathy noted in HSAN type IV, as both groups experience decreased pain perception.

METHODS

From a database of 547 patients with HSAN type III and 32 patients with HSAN type IV, we performed a retrospective chart review and radiographic analysis of all patients who presented with joint swelling and deformity. Underlying joint pathology was classified as either osteonecrosis or Charcot arthropathy.

RESULTS

In the HSAN type III population, 44 (8%; 22 males and 22 females) of the 547 patients had clinical evidence of arthropathy. In 42 patients, 48 joints demonstrated radiographic evidence of osteonecrosis; 45 (94%) of the 48 joints with osteonecrosis occurred in the lower extremity. In each case of osteonecrosis of the knee (n = 19), isolated involvement of the lateral distal femoral condyle was seen consisting of varying sizes of posterolateral osteochondral fragmentation. In the 32 patients comprising the HSAN type IV population, 18 (56%) were found to have radiographic findings consistent with Charcot arthropathy in a total of 30 affected joints. One patient demonstrated Charcot arthropathy of the spine and subsequent progressive spondylolisthesis. Nine patients (12 joints) also demonstrated osteomyelitis.

CONCLUSIONS

In patients with HSAN type III, osteonecrosis is the initial lesion preceding destructive arthropathy. Osteonecrosis and osteochondral fragmentation were always isolated at the lateral distal femoral condyle in the knee. This pathology may be amenable to surgical reconstruction and fixation to stabilize the knee and prevent further degeneration. Hereditary sensory and autonomic neuropathy type IV was most commonly associated with Charcot arthropathy or joint subluxation and dislocation. Late secondary changes at the articular surface may make radiographic distinction difficult. Charcot arthropathy affected both sides of the involved joint with evidence of collapse and fragmentation. With osteonecrosis, the articular process was found to be more focal.

摘要

背景

确定遗传性感觉和自主神经病变(HSAN)III型患儿外周关节潜在破坏性关节病的特征,并将其与HSAN IV型中观察到的关节病进行比较,因为这两组患者均存在痛觉减退。

方法

从一个包含547例HSAN III型患者和32例HSAN IV型患者的数据库中,我们对所有出现关节肿胀和畸形的患者进行了回顾性病历审查和影像学分析。潜在的关节病理被分类为骨坏死或夏科氏关节病。

结果

在HSAN III型患者群体中,547例患者中有44例(8%;男性22例,女性22例)有关节病的临床证据。在42例患者中,48个关节显示有骨坏死的影像学证据;48个有骨坏死的关节中有45个(94%)发生在下肢。在每例膝关节骨坏死(n = 19)中,均可见外侧股骨远端髁单独受累,表现为不同大小的后外侧骨软骨碎片。在包含HSAN IV型患者群体的32例患者中,18例(56%)在总共30个受累关节中发现有与夏科氏关节病一致的影像学表现。1例患者表现为脊柱夏科氏关节病及随后的进行性椎体滑脱。9例患者(12个关节)还表现为骨髓炎。

结论

在HSAN III型患者中,骨坏死是破坏性关节病之前的初始病变。骨坏死和骨软骨碎片总是孤立于膝关节外侧股骨远端髁。这种病理情况可能适合手术重建和固定,以稳定膝关节并防止进一步退变。遗传性感觉和自主神经病变IV型最常与夏科氏关节病或关节半脱位和脱位相关。关节表面的晚期继发性改变可能使影像学鉴别变得困难。夏科氏关节病累及受累关节的两侧,有塌陷和碎片的证据。对于骨坏死,关节病变更具局限性。

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