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采用Masquelet技术治疗先天性股骨假关节

Congenital Pseudoarthrosis of the Femur Managed with Masquelet Technique.

作者信息

Kantiwal Prabodh, Aggarwal Aakarsh, Elhence Abhay, Banerjee Sumit

机构信息

Department of Orthopaedics, All India Institute of Medical Sciences, Jodhpur, Rajasthan - 342005, India.

出版信息

J Orthop Case Rep. 2024 Oct;14(10):29-34. doi: 10.13107/jocr.2024.v14.i10.4800.

Abstract

INTRODUCTION

Congenital pseudoarthrosis is a rare disorder, and mostly occurs in the radius, ulna, tibia, and fibula, but is not reported in the femur. Congenital cases that were reported in the literature, most were associated with neurofibromatosis, cleidocranial dysostosis, congenital constriction band syndrome and fibrous dysplasia and the acquired cases followed fractures of bones or tuberculosis. Since the life span of the patient is affected rarely, clinical examination of these patients and serial radiographs can give us plenty of information about the limb abnormality, its clinical course, and the nature of the underlying disturbance of growth.

CASE REPORT

A 3 year female child presents to the outpatient department of a tertiary care hospital with complaints of pain, swelling and deformity thigh region right side for 5 months. On examination, Swelling was present [2x2 cm] at the junction of the mid and distal thigh, smooth surface, ill defined edges, soft and non tender. There was abnormal mobility which was noted at the right thigh at the junction of the middle and distal 1/3 right femurMRI reported circumferential periosteal reaction with cortical surface irregularity of the right femoral shaft was also noted. The findings were reported to be concerning for chronic osteomyelitis with non-united fracture & cortical resorption/chronic bone loss. Histopathological sections showed multiple bits of viable bony trabeculae with surrounding fibro-collagenous tissue displaying significant proliferation of fibroblasts, slit-like blood vessels, arterioles and moderate mixed inflammatory infiltrate of plasma cells, few neutrophils, lymphocytes, histiocytes and few multinucleated histiocytes.She was managed with resection of pseudoarthrosis and masquelet procedure stage 1 and later masquelet stage 2 (cement spacer removal, ipsilateral ileac crest bone grafting with fixation with 7-hole distal fibular anatomical plate and bone graft substitute placement [ChronOs]).

CONCLUSION

Idiopathic or primary congenital pseudoarthrosis can involve the femur as well as other long bones. It may or may not be associated with hip dysplasia and the outcome may not be as bad as previously reported in the pseudoarthrosis of other long bones.

摘要

引言

先天性假关节是一种罕见疾病,主要发生于桡骨、尺骨、胫骨和腓骨,但未见股骨发病的报道。文献报道的先天性病例大多与神经纤维瘤病、锁骨颅骨发育不全、先天性束带综合征和骨纤维发育不良有关,后天性病例则继发于骨折或结核。由于患者寿命很少受到影响,对这些患者进行临床检查和系列X线片检查能够为我们提供大量有关肢体异常、其临床病程以及潜在生长障碍性质的信息。

病例报告

一名3岁女童因右侧大腿疼痛、肿胀及畸形5个月就诊于一家三级医院门诊部。检查发现,大腿中、远端交界处有一[2×2厘米]肿块,表面光滑,边界不清,质地柔软,无压痛。右侧大腿中、远端1/3交界处有异常活动。MRI报告显示右侧股骨干有环形骨膜反应,皮质表面不规则。这些发现提示为慢性骨髓炎合并骨折不愈合及皮质吸收/慢性骨质丢失。组织病理学切片显示多个存活的骨小梁碎片,周围纤维胶原组织中可见成纤维细胞显著增生、裂隙样血管、小动脉以及中等程度的浆细胞、少量中性粒细胞、淋巴细胞、组织细胞和少量多核组织细胞混合性炎症浸润。她接受了假关节切除术及一期Masquelet手术,随后进行了二期Masquelet手术(取出骨水泥间隔物,取自体髂嵴骨移植,用7孔远端腓骨解剖钢板固定,并放置骨移植替代物[ChronOs])。

结论

特发性或原发性先天性假关节可累及股骨以及其他长骨。它可能与髋关节发育不良有关,也可能无关,其预后可能不像之前报道的其他长骨假关节那样差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d81/11458226/8b21b6cc5804/JOCR-14-29-g001.jpg

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