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儿童右肩胛带和颈椎进行性戈谢病1例罕见病例:10年随访及文献复习

A Rare Case of Progressive Gorham's Disease of Right Shoulder Girdle and Cervical Spine in A Child: 10 Year Follow-up and A Review of Literature.

作者信息

Pn Gedam, Ac Dhamangaonkar, An Parekh

机构信息

Department of Orthopaedics, BYL Nair Ch. Hosp. and Topiwala National Medical College, Mumbai-400008. Maharashtra. India.

Department of Orthopaedics, Lokmanya Tilak Municipal Medicl College & General Hospital, Sion, Mumbai-400022. Maharashtra. India.

出版信息

J Orthop Case Rep. 2015 Oct-Dec;5(4):30-3. doi: 10.13107/jocr.2250-0685.339.

DOI:10.13107/jocr.2250-0685.339
PMID:27299093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4845451/
Abstract

INTRODUCTION

'Vanishing Bone Disease' or Gorham's disease is a very rare form of primary idiopathic osteolysis with only around 200 cases being reported till date. We present in this case report a ten year follow-up of a patient who had progressive osteolysis of the right shoulder girdle and eventually involved the spine inspite of supplementary calcium and bisphosphonate therapy. We also report the utility of using an intra-medullary device is to attain acceptable union in case of pathological long bone fracture in Gorham's disease.

CASE

A four year old child presented to us with a spontaneous osteolysis of the right scapula ten years ago in 2003. Within two years, the osteolysis progressed to the entire scapula, clavicle and he had a clavicular fracture. The patient was treated conservatively, oral calcium and bisphosphonate therapy was initiated after ruling out any metabolic bone disease. The patient again sustained a pathological fracture humerus five years later, which was treated with open reduction and internal fixation with an intra-medullary K wire. The fracture united without any other supplementary treatment but osteolysis continued to progressively involve the entire scapula, proximal humerus, clavicle, upper two ribs and the cervical spine.

CONCLUSION

Gorham's disease is a rare disease with an unpredictable course without any satisfactory treatment. There is still a role for surgical intervention to treat long bone pathological fractures secondary to Gorham's disease with an intra-medullary device. The fractures unite without any other supplementary radio or chemotherapy.

摘要

引言

“骨质消失症”或戈勒姆病是一种非常罕见的原发性特发性骨质溶解症,迄今为止仅报告了约200例。在本病例报告中,我们对一名患者进行了为期十年的随访,该患者右肩胛带出现进行性骨质溶解,尽管进行了补充钙剂和双膦酸盐治疗,但最终仍累及脊柱。我们还报告了在戈勒姆病导致病理性长骨骨折的情况下,使用髓内装置实现可接受的骨愈合的效用。

病例

一名四岁儿童于十年前即2003年因右肩胛骨自发性骨质溶解前来就诊。两年内,骨质溶解进展至整个肩胛骨、锁骨,并发生了锁骨骨折。患者接受了保守治疗,在排除任何代谢性骨病后开始口服钙剂和双膦酸盐治疗。五年后患者再次发生肱骨病理性骨折,采用切开复位并用髓内克氏针内固定治疗。骨折未进行任何其他辅助治疗即愈合,但骨质溶解继续逐渐累及整个肩胛骨、肱骨近端、锁骨、上两根肋骨和颈椎。

结论

戈勒姆病是一种罕见疾病,病程不可预测,且没有任何令人满意的治疗方法。对于戈勒姆病继发的长骨病理性骨折,采用髓内装置进行手术干预仍有作用。骨折无需任何其他辅助放疗或化疗即可愈合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4845451/3e2248e11e12/JOCR-5-30-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4845451/301caa7b30eb/JOCR-5-30-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4845451/85685ab274f6/JOCR-5-30-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4845451/426e7d963818/JOCR-5-30-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4845451/3e2248e11e12/JOCR-5-30-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4845451/301caa7b30eb/JOCR-5-30-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4845451/85685ab274f6/JOCR-5-30-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4845451/426e7d963818/JOCR-5-30-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4845451/3e2248e11e12/JOCR-5-30-g004.jpg

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