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Osteochondroma of Dorsal Scapula: A Case Report and Review of Literature.肩胛背侧骨软骨瘤:一例报告并文献复习
J Orthop Case Rep. 2023 Jul;13(7):104-109. doi: 10.13107/jocr.2023.v13.i07.3772.
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3
Bilateral scapular osteochondroma in Multiple Hereditary Exostosis patient presented with bilateral shoulder pain treated with arthroscopic and open excision: Case report.多发性遗传性骨软骨瘤患者双侧肩胛部骨软骨瘤伴双侧肩部疼痛,经关节镜及开放切除术治疗:病例报告
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An unusual example of hereditary multiple exostoses: a case report and review of the literature.遗传性多发性外生骨疣的一个不寻常病例报告:病例报告及文献复习。
BMC Musculoskelet Disord. 2021 Jan 21;22(1):96. doi: 10.1186/s12891-021-03967-6.

本文引用的文献

1
Delayed presentation of osteochondroma on the ventral surface of the scapula.肩胛骨腹侧骨软骨瘤的延迟表现。
Int J Shoulder Surg. 2012 Apr;6(2):61-3. doi: 10.4103/0973-6042.96996.
2
Epidemiology of musculoskeletal tumors in Shiraz, south of Iran.伊朗南部设拉子肌肉骨骼肿瘤的流行病学
Indian J Med Paediatr Oncol. 2011 Oct;32(4):187-91. doi: 10.4103/0971-5851.95138.
3
Scapular osteochondromas treated with surgical excision.采用手术切除治疗的肩胛骨肉瘤。
Orthopedics. 2010 Nov 2;33(11):804. doi: 10.3928/01477447-20100924-09.
4
The surgical management of osteochondroma on the ventral surface of the scapula.肩胛骨腹面骨软骨瘤的手术治疗
J Pediatr Orthop B. 2009 Nov;18(6):304-7. doi: 10.1097/BPB.0b013e32832f06f4.
5
Pseudowinging of the scapula due to subscapular osteochondroma.
Orthopedics. 2005 Feb;28(2):171-2. doi: 10.3928/0147-7447-20050201-22.
6
Incomplete penetrance and expressivity skewing in hereditary multiple exostoses.遗传性多发性骨软骨瘤中的不完全外显率和表达性偏倚。
Clin Genet. 1997 Jul;52(1):12-6. doi: 10.1111/j.1399-0004.1997.tb02508.x.
7
The natural history of hereditary multiple exostoses.遗传性多发性骨软骨瘤的自然病史。
J Bone Joint Surg Am. 1994 Jul;76(7):986-92. doi: 10.2106/00004623-199407000-00005.
8
Natural history study of hereditary multiple exostoses.
Am J Med Genet. 1995 Jan 2;55(1):43-6. doi: 10.1002/ajmg.1320550113.

双侧夹入式肩胛骨:遗传性多发性骨软骨瘤的一种罕见表现。

Bilateral sandwiched scapulae: A rare presentation of hereditary multiple exostoses.

作者信息

Mozaffarian Kamran, Farahani Mohammad Javad, Vosoughi Amir Reza

机构信息

Bone and Joint Diseases Research Center, Department of Orthopedic Surgery, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

J Clin Orthop Trauma. 2016 Oct-Dec;7(Suppl 1):5-7. doi: 10.1016/j.jcot.2016.11.003. Epub 2016 Nov 22.

DOI:10.1016/j.jcot.2016.11.003
PMID:28018061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5167512/
Abstract

Hereditary multiple exostoses, an autosomal dominant condition, is a common benign tumor which is characterized by the development of multiple osteochondromas. Bilateral dorsal and ventral involvement of scapulae is extremely rare without any reported case in the literature. An 18-year-old girl was referred because of bilateral prominent scapulae and left-sided pain on shoulder girdle motion especially at more than 90° abduction and forward flexion. Radiograph evaluation showed multiple exostoses on ventral and dorsal surfaces of body of both scapulae; hence simple excision of the lesion was impossible. The patient was symptom-free about 18 months after partial scapulectomy of left side. Partial scapulectomy seems to be an effective treatment for the sandwiched scapula between dorsal and ventral benign tumors.

摘要

遗传性多发性骨软骨瘤是一种常染色体显性疾病,是一种常见的良性肿瘤,其特征是多发骨软骨瘤的形成。双侧肩胛背侧和腹侧受累极为罕见,文献中尚无报道病例。一名18岁女孩因双侧肩胛突出以及肩胛带活动时左侧疼痛(尤其是外展和前屈超过90°时)前来就诊。X线评估显示双侧肩胛骨体的腹侧和背侧表面有多个骨软骨瘤;因此无法对病变进行单纯切除。左侧部分肩胛骨切除术后约18个月,患者无症状。部分肩胛骨切除术似乎是治疗肩胛背侧和腹侧良性肿瘤夹在中间的肩胛骨的有效方法。