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颧骨的长期存在的软骨黏液样纤维瘤:一例罕见病例报告及文献复习

Long-lasting chondromyxoid fibroma of the zygoma: A rare case report and review of literature.

作者信息

Ashraf Mohammad Javad, Azarpira Negar, Omidifar Navid, Khademi Bijan

机构信息

Department of Pathology, Clinical Pathology Division, Department of Pathology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

J Educ Health Promot. 2017 Aug 9;6:78. doi: 10.4103/jehp.jehp_33_17. eCollection 2017.

DOI:10.4103/jehp.jehp_33_17
PMID:28852667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5561685/
Abstract

Chondromyxoid fibroma (CMF) is a benign tumor which usually occurs in skeletal long bones. Its presence in zygoma is extremely rare. The patient was a 47-year-old female, with chief complaint of painful swelling in the left side of zygoma since 1 month ago after a long-lasting painless swelling for about 15 years. Computed tomography scan showed an osteolytic lesion, in the body of left zygomatic bone with lobulated and well-demarcated margins. During surgery, the mass was completely excised and the histological feature of the tumor was in favor of CMF. CMF is benign tumor and complete resection is the treatment of choice.

摘要

软骨黏液样纤维瘤(CMF)是一种通常发生于骨骼长骨的良性肿瘤。其在颧骨出现极为罕见。该患者为一名47岁女性,主诉自1个月前左侧颧骨出现疼痛性肿胀,在此之前有长达约15年的无痛性肿胀。计算机断层扫描显示左侧颧骨体部有一个溶骨性病变,边缘呈分叶状且界限清晰。手术中,肿块被完整切除,肿瘤的组织学特征支持软骨黏液样纤维瘤的诊断。软骨黏液样纤维瘤是良性肿瘤,完整切除是首选的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a270/5561685/6422ede995e9/JEHP-6-78-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a270/5561685/6edd8e4eb496/JEHP-6-78-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a270/5561685/e123dce0f406/JEHP-6-78-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a270/5561685/b1d61133c419/JEHP-6-78-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a270/5561685/6422ede995e9/JEHP-6-78-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a270/5561685/6edd8e4eb496/JEHP-6-78-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a270/5561685/e123dce0f406/JEHP-6-78-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a270/5561685/b1d61133c419/JEHP-6-78-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a270/5561685/6422ede995e9/JEHP-6-78-g004.jpg

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引用本文的文献

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Chondromyxoid fibroma of the temporal bone: A rare case report.颞骨软骨黏液样纤维瘤:1例罕见病例报告

本文引用的文献

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Ann Maxillofac Surg. 2015 Jul-Dec;5(2):244-8. doi: 10.4103/2231-0746.175755.
2
Chondromyxoid fibroma of zygoma: A rare case report.颧骨软骨黏液样纤维瘤:1例罕见病例报告
J Oral Maxillofac Pathol. 2014 Jan;18(1):93-6. doi: 10.4103/0973-029X.131924.
3
A rare case of epiphyseal chondromyxoid fibroma of the proximal tibia.胫骨近端骨软骨黏液样纤维瘤 1 例罕见病例报告。
Medicine (Baltimore). 2020 Mar;99(11):e19487. doi: 10.1097/MD.0000000000019487.
Korean J Radiol. 2011 Nov-Dec;12(6):761-4. doi: 10.3348/kjr.2011.12.6.761. Epub 2011 Sep 27.
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Chondromyxoid fibroma of the skull base invading the occipitocervical junction: report of a unique case and discussion.侵犯枕颈交界区的颅底软骨黏液样纤维瘤:1例罕见病例报告及讨论
Skull Base. 2010 Mar;20(2):101-4. doi: 10.1055/s-0029-1225534.
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Chondromyxoid fibroma of bone; a distinctive benign tumor likely to be mistaken especially for chondrosarcoma.骨软骨黏液样纤维瘤;一种独特的良性肿瘤,尤其容易被误诊为软骨肉瘤。
Arch Pathol (Chic). 1948 Apr;45(4):541-51.
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Chondromyxoid fibroma of the skull base: differential diagnosis and radiotherapy: two case reports and a review of the literature.颅底软骨黏液样纤维瘤:鉴别诊断与放射治疗:两例病例报告及文献复习
Acta Oncol. 2005;44(6):545-53. doi: 10.1080/00365590500237846.
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Chondromyxoid fibroma of the parietal bone.顶骨软骨黏液样纤维瘤
Neuropathology. 2005 Mar;25(1):84-8. doi: 10.1111/j.1440-1789.2004.00576.x.
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Chondromyxoid fibromas: a study of 10 cases.软骨黏液样纤维瘤:10例病例研究
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