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肋骨孤立性、成人发病的骨内肌纤维瘤:一例报告及文献复习

Solitary, adult-onset, intraosseous myofibroma of the rib: a case report and literature review.

作者信息

Weidlich Anne, Pablik Jessica, Schaser Klaus-Dieter, Winkler Doreen, Mehnert Elisabeth, Fritzsche Hagen

机构信息

University Hospital Carl Gustav Carus Dresden, Dresden, Germany.

出版信息

SAGE Open Med Case Rep. 2023 Jun 21;11:2050313X231182791. doi: 10.1177/2050313X231182791. eCollection 2023.

DOI:10.1177/2050313X231182791
PMID:37359281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10288404/
Abstract

Myofibromas are rare benign tumors with myofibroblastic origin. They occur especially in cutis and subcutaneous tissue of the head and the neck, less frequently on the extremities. Myofibromas grow very slowly and are often painless, which is why patients often present relatively late. In the literature, there were many reports about intraosseous myofibromas of the craniofascial bones but reports of the trunk and extremities in adults are very rare. The authors present a very rare case of an intraosseous myofibroma of the ribs resulting in pathological fracture, including a research of literature from other cases of intraosseous myofibromas of the trunk or extremities.

摘要

肌纤维瘤是起源于肌成纤维细胞的罕见良性肿瘤。它们尤其发生在头颈部的皮肤和皮下组织,较少见于四肢。肌纤维瘤生长非常缓慢,通常无痛,这就是患者就诊往往相对较晚的原因。文献中有许多关于颅面骨骨内肌纤维瘤的报道,但关于成人躯干和四肢的报道非常罕见。作者报告了一例非常罕见的肋骨骨内肌纤维瘤导致病理性骨折的病例,并对其他躯干或四肢骨内肌纤维瘤病例的文献进行了研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe2/10288404/4b4907cfb67c/10.1177_2050313X231182791-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe2/10288404/3c37a7dc82cb/10.1177_2050313X231182791-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe2/10288404/4b4907cfb67c/10.1177_2050313X231182791-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe2/10288404/3c37a7dc82cb/10.1177_2050313X231182791-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe2/10288404/4b4907cfb67c/10.1177_2050313X231182791-fig2.jpg

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本文引用的文献

1
Intraosseous solitary myofibroma of the orbit in an adolescent woman.青少年女性眶内骨孤立性肌纤维瘤。
BMJ Case Rep. 2021 Oct 7;14(10):e244800. doi: 10.1136/bcr-2021-244800.
2
Myofibroma/myofibromatosis: MDCT and MR imaging findings in 24 patients with radiological-pathological correlation.肌纤维瘤/肌纤维母细胞瘤:24 例患者的 MDCT 和 MR 成像表现与放射病理学相关性。
BMC Med Imaging. 2020 Aug 26;20(1):100. doi: 10.1186/s12880-020-00498-9.
3
Aggressive Intraosseous Myofibroma of the Maxilla: Report of a Rare Case and Literature Review.
上颌骨侵袭性骨内肌纤维瘤:罕见病例报告及文献复习。
Head Neck Pathol. 2021 Mar;15(1):303-310. doi: 10.1007/s12105-020-01162-y. Epub 2020 Apr 25.
4
A Distinctive Genomic and Immunohistochemical Profile for NOTCH3 and PDGFRB in Myofibroma With Diagnostic and Therapeutic Implications.肌纤维瘤中NOTCH3和PDGFRB独特的基因组及免疫组化特征及其诊断和治疗意义
Int J Surg Pathol. 2020 Apr;28(2):128-137. doi: 10.1177/1066896919876703. Epub 2019 Sep 29.
5
Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis.血小板衍生生长因子受体B(PDGFRB)突变与儿童肌纤维瘤及肌纤维瘤病的关联
JAMA Dermatol. 2019 Aug 1;155(8):946-950. doi: 10.1001/jamadermatol.2019.0114.
6
Infantile myofibromatosis.婴儿肌纤维瘤病
An Bras Dermatol. 2017 Nov-Dec;92(6):854-857. doi: 10.1590/abd1806-4841.20175001.
7
[Myofibroma/myofibromatosis: a clinicopathologic analysis of 9 cases].[肌纤维瘤/肌纤维瘤病:9例临床病理分析]
Zhonghua Bing Li Xue Za Zhi. 2018 Jan 8;47(1):45-50. doi: 10.3760/cma.j.issn.0529-5807.2018.01.009.
8
Solitary intraosseous myofibroma of the ilium in an adult patient: A case report and literature review.成年患者髂骨孤立性骨内肌纤维瘤:一例报告及文献复习
J Orthop Sci. 2020 Jul;25(4):729-733. doi: 10.1016/j.jos.2017.10.010. Epub 2017 Nov 10.
9
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Am J Surg Pathol. 2017 Aug;41(8):1034-1044. doi: 10.1097/PAS.0000000000000862.
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Solitary intraosseous myofibroma of the tibia in an adult patient: A case report.一名成年患者胫骨的孤立性骨内肌纤维瘤:病例报告
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