[左下颌婴儿肌纤维瘤病：一例报告]
[Left mandibular infantile myofibromatosis: a case report].
作者信息
Ren Li-Zhi, Sun Rui
机构信息
Shanxi Medical University School and Hospital of Stomatology, Taiyuan 030001, China.
Dept. of Oral and Maxillofacial Surgery, Shanxi Provincial People's Hospital, Taiyuan 030012, China.
出版信息
Hua Xi Kou Qiang Yi Xue Za Zhi. 2020 Oct 1;38(5):594-597. doi: 10.7518/hxkq.2020.05.021.
Abstract
Infantile myofibromatosis is a rare benign childhood myofibroblastoma. A case of infantile myofibromatosis of the left mandible was reported, and relevant literature was reviewed to discuss the clinical characteristics, pathogenesis, imaging characteristics, pathological characteristics, differential diagnosis, and the treatment of the tumor to improve the understanding of the tumor.
摘要
婴儿肌纤维瘤病是一种罕见的儿童良性肌纤维母细胞瘤。本文报道1例左下颌骨婴儿肌纤维瘤病，并复习相关文献，以探讨该肿瘤的临床特征、发病机制、影像学特征、病理特征、鉴别诊断及治疗方法，以提高对该肿瘤的认识。
相似文献
1
[Left mandibular infantile myofibromatosis: a case report].[左下颌婴儿肌纤维瘤病：一例报告]
Hua Xi Kou Qiang Yi Xue Za Zhi. 2020 Oct 1;38(5):594-597. doi: 10.7518/hxkq.2020.05.021.
2
[Infantile myofibromatosis of the tongue - a case-report].[舌部婴儿肌纤维瘤病——一例报告]
Laryngorhinootologie. 2002 Jun;81(6):422-5. doi: 10.1055/s-2002-32206.
3
Infantile myofibromatosis involving the choroid plexus.累及脉络丛的婴儿肌纤维瘤病。
Pediatr Radiol. 2008 Jan;38(1):107-10. doi: 10.1007/s00247-007-0614-y. Epub 2007 Nov 6.
4
A rare case of infantile myofibromatosis and review of literature.一例罕见的婴儿肌纤维瘤病及文献综述。
J Pediatr Orthop B. 2010 Jan;19(1):122-6. doi: 10.1097/BPB.0b013e32832e4756.
5
Infantile myofibromatosis: case report of a solitary hand lesion with emphasis on differential diagnosis and management.婴儿肌纤维瘤病：一例孤立性手部病变的病例报告，重点在于鉴别诊断和治疗。
Ann Plast Surg. 2001 Jan;46(1):62-7. doi: 10.1097/00000637-200101000-00014.
6
Solitary infantile myofibromatosis in the lateral orbit floor showing spontaneous regression.外侧眶底孤立性婴儿肌纤维瘤病表现为自发消退。
J Laryngol Otol. 2001 May;115(5):419-21. doi: 10.1258/0022215011907811.
7
Infantile myofibromatosis treated by mandibulectomy and staged reconstruction with submental flap and free fibula flap: a case report.下颌骨切除术联合颏下瓣和游离腓骨瓣分期重建治疗婴儿肌纤维瘤病：病例报告。
J Otolaryngol Head Neck Surg. 2019 Mar 14;48(1):14. doi: 10.1186/s40463-019-0333-z.
8
[Infantile myofibromatosis--a case report].[婴儿肌纤维瘤病——病例报告]
Klin Monbl Augenheilkd. 1998 May;212(5):400-2. doi: 10.1055/s-2008-1034918.
9
Infantile myofibromatosis in a three-year-old boy presented as subdural hematoma.
Tumori. 2008 Nov-Dec;94(6):885-7. doi: 10.1177/030089160809400622.
10
[Solitary infantile myofibromatosis of bone].[骨孤立性婴儿肌纤维瘤病]
Ann Pathol. 1996;16(2):108-11.
引用本文的文献
1
[Analysis of 141 cases with benign upper airway occupying in infant].[141例婴幼儿上气道良性占位病例分析]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024 Apr;38(4):334-338. doi: 10.13201/j.issn.2096-7993.2024.04.014.
本文引用的文献
1
Infantile myofibromatosis treated by mandibulectomy and staged reconstruction with submental flap and free fibula flap: a case report.下颌骨切除术联合颏下瓣和游离腓骨瓣分期重建治疗婴儿肌纤维瘤病：病例报告。
J Otolaryngol Head Neck Surg. 2019 Mar 14;48(1):14. doi: 10.1186/s40463-019-0333-z.
2
[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.
3
Agressive pediatric myofibromatosis in a two-year-old child.两岁儿童侵袭性小儿肌纤维瘤病。
J Stomatol Oral Maxillofac Surg. 2018 Jun;119(3):216-219. doi: 10.1016/j.jormas.2017.11.018. Epub 2017 Dec 20.
4
[Infantile myofibroma: a neonate with a swelling on the arm].[婴儿肌纤维瘤：一名手臂有肿物的新生儿]
Ned Tijdschr Geneeskd. 2015;159:A8685.
5
Head and neck solitary infantile myofibroma: Clinicopathological and immunohistochemical features of a case series.头颈部孤立性婴儿肌纤维瘤：一组病例的临床病理及免疫组化特征
Acta Histochem. 2015 May-Jun;117(4-5):431-6. doi: 10.1016/j.acthis.2015.02.001. Epub 2015 Mar 3.
6
Aggressive fibromatosis of the head and neck in the pediatric population.儿童头颈部侵袭性纤维瘤病
Int J Pediatr Otorhinolaryngol. 2014 Jan;78(1):1-4. doi: 10.1016/j.ijporl.2013.10.058. Epub 2013 Nov 14.
7
Mutations in PDGFRB and NOTCH3 are the first genetic causes identified for autosomal dominant infantile myofibromatosis.血小板衍生生长因子受体B（PDGFRB）和Notch3基因的突变是常染色体显性遗传型婴儿肌纤维瘤病首次被确认的遗传病因。
Clin Genet. 2013 Oct;84(4):340-1. doi: 10.1111/cge.12238. Epub 2013 Jul 31.
8
Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis.PDGFRB 基因突变导致常染色体显性遗传婴儿肌纤维瘤病。
Am J Hum Genet. 2013 Jun 6;92(6):1001-7. doi: 10.1016/j.ajhg.2013.04.024. Epub 2013 May 23.
9
A recurrent PDGFRB mutation causes familial infantile myofibromatosis.一个反复出现的 PDGFRB 突变导致家族性婴儿肌纤维瘤病。
Am J Hum Genet. 2013 Jun 6;92(6):996-1000. doi: 10.1016/j.ajhg.2013.04.026. Epub 2013 May 23.
10
Desmoid fibromatosis in pediatric patients: management based on a retrospective analysis of 59 patients and a review of the literature.儿童患者的韧带样型纤维瘤病：基于59例患者的回顾性分析及文献复习的治疗方法
Sarcoma. 2012;2012:475202. doi: 10.1155/2012/475202. Epub 2012 Aug 5.
Zotero 插件