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Pediatric Subcutaneous Scalp Mass: A Case Report and Review.小儿头皮下肿块:病例报告与复习。
Perm J. 2022 Jun 29;26(2):149-152. doi: 10.7812/TPP/21.184. Epub 2022 Jun 15.
2
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Solitary cutaneous infantile myofibroma as a hallmark of myofibromatosis: Two cases and review of the literature.孤立性皮肤幼年性肌纤维瘤作为肌纤维瘤病的特征:两例病例并文献复习。
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Infantile myofibroma: a firm, round plaque in an infant.婴儿肌纤维瘤:婴儿身上的一个坚硬、圆形斑块。
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Precursor B-cell lymphoblastic lymphoma presenting as concurrent enlarging masses on the scalp and postauricular region in a 13-year-old boy.一名13岁男孩患前驱B细胞淋巴母细胞淋巴瘤,表现为头皮和耳后区域同时出现进行性增大的肿块。
Kaohsiung J Med Sci. 2024 May;40(5):509-510. doi: 10.1002/kjm2.12811. Epub 2024 Feb 16.

本文引用的文献

1
Diverse presentation and tailored treatment of infantile myofibromatosis: A single-center experience.婴儿肌纤维瘤病的多样化表现和针对性治疗:单中心经验。
Pediatr Blood Cancer. 2021 Feb;68(2):e28769. doi: 10.1002/pbc.28769. Epub 2020 Oct 16.
2
CARE guidelines for case reports: explanation and elaboration document.病例报告的CARE指南:解释与阐述文件。
J Clin Epidemiol. 2017 Sep;89:218-235. doi: 10.1016/j.jclinepi.2017.04.026. Epub 2017 May 18.
3
Infantile myofibromatosis: a series of 28 cases.婴儿肌纤维瘤病:28 例系列病例。
J Am Acad Dermatol. 2014 Aug;71(2):264-70. doi: 10.1016/j.jaad.2014.03.035. Epub 2014 Jun 2.
4
Myofibromatosis: imaging characteristics.肌纤维瘤病:影像学特征
Pediatr Radiol. 2005 Apr;35(4):374-80. doi: 10.1007/s00247-004-1357-7. Epub 2004 Nov 19.
5
Congenital fibrosarcoma; report of a case in a newborn infant.先天性纤维肉瘤:一例新生儿病例报告。
AMA Arch Pathol. 1951 May;51(5):548-52.
6
Pediatric myofibromatosis of the head and neck.头颈部小儿肌纤维瘤病
Arch Otolaryngol Head Neck Surg. 1999 Jan;125(1):39-44. doi: 10.1001/archotol.125.1.39.
7
Massive apoptosis in infantile myofibromatosis. A putative mechanism of tumor regression.婴儿肌纤维瘤病中的大量细胞凋亡。肿瘤消退的一种可能机制。
Am J Pathol. 1994 Mar;144(3):480-5.
8
Infantile hemangiopericytoma versus infantile myofibromatosis. Study of a series suggesting a continuous spectrum of infantile myofibroblastic lesions.婴儿血管外皮细胞瘤与婴儿肌纤维瘤病。一项系列研究提示婴儿肌纤维母细胞性病变存在连续谱。
Am J Surg Pathol. 1994 Sep;18(9):922-30. doi: 10.1097/00000478-199409000-00007.
9
Infantile myofibromatosis.婴儿肌纤维瘤病
Cancer. 1981 Oct 15;48(8):1807-18. doi: 10.1002/1097-0142(19811015)48:8<1807::aid-cncr2820480818>3.0.co;2-g.

小儿头皮下肿块:病例报告与复习。

Pediatric Subcutaneous Scalp Mass: A Case Report and Review.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Kaiser Permanente Oakland Medical Center, CA, USA.

Department of Pathology, Kaiser Permanente Oakland Medical Center, CA, USA.

出版信息

Perm J. 2022 Jun 29;26(2):149-152. doi: 10.7812/TPP/21.184. Epub 2022 Jun 15.

DOI:10.7812/TPP/21.184
PMID:35933658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9662248/
Abstract

Infantile myofibroma is a unique fibrous tumor encountered in the head and neck. Although the majority of cases are solitary nodules that require only conservative management, awareness of the possibility of multicentric disease is important considering its substantial morbidity. A 3-month-old girl presenting with an enlarging 2.5-cm firm, mobile, nontender subcutaneous scalp mass was evaluated with magnetic resonance imaging and biopsy, revealing a diagnosis of infantile myofibroma. The literature was reviewed for supporting evidence of recommended management in a disease with no official treatment guidelines. Histological, genetic, and imaging characteristics are reviewed. Although biopsy is mandatory, conservative management can be employed for cases without multicentric involvement. Although there are no official guidelines for the evaluation of visceral involvement, skeletal radiograph and abdominal ultrasound are recommended. Infantile myofibroma is a distinct clinical entity with predilection for the head and neck. Its unique immunohistopathology and clinical course should be well understood and should be included in the differential diagnosis of infantile skin and subcutaneous masses.

摘要

婴儿肌纤维瘤是一种在头颈部发现的独特纤维性肿瘤。尽管大多数病例是仅需保守治疗的孤立性结节,但鉴于其发病率较高,了解多中心疾病的可能性很重要。一名 3 个月大的女婴因 2.5 厘米大的、坚实的、可移动的、无触痛的头皮皮下肿块而就诊,经磁共振成像和活检发现婴儿肌纤维瘤的诊断。对文献进行了回顾,以寻找在没有官方治疗指南的疾病中推荐管理的支持证据。回顾了组织学、遗传学和影像学特征。尽管活检是强制性的,但对于没有多中心受累的病例,可以采用保守治疗。虽然没有评估内脏受累的官方指南,但建议进行骨骼 X 线摄影和腹部超声检查。婴儿肌纤维瘤是一种具有头颈部偏好的独特临床实体。其独特的免疫组织病理学和临床病程应得到很好的理解,并应包括婴儿皮肤和皮下肿块的鉴别诊断。