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Pediatric Subcutaneous Scalp Mass: A Case Report and Review

机译:小儿皮下头皮肿块:病例报告和回顾

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摘要

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.
机译:婴儿肌纤维瘤是一种发生在头部和颈部的独特纤维瘤。尽管大多数病例是孤立性结节,只需要保守治疗,但考虑到其发病率高,认识多中心疾病的可能性很重要。一名 3 个月大的女孩表现为 2.5 cm 坚硬、可移动、无触痛的皮下肿块,通过磁共振成像和活检进行评估,揭示婴儿肌纤维瘤的诊断。对文献进行了综述,以寻找在没有官方治疗指南的疾病中推荐治疗的支持证据。总结组织学、遗传学和影像学特征。虽然活检是强制性的,但对于没有多中心参与的病例,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 线检查和腹部超声检查。婴儿肌纤维瘤是一种独特的临床疾病,好发于头部和颈部。应充分了解其独特的免疫组病理学和临床病程,并应纳入婴儿皮肤和皮下肿块的鉴别诊断中。

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