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首页> 外文期刊>Internet Journal of Pediatrics and Neonatology >Midfacial degloving approach to myxoid type nodular fasciitis of the maxilla in a 16-month-old female
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Midfacial degloving approach to myxoid type nodular fasciitis of the maxilla in a 16-month-old female

机译:一名16个月大女性的上颌黏液样结节性筋膜炎的面部脱脂方法

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Nodular fasciitis is a rare, benign tumor of mesenchymal fibroblasts arising from the deep fascia or bony periostium and presents as a mass in the subcutaneous tissues. Due to its rapid growth, it may mimic a malignant lesion. In children, the myxoid type of nodular fasciitis (also termed infiltrative fasciitis, pseudosarcomatous fasciitis, or pseudosarcomatous fibromatosis) is most common with involvement of the head and neck. To date, four cases of nodular fasciitis specifically involving the maxilla have been reported, only one of which includes a description of the surgical approach. This case report describes a 16-month-old female with nodular fasciitis of the nasolabial groove arising from the maxilla. The objective is to discuss and illustrate the imaging appearance of this rare maxillary location of myxoid fasciitis and to describe the successful resection of the mass utilizing the midfacial degloving approach. Introduction Nodular fasciitis is a rare, benign tumor of fibroblastic growth that most often presents in patients between 20 and 40 years of age but may also affect children [123]. While the specific cause for nodular fasciitis is unknown, it is thought to be part of a spectrum of “quasi-neoplastic” lesions [4]. Interestingly, but of unknown significance, is the fact that a history of trauma has been reported to precede the occurrence of the lesion in some cases [5]. In addition to the relationship with trauma, chromosomal abnormalities have been described and may suggest a neoplastic origin [6]. The misdiagnosis as a sarcoma stems from the rapid growth, mitotic activity, and numerous spindle cells [1]. The exact rate of occurrence is unknown because of the common misdiagnosis as a sarcoma [4]. Case Report A 16-month-old girl presented to our children’s tertiary referral center with a rapidly enlarging mass that had been present for 2 weeks. The patient had no pain, fever or epiphora. The parents did not recall any specific trauma (major or minor) recently involving the child’s face. The past medical history was unremarkable and development was age appropriate.Physical exam revealed an overall healthy and active 16-month-old child with a firm 2.0 cm mass obscuring the left nasolabial fold. Anterior rhinoscopy revealed the mass nearly obstructing the left nasal cavity. The mucosa of the nasal cavity and overlying facial skin were uninvolved. The remainder of the physical exam, including the eye exam, was unremarkable.Since the lesion was initially thought to involve the lacrimal sac, the young girl was first seen by ophthalmology. The nasolacrimal duct was probed and flushed intra-operatively, revealing no obstruction. The solid intranasal mass was biopsied, but not resected. The pathology suggested nodular fasciitis (Figure 1).
机译:结节性筋膜炎是由深筋膜或骨性骨膜形成的间充质成纤维细胞罕见的良性肿瘤,在皮下组织中呈肿块状。由于其快速生长,它可能模仿恶性病变。在儿童中,黏液样结节性筋膜炎(也称为浸润性筋膜炎,假性肉瘤性筋膜炎或假性肉瘤性纤维瘤病)最常见于头颈部。迄今为止,已经报告了四例特别涉及上颌的结节性筋膜炎,其中只有一例描述了手术方法。该病例报告描述了一名16个月大的女性,患有上颌骨引起的鼻唇沟结节性筋膜炎。目的是讨论和说明这种罕见的上颌黏液样筋膜炎的影像学表现,并描述使用表面脱脂方法成功切除肿块的方法。引言结节性筋膜炎是一种罕见的成纤维细胞生长的良性肿瘤,多见于20至40岁的患者中,但也可能影响儿童[123]。虽然结节性筋膜炎的具体原因尚不清楚,但它被认为是“准肿瘤性”病变的一部分[4]。有趣的是,但在未知的意义下,事实是,在某些情况下,有创伤史的报道早于创伤的发生[5]。除了与创伤的关系外,还描述了染色体异常,并可能提示肿瘤起源[6]。肉瘤的误诊源于生长迅速,有丝分裂活性和大量梭形细胞[1]。由于常见的误诊为肉瘤,确切的发生率尚不清楚[4]。病例报告一名16个月大的女孩出现在我们孩子的三级转诊中心,其肿块迅速增大,持续了2周。该患者没有疼痛,发烧或癫痫发作。父母没有回想起最近涉及孩子脸部的任何具体创伤(严重或轻微)。既往病史不明显,发展情况适合年龄。体格检查显示,一个整体健康,活跃的16个月大儿童,有2.0厘米的肿块,遮盖了左鼻唇沟。前鼻腔镜检查发现肿物几乎阻塞了左鼻腔。鼻腔粘膜和面部皮肤未受累。其余的身体检查,包括眼科检查,都没有什么变化。由于最初认为病变累及泪囊,因此第一次在眼科就诊了这名年轻女孩。术中探查并冲洗了鼻泪管,未发现阻塞。对该鼻腔内肿物进行活检,但未切除。病理提示结节性筋膜炎(图1)。

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