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头颈部小儿结节性筋膜炎:评估与管理

Pediatric nodular fasciitis in the head and neck: evaluation and management.

作者信息

Hseu Anne, Watters Karen, Perez-Atayde Antonio, Silvera V Michelle, Rahbar Reza

机构信息

Department of Otolaryngology and Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts.

Department of Pathology, Boston Children's Hospital, Boston, Massachusetts.

出版信息

JAMA Otolaryngol Head Neck Surg. 2015 Jan;141(1):54-9. doi: 10.1001/jamaoto.2014.2797.

Abstract

IMPORTANCE

Nodular fasciitis is a rare benign tumor that can present in the head and neck in children. A better understanding of this rare condition is critical to optimize management.

OBJECTIVE

To review the presentation, evaluation, diagnosis, and management of pediatric nodular fasciitis of the head and neck.

DESIGN, SETTING, AND PARTICIPANTS: Retrospective review of all patients treated for nodular fasciitis of the head and neck over a 20-year period at a pediatric tertiary care center.

INTERVENTION

Surgical excision.

MAIN OUTCOMES AND MEASURES

Clinical data, including age, presenting symptoms, anatomical site(s), evaluation, treatment, and complications.

RESULTS

Fifteen children with pathologically confirmed nodular fasciitis of the head and neck were identified, including 8 boys and 7 girls. The median (range) age at diagnosis was 9.3 years (2 months to 18 years). Patients most commonly presented with a firm, enlarging soft-tissue mass. Two patients reported pain, and 1 patient presented with erythema. The most common location was the maxillofacial region (5 patients). Other locations included the scalp (3 patients), forehead (2 patients), neck (2 patients), mandible (1 patient), postauricular region (1 patient), and nasal dorsum (1 patient). One patient reported a preceding trauma, and 1 patient, a preceding infection. Presurgical imaging varied; imaging modalities used included computed tomography, magnetic resonance imaging, radiography, ultrasound, and sialography. All patients underwent surgical excision, which focused on excising the mass while preserving surrounding normal tissues. Mean (range) follow-up was 7.69 (0-46) months. Two minor complications were reported: 1 patient who underwent a near-total excisional biopsy experienced residual firmness and tenderness at the site of the lesion and another patient was left with an unfavorable cosmetic scar that necessitated intralesional steroid injection. No patient demonstrated recurrence at follow-up.

CONCLUSIONS AND RELEVANCE

Although an uncommon diagnosis, nodular fasciitis should be considered in the evaluation and treatment of head and neck soft-tissue masses in children. Preoperative imaging is nonspecific and variable. Pathological findings are necessary for diagnosis. Surgical excisional biopsy is curative, with no instances of recurrence in our series.

摘要

重要性

结节性筋膜炎是一种罕见的良性肿瘤,可发生于儿童的头颈部。更好地了解这种罕见疾病对于优化治疗至关重要。

目的

回顾儿童头颈部结节性筋膜炎的临床表现、评估、诊断和治疗。

设计、地点和参与者:对一家儿科三级护理中心20年间所有接受头颈部结节性筋膜炎治疗的患者进行回顾性研究。

干预措施

手术切除。

主要结局和指标

临床数据,包括年龄、首发症状、解剖部位、评估、治疗和并发症。

结果

确定了15例经病理证实的头颈部结节性筋膜炎患儿,其中8例男孩,7例女孩。诊断时的中位(范围)年龄为9.3岁(2个月至18岁)。患者最常见的表现是一个质地坚硬、不断增大的软组织肿块。2例患者报告有疼痛,1例患者有红斑。最常见的部位是颌面区域(5例)。其他部位包括头皮(3例)、前额(2例)、颈部(2例)、下颌骨(1例)、耳后区域(1例)和鼻背(1例)。1例患者报告有先前的创伤,1例患者有先前的感染。术前影像学检查结果各异;使用的影像学检查方法包括计算机断层扫描、磁共振成像、X线摄影、超声和唾液造影。所有患者均接受了手术切除,重点是在保留周围正常组织的同时切除肿块。平均(范围)随访时间为7.69(0 - 46)个月。报告了2例轻微并发症:1例接受了近乎全切活检的患者在病变部位出现残留的硬结和压痛,另1例患者留下了不理想的美容瘢痕,需要进行病灶内类固醇注射。随访期间无患者复发。

结论及意义

尽管结节性筋膜炎是一种不常见的诊断,但在评估和治疗儿童头颈部软组织肿块时应予以考虑。术前影像学检查缺乏特异性且结果各异。诊断需要病理检查结果。手术切除活检具有治愈性,在我们系列研究中无复发病例。

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