Fibromatosis colli: A rare neck mass of the sternocleidomastoid muscle in an infant: A case report

IF 0.3 Q4 OTORHINOLARYNGOLOGY
Otolaryngology Case Reports Pub Date : 2026-03-01 Epub Date: 2025-11-17 DOI:10.1016/j.xocr.2025.100714
Tesfa G/Meskel , Mesfin Wubishet , Nuri Mama , Ayalneh Demissie
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Abstract

Background

Fibromatosis colli (FC), also known as sternocleidomastoid pseudotumor of infancy, is a rare benign proliferation of fibrous tissue within the sternocleidomastoid muscle. It typically presents as a unilateral neck mass during the first weeks of life. Although self-limiting, early recognition is essential to prevent unnecessary investigations and to reduce the risk of complications such as congenital torticollis.

Case presentation

We report the case of a 3-week-old female neonate who presented with a painless, left-sided neck swelling of one week’s duration. Clinical examination revealed a firm, non-tender mass along the sternocleidomastoid muscle. Ultrasonography confirmed the diagnosis of Fibromatosis colli. The patient was managed conservatively with physiotherapy, resulting in near-complete resolution of the mass and restoration of normal neck mobility within three months.

Conclusion

Fibromatosis colli is an uncommon but clinically significant cause of neck swelling in neonates and may closely mimic neoplastic lesions. It should be considered in the differential diagnosis of unilateral neck masses in early infancy. Accurate diagnosis is typically achieved through targeted clinical examination complemented by ultrasonography. Early initiation of physiotherapy is highly effective, typically resulting in complete recovery without the need for surgical intervention. Timely recognition and differentiation from other neonatal neck masses are crucial to avoid unnecessary invasive procedures, alleviate parental anxiety, and prevent complications such as persistent torticollis and craniofacial asymmetry.
结缔组织瘤病:婴儿胸锁乳突肌罕见颈部肿块1例报告
背景:乳突纤维瘤病(FC),也称为婴儿期胸锁乳突假瘤,是一种罕见的胸锁乳突肌内纤维组织的良性增生。在生命的最初几周,它通常表现为单侧颈部肿块。虽然有局限性,但早期识别对于防止不必要的调查和减少并发症(如先天性斜颈)的风险至关重要。病例介绍我们报告的情况下,3周大的女性新生儿谁提出了无痛,左侧颈部肿胀的一个星期的时间。临床检查发现沿胸锁乳突肌有一坚固无压痛肿块。超声检查证实为大肠纤维瘤病。患者接受了保守的物理治疗,三个月内肿块几乎完全消退,颈部活动恢复正常。结论大肠纤维瘤病是一种罕见但临床意义重大的新生儿颈部肿胀病因,与肿瘤病变相似。在婴儿期早期单侧颈部肿块的鉴别诊断中应予以考虑。准确的诊断通常通过有针对性的临床检查和超声检查来实现。早期开始物理治疗是非常有效的,通常导致完全恢复而不需要手术干预。及时识别和区分其他新生儿颈部肿块对于避免不必要的侵入性手术,减轻父母的焦虑,防止并发症如持续性斜颈和颅面不对称是至关重要的。
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来源期刊
Otolaryngology Case Reports
Otolaryngology Case Reports Medicine-Otorhinolaryngology
CiteScore
0.50
自引率
0.00%
发文量
99
审稿时长
21 weeks
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