Congenital torticollis in an infant

IF 0.1 Q4 PEDIATRICS
Priyantha Pang, Jeyasakthy Saniasiaya, Jeyanthi Kulasegarah
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引用次数: 0

Abstract

Introduction: Fibromatosis colli is an uncommon congenital infantile tumour occurring in 0.4–1.3% of live births. They are non-malignant, however early detection and treatment are crucial. This is because, if left untreated, fibromatosis colli tumours can cause permanent disfigurements to the skull and spine of the infant. The main aetiology that causes congenital fibromatosis colli is believed to be muscle injury, either intrauterine or during childbirth. A common symptom of congenital fibromatosis colli is head tilting toward the affected side. Case report: This case report discusses the management of an 82-day-old infant with fibromatosis colli. Discussion: Clinical examination including palpation and examination of the range of movement of the sternocleidomastoid muscle is the key to diagnosing fibromatosis colli. Early physiotherapy represents the first-line treatment in affected infants.
婴儿先天性斜颈
大肠纤维瘤病是一种罕见的先天性婴儿肿瘤,发生率为活产婴儿的0.4-1.3%。它们是非恶性的,但早期发现和治疗至关重要。这是因为,如果不及时治疗,纤维瘤病会导致婴儿的头骨和脊柱永久性毁容。引起先天性大肠纤维瘤病的主要病因被认为是子宫内或分娩时的肌肉损伤。先天性结肠纤维瘤病的常见症状是头部向患病一侧倾斜。病例报告:本病例报告讨论了一例82日龄婴儿结肠炎纤维瘤病的处理。讨论:临床检查包括触诊及胸锁乳突肌活动范围检查是诊断大肠纤维瘤病的关键。早期物理治疗是患病婴儿的一线治疗。
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
33
审稿时长
20 weeks
期刊介绍: PEDIATRIA I MEDYCYNA RODZINNA is a peer-reviewed scientific journal publishing original articles that constitute significant contributions to the advancements of paediatrics and family medicine. In addition, PEDIATRIA I MEDYCYNA RODZINNA, publishes information from the medical associations, reports and materials from international congresses, letters to the Editor, information on new medical products as well as abstracts and discussions on papers published in other scientific journals, reviews of books and other publications.
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