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纤维瘤病导致的斜头畸形伴大体解剖和超声相关性。

Fibromatosis colli leading to positional plagiocephaly with gross anatomical and sonographic correlation.

机构信息

Diagnostic Radiology, Tripler Army Medical Center, Honolulu, Hawaii, USA

Neuroscience, Duke University, Durham, North Carolina, USA.

出版信息

BMJ Case Rep. 2021 Jan 11;14(1):e239236. doi: 10.1136/bcr-2020-239236.

Abstract

Fibromatosis colli, also known as 'sternocleidomastoid tumour of infancy' or 'pseudotumour of infancy', is a rare condition involving fibrosis and swelling, or 'tumour' of the sternocleidomastoid muscle in newborns that typically occurs after a traumatic delivery. Although usually self-limited, fibromatosis colli can lead to congenital muscular torticollis and positional plagiocephaly due to uneven forces on the neonatal skull. Ultrasound is the diagnostic imaging modality of choice and can prevent additional imaging and unnecessary intervention.

摘要

纤维瘤病颈,又称“婴儿胸锁乳突肌肿瘤”或“婴儿假瘤”,是一种罕见疾病,涉及纤维化和肿胀,或新生儿胸锁乳突肌“肿瘤”,通常发生在创伤性分娩后。虽然通常是自限性的,但纤维瘤病颈可导致先天性肌性斜颈和位置性扁头畸形,因为新生儿颅骨受力不均。超声是首选的诊断成像方式,可以防止额外的成像和不必要的干预。

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Fibromatosis colli of infancy: variability of sonographic appearance.婴儿期颈部纤维瘤病:超声表现的变异性
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本文引用的文献

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Congenital muscular torticollis.先天性肌性斜颈
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The presentation and management of fibromatosis colli.婴儿肌性斜颈的临床表现与治疗
Ear Nose Throat J. 2010 Sep;89(9):E4-8. doi: 10.1177/014556131008900902.
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