Fibromatosis colli

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Imaging description A one-month-old male presented with a palpable right neck mass, which had been noticed 10 days previously. The mass was not perceived to be painful or bothersome to the patient. There was no reported fever or weight loss. He was feeding normally and there was ipsilateral mild torticollis. He was born at 37 weeks by cesarean section due to cardiac decelerations during labor. Imaging evaluation with ultrasound (US) (Fig. 2.1a) demonstrated heterogeneous, mass-like enlargement involving the right inferior sternocleidomastoid muscle (SCM). The mass tapered gently toward the SCM and was surrounded by normal appearing SCM. The fascial planes surrounding the muscle were preserved. There were morphologically normal appearing prominent ipsilateral cervical chain lymph nodes. The lesion did demonstrate moderate internal vascularity on Doppler ultrasound (Fig. 2.1b).An MRI was also performed in spite of the fact that the US appearance was strongly suggestive of fibromatosis colli. This demonstrated enlargement of the inferior right SCM, with intact surrounding fascial planes. The process was confined to the inferior SCM. There was increased T2 signal and heterogeneous enhancement of the involved muscle (Fig. 2.1c, d, e). There were no calcifications present in the lesion. The MRI findings also supported the diagnosis of fibromatosis colli.

Original languageEnglish (US)
Title of host publicationPearls and Pitfalls in Pediatric Imaging
Subtitle of host publicationVariants and Other Difficult Diagnoses
PublisherCambridge University Press
Pages7-9
Number of pages3
Volume9781107017498
ISBN (Electronic)9781139084239
ISBN (Print)9781107017498
DOIs
StatePublished - Jan 1 2012

Bibliographical note

Publisher Copyright:
© Heike Daldrup-Link and Beverley Newman 2014.

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