Prenatal sonography of multicentric infantile myofibromatosis: Case report and review of the literature

Scant literature exists on prenatally diagnosed infantile myofibromatosis (IM). We report a case of multicentric IM, which was first recognized as a soft‐tissue paraspinal mass on prenatal sonography and subsequently characterized by MRI with pathological confirmation.

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Bibliographic Details
Published inJournal of clinical ultrasound Vol. 47; no. 8; pp. 490 - 493
Main Authors Rekawek, Patricia, Coleman, Beverly G., Kamath, Amita, Stone, Joanne L.
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.10.2019
Wiley Subscription Services, Inc
Subjects
Adult
Case reports
Connective tissue diseases
Diagnosis, Differential
Female
Humans
Infant, Newborn
infantile myofibromatosis
Literature reviews
Magnetic resonance imaging
Male
MRI
Myofibromatosis - congenital
Myofibromatosis - diagnosis
obstetrics
Pregnancy
soft tissue mass
sonography
Ultrasonic imaging
Ultrasonography, Prenatal - methods
soft tissue mass
infantile myofibromatosis
obstetrics
MRI
sonography
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Summary:Scant literature exists on prenatally diagnosed infantile myofibromatosis (IM). We report a case of multicentric IM, which was first recognized as a soft‐tissue paraspinal mass on prenatal sonography and subsequently characterized by MRI with pathological confirmation.
Bibliography:ObjectType-Case Study-3
SourceType-Scholarly Journals-1
content type line 23
ObjectType-Review-1
ObjectType-Feature-5
ObjectType-Report-2
ObjectType-Article-4
ISSN:0091-2751
1097-0096
DOI:10.1002/jcu.22731