The Importance of Follow-Up: Juvenile Xanthogranuloma Mimicking Cephalohematoma

Authors

  • Elizabeth Rooks John A Burns School of Medicine, Honolulu, HI, USA https://orcid.org/0000-0001-6763-4081
  • Megan Buras University of Miami, Miami, FL, USA
  • Andrea Stephenson MD Brian D Allgood Army Community Hospital, Seoul, Korea
  • Elianna Goldstein MD Department of Radiology, Tripler Army Medical Center, HI, USA

DOI:

https://doi.org/10.3941/jrcr.4829

Keywords:

Juvenile Xanthogranuloma, Cephalohematoma, Follow-up care, Ultrasonography

Abstract

Juvenile xanthogranuloma is a type of non-Langerhans cell histiocytosis primarily affecting infants and young children. It is an uncommon disease and is rarely considered in the differential in radiological studies of infants. A case of juvenile xanthogranuloma mimicking a cephalohematoma in an otherwise healthy 3-month-old infant born via vacuum assisted delivery is presented here. At a follow-up appointment, interval growth and internal color Doppler flow with arterial waveform were noted on ultrasound. The differential diagnosis was expanded to include other well-circumscribed hypoechoic scalp lesions. At 8 months of age the lesion was surgically excised, and immunohistochemistry established the definitive diagnosis of juvenile xanthogranuloma. This case emphasizes the importance of following cephalohematomas clinically to resolution in order to exclude an alternate underlying pathology.

Author Biographies

Elizabeth Rooks, John A Burns School of Medicine, Honolulu, HI, USA

Medical Student

Megan Buras, University of Miami, Miami, FL, USA

Undergraduate Student

A 3-month-old male patient with juvenile xanthogranuloma.

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Published

2025-06-30

Issue

Section

Pediatric Radiology