Taiwanese Journal of Obstetrics & Gynecology (Mar 2014)

Complete involution of prenatally-diagnosed fetal scalp hemangioma

  • Eun Ju Jo,
  • Suk-Joo Choi,
  • Soo-young Oh,
  • Byung Kwan Park,
  • Cheong-Rae Roh,
  • Jong-Hwa Kim

DOI
https://doi.org/10.1016/j.tjog.2013.10.038
Journal volume & issue
Vol. 53, no. 1
pp. 86 – 89

Abstract

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Objective: Scalp hemangioma is a rare benign fetal tumor. Here, we describe the detailed imaging features and natural course of a fetal scalp hemangioma until 1 year of age. Case report: We encountered a case of scalp hemangioma at 23 weeks’ gestation by prenatal ultrasonography and magnetic resonance imaging. The mass persisted postnatally, but spontaneously regressed after birth. Conclusion: Proper diagnosis with prenatal ultrasonography and magnetic resonance imaging is important when a scalp mass is suspected in utero. Continuation of the pregnancy after appropriate counseling is prudent, considering the favorable prognosis and the rate of spontaneous regression of uncomplicated cases.

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