Infantile Hemangioma of the Genital Region: A Case Report



Biljana Choneska Jovanova1,2*, Aneta Demerdzieva2, Marija Dimitrovska-Ivanova2,3, Snezana Palcevska Kocevska1,2, Natasha Nikchevska1, Aleksandra Jovanovska4

1Acibadem Sistina Hospital, Skopje, Republic of Macedonia.

2Faculty of Medical Sciences, Goce Delcev University, Stip, North Macedonia.

3Clinical Hospital, Stip, North Macedonia.

4University Clinic for Children diseases, Faculty of Medicine, Ss. Cyril and Methodius University in Skopje, Republic of North Macedonia.

*Corresponding Author: Biljana Choneska Jovanova, Acibadem Sistina Hospital in Skopje, Faculty of Medical Sciences Goce Delcev University, Stip; North Macedonia.

https://doi.org/10.58624/SVOAPD.2026.05.018

Received: May 17, 2026

Published: June 26, 2026

Citation: Choneska Jovanova B, Demerdzieva A, Dimitrovska-Ivanova M, Palcevska Kocevska S, Nikchevska N, Jovanovska A. Infantile Hemangioma of the Genital Region: A Case Report. SVOA Paediatrics 2026, 5:3, 126-130. doi: 10.58624/SVOAPD.2026.05.018

 

Abstract

Background: Infantile hemangiomas (IH) are the most common benign tumors in infancy, with a prevalence of 4.5%; less than 1% of these tumors are located in the genital region. This is a case of a 6 weeks old infant presenting with IH in the genital region.

Case presentation: Physical examination revealed a large genital cavernous hemangioma measuring 5 × 4 cm, which involved the labia majora, labia minora, and clitoris. Additionally, several hemangiomas were observed in the lower abdominal wall. A non-indurated ulcer measuring 1 × 1 cm with well-defined margins and a base covered with granulation tissue was observed on the right labia majora of the patient. Ultrasonography of the abdomen, brain, and heart and ECG were normal. We initiated therapy with propranolol (1 mg/kg) in an inpatient setting, with 24h monitoring of possible side effects. The therapy was well tolerated and no adverse effects were observed. After one week, the dose of propranolol was increased to 2 mg/kg in an outpatient setting. After two weeks, there was a great response to the therapy; the hemangioma started to decrease in volume, and the ulceration disappeared. At the age of 16 months, we stopped propranolol therapy when the hemangioma had almost completely disappeared.

Conclusion: Genital IH is rare but is associated with a high risk of ulceration and possible functional impairment. If therapy is indicated, propranolol is effective in the treatment of IH; however, it should be used cautiously, and patients must be closely monitored for adverse effects.

Keywords: Infantile hemangioma, Genital hemangioma, Propranolol