Unusual Case of Diffuse Neonatal Hemangiomatosis Case Report and Literature Review
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Updated: May 10, 2026

Isolation of Neonatal Extrahepatic Cholangiocytes
Published on: June 5, 2014
Fatima Zahrae El Mansoury1, Zakia El Yousfi1, Mohamed Ismail Halfi1
1Radiology Department Mother and Child Hospital IBN SINA, Rabat, Morocco.
Abstract:
Diffuse neonatal hemangiomatosis (DNH) is an infrequent condition characterized by the simultaneous occurrence of multiple cutaneous hemangiomas and the involvement of 3 or more organs. DNH is suspected when multiple hemangiomas are identified on the skin of the infant. Although it is benign in nature, DNH can lead to critical and life-threatening complications. Diagnosis primarily relies on clinical evaluation with a significant emphasis on imaging techniques. In this case report, we present an unusual pediatric case of diffuse infantile hemangioendothelioma, for which the investigative approach included ultrasound and CT scans. These imaging methods were instrumental in revealing the presence of lesions in the liver, thyroid, and brain, ultimately playing a pivotal role in making the diagnosis of DNH. A positive clinical and biological improvement was observed with corticosteroid treatment during a 3-month follow-up.
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