Multisystem Infantile Hemangiomatosis with Cutaneous, Hepatic, and Splenic Involvement
The present case illustrates the rarity and complexity of multifocal infantile haemangiomatosis and highlights the importance of early diagnosis, comprehensive organ evaluation, and tailored multidisciplinary management. It clearly demonstrates that prompt intervention and careful therapy adjustment can lead to favorable outcomes even in the setting of extensive visceral involvement.
Authors
- Cristina Blag (ORCID: https://orcid.org/0000-0003-4111-1295)
- Tudor Lucian Pop (ORCID: https://orcid.org/0000-0002-4931-1219)
- Otilia Fufezan
- Gabriel Bența (ORCID: https://orcid.org/0000-0002-2099-8379)
- Alexandra Mititelu (ORCID: https://orcid.org/0000-0002-0955-4486)
- Alina Grama (ORCID: https://orcid.org/0000-0001-7022-6345)
- Mădălina Bota
- Elvira Ioana Buda
- Diana Borcău
Institutions
- Iuliu Hațieganu University of Medicine and Pharmacy (RO)
- Clinical Emergency Hospital Bucharest (RO)
Publication Details
- Journal
- Pediatric Reports
- Published
- 2025-10-03
- DOI
- https://doi.org/10.3390/pediatric17050102
- Citations
- 1
- Primary Topic
- Vascular Malformations and Hemangiomas
- Type
- article
- Field-Weighted Citation Impact
- 2.01