| Literature DB >> 27317759 |
Erica Torres1, João Rosa1, Christine Leaute-Labreze2, Luis Soares-de-Almeida3.
Abstract
We describe a case of a newborn who presented with multiple dark red macules that developed into red-to-purple papules associated with thrombocytopaenia. Abdominal ultrasound showed multiple hyperechoic papules and nodules. Endothelial cells from a skin biopsy stained positively for endothelial cell glucose transporter 1, which was consistent with a diagnosis of multifocal infantile haemangioma. At the age of 2 months, the child developed intestinal bleeding and anaemia. Upper and lower endoscopies showed no intestinal haemangiomas. Oral treatment with propranolol (3 mg/kg/day) resulted in complete involution of the skin and hepatic haemangiomas over the period of treatment, which lasted until the child was aged 15 months. This is a rare case of multifocal cutaneous haemangioma with hepatic and probable intestinal involvement, successfully treated with propranolol. 2016 BMJ Publishing Group Ltd.Entities:
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Year: 2016 PMID: 27317759 PMCID: PMC4932334 DOI: 10.1136/bcr-2016-214827
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X