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Published on: June 15, 2020
Propranolol-resistant infantile haemangiomas
S Caussé1, H Aubert, M Saint-Jean
1Department of Dermatology, Centre Hospitalier Universitaire Hôtel-Dieu, 1 place Alexis-Ricordeau, 44093 Nantes Cedex 1, France.
Insights
Propranolol-resistant infantile haemangiomas (PRIH) are rare, affecting less than 1% of patients. This study characterizes PRIH, noting its occurrence across various ages and proliferation stages.
Area of Science:
- Pediatric Dermatology
- Pharmacology
- Clinical Research
Background:
- Propranolol is a standard treatment for severe infantile haemangiomas (IHs).
- Propranolol-resistant infantile haemangiomas (PRIH) are infrequently documented in medical literature.
Purpose of the Study:
- To characterize the clinical features of infantile haemangiomas resistant to propranolol treatment.
- To investigate the prevalence and presentation of PRIH.
Main Methods:
- A national, multicentre, retrospective, observational study was conducted.
- Data were collected from patients evaluated between January 2007 and December 2011.
Main Results:
- Out of 1130 patients treated with propranolol for IH, 10 (0.9%) exhibited PRIH.
- PRIH was observed in children of all ages and at any stage of haemangioma proliferation.
Conclusions:
- Propranolol-resistant infantile haemangioma is a rare clinical entity.
- Further research is warranted to understand the mechanisms and management of PRIH.
Background:
Propranolol is now widely used to treat severe infantile haemangiomas (IHs). Very few cases of propranolol-resistant IH (PRIH) are mentioned in the literature.
Objectives:
To describe the characteristics of PRIHs.
Methods:
A national, multicentre, retrospective, observational study was conducted from February 2011 to December 2011. All patients with PRIH evaluated by the members of the Groupe de Recherche Clinique en Dermatologie Pédiatrique from 1 January 2007 to 1 December 2011 were eligible.
Results:
Among 1130 patients treated with propranolol for infantile haemangioma, 10 (0.9%) had PRIHs. Haemangioma propranolol resistance was observed at all ages during early childhood and at any proliferation stage.
Conclusions:
PRIH is a rare phenomenon that raises questions and merits further investigation.
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