Congenital haemangiomas: a single-centre retrospective review

Objective Congenital haemangiomas (CHs) are rare, benign vascular tumours that are fully developed at birth. Three subtypes of CHs have been described based on clinical behaviour: rapidly involuting CHs (RICHs), non-involuting CHs (NICHs) and partially involuting CHs (PICHs). We explore in our study...

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Main Authors: Nicolas Grenier, Victoire Braun, Sorilla Prey, Carlotta Gurioli, Franck Boralevi, Alain Taieb, Maya Loot, Marie-Laure Jullie, Christine Léauté-Labrèze
Format: Article
Language:English
Published: BMJ Publishing Group 2020-04-01
Series:BMJ Paediatrics Open
Online Access:https://bmjpaedsopen.bmj.com/content/4/1/e000816.full
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spelling doaj-56e263432240453faa2ce113a84cdd6d2021-05-24T11:01:08ZengBMJ Publishing GroupBMJ Paediatrics Open2399-97722020-04-014110.1136/bmjpo-2020-000816Congenital haemangiomas: a single-centre retrospective reviewNicolas Grenier0Victoire Braun1Sorilla Prey2Carlotta Gurioli3Franck Boralevi4Alain Taieb5Maya Loot6Marie-Laure Jullie7Christine Léauté-Labrèze84 Department of Radiology, CHU de Bordeaux, Bordeaux, Aquitaine, France1 Dermatology, CHU de Bordeaux, Bordeaux, France1 Dermatology, CHU de Bordeaux, Bordeaux, France 3 Department of Specialized, Experimental and Diagnostic Medicine, Dermatology, University of Bologna, University of Bologna, Bologna, Emilia-Romagna, Italy1 Dermatology, CHU de Bordeaux, Bordeaux, France 1 Dermatology, CHU de Bordeaux, Bordeaux, France 5 Paediatric Surgery Department, CHU de Bordeaux, Bordeaux, Aquitaine, France6 Pathology Department, CHU de Bordeaux, PESSAC, Aquitaine, France1 Dermatology, CHU de Bordeaux, Bordeaux, France Objective Congenital haemangiomas (CHs) are rare, benign vascular tumours that are fully developed at birth. Three subtypes of CHs have been described based on clinical behaviour: rapidly involuting CHs (RICHs), non-involuting CHs (NICHs) and partially involuting CHs (PICHs). We explore in our study clinical, evolutionary and paraclinical characteristics of the three CH subtypes.Design Children with CH attending our department of paediatric dermatology at Bordeaux University Hospital over a 13-year period were retrospectively included. Epidemiological, clinical and evolutionary data, photographs and imaging results were reviewed. All available tissue samples were histologically examined.Results We included 57 patients: 22 with RICH, 22 with NICH and 13 with PICH. Males predominated (ratio 1.7); the most common CH location was on the limbs. RICH, NICH and PICH exhibited overlapping characteristics; all were single telangiectatic lesions with pale peripheral halos. At birth, NICHs were flat but RICHs and PICHs bulky. The median age at complete RICH involution was 12 months. One-third of CHs that appeared RICH-like at birth underwent incomplete involution to become PICHs. Heart failure and thrombocytopenia were rare complications. PICHs were frequently ulcerated. Pain was common for NICH and PICH. The imaging and histological data of the three CH subtypes were rather similar.Conclusions We describe the characteristics and evolution of the three CH subtypes using a case series. Certain overlapping features were apparent, reinforcing the hypothesis that RICH, NICH and PICH lie on the same pathological spectrum.https://bmjpaedsopen.bmj.com/content/4/1/e000816.full
collection DOAJ
language English
format Article
sources DOAJ
author Nicolas Grenier
Victoire Braun
Sorilla Prey
Carlotta Gurioli
Franck Boralevi
Alain Taieb
Maya Loot
Marie-Laure Jullie
Christine Léauté-Labrèze
spellingShingle Nicolas Grenier
Victoire Braun
Sorilla Prey
Carlotta Gurioli
Franck Boralevi
Alain Taieb
Maya Loot
Marie-Laure Jullie
Christine Léauté-Labrèze
Congenital haemangiomas: a single-centre retrospective review
BMJ Paediatrics Open
author_facet Nicolas Grenier
Victoire Braun
Sorilla Prey
Carlotta Gurioli
Franck Boralevi
Alain Taieb
Maya Loot
Marie-Laure Jullie
Christine Léauté-Labrèze
author_sort Nicolas Grenier
title Congenital haemangiomas: a single-centre retrospective review
title_short Congenital haemangiomas: a single-centre retrospective review
title_full Congenital haemangiomas: a single-centre retrospective review
title_fullStr Congenital haemangiomas: a single-centre retrospective review
title_full_unstemmed Congenital haemangiomas: a single-centre retrospective review
title_sort congenital haemangiomas: a single-centre retrospective review
publisher BMJ Publishing Group
series BMJ Paediatrics Open
issn 2399-9772
publishDate 2020-04-01
description Objective Congenital haemangiomas (CHs) are rare, benign vascular tumours that are fully developed at birth. Three subtypes of CHs have been described based on clinical behaviour: rapidly involuting CHs (RICHs), non-involuting CHs (NICHs) and partially involuting CHs (PICHs). We explore in our study clinical, evolutionary and paraclinical characteristics of the three CH subtypes.Design Children with CH attending our department of paediatric dermatology at Bordeaux University Hospital over a 13-year period were retrospectively included. Epidemiological, clinical and evolutionary data, photographs and imaging results were reviewed. All available tissue samples were histologically examined.Results We included 57 patients: 22 with RICH, 22 with NICH and 13 with PICH. Males predominated (ratio 1.7); the most common CH location was on the limbs. RICH, NICH and PICH exhibited overlapping characteristics; all were single telangiectatic lesions with pale peripheral halos. At birth, NICHs were flat but RICHs and PICHs bulky. The median age at complete RICH involution was 12 months. One-third of CHs that appeared RICH-like at birth underwent incomplete involution to become PICHs. Heart failure and thrombocytopenia were rare complications. PICHs were frequently ulcerated. Pain was common for NICH and PICH. The imaging and histological data of the three CH subtypes were rather similar.Conclusions We describe the characteristics and evolution of the three CH subtypes using a case series. Certain overlapping features were apparent, reinforcing the hypothesis that RICH, NICH and PICH lie on the same pathological spectrum.
url https://bmjpaedsopen.bmj.com/content/4/1/e000816.full
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