A5057477803- Vascular Malformations and Hemangiomas
- Vascular Tumors and Angiosarcomas
- Cutaneous lymphoproliferative disorders research
- Histiocytic Disorders and Treatments
- Contact Dermatitis and Allergies
- Vascular Malformations Diagnosis and Treatment
- Skin and Cellular Biology Research
- Cardiac tumors and thrombi
- Autoimmune Bullous Skin Diseases
- Tumors and Oncological Cases
- Nail Diseases and Treatments
- Dermatology and Skin Diseases
- Sarcoma Diagnosis and Treatment
- Infectious Diseases and Mycology
- Eosinophilic Disorders and Syndromes
- Occupational exposure and asthma
- Genetic and rare skin diseases.
- Drug-Induced Adverse Reactions
- Tuberous Sclerosis Complex Research
- Cancer and Skin Lesions
- PI3K/AKT/mTOR signaling in cancer
- Chronic Lymphocytic Leukemia Research
- Sympathectomy and Hyperhidrosis Treatments
- Autoimmune and Inflammatory Disorders Research
- Parvovirus B19 Infection Studies
Cliniques Universitaires Saint-Luc
2013-2024
Queen Fabiola Children's University Hospital
2023
Centre Hospitalier Universitaire de Bordeaux
2020
Hôpital Necker-Enfants Malades
2011-2012
Abstract Background and purpose Sturge–Weber syndrome (SWS) is a neurocutaneous disorder characterized by clinical manifestations involving the brain, eye skin. SWS commonly caused somatic mutations in G protein subunit Alpha Q ( GNAQ ). Five cases of s ubunit 11 GNA11 ) have been reported. We studied phenotypic features GNA11‐SWS compared them with those classic SWS. Methods Within two European multidisciplinary centers we looked for patients characteristics mutation. Clinical radiological...
Punctate palmoplantar keratoderma (PPKP1; Buschke-Fischer-Brauer) is a rare autosomal dominant inherited skin disease characterized by multiple hyperkeratotic papules involving the palms and soles. Mutations have been found at 2 loci, on chromosomes 15q22-15q24 8q24.13-8q24.21. We recently identified mutations in 3 families, AAGAB gene 15q, which encodes alpha- gamma-adaptin-binding protein p34. The current study examined 14 additional comprising total of 26 affected individuals 8 novel 9...
Background: To assess the impact of propranolol as first-line treatment infantile hemangioma (IH) on need for surgery in management IH. Methods: Retrospective study 420 patients, with IH, referred to our multidisciplinary center between January 2005 and August 2014. Clinical data including sex, age at first consultation initiation, location, size, number, aspect, complication well type were collected. Statistical analyses conducted considering each patient tumor independently. Results: A...
Abstract We herein report the case of a 3‐year‐old girl with atypical congenital right upper limb lymphedema who developed an angiosarcoma. Only few cases have been reported following form and only 4 in such young child. also summarize all angiosarcoma associated literature.
Background: Our objective was to describe the clinical, histological characteristics, and disease outcome of a cohort mycosis fungoides (MF) diagnosed during childhood including status at adulthood. Methods: This is retrospective multicentre survey patients aged under 18 years diagnosis with histologically confirmed MF. Patients’ clinical treatments, (for followed for more than 12 months) were analysed. Results: Forty-six included (median age diagnosis: 11 years; M:F sex ratio: 3:1) 39 (85%)...
Schnitzler syndrome is an underdiagnosed clinical condition characterized by 2 major criteria: chronic recurrent urticarial eruption and monoclonal IgM gammopathy, as well at least of the following minor (1) fever, (2) high C-reactive protein (CRP) levels, (3) signs abnormal bone remodeling with or without pain, (4) neutrophilic infiltrates on skin biopsy.1 We report case a patient history hairy cell leukemia who exhibited atypical presentation urticaria for years before final diagnosis was...