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The scalp hair collar and tuft signs: A retrospective multicenter study of 78 patients with a systematic review of the literature.
Bessis, Didier; Bigorre, Michèle; Malissen, Nausicaa; Captier, Guillaume; Chiaverini, Christine; Abasq, Claire; Barbarot, Sébastien; Boccara, Olivia; Bourrat, Emmanuelle; El Fertit, Hassan; Eschard, Catherine; Hubiche, Thomas; Lacour, Jean-Philippe; Leboucq, Nicolas; Mahé, Emmanuel; Mallet, Stéphanie; Marque, Myriam; Martin, Ludovic; Mazereeuw-Hautier, Juliette; Milla, Nathalie; Phan, Alice; Plantin, Patrice; Picot, Marie-Christine; Puzenat, Eve; Rigau, Valérie; Vabres, Pierre; Fraitag, Sylvie; Boralevi, Franck.
Afiliação
  • Bessis D; Department of Dermatology, Saint-Eloi Hospital, Montpellier, France; Montpellier University Hospital and Institut National de la Santé et de la Recherche Médicale (INSERM) U1058, Montpellier, France. Electronic address: d-bessis@chu-montpellier.fr.
  • Bigorre M; Department of Infantile Plastic Surgery, Lapeyronie Hospital, Montpellier, France.
  • Malissen N; Department of Dermatology, Saint-Eloi Hospital, Montpellier, France.
  • Captier G; Department of Infantile Plastic Surgery, Lapeyronie Hospital, Montpellier, France.
  • Chiaverini C; Department of Dermatology, Archet-2 Hospital, Nice, France.
  • Abasq C; Department of Dermatology, Brest University Hospital, Brest, France.
  • Barbarot S; Department of Dermatology, Hôtel-Dieu Hospital, Nantes, France.
  • Boccara O; Department of Pediatric Dermatology, Necker-Enfants Malades Hospital, Paris, France.
  • Bourrat E; Department of Pediatric Dermatology, Robert-Debré Hospital, Paris, France.
  • El Fertit H; Department of Infantile Neurosurgery, Caremeau Hospital, Nîmes, France.
  • Eschard C; Department of Dermatology, Robert-Debré Hospital, Reims, France.
  • Hubiche T; Department of Dermatology and Infectious Diseases, Fréjus Hospital, Fréjus, France.
  • Lacour JP; Department of Dermatology, Archet-2 Hospital, Nice, France.
  • Leboucq N; Department of Neuroradiology, Gui de Chauliac Hospital, Montpellier, France.
  • Mahé E; Department of Dermatology, Argenteuil Hospital, Argenteuil, France.
  • Mallet S; Department of Dermatology, Timone Hospital, Marseille, France.
  • Marque M; Department of Dermatology, Caremeau Hospital, Nîmes, France.
  • Martin L; Department of Dermatology, Angers University Hospital, Angers, France.
  • Mazereeuw-Hautier J; Department of Dermatology, National Center for Rare Skin Disorders, Larrey Hospital, Toulouse, France.
  • Milla N; Department of Dermatology, Saint-Eloi Hospital, Montpellier, France.
  • Phan A; Department of Pediatric Dermatology, Femme-Mère-Enfant Hospital and Claude-Bernard Lyon 1 University, Lyonm, France.
  • Plantin P; Department of Dermatology, Quimper Hospital, Quimper, France.
  • Picot MC; Unit of Clinical Research and Epidemiology, Department of Medical Information, Antonin Balmes Hospital, Montpellier, France.
  • Puzenat E; Department of Dermatology, Besançon University Hospital, Besançon, France.
  • Rigau V; Department of Pathology, Montpellier University Hospital, Montpellier, France.
  • Vabres P; Department of Dermatology, Bocage Hospital and Bourgogne Medical University, Dijon, France.
  • Fraitag S; Department of Pathology, Necker-Enfants Malades University Hospital, Paris, France.
  • Boralevi F; Department of Pediatric Dermatology, National Center for Rare Skin Disorders-Institut National de la Santé et de la Recherche Médicale (INSERM) U1035, Bordeaux, France.
J Am Acad Dermatol ; 76(3): 478-487, 2017 Mar.
Article em En | MEDLINE | ID: mdl-27742172
BACKGROUND: Hair collar sign (HCS) and hair tuft of the scalp (HTS) are cutaneous signs of an underlying neuroectodermal defect, but most available data are based on case reports. OBJECTIVE: We sought to define the clinical spectrum of HCS and HTS, clarify the risk for underlying neurovascular anomalies, and provide imaging recommendations. METHODS: A 10-year multicenter retrospective and prospective analysis of clinical, radiologic, and histopathologic features of HCS and HTS in pediatric patients was performed. RESULTS: Of the 78 patients included in the study, 56 underwent cranial and brain imaging. Twenty-three of the 56 patients (41%) had abnormal findings, including the following: (1) cranial/bone defect (30.4%), with direct communication with the central nervous system in 28.6%; (2) venous malformations (25%); or (3) central nervous system abnormalities (12.5%). Meningeal heterotopia in 34.6% (9/26) was the most common neuroectodermal association. Sinus pericranii, paraganglioma, and combined nevus were also identified. LIMITATIONS: The partial retrospective design and predominant recruitment from the dermatology department are limitations of this study. CONCLUSIONS: Infants with HCS or HTS are at high risk for underlying neurovascular anomalies. Magnetic resonance imaging scans should be performed in order to refer the infant to the appropriate specialist for management.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Crânio / Veias / Anormalidades Múltiplas / Encéfalo / Coristoma / Cabelo / Meninges Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Am Acad Dermatol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Crânio / Veias / Anormalidades Múltiplas / Encéfalo / Coristoma / Cabelo / Meninges Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Am Acad Dermatol Ano de publicação: 2017 Tipo de documento: Article