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Proposal for a 6-step approach for differential diagnosis of neonatal erythroderma.
Cuperus, E; Bygum, A; Boeckmann, L; Bodemer, C; Bolling, M C; Caproni, M; Diociaiuti, A; Emmert, S; Fischer, J; Gostynski, A; Guez, S; van Gijn, M E; Hannulla-Jouppi, K; Has, C; Hernández-Martín, A; Martinez, A E; Mazereeuw-Hautier, J; Medvecz, M; Neri, I; Sigurdsson, V; Suessmuth, K; Traupe, H; Oji, V; Pasmans, S G M A.
Afiliação
  • Cuperus E; Department of Dermatology, Center of Pediatric Dermatology, Erasmus MC University Medical Center Rotterdam-Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Bygum A; Department of Clinical Genetics, Clinical Institute, Denmark & Odense University Hospital, University of Southern Denmark, Odense, Denmark.
  • Boeckmann L; Clinic and Policlinic for Dermatology and Venereology, University Medical Center Rostock, Rostock, Germany.
  • Bodemer C; Department of Dermatology, Reference Center for Genodermatoses (MAGEC), Necker-Enfants Malades Hospital (AP-HP5), Imagine Institute, INSERM, Paris-Centre University, Paris, France.
  • Bolling MC; Department of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Caproni M; Department of Health Sciences, Section of Dermatology, USL Toscana Centro, Rare Diseases Unit, University of Florence, Florence, Italy.
  • Diociaiuti A; Dermatology Unit and Genodermatosis Unit, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Emmert S; Clinic and Policlinic for Dermatology and Venereology, University Medical Center Rostock, Rostock, Germany.
  • Fischer J; Institute of Human Genetics, Medical Faculty and Medical Center, University of Freiburg, Freiburg, Germany.
  • Gostynski A; Department of Dermatology, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Guez S; GROW School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, The Netherlands.
  • van Gijn ME; Pediatrics Department, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.
  • Hannulla-Jouppi K; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Has C; Department of Dermatology and Allergology, University of Helsinki and Helsinki University Central Hospital, HUS, Helsinki, Finland.
  • Hernández-Martín A; Department of Dermatology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Martinez AE; Department of Dermatology, Hospital Infantil Niño Jesús, Madrid, Spain.
  • Mazereeuw-Hautier J; Pediatric Dermatology, NHS Foundation Trust, London, UK.
  • Medvecz M; Dermatology Department, Reference Center for Rare Skin Diseases, Toulouse, France.
  • Neri I; Department of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
  • Sigurdsson V; Dermatology - IRCCS Policlinico di Sant'Orsola - Department of Experimental, Diagnostic and Specialty Medicine (DIMES) Alma Mater, Studiorum University of Bologna, Bologna, Italy.
  • Suessmuth K; Department of Dermatology, University Medical Center Utrecht and Utrecht University, Utrecht, The Netherlands.
  • Traupe H; Department of Dermatology, University Hospital of Münster, Münster, Germany.
  • Oji V; Department of Dermatology, University Hospital of Münster, Münster, Germany.
  • Pasmans SGMA; Department of Dermatology, University Hospital of Münster, Münster, Germany.
J Eur Acad Dermatol Venereol ; 36(7): 973-986, 2022 Jul.
Article em En | MEDLINE | ID: mdl-35238435
ABSTRACT
The broad differential diagnosis of neonatal erythroderma often poses a diagnostic challenge. Mortality of neonatal erythroderma is high due to complications of the erythroderma itself and the occasionally severe and life-threatening underlying disease. Early correct recognition of the underlying cause leads to better treatment and prognosis. Currently, neonatal erythroderma is approached on a case-by-case basis. The purpose of this scoping review was to develop a diagnostic approach in neonatal erythroderma. After a systematic literature search in Embase (January 1990 - May 2020, 74 cases of neonatal erythroderma were identified, and 50+ diagnoses could be extracted. Main causes were the ichthyoses (40%) and primary immunodeficiencies (35%). Congenital erythroderma was present in 64% (47/74) of the cases, predominantly with congenital ichthyosis (11/11; 100%), Netherton syndrome (12/14, 86%) and Omenn syndrome (11/23, 48%). Time until diagnosis ranged from 102 days to 116 days for cases of non-congenital erythroderma and congenital erythroderma respectively. Among the 74 identified cases a total of 17 patients (23%) died within a mean of 158 days and were related to Omenn syndrome (35%), graft-versus-host disease (67%) and Netherton syndrome (18%). Disease history and physical examination are summarized in this paper. Age of onset and a collodion membrane can help to narrow the differential diagnoses. Investigations of blood, histology, hair analysis, genetic analysis and clinical imaging are summarized and discussed. A standard blood investigation is proposed, and the need for skin biopsies with lympho-epithelial Kazal-type related Inhibitor staining is highlighted. Overall, this review shows that diagnostic procedures narrow the differential diagnosis in neonatal erythroderma. A 6-step flowchart for the diagnostic approach for neonatal erythroderma during the first month of life is proposed. The approach was made with the support of expert leaders from international multidisciplinary collaborations in the European Reference Network Skin-subthematic group Ichthyosis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunodeficiência Combinada Severa / Ictiose Lamelar / Dermatite Esfoliativa / Síndrome de Netherton / Ictiose Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunodeficiência Combinada Severa / Ictiose Lamelar / Dermatite Esfoliativa / Síndrome de Netherton / Ictiose Idioma: En Ano de publicação: 2022 Tipo de documento: Article