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Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma

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 ca...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310754/
https://www.ncbi.nlm.nih.gov/pubmed/35238435
http://dx.doi.org/10.1111/jdv.18043
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author 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.
author_facet 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.
author_sort Cuperus, E.
collection PubMed
description 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.
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spelling pubmed-93107542022-07-29 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. J Eur Acad Dermatol Venereol Review Articles 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. John Wiley and Sons Inc. 2022-03-15 2022-07 /pmc/articles/PMC9310754/ /pubmed/35238435 http://dx.doi.org/10.1111/jdv.18043 Text en © 2022 The Authors. Journal of the European Academy of Dermatology and Venereology published by John Wiley & Sons Ltd on behalf of European Academy of Dermatology and Venereology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
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.
Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma
title Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma
title_full Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma
title_fullStr Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma
title_full_unstemmed Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma
title_short Proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma
title_sort proposal for a 6‐step approach for differential diagnosis of neonatal erythroderma
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310754/
https://www.ncbi.nlm.nih.gov/pubmed/35238435
http://dx.doi.org/10.1111/jdv.18043
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