Literature DB >> 10890989

Neonatal and infantile erythrodermas: a retrospective study of 51 patients.

A Pruszkowski1, C Bodemer, S Fraitag, D Teillac-Hamel, J C Amoric, Y de Prost.   

Abstract

OBJECTIVE: To determine the frequency of the various underlying causes of erythroderma in newborns or infants, as well as which clinical or laboratory findings were relevant for the etiological diagnosis. PATIENTS: Fifty-one patients who presented with exfoliative erythroderma during their first year of life were included in this retrospective study.
SETTING: Department of Pediatric Dermatology at a university hospital.
RESULTS: On average, the etiological diagnosis was established 11 months after the onset of erythroderma. The underlying causes observed included immunodeficiency (30%), simple or complex ichthyosis (24%), Netherton syndrome (18%), and eczematous or papulosquamous dermatitis (20%). Five patients (10%) had erythroderma of unknown origin. The following parameters were of value in determining the underlying cause of erythroderma: congenital onset, skin induration and the presence of large scaling plaques, alopecia with or without hair dysplasia, evolution, response to topical corticosteroid therapy, presence of infections, and failure to thrive. Histological analysis confirmed the diagnosis in only 19 (45%) of 42 cases. However, it proved of great value for the detection of significant lymphocyte infiltration or keratinocyte necrosis indicating a diagnosis of Omenn syndrome or immunodeficiency. The prognosis was poor in this series: the mortality rate was 16%, and severe dermatosis persisted in 29 (67%) of the survivors.
CONCLUSIONS: The etiological diagnosis of neonatal erythroderma is difficult to make; some clinical features may be helpful, but no one feature is characteristic of a cause. An immunodeficiency must be suspected in cases of severe erythroderma with skin induration, severe alopecia, failure to thrive, infectious complications, or evocative histological findings. The prognosis is poor, with a high rate of mortality in immunodeficiency disorders and severe chronic disease in Netherton syndrome and psoriasis.

Entities:  

Mesh:

Year:  2000        PMID: 10890989     DOI: 10.1001/archderm.136.7.875

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  11 in total

Review 1.  [Red, scaly baby: a pediatric dermatological emergency : Clinical and differential diagnoses of neonatal erythroderma].

Authors:  H Ott; J Grothaus
Journal:  Hautarzt       Date:  2017-10       Impact factor: 0.751

Review 2.  Netherton Syndrome: A Genotype-Phenotype Review.

Authors:  Constantina A Sarri; Angeliki Roussaki-Schulze; Yiannis Vasilopoulos; Efterpi Zafiriou; Aikaterini Patsatsi; Costas Stamatis; Polyxeni Gidarokosta; Dimitrios Sotiriadis; Theologia Sarafidou; Zissis Mamuris
Journal:  Mol Diagn Ther       Date:  2017-04       Impact factor: 4.074

3.  Netherton syndrome: report of identical twins presenting with severe atopic dermatitis.

Authors:  Gurkan Kilic; Nermin Guler; Ulker Ones; Zeynep Tamay; Pinar Guzel
Journal:  Eur J Pediatr       Date:  2006-05-03       Impact factor: 3.183

4.  Netherton syndrome with pili torti.

Authors:  Sahana M Srinivas; Ravi Hiremagalore; Swetha Suryanarayan; Leelavathy Budamakuntala
Journal:  Int J Trichology       Date:  2013-10

5.  Intercellular skin barrier lipid composition and organization in Netherton syndrome patients.

Authors:  Jeroen van Smeden; Michelle Janssens; Walter A Boiten; Vincent van Drongelen; Laetitia Furio; Rob J Vreeken; Alain Hovnanian; Joke A Bouwstra
Journal:  J Invest Dermatol       Date:  2013-11-29       Impact factor: 8.551

6.  Madarosis: a marker of many maladies.

Authors:  Annapurna Kumar; Kaliaperumal Karthikeyan
Journal:  Int J Trichology       Date:  2012-01

7.  [Neonatal erythroderma: do not ignore an immune deficiency].

Authors:  Aziza El Ouali; Yousra El Boussaadni; Fatima Ailal; Ahmed Aziz Bousfiha; Sihame Dikhaye; Noufissa Benajiba
Journal:  Pan Afr Med J       Date:  2014-08-21

8.  Severe erytrodermic psoriasis in child twins: from clinical-pathological diagnosis to treatment of choice through genetic analyses: two case reports.

Authors:  Elena Campione; Laura Diluvio; Alessandro Terrinoni; Augusto Orlandi; Maria Paola Latino; Claudia Torti; Lucia Pietroleonardo; Elisabetta Botti; Sergio Chimenti; Luca Bianchi
Journal:  BMC Res Notes       Date:  2014-12-17

9.  Outcomes of Systemic Treatment in Children and Adults With Netherton Syndrome: A Systematic Review.

Authors:  Anouk E M Nouwen; Renske Schappin; N Tan Nguyen; Aviël Ragamin; Anette Bygum; Christine Bodemer; Virgil A S H Dalm; Suzanne G M A Pasmans
Journal:  Front Immunol       Date:  2022-03-30       Impact factor: 8.786

10.  Neonatal erythroderma: diagnostic and therapeutic challenges.

Authors:  Sandipan Dhar; Raghubir Banerjee; Rajib Malakar
Journal:  Indian J Dermatol       Date:  2012-11       Impact factor: 1.494

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