Department of Dermatology, Center of Pediatric Dermatology, Erasmus MC University Medical Center Rotterdam-Sophia Children's Hospital, Rotterdam, The Netherlands.
Department of Clinical Genetics, Clinical Institute, Denmark & Odense University Hospital, University of Southern Denmark, Odense, Denmark.
J Eur Acad Dermatol Venereol. 2022 Jul;36(7):973-986. doi: 10.1111/jdv.18043. Epub 2022 Mar 15.
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.
新生儿红斑的广泛鉴别诊断通常具有挑战性。由于红斑本身以及偶尔严重和危及生命的基础疾病的并发症,新生儿红斑的死亡率很高。早期正确识别基础病因可导致更好的治疗和预后。目前,新生儿红斑是逐个病例进行处理的。本综述的目的是制定新生儿红斑的诊断方法。在对 Embase 进行系统文献检索(1990 年 1 月至 2020 年 5 月)后,确定了 74 例新生儿红斑病例,并从中提取了 50 多种诊断。主要原因是鱼鳞病(40%)和原发性免疫缺陷(35%)。先天性红斑见于 64%(74 例中的 47 例)的病例,主要是先天性鱼鳞病(11/11;100%)、 Netherton 综合征(12/14,86%)和 Omenn 综合征(23/23,48%)。非先天性红斑和先天性红斑的诊断时间分别为 102 天至 116 天。在确定的 74 例病例中,共有 17 例(23%)患者在平均 158 天内死亡,与 Omenn 综合征(35%)、移植物抗宿主病(67%)和 Netherton 综合征(18%)有关。本文总结了疾病病史和体检。发病年龄和胶状膜有助于缩小鉴别诊断范围。血液检查、组织学检查、毛发分析、基因分析和临床成像检查均进行了总结和讨论。提出了标准血液检查建议,并强调了进行皮肤活检和淋巴上皮 Kazal 型相关抑制剂染色的必要性。总的来说,本综述表明,诊断程序可缩小新生儿红斑的鉴别诊断范围。提出了一种用于生命第一个月新生儿红斑的诊断方法 6 步流程图。该方法得到了欧洲参考网络皮肤亚专题组鱼鳞病国际多学科合作的专家领导的支持。