Department of Plastic, Reconstructive and Hand Surgery, Amsterdam University Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
Department of Dermatology, Amsterdam Public Health, Amsterdam University Medical Center, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
Orphanet J Rare Dis. 2022 Mar 2;17(1):95. doi: 10.1186/s13023-022-02234-8.
A congenital melanocytic naevus (CMN) is a rare skin condition that can be associated with abnormalities of the central nervous system (CNS). These anomalies can sometimes cause severe complications, and rarely death. Adequate information about aetiology and management is therefore crucial. To identify how to monitor patients with CMN, we aimed to estimate the prevalence of neurological involvement in patients with CMN and to summarize what specific neurological signs and symptoms and MRI abnormalities are reported in the medical literature. In addition, we summarized and evaluated the recommendations regarding MRI-screening reported in the medical literature.
This review was registered in PROSPERO and reported according to the MOOSE checklist. A search was conducted in EMBASE (Ovid), PubMed, and the Cochrane Library. We included studies with 10 or more patients with CMN, reporting on neurological signs and symptoms or CNS MRI. Study selection, data extraction and methodological quality assessment were performed by two independent reviewers. A meta-analysis was used to assess the prevalence of neurological signs and symptoms.
Out of 1287 studies, fourteen studies were eligible for inclusion of which eight were included in the meta-analysis. Neurological signs and symptoms prevalence was 7.04% (CI 95% 4.47-10.93%) in the meta-analysis group and 6.26% (95% CI 3.85-10%) in a subgroup of patients with a CMN > 6 cm, evaluated in seven studies. Neurodevelopmental delay and seizures were the most frequently reported signs and symptoms. CNS melanocytosis and hydrocephalus were the most frequently reported MRI abnormalities. It was not possible to estimate the increased risk of neurological involvement in patients with CMN due to low quality of evidence and clinical heterogeneity.
Standardization in CMN studies and a multi-centre prospective study are needed to evaluate neurological involvement. Based on current literature, it is not possible to make strong recommendations on routine MRI-screening. For now, every clinical centre should decide on its own policy and weigh the advantages and disadvantages of routine MRI.
先天性黑素细胞痣(CMN)是一种罕见的皮肤疾病,可能与中枢神经系统(CNS)异常有关。这些异常有时会导致严重的并发症,甚至死亡。因此,充分了解病因和治疗方法至关重要。为了确定如何监测 CMN 患者,我们旨在评估 CMN 患者神经受累的患病率,并总结医学文献中报道的特定神经体征和症状以及 MRI 异常。此外,我们总结并评估了医学文献中报道的 MRI 筛查建议。
本综述在 PROSPERO 中进行了注册,并按照 MOOSE 清单进行了报告。在 EMBASE(Ovid)、PubMed 和 Cochrane 图书馆中进行了搜索。我们纳入了 10 例或 10 例以上 CMN 患者报告神经体征和症状或 CNS MRI 的研究。两名独立评审员进行了研究选择、数据提取和方法学质量评估。使用荟萃分析评估神经体征和症状的患病率。
在 1287 项研究中,有 14 项研究符合纳入标准,其中 8 项研究纳入荟萃分析。荟萃分析组中神经体征和症状的患病率为 7.04%(95%CI 95% 4.47-10.93%),而在纳入的 7 项研究中,7 项研究中有 6 项以上 CMN 患者的亚组中,患病率为 6.26%(95%CI 3.85-10%)。神经发育迟缓与癫痫发作是最常报告的体征和症状。CNS 黑素细胞增多症和脑积水是最常报告的 MRI 异常。由于证据质量低和临床异质性,无法估计 CMN 患者神经受累的风险增加。
需要在 CMN 研究中进行标准化,并开展多中心前瞻性研究,以评估神经受累情况。基于目前的文献,不可能对常规 MRI 筛查提出强有力的建议。目前,每个临床中心都应自行制定政策,并权衡常规 MRI 的利弊。