Emerging insights into cephalic neural crest disorders: A single center experience

M. Nayak, B. Mishra, Sebastian Levejoseph, Ajay Garg, Kalyan Sarma, Biswajit Sahoo, Manjari Tripathi, Shailesh B. Gaikwad
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Abstract

Neural crest cells (NCCs) are transient structures in the fetal life in vertebrates, which develop at the junctional site of the non-neural and neural ectoderm, sharing a common developmental origin for diverse diseases. After Epithelio-mesenchymal (EMT) of the NCCs within the neural tube, delamination of NCCs occurs. After delamination, the transformation of these cells into various cell lineages produces melanocytes, bones, and cartilage of the skull, cells of the enteric and peripheral nervous system. After the conversion, these cells migrate into various locations of the entire body according to the cell lineage. Abnormalities in neural crest (NC) formation and migration result in various malformations and tumors, known as neurocristopathy. Herein, this case series describes a single-center experience in cephalic NC disorders over the past 3 years, including 17 cases of varying composition (i.e., vascular, dysgenetic, mixed, and neoplastic forms) involving the brain and occasionally skin, eyes, and face of the patients. In our study of 17 patients with cephalic NC disease, 6 (35.3%) patients had vascular form, 5 (29.4%) had dysgenetic form, 4 (23.5%) had mixed form, and 2 (11.7%) had neoplastic form. Brain involvement in the form of vascular or parenchyma or both vascular and parenchymal was seen in all of our patients (100%), skin in 6 (35.3%) patients, eye in 2 (11.7%), and face in 1 (5.9%) patient. Treatment was planned according to the various manifestations of the disease. Neural crest diseases (NCDs) are a rare and under-recognized group of disorders in the literature and may have been under-reported due to a lack of awareness regarding the same. More such reporting may increase the repertoire of these rare disorders such that clinicians can have a high degree of suspicion leading to early detection and timely counseling and also improve preventive strategies and help in developing new drugs for these disorders or prevent them.
对头神经嵴疾病的新认识:单中心经验
神经嵴细胞(NCCs)是脊椎动物胎儿时期的瞬时结构,发育在非神经外胚层和神经外胚层的交界处,是多种疾病的共同发育起源。神经管内的 NCC 上皮-间充质化(EMT)后,NCC 发生分层。分层后,这些细胞转变为各种细胞系,产生黑色素细胞、骨骼、颅骨软骨、肠道和周围神经系统细胞。转化后,这些细胞会根据细胞系迁移到全身的不同位置。神经嵴(NC)形成和迁移的异常会导致各种畸形和肿瘤,即所谓的神经嵴病。在此,本病例系列描述了过去 3 年中单中心在头颅神经嵴病方面的经验,包括 17 例不同组成的病例(即:血管性、遗传性、混合性)、在我们对 17 例头面部 NC 疾病患者的研究中,6 例(35.3%)患者为血管型,5 例(29.4%)为遗传障碍型,4 例(23.5%)为混合型,2 例(11.7%)为肿瘤型。所有患者(100%)的脑部受累表现为血管或实质受累,或血管和实质均受累;6 名患者(35.3%)的皮肤受累;2 名患者(11.7%)的眼部受累;1 名患者(5.9%)的面部受累。神经嵴疾病(NCDs)在文献中是一类罕见且未得到充分认识的疾病,可能是由于缺乏对该疾病的认识而导致报告不足。更多这样的报告可能会增加这些罕见疾病的病例,使临床医生能够高度怀疑,从而及早发现并及时提供咨询,还能改善预防策略,帮助开发治疗或预防这些疾病的新药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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