Coberly S, Lammer E, Alashari M
Department of Medical Genetics, Children's Hospital Oakland, California, USA.
Pediatr Pathol Lab Med. 1996 Sep-Oct;16(5):823-36.
Isotretinoin use as a treatment for acne has increased tremendously and, with it, the problems of associated birth defects. We feel that pathologists should be familiar with isotretinoin embryopathy and its pathogenesis in order to assist in differentiating this syndrome from other genetic syndromes that involve branchial arch defects, such as DiGeorge syndrome or velocardiofacial syndrome. Although selected autopsy findings have been presented in epidemiologic reports, to our knowledge a detailed autopsy report has not been published. We therefore wish to present a complete case study of isotretinoin embryopathy that illustrates the pathologic diagnostic criteria and correlates these with the clinical findings. Although the syndrome's major features are explained by the drug's effect on neural crest cells, it has been postulated that isotretinoin also affects other cells in the central nervous system. Our current case supports this theory and shows that these changes in the nervous system may present significant functional impairment, while not presenting visible anatomic changes on either imaging studies or routine histologic examinations.
异维甲酸用于治疗痤疮的情况急剧增加,与之相关的出生缺陷问题也随之出现。我们认为,病理学家应该熟悉异维甲酸胚胎病及其发病机制,以便协助将该综合征与其他涉及鳃弓缺陷的遗传综合征(如迪乔治综合征或心脏颜面综合征)区分开来。尽管在流行病学报告中已经介绍了部分尸检结果,但据我们所知,尚未发表详细的尸检报告。因此,我们希望展示一个完整的异维甲酸胚胎病病例研究,阐述病理诊断标准,并将其与临床发现相关联。尽管该综合征的主要特征可以通过药物对神经嵴细胞的作用来解释,但据推测异维甲酸也会影响中枢神经系统中的其他细胞。我们目前的病例支持这一理论,并表明神经系统的这些变化可能会导致显著的功能损害,而在影像学研究或常规组织学检查中却未呈现出明显的解剖学变化。