墨西哥2型神经性Ceroid脂褐菌病患者的临床、病理和分子表现:支持c.1226致病性g>t变异与樱桃红斑病发生的关系

IF 1.3 4区 医学 Q3 PATHOLOGY
Pediatric and Developmental Pathology Pub Date : 2025-01-01 Epub Date: 2024-12-23 DOI:10.1177/10935266241286723
Celso Tomás Corcuera-Delgado, Alfonso Gilberto Ramírez-Ristori, Estela Pérez-Muñoz, María Emilia Mendizábal-Rodríguez, Camilo E Villarroel
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引用次数: 0

摘要

2型神经元类脂褐素病(CLN2)由TPP1基因的双等位致病变异引起,导致溶酶体酶三肽基肽酶1活性不足。我们报告一个CLN2在分子水平上的尸检病例。患者表现出一系列神经系统症状,包括癫痫、行为改变、认知衰退、运动障碍和视力丧失。眼底检查见樱桃红色斑点。她死于7岁,尸检显示大脑和小脑严重萎缩,伴有神经元丢失和神经胶质瘤。自荧光蜡样脂褐素使神经元呈细颗粒状和粗圆体两种类型的扩张。此外,电子显微镜研究显示特征曲线轮廓。尸体解剖后,进行了种系分子测试,发现了c.1226纯合状态下的G >t变异。这一变种曾在一份不详细的报告中提及,并被归类为意义不确定。我们的研究结果支持了樱桃红斑在CLN2中存在,并证实了c.1226的致病性G > T变体。目前的CLN2管理包括需要早期诊断的酶替代,这可以通过疾病的临床描述和适当的分类和公开报告TPP1变异来促进。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical, Pathological, and Molecular Findings in a Mexican Patient With Neuronal Ceroid Lipofuscinosis Type 2: Support for Pathogenicity of the c.1226 G>T Variant and for Presence of Cherry-Red Spot in This Disease.

Neuronal ceroid lipofuscinosis type 2 (CLN2) results from biallelic pathogenic variants in the TPP1 gene, leading to deficient activity of the lysosomal enzyme tripeptidyl peptidase 1. We report an autopsy case of CLN2 characterized at molecular level. The patient exhibited a spectrum of neurologic symptoms including epilepsy, behavioral alterations, cognitive regression, motor impairment, and visual loss. In fundus exam, a cherry-red spot was observed. She died at 7 years old, autopsy demonstrated severe atrophy of the brain and cerebellum with neuronal loss and gliosis. Neurons were distended by autofluorescent ceroid lipofuscin of 2 types: fine granular deposits and coarse round bodies. In addition, electron microscopy study revealed characteristic curvilinear profiles. After autopsy, a germline molecular test was performed that found the c.1226 G>T variant in a homozygous state. This variant has been referenced in a single undetailed report and is classified as of uncertain significance. Our findings support that cherry-red spot can be present in CLN2 and confirm the pathogenicity of the c.1226 G>T variant. Current management of CLN2 includes enzyme replacement that requires early diagnosis, which can be facilitated by clinical delineation of the disease and appropriate classification and public reporting of TPP1 variants.

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来源期刊
CiteScore
3.70
自引率
5.30%
发文量
59
审稿时长
6-12 weeks
期刊介绍: The Journal covers the spectrum of disorders of early development (including embryology, placentology, and teratology), gestational and perinatal diseases, and all diseases of childhood. Studies may be in any field of experimental, anatomic, or clinical pathology, including molecular pathology. Case reports are published only if they provide new insights into disease mechanisms or new information.
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