Extensive and persistent tongue ulceration is an early character of dyskeratosis congenita.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Xuefeng Zhang, Hongxia Dan, Yu Zhou, Wanxin Sun, Wanchun Yang, Xin Zeng
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引用次数: 0

Abstract

Background: Dyskeratosis congenita (DC) is a rare and fatal disease, presenting with a classic triad of skin pigmentation, nail dystrophy and oral leukoplakia. However, diagnosing DC is challenging based solely on the protean manifestations and multisystemic involvement. Therefore, it is urgent to identify an early feature facilitating initial suspicion of DC.

Results: In this study, we enrolled a cohort of six male children diagnosed with DC, all of whom exhibited erosions or ulcers on the tongue, while five of them did not display the complete classic triad. Strikingly, oral erosions or ulcers have never been included in any existing clinical diagnostic criteria for DC. Through a retrospective analysis, we further demonstrated that extensive and persistent tongue ulceration emerges as an early and practicable clinical marker, provoking suspicion of DC even in the absence of the classic triad.

Conclusions: Our findings challenge prevailing diagnostic criteria and advocates for an expanded consideration of tongue ulceration as a primary and indicative manifestation of DC, thereby affording a strategic advantage for early detection and intervention of this lethal disease.

广泛和持续的舌溃疡是先天性角化不良的早期特征。
背景:先天性角化不良症(DC)是一种罕见且致命的疾病,表现为典型的皮肤色素沉着、指甲营养不良和口腔白斑。然而,仅根据多种表现和多系统累及诊断DC是具有挑战性的。因此,迫切需要识别一个早期特征,以便对DC进行初步怀疑。结果:在这项研究中,我们招募了6名诊断为DC的男性儿童,他们都表现出舌头上的糜烂或溃疡,而其中5人没有表现出完整的经典三联征。引人注目的是,口腔糜烂或溃疡从未包括在任何现有的DC临床诊断标准中。通过回顾性分析,我们进一步证明,广泛和持续的舌溃疡是早期和切实可行的临床标志,即使在没有经典的三联征的情况下,也会引起DC的怀疑。结论:我们的研究结果挑战了现行的诊断标准,并倡导将舌溃疡作为DC的主要和指示性表现进行扩大考虑,从而为这种致命疾病的早期发现和干预提供了战略优势。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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