Diffuse familial adenomatous intestinal polyposis in childhood: current state of the problem and case report.

Q4 Medicine
Tetiana Shatynska, Iryna Lembryk, Orysia Tsytsiura, Oleksandra Zhyliak, Anastasiya Stefanyshyn, Nataliia Kostyrko, Yuliia Bodnarchuk
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引用次数: 0

Abstract

Objective: Aim: To explore the prevalence, clinical characteristics, and diagnostic aspects of diffuse familial adenomatous polyposis in childhood. This objective is accomplished through an extensive review of recent literature, and the presentation of case report from our clinical practice.

Patients and methods: Materials and Methods: We analyzed 75 scientific papers, the findings of which have been documented in the PubMed database. Our search criteria included keywords such as ≪diffuse familial adenomatous intestinal polyposis,≫ ≪children,≫ and ≪diagnosis.≫ Then we conducted a second-stage analysis that involved a detailed review of a practical case - the medical records of inpatient Kh.V. who had been diagnosed with familial adenomatous polyposis.

Conclusion: Conclusions: The analysis of the literature data is consistent with the findings from our clinical observations of familial adenomatous polyposis in a patient with complicated family anamnesis. It is worth noting that clinical features do not significantly differ across various types of polyposis. In cases of suspected familial adenomatous polyposis in adolescents, genetic testing is crucial.

儿童期弥漫性家族性腺瘤性肠息肉病:问题现状和病例报告。
目的:探讨儿童弥漫性家族性腺瘤性息肉病的发病率、临床特征和诊断方法:目的:探讨儿童弥漫性家族性腺瘤性息肉病的发病率、临床特征和诊断方法。为了实现这一目标,我们对近期的文献进行了广泛的综述,并介绍了我们临床实践中的病例报告:材料与方法:我们分析了 75 篇发表在 PubMed 数据库中的科学论文。我们的搜索标准包括≪弥漫性家族性腺瘤性肠息肉病≫、≪儿童≫和≪诊断≫等关键词,然后我们进行了第二阶段分析,详细回顾了一个实际病例--被诊断为家族性腺瘤性息肉病的住院病人 Kh.V. 的病历:结论:结论:对文献资料的分析与我们对一名家族病史复杂的患者家族性腺瘤性息肉病的临床观察结果一致。值得注意的是,不同类型息肉病的临床特征并无明显差异。对于疑似家族性腺瘤性息肉病的青少年病例,基因检测至关重要。
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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来源期刊
Wiadomosci lekarskie
Wiadomosci lekarskie Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
482
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