Deep Phenotyping of Pathology-Confirmed Benign Lesions in PTEN Hamartoma Tumor Syndrome Patients

IF 2.3 3区 医学 Q2 GENETICS & HEREDITY
Ane J. Schei-Andersen, Janneke H. M. Schuurs-Hoeijmakers, Rachel van der Post, Arjen R. Mensenkamp, Jolanda Schieving, PTEN Study Group, Janet R. Vos, Nicoline Hoogerbrugge
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Abstract

PTEN Hamartoma Tumor Syndrome (PHTS) is a rare hereditary syndrome. PHTS has a variable phenotype characterized by benign lesions and increased cancer risks. Clarifying the extent of the benign phenotype could facilitate early recognition of PHTS patients before cancer development. Therefore, we assessed the spectrum, frequency, and age of excerpt of pathology-confirmed benign lesions in PHTS patients. Pathology reports were collected for 379 patients with a pathogenic PTEN variant from the Dutch nationwide pathology databank (Palga). Benign lesions were classified as PHTS-related based on current clinical diagnostic guidelines and non-PHTS-related lesions by ICD-10 codes. Age of last follow-up was year of pathology request minus birth year. Analyses were stratified by sex and index status. Patients presented mainly with gastrointestinal (54%), skin (47%), thyroid (31%) and vascular lesions (26%). Males developed lipomas at an early age (9 years (5–34)). Females developed endometrial hyperplasia (16%) at an earlier age (41 years (35–49)) and uterine polyps (13%) more often than the general population. No significant differences were observed between sexes or index and non-index patients. The results are reflective of current diagnostic guidelines. Early-onset lipomas may be useful for early detection of PHTS patients. Additionally, uterine polyps should be considered for inclusion as a PHTS-related lesion.

Abstract Image

病理证实的PTEN错构瘤肿瘤综合征患者良性病变的深度表型分析。
PTEN错构瘤肿瘤综合征(PHTS)是一种罕见的遗传性综合征。PHTS具有可变表型,其特征是良性病变和癌症风险增加。阐明PHTS良性表型的程度有助于在癌症发展前早期识别PHTS患者。因此,我们评估了PHTS患者病理证实的良性病变摘取的频谱、频率和年龄。从荷兰全国病理数据库(Palga)收集了379例PTEN致病性变异患者的病理报告。根据现行临床诊断指南将良性病变分为phts相关病变和ICD-10编码的非phts相关病变。最后一次随访年龄为病理要求年份减去出生年份。分析按性别和指标状况分层。患者主要表现为胃肠道(54%)、皮肤(47%)、甲状腺(31%)和血管病变(26%)。男性发生脂肪瘤的年龄较早(9岁(5-34岁))。女性在较早的年龄(41岁(35-49岁))出现子宫内膜增生(16%),子宫息肉(13%)比一般人群更常见。性别、指数和非指数患者之间无显著差异。结果反映了当前的诊断指南。早发性脂肪瘤可能有助于PHTS患者的早期发现。此外,子宫息肉应考虑纳入phts相关病变。
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来源期刊
Clinical Genetics
Clinical Genetics 医学-遗传学
CiteScore
6.50
自引率
0.00%
发文量
175
审稿时长
3-8 weeks
期刊介绍: Clinical Genetics links research to the clinic, translating advances in our understanding of the molecular basis of genetic disease for the practising clinical geneticist. The journal publishes high quality research papers, short reports, reviews and mini-reviews that connect medical genetics research with clinical practice. Topics of particular interest are: • Linking genetic variations to disease • Genome rearrangements and disease • Epigenetics and disease • The translation of genotype to phenotype • Genetics of complex disease • Management/intervention of genetic diseases • Novel therapies for genetic diseases • Developmental biology, as it relates to clinical genetics • Social science research on the psychological and behavioural aspects of living with or being at risk of genetic disease
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