Pik3ca体细胞突变的死胎胸部巨静脉畸形。

IF 0.7 4区 医学 Q4 PATHOLOGY
Fetal and Pediatric Pathology Pub Date : 2025-05-01 Epub Date: 2025-04-24 DOI:10.1080/15513815.2025.2493721
Nunzio Cosimo Mario Salfi, Sabrina Gismondi, Anna Martinelli, Elisa Tidu, Patrizio Giovanni Maria Antonazzo, Stefano Faiola, Mariano Matteo Lanna, Elisa Cattaneo, Enrico Farnetti, Davide Nicoli, Maria Paola Bonasoni
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引用次数: 0

摘要

简介:先天性静脉畸形(vm)通常位于头颈部皮肤,但也可能延伸到深部组织和内脏器官。在20%的病例中,散发性vm是由PIK3CA基因的体细胞突变引起的,该基因决定了异常的血管生成。病例报告:28周+ 6天发生一例已知右半胸广泛血管病变的胎儿宫内死亡。尸检显示大量双侧胸腔积液,组织学显示VM。PIK3CA和TEK对羊膜细胞的高深度下一代测序结果为阴性。对病变石蜡包埋样品进行PIK3CA的死后实时聚合酶链反应显示,体细胞p.H1047X外显子20发生热点突变。结论:据我们所知,这是首例VM死产病例。广泛的病变携带胎儿死亡的高风险,由于高输出心力衰竭。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thoracic Giant Venous Malformation in a Stillbirth with Pik3ca Somatic Mutation.

Introduction: Congenital venous malformations (VMs) are typically located in the skin of the head and neck, but extension to deep tissues and visceral organs may occur. In 20% of cases, sporadic VMs are caused by somatic mutations in the PIK3CA gene, which determines aberrant angiogenesis. Case report: Intrauterine death of a fetus with a known extensive vascular lesion of the right hemithorax occurred at 28 weeks + 6 days. Autopsy revealed abundant bilateral pleural effusions, and histology showed a VM. High-depth next-generation sequencing for PIK3CA and TEK on amniocytes was negative. Postmortem real-time polymerase chain reaction for PIK3CA on paraffin-embedded samples of the lesion revealed somatic p.H1047X hotspot mutation in the exon 20. Conclusion: To the best of our knowledge, this is the first case of a VM in a stillbirth. Extensive lesions carry a high risk of fetal demise due to high-output cardiac failure.

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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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