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患有DICER1综合征婴儿的先天性中线脊髓错构瘤:一例报告

Congenital midline spinal hamartoma in an infant with DICER1 syndrome: A case report.

作者信息

Hammad Rawan, Lo Winnie, Chen Haiying, Shroff Manohar, Malkin David, Villani Anita, Denburg Avram

机构信息

Division of Pediatric Hematology and Oncology, The Hospital for Sick Children, Toronto, ON, Canada.

Division of Hematology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.

出版信息

Front Oncol. 2022 Aug 18;12:963768. doi: 10.3389/fonc.2022.963768. eCollection 2022.

Abstract

Congenital spinal hamartomas are rare benign tumors. They are mostly seen in infants and are typically asymptomatic at presentation. Spinal hamartomas have not been associated with any known cancer predisposition syndrome. DICER1 syndrome is a well-characterized cancer predisposition syndrome caused by a germline mutation in the gene, which shows variable expressivity. To our knowledge, spinal hamartoma has never been described in individuals with DICER1 syndrome. Here, we describe a rare association of congenital spinal hamartoma and DICER1 syndrome in a 5-week-old infant, with molecular findings suggestive of the implication of in the pathogenesis of this tumor.

摘要

先天性脊柱错构瘤是罕见的良性肿瘤。它们多见于婴儿,通常在发病时无症状。脊柱错构瘤与任何已知的癌症易感综合征均无关联。DICER1综合征是一种特征明确的癌症易感综合征,由该基因的种系突变引起,表现出可变的表达性。据我们所知,DICER1综合征患者中从未有过脊柱错构瘤的描述。在此,我们描述了一名5周大婴儿中先天性脊柱错构瘤与DICER1综合征的罕见关联,分子学研究结果提示该基因在这种肿瘤的发病机制中具有一定作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c3e/9433698/edd5457d090b/fonc-12-963768-g001.jpg

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