Department of Surgery, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA.
Center for Bioinformatics and Computational Biology, University of Iowa College of Engineering, Iowa City, Iowa, USA.
Am J Med Genet A. 2021 May;185(5):1582-1588. doi: 10.1002/ajmg.a.62145. Epub 2021 Mar 1.
Currarino syndrome (CS) is an autosomal dominant syndrome caused by mutations in MNX1 and characterized by anorectal abnormalities, partial sacral agenesis, and presacral masses. The presacral masses are typically benign; however, malignant degeneration can occur, and presacral neuroendocrine tumors (NETs) have been reported in six cases. We report three individuals from two families affected by CS in which multiple individuals developed presacral NETs. The first family, 491, had six members with features of CS, including two siblings who presented with presacral, Grade 2 NETs, one of which had metastasized to bone and lymph nodes. A germline c.874C>T (p.Arg292Trp) mutation was found in a highly conserved region of MNX1 in three affected members who underwent sequencing. A second somatic variant/deletion in MNX1 was not detected in either patient's tumor. In the second family, 342, the proband presented with an incidentally discovered presacral NET. The proband's father had previously undergone resection of a presacral NET, and so genetic testing was performed, which did not reveal an MNX1 mutation or copy number variants. The lack of a second, somatic mutation in the tumors from family 491 argues against MNX1 acting as a tumor suppressor, and the absence of a germline MNX1 mutation in family 342 suggests that other genetic and anatomic factors contribute to the development of presacral NETs. These cases highlight the variable presentation of CS, and the potential for malignancy in these patients.
库拉里诺综合征(CS)是一种常染色体显性综合征,由 MNX1 基因突变引起,其特征为肛肠异常、部分骶骨发育不全和骶前肿块。骶前肿块通常为良性,但也可能发生恶性转化,已有 6 例报道为骶前神经内分泌肿瘤(NET)。我们报告了两个家系中的 3 例 CS 患者,其中多个个体发生了骶前 NET。第一家系 491 有 6 名成员具有 CS 的特征,包括 2 名出现骶前 2 级 NET 的兄弟姐妹,其中 1 例发生骨和淋巴结转移。在接受测序的 3 名受影响成员中,MNX1 的一个高度保守区域发现了一个胚系 c.874C>T(p.Arg292Trp)突变。在这两个患者的肿瘤中均未检测到 MNX1 的第二个体细胞变异/缺失。在第二家系 342 中,先证者偶然发现骶前 NET。先证者的父亲曾接受过骶前 NET 切除术,因此进行了基因检测,但未发现 MNX1 突变或拷贝数变异。家系 491 中的肿瘤缺乏第二个体细胞突变,这表明 MNX1 可能不是肿瘤抑制基因,而家系 342 中的肿瘤缺乏胚系 MNX1 突变,则提示其他遗传和解剖因素也可能导致骶前 NET 的发生。这些病例突出了 CS 的多变表现以及这些患者发生恶性肿瘤的可能性。