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首页> 外文期刊>The journal of obstetrics and gynaecology research >Parasitic myomas after laparoscopic-assisted myomectomy in multiple endocrine neoplasia type 1
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Parasitic myomas after laparoscopic-assisted myomectomy in multiple endocrine neoplasia type 1

机译：腹腔镜辅助子宫肌瘤切除术在多发性内分泌肿瘤1型中的寄生性肌瘤

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摘要

Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary disorder that develops multiple tumors arising from various endocrine organs, including the parathyroid gland, endocrine pancreas and pituitary gland. Although mesenchymal tumors can be an integral part of the syndrome, parasitic peritoneal myomas have never been described in an MEN1 patient. Seven years after laparoscopic-assisted myomectomy, parasitic peritoneal myomas were diagnosed in a 31-year-old woman with situs inversus totalis and previous history of parathyroid adenoma. Subsequently, MEN1 was clinically diagnosed by identification of endocrine pancreatic, adrenal and pituitary tumors. Genetic analysis revealed a heterozygous germline mutation in the splice donor sequence of intron 6 of the MEN1 gene. Although rare, parasitic peritoneal myomas could potentially be associated with MEN1 syndrome.
机译：1型多发性内分泌肿瘤（MEN1）是一种罕见的常染色体显性遗传性疾病，可发展出由各种内分泌器官（包括甲状旁腺，内分泌胰腺和垂体）引起的多种肿瘤。尽管间充质肿瘤可能是该综合征的组成部分，但从未在MEN1患者中描述过寄生性腹膜肌瘤。腹腔镜辅助子宫肌瘤切除术七年后，在一名31岁女性，总眼睑内翻及甲状旁腺腺瘤病史中，诊断出寄生虫腹膜肌瘤。随后，通过鉴定内分泌胰腺，肾上腺和垂体肿瘤对MEN1进行临床诊断。遗传分析显示，MEN1基因内含子6的剪接供体序列中杂合了种系突变。尽管罕见，但寄生虫性腹膜肌瘤可能与MEN1综合征有关。

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