库拉里诺三联征：一例48岁神经内分泌肿瘤患者的病例报告。
Currarino triad: A case report of a 48-year-old patient with a neuroendocrine tumor.
作者信息
Rebelo João, Marques Ana, Vilares Teresa, Silva Nuno, Silva Roberto, Cunha Rui, Madureira António
机构信息
Radiology Department, Centro Hospitalar Universitário de São João, Alameda Prof. Hernâni Monteiro, Porto 4200-319, Portugal.
Pathology Department, Centro Hospitalar Universitário de São João, Porto, Portugal.
出版信息
Radiol Case Rep. 2020 Jul 6;15(9):1555-1561. doi: 10.1016/j.radcr.2020.06.039. eCollection 2020 Sep.
Currarino triad is a rare syndrome, with less than 250 cases reported, and it includes a combination of sacrococcigeal bony abnormalities, anorectal malformations and the presence of a presacral mass. Here we present a case of a 48-year-old male patient with history of severe chronic constipation, who was incidentally diagnosed with a presacral during imagiological investigation, which was histologically proven to be a neurendocrine tumor.
库里亚里诺三联征是一种罕见综合征，报告病例少于250例，它包括骶尾部骨质异常、肛门直肠畸形以及骶前肿块。我们在此报告一例48岁男性患者，有严重慢性便秘病史，在影像学检查中偶然诊断出骶前肿物，组织学检查证实为神经内分泌肿瘤。
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