Aldabbab Habib Y, Al Ghadeer Hussain A, Alnosair Ashraf A, Al Jabran Hussain A, Alqattan Maram H, Abdulrahman Chadi M, Alabbad Mohammed R
Orthopedic Surgery, King Faisal University, AlAhsa, SAU.
Pediatrics, Maternity and Children Hospital, AlAhsa, SAU.
Cureus. 2022 Apr 1;14(4):e23743. doi: 10.7759/cureus.23743. eCollection 2022 Apr.
Currarino syndrome (CS) is a congenital disorder that is characterized by the triad of anorectal malformation, sacrococcygeal anomalies, and a presacral mass. The inheritance of CS is autosomal dominant. Chronic constipation is the most common symptom of CS. MRI is considered the most sensitive test to diagnose CS. The report describes an eight-month-old baby girl who presented with chronic constipation. Physical examination showed abdominal distension and anal stenosis. Plain radiographs and MRI revealed sacrococcygeal abnormalities with a presacral mass. A patient was diagnosed with Currarino syndrome and managed surgically with excision of the presacral mass and an anorectoplasty via a posterior sagittal midline incision.
库拉里诺综合征（CS）是一种先天性疾病，其特征为肛门直肠畸形、骶尾骨异常和骶前肿块三联征。CS的遗传方式为常染色体显性遗传。慢性便秘是CS最常见的症状。MRI被认为是诊断CS最敏感的检查。该报告描述了一名8个月大的女婴，她因慢性便秘前来就诊。体格检查显示腹胀和肛门狭窄。X线平片和MRI显示骶尾骨异常并伴有骶前肿块。一名患者被诊断为库拉里诺综合征，并通过后矢状中线切口手术切除骶前肿块并行肛门直肠成形术进行治疗。
