부신종양을 동반한 Beckwith-Wiedemann 증후군

Beckwith-Wiedemann Sydrome with Left Adrenal Cortical Neoplasm

  • 정재희 (가톨릭대학교 의과대학 외과학교실) ;
  • 고재경 (가톨릭대학교 의과대학 해부병리학교실) ;
  • 송영택 (가톨릭대학교 의과대학 외과학교실)
  • Jung, Jae-Hee (Department of Surgery, St. Mary's Hospital, The Catholic University of Korea) ;
  • Ko, Jae-Kyoung (Department of Pathology, St. Mary's Hospital, The Catholic University of Korea) ;
  • Song, Young-Tack (Department of Surgery, St. Mary's Hospital, The Catholic University of Korea)
  • 발행 : 2000.12.30

초록

저자들은 확정되지 않은 악성의 가능성을 가진 부신 피질 방추세포 종양 (adrenal cortical spindle cell neoplasm of indeterminate malignant potential)을 동반한 Beckwith-Wiedemann 증후군을 경험하였기에 문헌고찰과 함께 보고하는 바이다.

Beckwith-Wiedemann syndrome presents with multisystemic patterns of congenital anomalies and macrosomia. This syndrome was independently described by Beckwith in 1963 and by Wiedemann in 1964. There is wide spectrum of clinical manifestations, including prenatal or postnatal overgrowth, neonatal hypoglycemia, macroglossia, visceromegaly, omphalocele, hemihypertrophy and a predisposition for embryonal tumors, most frequently Wilms' tumor. We managed a case of Beckwith-Wiedemann syndrome with left adrenal cortical neoplasm of undetermined malignancy.

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