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카테콜아민치가 정상인 발작성 갈색세포종 1예

A Case of Paroxysmal Pheochromocytoma with Normal Catecholamine Levels

  • 유정래 (제주대학교병원 내과학교실) ;
  • 진현정 (한국병원 내과) ;
  • 김미연 (제주대학교병원 내과학교실) ;
  • 정우성 (제주대학교병원 내과학교실) ;
  • 이상아 (제주대학교병원 내과학교실) ;
  • 이대호 (제주대학교병원 내과학교실) ;
  • 고관표 (제주대학교병원 내과학교실)
  • Yu, Jung-Re (Department of Internal Medicine, Jeju National University Hospital, Jeju National University School of Medicine) ;
  • Chin, Hyoun-Jung (Department of Internal Medicine, Hankook General Hospital) ;
  • Kim, Mi-Yeon (Department of Internal Medicine, Jeju National University Hospital, Jeju National University School of Medicine) ;
  • Jeong, Woo-Seong (Department of Internal Medicine, Jeju National University Hospital, Jeju National University School of Medicine) ;
  • Lee, Sang-Ah (Department of Internal Medicine, Jeju National University Hospital, Jeju National University School of Medicine) ;
  • Lee, Dae-Ho (Department of Internal Medicine, Jeju National University Hospital, Jeju National University School of Medicine) ;
  • Koh, Gwan-Pyo (Department of Internal Medicine, Jeju National University Hospital, Jeju National University School of Medicine)
  • 발행 : 2012.10.01

초록

갈색세포종의 특징적인 임상증상을 주소로 내원한 53세 여자 환자에서 혈장과 24시간 소변에서 생화학적 검사는 정상이었지만 MIBG 스캔을 시행하여 복부 CT의 위치와 병변이 일치하는 갈색세포종을 진단하였다. 부신적출술 시행 후 조직학적으로 갈색세포종을 확진했으며 발작적인 증상과 고혈압은 호전되었다. 따라서 카테콜아민치가 정상이더라도 임상증상이 갈색세포종에 합당하다면 핵의학 영상검사가 필요하다고 말할 수 있다.

A 53-year-old woman had a 1.7 cm left adrenal mass on an abdominal computed tomography (CT) scan. She presented with paroxysmal headache, palpitation, sweating, and hypertension. The patient was highly suspected of having a pheochromocytoma, but measurements of 24-hour urinary metanephrine, catecholamines, and vanillylmandelic acid were normal. Plasma and urine catecholamine levels were within the normal range even during paroxysmal episodes. A scintigraphic study with $^{131}I$-metaiodo-benzylguanidine (MIBG) revealed selective concentration of the radiotracer, corresponding to the CT mass. The patient underwent a left adrenalectomy and the pathological examination confirmed the diagnosis of pheochromocytoma. In this report, we describe a rare case of a symptomatic pheochromocytoma with normal catecholamine levels. Our case illustrates that routine nuclear scintigraphy, such as $^{131}I$-MIBG, should be performed even in cases with normal hormonal testing for all patients with high clinical suspicion of pheochromocytoma.

키워드

참고문헌

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