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Case Report
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Korean J Med. 2014;87(5):619-624. Published online November 1, 2014.
DOI: https://doi.org/10.3904/kjm.2014.87.5.619
- 무도병을 주소로 내원한 진성적혈구증가증 1예
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김선웅1, 유형민1, 이윤정1, 김희진2, 허미나3, 이홍기1
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1건국대학교 의학전문대학원 건국대학교병원 내과
2건국대학교 의학전문대학원 건국대학교병원 신경과
3건국대학교 의학전문대학원 건국대학교병원 진단검사의학과
- Polycythemia Vera Presenting with Generalized Chorea: A Case Report and Review of the Literature
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Sun Woong Kim1, Hyung Min Yu1, Yoon Jeong Lee1, Hee Jin Kim2, Mina Hur3, Hong Ghi Lee1
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1Departments of Internal Medicine, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea
2Departments of Neurology, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea
3Departments of Laboratoy Medicine, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea
- Corresponding author: Hong Ghi Lee ,Tel: +82-2-2030-7538, Fax: +82-2-2030-7748, Email: mlee@kuh.ac.kr
- Received: October 16, 2013; Revised: December 30, 2013 Accepted: January 15, 2014.
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߽ɾ :진성적혈구증가증; 무도병
- Abstract
- Polycythemia vera (PV) is a myeloproliferative neoplasm characterized by erythrocytosis. Clinical symptoms can range in severity from headache and tinnitus to thrombohemorrhagic complications. Neurologic symptoms are common at the onset of polycythemia; however, chorea due to PV is a rare complication. We present the case of a 77-year-old female who was referred to our hospital because of choreic movement of the limbs, head and face. She was diagnosed with JAK2V617F mutation-positive PV. Her chorea was completely resolved by phlebotomy combined with hydroxyurea and aspirin.
Keywords :Polycythemia vera, Chorea disorders
