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8, 9번 삼염색체를 가진 골수형성이상증후군과 정신분열증을 동반한 베체트병
백정훈 ( Jung Hoon Baek ),전현정 ( Hyun Jung Chun ),박윤희 ( Youn Hee Park ),조정현 ( Jeong Hyeon Cho ),배상균 ( Sang Kyun Bae ),하유정 ( You Jung Ha ) 대한류마티스학회 2013 대한류마티스학회지 Vol.20 No.6
Behcet`s disease (BD) is a multi-systemic inflammatory disease of unknown origin that affects nearly all organs. Recent reports of BD with myelodysplastic syndrome (MDS) often note an association with gastrointestinal involvement and trisomy 8. We herein report on a case of a 51-year-old man who had refractory schizophrenia and developed gastrointestinal BD and MDS with trisomy 8 and 9. He visited our hospital due to fever and abdominal pain. Multiple ulcerations in the colorectum were observed on colonoscopy, and he was diagnosed with intestinal BD. During the treatment of intestinal BD, anemia and thrombocytopenia developed. His bone marrow study revealed myelodysplastic syndrome (refractory anemia with ringed sideroblast) with trisomy 8 and trisomy 9. We report a rare case of intestinal BD accompanied by schizophrenia and myelodysplastic syndrome with trisomy 8 and 9.