Edwards P D, Prosser R, Wells C E
J Neurol Neurosurg Psychiatry. 1975 Aug;38(8):729-39. doi: 10.1136/jnnp.38.8.729.
Two cases of polycythaemic chorea are described, both of which were complicated by severe heart disease. The first was a child with patent ductus arteriosus and coarctation of the aorta causing severe cyanosis and secondary polycythaemia. Chorea began intermittently at an early age, becoming continuous by his fifth birthday. The second was a middle-aged male with tight mitral stenosis and a story of paralytic chorea in his teens. Polycythaemia rubra vera was eventually diagnosed two years after mitral valvotomy, some seven years after the onset of chorea.
本文描述了两例红细胞增多性舞蹈病,两例均伴有严重心脏病。第一例是一名患有动脉导管未闭和主动脉缩窄的儿童,导致严重发绀和继发性红细胞增多症。舞蹈病在幼年时开始间歇性发作,到五岁生日时变为持续性发作。第二例是一名中年男性,患有严重二尖瓣狭窄,十几岁时曾患过麻痹性舞蹈病。二尖瓣切开术后两年,即舞蹈病发作约七年后,最终诊断为真性红细胞增多症。