先天性多囊肾,无特异临床表现,常易误诊。我院1972～1984年8月共收治33例,在院内外误诊23例。本文分析了误诊的原因,以期引起重视,并提出早期诊断的几点意见。 临床资料 一般资料 本组33例,婴儿型1例(4岁),成人型32例;男19例,女14例,30岁以上者30例,占94%。出现首发症状平均年龄37岁,最小18岁,最大53岁。获得诊断平均年龄为44岁,最小22岁,最大58岁。 Congenital polycystic kidney disease, no specific clinical manifestations, often misdiagnosed. Our hospital from 1972 to August 1984 were treated 33 cases, misdiagnosed 23 cases in the hospital. This article analyzes the causes of misdiagnosis, with a view to attracting attention, and put forward some views of early diagnosis. Clinical data General information The group of 33 cases, 1 infants (4 years old), adult type 32 cases; 19 males and 14 females, 30 years of age over 30, accounting for 94%. The first symptom of onset of the average age of 37 years, minimum 18 years old, maximum 53 years old. The average age of diagnosis was 44 years old, the youngest 22 years old and the oldest 58 years old.