摘要
软斑病是一种罕见的慢性肉芽肿性疾病,最常发生于泌尿系统。临床上易有可能被误为肿瘤,确诊需依靠活检。其病变特点是在炎症的背景中,出现大量软斑细胞呈肿瘤样聚集,并可见 M-G 小体。本文报告了二例:一例发生于膀胱,另一例发生于肠道和会阴部。本文就软斑病的病因、发病机制、病理诊断和预后等问题进行了讨论。
Malakoplakia is a rare granulomatous disease mainly involving urinary tract,Thedisease appears as a tumor-like mass grossly.Microscopically,the diagnostic featuresof the lesion are(1)in an inflammatory background,there are a number of malako-plakia ceils(a variety of macrophages),and(2)within and without the malakoplakiacells there are some M-G bodies containing calcium and iron.Two of such casesare reported here,one was in the urinary bladder,and the other in the intestine andperineum.The cause,pathogenesis,pathologic diagnosis and prognosis of the diseaseare discussed.
出处
《天津医药》
CAS
1990年第5期291-293,共3页
Tianjin Medical Journal
