Lakshmanan Y, Wills M L, Gearhart J P
Division of Pediatric Urology, James Buchanan Brady Urological Institute, Johns Hopkins Hospital, Baltimore, Maryland 21287-2101, USA.
Urology. 1997 Aug;50(2):285-8. doi: 10.1016/S0090-4295(97)00192-1.
We present a case of inflammatory (pseudosarcomatous) myofibroblastic tumor of the bladder in a child, along with a review of the literature. The benign nature of this rare disorder needs to be recognized so that superfluous radical therapy can be avoided. The clinical features and microscopic, ultrastructural, and immunohistochemical characteristics that help to identify this entity are described. To date, 72 such cases involving the bladder have been reported in the literature including the present one.
我们报告一例儿童膀胱炎性(假肉瘤样)肌成纤维细胞瘤病例,并对相关文献进行综述。需要认识到这种罕见疾病的良性本质,以免进行不必要的根治性治疗。本文描述了有助于识别该疾病的临床特征以及显微镜、超微结构和免疫组化特征。迄今为止,包括本病例在内,文献中已报道72例累及膀胱的此类病例。