Hautmann R E, Bachor R
Department of Urology, Faculty of Medicine, University of Ulm, Germany.
J Urol. 1993 Aug;150(2 Pt 1):456-7. doi: 10.1016/s0022-5347(17)35509-x.
Although juvenile xanthogranulomas are frequently seen by pediatricians and dermatologists, urological data are extremely rare. To our knowledge we report the first case of juvenile xanthogranuloma of the penis. Differentiation from other, similar lesions with more ominous prognostic significance, such as xanthosarcoma, malignant fibrous histiocytoma or histiocytic reticulosarcoma, is essential. This well documented case is noteworthy, since proper ad hoc diagnosis would have allowed us to perform a small biopsy rather than 2 surgical procedures. Our data support the currently held belief that juvenile xanthogranulomas are generally benign, self-limiting lesions.
尽管儿科医生和皮肤科医生经常能见到幼年性黄色肉芽肿,但泌尿外科方面的数据却极为罕见。据我们所知,我们报告了首例阴茎幼年性黄色肉芽肿病例。将其与其他具有更不祥预后意义的类似病变,如黄色肉瘤、恶性纤维组织细胞瘤或组织细胞性网状肉瘤相鉴别至关重要。这个记录详实的病例值得关注,因为恰当的临时诊断本可让我们进行一次小活检而非两次外科手术。我们的数据支持了目前普遍认为的幼年性黄色肉芽肿通常是良性、自限性病变的观点。