Townsend Tiffany C, Bowen Anneli R, Nobuhara Kerilyn K
Division of Pediatric Surgery, Department of Surgery,University of California at San Francisco, 94143, USA.
J Pediatr. 2004 Jul;145(1):131-3. doi: 10.1016/j.jpeds.2004.03.048.
We report a case of syringocystadenoma papilliferum, a rare cutaneous adnexal neoplasm, occurring synchronously in two distinct unusual locations in a 22-month-old child with lesions on the lower leg and back.
我们报告一例乳头状汗管囊腺瘤，这是一种罕见的皮肤附属器肿瘤，在一名22个月大的儿童中，小腿和背部出现了两个不同寻常部位的同步病变。
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