Goodden J R, Marven S S, Cohen M, de Ville McMullan P J, Smith M F
Department of Neurological Surgery, Sheffield Children's Hospital, Sheffield, United Kingdom.
Eur J Pediatr Surg. 2008 Aug;18(4):282-4. doi: 10.1055/s-2007-965789. Epub 2008 Jul 15.
We report a rare congenital scalp tumour with histological diagnosis of a congenital apocrine adenoma with features of a tubular adenoma. Following cranial CT and MRI, the tumour was serially excised. The macroscopic and microscopic appearances and management are discussed. To our knowledge, such a case has not been previously reported.
我们报告了一例罕见的先天性头皮肿瘤，经组织学诊断为具有管状腺瘤特征的先天性大汗腺腺瘤。经头颅CT和MRI检查后，对该肿瘤进行了系列切除。本文讨论了该肿瘤的大体及显微镜下表现及治疗方法。据我们所知，此前尚无此类病例的报道。
