Kaygusuz Ecmel Işık, Çetiner Handan, Moralıoğlu Serdar, Bosnalı Oktav, Celayir Ayşenur
Departments of Pathology, Zeynep Kamil Maternity and Children's Training and Research Hospital, Istanbul, Turkey.
Turk J Pediatr. 2015 Nov-Dec;57(6):632-634.
Childhood malignant testicle tumors are very rare. In the literature to date, it has been reported that there are only 24 cavernous hemangioma cases existing in English literature. In this study, we discuss a testicular mass case which was diagnosed as cavernous hemangioma. The patient, who followed for left multicystic dysplastic kidney since his birth, was admitted to our clinic with complaints of left testicular mass and pain at 1-year of age. Histopathological investigation revealed cavernous hemagioma. Even if it has its characteristic ultrasonographic findings, radiology is too far beyond to eliminate the malignancy, final diagnosis can only be made after orchiectomy.
儿童恶性睾丸肿瘤非常罕见。在迄今为止的文献中，据报道英文文献中仅存在24例海绵状血管瘤病例。在本研究中，我们讨论了一例被诊断为海绵状血管瘤的睾丸肿块病例。该患者自出生起就患有左多囊性发育不良肾，1岁时因左侧睾丸肿块和疼痛入住我们的诊所。组织病理学检查显示为海绵状血管瘤。即使它有其特征性的超声表现，放射学检查也远不足以排除恶性肿瘤，最终诊断只能在睾丸切除术后才能做出。
