Paruliya Dipak, Sharma Shaleen, Gokhroo Sunil, Yadav Sher S, Sharma Krishan K, Sadasukhi Trilok C
Department of Urology, Sawai Man Singh Medical College, Jaipur, Rajasthan, India.
Urology. 2007 Oct;70(4):811.e9-10. doi: 10.1016/j.urology.2007.07.031.
Primary neuroectodermal tumor (PNET) is a rare entity with high malignant potential. It usually affects the skeletal system and primary extraskeletal involvement is uncommon. Because of rarity of tumor in the penis, only a few cases have been reported. A 17-year-old male adolescent presented with painless penile swelling of 4 weeks' duration. Clinical examination revealed multiple, 1 cm hard nodules palpable on penile shaft. Open incisional biopsy of the penile nodule revealed an undifferentiated malignant round cell tumor and on immunohistochemistry a diagnosis of PNET was made. Metastatic workup was negative. Total penectomy and perineal urethrostomy was performed, and subsequently adjuvant chemotherapy was given.
原发性神经外胚层肿瘤(PNET)是一种罕见的具有高度恶性潜能的实体瘤。它通常累及骨骼系统,原发性骨骼外受累情况并不常见。由于阴茎肿瘤罕见,仅有少数病例报道。一名17岁男性青少年出现持续4周的无痛性阴茎肿胀。临床检查发现阴茎体可触及多个1厘米的硬结节。阴茎结节的开放切口活检显示为未分化恶性圆形细胞瘤,免疫组化检查后诊断为PNET。转移灶检查为阴性。实施了阴茎全切术和会阴尿道造口术,随后给予辅助化疗。