Cholakkal Shanavas, V C Subhash, Nachiketh Gokul
Department of General Surgery, MIMS Hospital, Kozhikode, Kerala 673016 India.
Indian J Surg. 2018 Feb;80(1):90-92. doi: 10.1007/s12262-017-1669-0. Epub 2017 Jul 3.
Solitary plexiform neurofibroma of the penis is an extremely rare peripheral nerve lesion with only about 20 cases reported all around the world. Here, we are reporting a case of solitary penile plexiform neurofibroma with sexual dysfunction due to difficulty in penetration. This 47-year-old gentleman presented with a swelling on the dorsal side of the penis. He was aware of the swelling for the last 15 years. The swelling was slow growing and there was no associated loss of sensation or sexual dysfunction. For the last 2 months, he noticed that the tumour is rapidly increasing in size. He was also having difficulty in penetration during sexual intercourse which forced him to seek medical attention. He underwent excision of the swelling from our department. After 18 months of follow-up following excision, there has been no evidence of recurrence of the tumour.
Penile plexiform neurofibromas are a rare type of lesions and are usually associated with neurofibromatosis. Solitary penile plexiform neurofibromas are extremely rare. Excision, when done properly, gives good results, without erectile dysfunction.
阴茎孤立性丛状神经纤维瘤是一种极为罕见的周围神经病变,全球报道的病例仅有约20例。在此,我们报告一例因阴茎勃起功能障碍导致性交困难的孤立性阴茎丛状神经纤维瘤病例。这位47岁的男性患者阴茎背侧出现肿物。在过去15年里他一直知晓该肿物。肿物生长缓慢,且无相关感觉丧失或性功能障碍。在过去2个月里,他注意到肿瘤大小迅速增加。他在性交时也出现勃起功能障碍,这迫使他前来就医。他在我们科室接受了肿物切除手术。切除术后随访18个月,未见肿瘤复发迹象。
阴茎丛状神经纤维瘤是一种罕见的病变类型,通常与神经纤维瘤病相关。孤立性阴茎丛状神经纤维瘤极为罕见。正确进行切除手术可取得良好效果,且不会导致勃起功能障碍。