Abbas Zaheer, Khani Sepideh, Zare Javad
Paydar Skin, Hair and Laser Clinic, Bandar Abbas, Iran.
Department of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Shahryar, Tehran, Iran.
Indian Dermatol Online J. 2017 Mar-Apr;8(2):128-130. doi: 10.4103/2229-5178.202272.
Vascular abnormalities associated with neurofibromatosis type 1 are well described in the literature, however, arteriovenous malformation is a very rare finding in neurofibromatosis type 1. We report the case of an 11-year-old girl who presented with a soft mass on the right flank. Provisional diagnosis of plexiform neurofibroma was made on the basis of clinical and histological observations. Because the lesion was warm on palpation, imaging studies were performed to evaluate further and arteriovenous malformation was detected underlying the plexiform neurofibroma. This report emphasizes the importance of careful examination and proper investigations of the plexiform neurofibroma prior to treatment strategies to avoid future complications. The rarity of plexiform neurofibroma in association with arteriovenous malformation at the same site was also highlighted in this report.
1型神经纤维瘤病相关的血管异常在文献中有充分描述,然而,动静脉畸形在1型神经纤维瘤病中是非常罕见的发现。我们报告一例11岁女孩,其右侧腹出现一个柔软肿块。根据临床和组织学观察做出了丛状神经纤维瘤的初步诊断。由于触诊时病变部位发热,进行了影像学检查以进一步评估,结果在丛状神经纤维瘤下方检测到动静脉畸形。本报告强调了在制定治疗策略之前对丛状神经纤维瘤进行仔细检查和适当调查的重要性,以避免未来出现并发症。本报告还突出了同一部位丛状神经纤维瘤合并动静脉畸形的罕见性。