Kołodziejek Anna, Pronobis Katarzyna, Derlatka Pawel, Grabowska-Derlatka Kamila, Grabowska-Derlatka Laretta
Students' Scientific Group Affiliated to 2nd Department of Radiology, Medical University of Warsaw, Banacha 1a st, 02-097 Warsaw, Poland.
2nd Department of Radiology, Medical University of Warsaw, Banacha 1a st. Warsaw, Poland.
Radiol Case Rep. 2020 Aug 21;15(10):1983-1987. doi: 10.1016/j.radcr.2020.06.028. eCollection 2020 Oct.
Ganglioneuroma is a rare tumour originating from neural crest cells, occurring mainly within children older than 7 years. It can be localised in pelvic; however, this localisation is extremely rare. This paper presents the case of a 39-year-old woman, at whom the pelvic localisation of the lesion and the unspecific symptoms associated with the digestive and genital tract impeded the recognition of the actual disease. The immensely slow growth of the tumour, combined with gradual fading of the symptoms, indicated its benign character. Only the CT-controlled biopsy enabled the recognition of the ganglioneuroma. Taking under consideration the histopathologic result and the cease of the symptoms, we decided to leave the patient under observation. After 6 years of observation, no progression signs have been recorded.
神经节神经瘤是一种起源于神经嵴细胞的罕见肿瘤，主要发生在7岁以上的儿童中。它可位于盆腔；然而，这种定位极其罕见。本文介绍了一名39岁女性的病例，其病变的盆腔定位以及与消化道和生殖道相关的非特异性症状妨碍了对实际疾病的识别。肿瘤生长极其缓慢，加上症状逐渐消退，表明其具有良性特征。只有CT引导下的活检才得以识别神经节神经瘤。考虑到组织病理学结果和症状的缓解，我们决定对患者进行观察。经过6年的观察，未记录到进展迹象。
