Shin Dong-Won, Kim Jeong Hoon, Song Sang Woo, Kim Young-Hoon, Cho Young Hyun, Hong Seok Ho, Nam Soo Jeong
Department of Neurosurgery, Asan Medical Center, College of Medicine, University of Ulsan, Seoul, Korea.
Department of Pathology, Asan Medical Center, College of Medicine, University of Ulsan, Seoul, Korea.
J Korean Neurosurg Soc. 2021 Nov;64(6):975-982. doi: 10.3340/jkns.2020.0343. Epub 2021 Sep 15.
The occurrence of posterior fossa teratomas in adulthood is extremely rare. In this study, we aimed to report our experience with two cases of posterior fossa mature teratoma in adults who underwent surgical resection. We also performed a systematic review of published papers available to date.
We retrospectively reviewed the electronic medical records of patients who had onset of posterior fossa teratomas in adulthood at our institute between 1995 and 2020. We evaluated the clinical, radiographic, and pathological features of mature teratomas at the posterior fossa in adulthood. Furthermore, we searched the PubMed, EMBASE, and Web of Science database and reviewed published articles.
We found 507 articles on database review; of them, 102 were duplicates and 389 were excluded based on the inclusion criteria. Finally, 16 cases of posterior fossa from the web search and related articles. Subsequently, we added two cases that underwent surgery at our institute. We analyzed a total of 18 cases of mature teratomas. Headache was the most common (55.6%) symptom. The teratomas showed heterogeneous signals on magnetic resonance imaging. Thirteen patients (72.2%) had lesion at midline, five patients (27.8%) had calcification. Surgical resection was performed in all patients. No studies reported recurrence after resection.
The occurrence of posterior fossa teratomas in adulthood is difficult to diagnose at the initial stage. Radiographic diagnosis alone can lead to misdiagnosis. Pathological confirmation is essential. Surgical resection is a curative option for posterior fossa teratomas in adulthood.
成人后颅窝畸胎瘤的发生极为罕见。在本研究中,我们旨在报告两例接受手术切除的成人后颅窝成熟畸胎瘤的治疗经验。我们还对迄今为止已发表的论文进行了系统综述。
我们回顾性分析了1995年至2020年间在我院发病的成人后颅窝畸胎瘤患者的电子病历。我们评估了成人后颅窝成熟畸胎瘤的临床、影像学和病理特征。此外,我们检索了PubMed、EMBASE和科学网数据库,并查阅了已发表的文章。
我们在数据库检索中发现了507篇文章;其中102篇为重复文章,389篇根据纳入标准被排除。最后,通过网络搜索和相关文章找到了16例后颅窝病例。随后,我们补充了在我院接受手术的两例病例。我们共分析了18例成熟畸胎瘤。头痛是最常见的症状(55.6%)。畸胎瘤在磁共振成像上表现为不均匀信号。13例患者(72.2%)病变位于中线,5例患者(27.8%)有钙化。所有患者均接受了手术切除。没有研究报告切除后复发。
成人后颅窝畸胎瘤在初始阶段难以诊断。仅靠影像学诊断可能导致误诊。病理确诊至关重要。手术切除是成人后颅窝畸胎瘤的一种治愈性选择。