Horikoshi Ko, Iimura Yasushi, Suzuki Hiroharu, Suzuki Mario, Sugano Hidenori, Kondo Akihide
Department of Neurosurgery, Juntendo University, 2-1-1Bunkyo-Ku, Hongo, Tokyo, 113-8421, Japan.
Sugano Neurosurgery Clinic, Tokyo, Japan.
Childs Nerv Syst. 2025 Mar 14;41(1):129. doi: 10.1007/s00381-025-06789-2.
Pilocytic astrocytoma (PA) is the most common pediatric tumor, typically located in the cerebellum, with spontaneous regression observed mainly in patients with neurofibromatosis type 1 (NF1). However, spontaneous regression of PA without NF1 is rarely reported.
Here, we describe a case of spontaneous regression of PA without NF1, located in the left frontal lobe with FGFR1-TACC1 fusion, in a 14-year-old boy who presented with epilepsy. Initial MRI revealed a lesion in the left middle frontal gyrus, and subsequent follow-up MRI demonstrated spontaneous regression. Despite this regression, the patient's seizures persisted, leading to epileptic focus resection. Pathological examination confirmed PA with characteristic histological findings and FGFR1-TACC1 fusion.
This case suggests that FGFR1-TACC1 fusion may be linked to spontaneous regression of PA, even in the absence of NF1. Surgical intervention may remain necessary in cases of epilepsy associated with PA, regardless of tumor regression.
毛细胞型星形细胞瘤(PA)是最常见的儿童肿瘤,通常位于小脑,主要在1型神经纤维瘤病(NF1)患者中观察到自发消退。然而,无NF1的PA自发消退的报道很少。
在此,我们描述了一例无NF1的PA自发消退病例,该肿瘤位于一名14岁患癫痫男孩的左额叶,伴有FGFR1-TACC1融合。最初的MRI显示左额中回有病变,随后的随访MRI显示肿瘤自发消退。尽管肿瘤消退,但患者的癫痫发作仍持续,导致癫痫灶切除。病理检查证实为PA,具有特征性组织学表现及FGFR1-TACC1融合。
该病例提示,即使没有NF1,FGFR1-TACC1融合也可能与PA的自发消退有关。对于与PA相关的癫痫病例,无论肿瘤是否消退,手术干预可能仍然必要。