Rancilio Nicholas, Drozd Mary, Donaldson Logan, Harm Tyler, Murakami Keiko
Department of Veterinary Clinical Sciences, Iowa State University, Ames, IA, United States.
School of Veterinary Medicine and Biomedical Sciences, University of Nebraska-Lincoln, Lincoln, NE, United States.
Front Vet Sci. 2025 May 9;12:1572808. doi: 10.3389/fvets.2025.1572808. eCollection 2025.
Pseudoprogression is a clinical and imaging phenomenon characterized by an increase in the size and contrast enhancement pattern of a glioma lesion following treatment with radiotherapy. In human beings, a substantial body of literature describes the phenomenon of pseudoprogression in glioblastoma after radiotherapy. The occurrence of gliomas in the cranial nerves has been reported in human beings as a clinically rare entity. A 7-year-old spayed female French Bulldog was presented with left-sided craniofacial muscle atrophy for a duration of 3 months and episodes of compulsive circling to the left. After a neurological examination, a magnetic resonance (MR) imaging scan of the brain was performed. A T2-and T2 FLAIR-weighted hyperintense, non-contrast-enhancing, T1-weighted hypointense intra-axial suprasellar lesion was found. In addition, an extra-axial, T1-weighted hyperintense, contrast-enhancing mass was identified at the level of the left trigeminal nerve. The lesions were presumptively diagnosed as a glioma and a left trigeminal nerve sheath tumor based on their imaging characteristics and the breed of the patient. A course of stereotactic radiotherapy (SRT) was prescribed, and 3 months after treatment, there was significant progression in the size of the suprasellar mass, indicative of either true progression or pseudoprogression. The left trigeminal nerve mass remained stable in size. Treatment with glucocorticoids resulted in a reduction in the size of the suprasellar mass, as observed on MR imaging 7 months after treatment. The left trigeminal nerve mass remained stable in size. Progression in the size of the suprasellar mass and the left trigeminal nerve mass occurred 9 months after the first course of treatment, and a second course of stereotactic radiotherapy was administered. Sixteen months after the first course of radiotherapy, a necropsy was performed. The suprasellar lesion and the left trigeminal nerve lesion were diagnosed as oligodendrogliomas on histopathology. Trigeminal nerve oligodendrogliomas and pseudoprogression following radiotherapy have not been previously described in dogs. Pseudoprogression should be considered a differential diagnosis for the progression of presumed or confirmed glioma lesions after treatment with radiotherapy. Concurrent oligodendroglioma lesions in the trigeminal nerve are also possible and should be included in the list of differential diagnoses for dogs with concurrent brain lesions.
假性进展是一种临床和影像学现象,其特征为胶质瘤病灶在接受放射治疗后,大小和对比增强模式出现增加。在人类中,大量文献描述了胶质母细胞瘤放疗后的假性进展现象。人类中已有颅神经胶质瘤发生的报道,这是一种临床罕见的病症。一只7岁已绝育的雌性法国斗牛犬出现左侧颅面肌萎缩3个月,并伴有向左强迫性转圈发作。经神经学检查后,对脑部进行了磁共振(MR)成像扫描。发现鞍上轴内有一个T2加权和T2液体衰减反转恢复序列(FLAIR)加权高信号、无对比增强、T1加权低信号的病灶。此外,在左侧三叉神经水平发现一个轴外T1加权高信号、有对比增强的肿块。根据病灶的影像学特征及患犬品种,初步诊断为胶质瘤和左侧三叉神经鞘瘤。给予立体定向放射治疗(SRT)疗程,治疗3个月后,鞍上肿块大小显著进展,提示可能为真性进展或假性进展。左侧三叉神经肿块大小保持稳定。糖皮质激素治疗后,治疗7个月时MR成像显示鞍上肿块大小缩小。左侧三叉神经肿块大小保持稳定。第一个疗程治疗9个月后,鞍上肿块和左侧三叉神经肿块大小均出现进展,于是给予第二个立体定向放射治疗疗程。第一个放射治疗疗程16个月后进行了尸检。组织病理学诊断鞍上病灶和左侧三叉神经病灶为少突胶质细胞瘤。此前尚未有犬三叉神经少突胶质细胞瘤及放疗后假性进展的报道。假性进展应被视为放疗后假定或确诊的胶质瘤病灶进展的鉴别诊断。三叉神经同时存在少突胶质细胞瘤病灶也是可能的,应列入并发脑部病灶犬的鉴别诊断清单中。