Recurrent symptomatic intracranial hemorrhage in high-grade astrocytoma with piloid features: illustrative case

被引:0
作者
Niwa, Hirotaka [1 ]
Kato, Takenori [1 ]
Hasegawa, Toshinori [1 ]
Kuwabara, Kyoko [2 ]
Ohka, Fumiharu [3 ]
Hirato, Junko [4 ]
Sasaki, Shoh [5 ]
Ichimura, Koichi [6 ]
Yoshioka, Takako
Naito, Takehiro [1 ,7 ]
Mizuno, Akihiro [1 ]
Kageyama, Akinori [1 ]
Oishi, Hiroyuki [1 ]
Saito, Ryuta [3 ]
机构
[1] Komaki City Hosp, Dept Neurosurg, Komaki, Aichi, Japan
[2] Komaki City Hosp, Dept Pathol, Komaki, Aichi, Japan
[3] Nagoya Univ, Grad Sch Med, Dept Neurosurg, Nagoya, Aichi, Japan
[4] Publ Tomioka Gen Hosp, Dept Pathol, Tomioka, Gunma, Japan
[5] Nara Med Univ, Dept Diagnost Pathol, Kashihara, Nara, Japan
[6] Juntendo Univ, Grad Sch Med, Dept Brain Dis Translat Res, Bunkyo, Tokyo, Japan
[7] Natl Ctr Child Hlth & Dev, Dept Pathol, Tokyo, Tokyo, Japan
来源
JOURNAL OF NEUROSURGERY-CASE LESSONS | 2024年 / 8卷 / 15期
关键词
high-grade astrocytoma with piloid features; intracranial hemorrhage; methylation-based classification; ENDOTHELIAL GROWTH-FACTOR; PILOCYTIC ASTROCYTOMA; FACTOR RECEPTOR; OVEREXPRESSION; ANGIOGENESIS; RESISTANCE;
D O I
10.3171/CASE24395
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND High-grade astrocytoma with piloid features (HGAP) is a novel condition introduced in the 2021 World Health Organization classification. Given that it has been recently classified, reports clarifying its clinical features or diagnostic criteria are lacking, especially in cases of atypical presentation. Herein, the authors present a rare case of HGAP with repeated symptomatic hemorrhages. OBSERVATIONS A woman in her 20s presented with an acute headache and vertigo. Computed tomography and magnetic resonance imaging revealed a 2.5 x 2.8 x 2.3-cm hemorrhagic cerebellar mass with calcifications. After moderate improvement of her symptoms, she developed recurrent hemorrhage, and the tumor size increased (3.0 x 3.6 x 4.0 cm) 18 days later, necessitating resection. Pathological and molecular analyses confirmed the diagnosis of HGAP with an FGFR1-TACC1 fusion, MTAP/CDKN2A/B deletion, and SETD2 rearrangement. Radiologically, the presence of calcification and cystic components and the absence of perilesional edema were atypical features of previously reported HGAP. LESSONS Although recurrent symptomatic intracranial hemorrhages are rare in HGAP, enhancing lesions on magnetic resonance imaging suggest the need for resection to obtain tissue for molecular diagnosis and guide adjuvant treatment strategies.
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