Soler-Rico Morgane, Daoud Lina, Fomekong Edward
Neurosurgery, Cliniques Universitaires Saint-Luc (UCLouvain Saint-Luc), Brussels, BEL.
Pathology and Laboratory Medicine, Cliniques Universitaires Saint-Luc (UCLouvain Saint-Luc), Brussels, BEL.
Cureus. 2024 Sep 26;16(9):e70296. doi: 10.7759/cureus.70296. eCollection 2024 Sep.
Spinal cord pilocytic astrocytoma (PA) is a rare, low-grade tumor in adults, typically presenting with a cystic component. Correct diagnosis is crucial, as gross total resection may improve survival rates. We report the case of a 44-year-old patient with chronic neck and arm pain, along with hypoesthesia on the left side, initially suspected of having myelitis based on MRI findings. Surgical exploration enabled near-complete resection, and histopathology confirmed the diagnosis of PA. This case highlights the importance of considering PA in the differential diagnosis of inflammatory and degenerative spinal cord disorders and suggests that further investigation is needed into its treatment and potential recurrence.
脊髓毛细胞型星形细胞瘤(PA)是成人中一种罕见的低级别肿瘤,通常伴有囊性成分。正确诊断至关重要,因为全切除可能提高生存率。我们报告了一例44岁患者,有慢性颈部和手臂疼痛以及左侧感觉减退,最初根据MRI表现怀疑患有脊髓炎。手术探查实现了近全切除,组织病理学确诊为PA。该病例强调了在炎症性和退行性脊髓疾病的鉴别诊断中考虑PA的重要性,并表明需要对其治疗和潜在复发进行进一步研究。