Nisiro Abebe Melis, Geremew Teketel Tadesse
Pathology Department, College of Medicine and Health Science, Hawassa University, Hawassa, Ethiopia.
Case Rep Pathol. 2025 Apr 11;2025:8927598. doi: 10.1155/crip/8927598. eCollection 2025.
Choroid plexus tumors (CPTs) are rare neoplasms. Patient presentation varies depending on the location of the lesions. Gross total resection of primary lesions remains the gold standard for surgical treatment of CPTs. Here, we present the case of a 22-year-old male patient with 2-day history of abnormal body movement and headache who was found to have an enhancing mass of the lateral ventricle. The patient underwent craniotomy for gross-total resection of the lesion, with final histopathology demonstrating WHO Grade II aCPP.
脉络丛肿瘤(CPTs)是罕见的肿瘤。患者的表现因病变位置而异。原发性病变的全切除仍然是CPTs手术治疗的金标准。在此,我们报告一例22岁男性患者,有2天身体异常运动和头痛病史,经检查发现侧脑室有一强化肿块。该患者接受了开颅手术以完全切除病变,最终组织病理学显示为世界卫生组织II级非典型脉络丛乳头状瘤(aCPP)。