Ivanova Nora I, Kyuchukova Dayana M, Tsalta-Mladenov Mihael E, Georgieva Darina K, Andonova Silva P
Department of Neurology and Neuroscience, Medical University "Prof. Paraskev Stoyanov", Varna, BGR.
Second Clinic of Neurology With Intensive Care Unit and Stroke Unit, University Hospital "St. Marina", Varna, BGR.
Cureus. 2024 Mar 1;16(3):e55349. doi: 10.7759/cureus.55349. eCollection 2024 Mar.
Prosopagnosia, also referred to as "face blindness," is a type of visual agnosia characterized by a decreased capacity to recognize familiar faces with a preserved ability to identify individuals based on non-facial visual traits or voice. Prosopagnosia can be categorized as developmental (DP) or acquired (AP) owing to a variety of underlying conditions, including trauma, neurodegenerative diseases, stroke, neuroinfections, and, less frequently, malignancies. Facial recognition is a complex process in which different neuronal networks are involved. The infrequent but notable higher visual-processing abnormalities can be caused by lesions of the inferior longitudinal fasciculus (ILF) in the non-dominant temporal lobe. We report a rare case of AP in a 69-year-old patient who is right-hand dominant with rectal carcinoma cerebral metastases. The patient complained of dizziness, vertigo, falls, and trouble recognizing her family members' faces. The CT scan of the head with contrast revealed two metastatic brain lesions with vasogenic edema, as one of them was in the right cerebellar hemisphere, causing dislocation and compression of the ILF. Corticosteroids and osmotherapy were utilized as a conservative treatment approach, which resulted in the prosopagnosia being completely withdrawn. In conclusion, patients with primary brain tumors or metastatic disease rarely present with an isolated cognitive deficit such as prosopagnosia. Based on the anatomical features and the personalized approach, a conservative or surgical approach may be useful to improve higher cortical functioning.
面孔失认症,也被称为“脸盲症”,是一种视觉失认症,其特征是识别熟悉面孔的能力下降,而基于非面部视觉特征或声音识别个体的能力保持完好。由于多种潜在病症,包括创伤、神经退行性疾病、中风、神经感染以及较少见的恶性肿瘤,面孔失认症可分为发育性(DP)或后天性(AP)。面部识别是一个涉及不同神经网络的复杂过程。非优势颞叶的下纵束(ILF)损伤可导致罕见但显著的高级视觉处理异常。我们报告一例69岁右利手直肠癌脑转移患者的罕见后天性面孔失认症病例。患者主诉头晕、眩晕、跌倒以及难以识别家人的面孔。头颅增强CT扫描显示两个伴有血管源性水肿的脑转移瘤,其中一个位于右侧小脑半球,导致ILF移位和受压。采用皮质类固醇和渗透性疗法作为保守治疗方法,结果面孔失认症完全消失。总之,原发性脑肿瘤或转移性疾病患者很少仅表现出如面孔失认症这样的孤立认知缺陷。基于解剖特征和个体化方法,保守或手术方法可能有助于改善高级皮质功能。