Castro-del Río M, Seijo-Martínez M, Iglesias A, Vázquez F, Arán I, Cebrián-Pérez E M
Servicio de Neurología, Complejo Hospitalario de Pontevedra, Pontevedra, Spain.
Rev Neurol. 2004;39(1):37-40.
Superficial siderosis of the central nervous system (CNS) is a rare disease characterized by deafness, ataxia and pyramidal dysfunction. It is due to hemosiderin deposition in the subpial membranes of the brain, spinal cord and cranial nerves. Most cases are secondary to chronic or recurrent bleeding into the subarachnoid space. Diagnosis is permitted by magnetic resonance imaging (MRI).
We report two patients with a chronic, slowly progressive cerebellar ataxia and hearing loss. MRI showed T2 hypointense signals in the brain, cerebellum and spinal cord diagnostic of superficial siderosis of the CNS. Xanthochromia was present in one patient. Evoked potentials showed retrochoclear hearing loss. Extensive vascular studies were negative for bleeding sources. One patient, treated with oral anticoagulants, benefited from reduction of the International Normalized Ratio.
Due to its rarity, clinical suspicion is essential for diagnosis of superficial siderosis of the CNS.
中枢神经系统(CNS)浅表性铁沉积症是一种罕见疾病,其特征为耳聋、共济失调和锥体功能障碍。它是由于含铁血黄素沉积于脑、脊髓和颅神经的软膜下。大多数病例继发于蛛网膜下腔的慢性或反复出血。磁共振成像(MRI)可用于诊断。
我们报告了两名患有慢性、缓慢进展性小脑共济失调和听力丧失的患者。MRI显示脑、小脑和脊髓的T2低信号,诊断为中枢神经系统浅表性铁沉积症。其中一名患者存在黄变症。诱发电位显示蜗后听力丧失。广泛的血管检查未发现出血源。一名接受口服抗凝剂治疗的患者因国际标准化比值降低而获益。
由于其罕见性,临床怀疑对于中枢神经系统浅表性铁沉积症的诊断至关重要。