Finsterer Josef, Rathkolb Victor
Neurology Neurophysiology Center, Vienna, Austria.
3rd Medical Department, Hanusch Krankenhaus, Vienna, Austria.
J Med Life. 2024 Nov;17(11):1020-1022. doi: 10.25122/jml-2024-0321.
Central nervous system (CNS) involvement in chronic lymphocytic leukemia (CLL) is rare, and spinal cord infiltration as a presenting manifestation has only rarely been described. We present the case of a 65-year-old man with CLL, initially diagnosed at the age of 54, who had not received prior treatment. He presented with a six-week history of thoracic and epigastric pressure. Mild ataxia was found in the clinical exam. Clinical evaluation revealed leukocytosis (163 G/L; normal range: 4-10 G/L). MRI of the spine showed a mildly enhancing, T2 hyperintense central lesion extending between C3 and T8. There was a pleocytosis of 105 /micro/l consisting of neoplastic B-lymphocytes. The bone marrow biopsy diagnosed a relapse of CLL, and the patient was started on ibrutinib, which had a positive effect. This case highlights spinal cord infiltration as a rare initial manifestation of CLL relapse, presenting with non-specific symptoms such as thoracic and epigastric pressure and mild spinal ataxia.
中枢神经系统(CNS)受累于慢性淋巴细胞白血病(CLL)较为罕见,而脊髓浸润作为首发表现仅有极少的病例报道。我们报告一例65岁男性CLL患者,最初于54岁时确诊,此前未接受过治疗。他因胸部和上腹部有压迫感6周前来就诊。临床检查发现轻度共济失调。临床评估显示白细胞增多(163 G/L;正常范围:4 - 10 G/L)。脊柱MRI显示一个轻度强化、T2高信号的中央病变,范围从C3延伸至T8。脑脊液检查显示每微升有105个肿瘤性B淋巴细胞。骨髓活检诊断为CLL复发,患者开始使用伊布替尼治疗,治疗效果良好。该病例突出了脊髓浸润作为CLL复发罕见的初始表现,伴有胸部和上腹部压迫感以及轻度脊髓性共济失调等非特异性症状。