Eto M, Toyooka K, Kosugi S, Ota T, Ogawa M, Tamaki T, Kishino B, Fujimura H
Department of Neurology, Izumisano Municipal Hospital.
Rinsho Shinkeigaku. 2001 Feb-Mar;41(2-3):107-12.
We report a 73-year-old woman with intravascular malignant lymphomatosis (IML) who showed generalized telangiectasia as well as various neurological symptoms. In July 1998, she developed fever, dizziness, and confusion followed by left hemiparesis, and was admitted to our hospital on August 11, 1998. Laboratory tests indicated a normochromic normocytic anemia, thrombocytopenia, elevated serum lactic dehydrogenase (LDH), C-reactive protein (CRP), and cerebrospinal fluid protein. Magnetic resonance imaging (MRI) of the brain revealed an infarct-like lesion in the left frontal lobe and multiple white matter lesions. After admission, her neurological status deteriorated and lapsed into coma and quadriplegia. At the end of September 1998, generalized telangiectasia appeared, and she was diagnosed as IML on skin biopsy. Although combination chemotherapy failed to improve her neurological symptoms, telangiectasia disappeared in a few days, and the infarct-like lesion on MRI decreased in size. Serum LDH, CRP, and thrombocyte counts were normalized. Autopsy findings revealed perivascular clustering of B cell type lymphoma cells in the left frontal lobe where abnormal signal intensity was found on MRI, as well as the spleen and the bone marrow. This case emphasizes the importance of early diagnosis and treatment in IML.
我们报告了一名73岁患有血管内恶性淋巴瘤(IML)的女性,她出现了全身性毛细血管扩张以及各种神经症状。1998年7月,她出现发热、头晕和意识模糊,随后出现左侧偏瘫,并于1998年8月11日入住我院。实验室检查显示为正色素正细胞性贫血、血小板减少、血清乳酸脱氢酶(LDH)、C反应蛋白(CRP)升高以及脑脊液蛋白升高。脑部磁共振成像(MRI)显示左侧额叶有梗死样病变以及多个白质病变。入院后,她的神经状态恶化,陷入昏迷和四肢瘫痪。1998年9月底,出现全身性毛细血管扩张,皮肤活检诊断为IML。尽管联合化疗未能改善她的神经症状,但毛细血管扩张在数天内消失,MRI上的梗死样病变大小减小。血清LDH、CRP和血小板计数恢复正常。尸检结果显示,在MRI上发现异常信号强度的左侧额叶以及脾脏和骨髓中,有B细胞型淋巴瘤细胞的血管周围聚集。该病例强调了IML早期诊断和治疗的重要性。