Iwahashi T, Koh C S, Ohara S, Inoue A, Yanagisawa N
Third Department of Internal Medicine (Neurology), Shinshu University School of Medicine.
Rinsho Shinkeigaku. 1992 Nov;32(11):1232-7.
A case of B cell lymphoma with clinical and histological features of malignant histiocytosis was described. A 57-year-old male was admitted to Shinshu University Hospital because of transverse myelopathy. Five months before admission, he noticed urinary disturbance, which progressed to urinary obstruction. The following month, bilateral muscular weakness appeared in his legs. A few days later he could not stand up, and was admitted to a local hospital. Neurological examination revealed sensory disturbances below the level of Th12 in all modalities, and marked weakness and hyperreflexia in the lower limbs. A spinal tumor was suspected. However, myelography showed no abnormality. The patient's condition worsened and he became bed-ridden in February 1990. He was transferred to Shinshu University Hospital for further evaluation. On admission he was poorly nourished with fever, anemia, hepatomegaly, and bilateral pretibial pitting edema. No lymphadenopathy was observed. Neurological examination showed total sensory loss below the level of Th12, spastic paraplegia, hyperreflexia in the legs, and urinary obstruction. Laboratory findings revealed an elevated erythrocyte sedimentation rate, increased CRP, pancytopenia, and hypoalbuminemia. Serum level of IgG, IgA, IgM, LDH, ALP, GPT and total bilirubin were increased. CSF and MRI imaging of the spinal cord were normal. Proliferation of atypical histiocytes with marked erythrophagocytosis, which is a characteristic pathological feature of malignant histiocytosis, was observed in peripheral blood and aspirated bone marrow. Immunoenzyme staining of bone marrow using monoclonal antibody L-26, which is a B-cell marker, revealed B-cell lymphoma.(ABSTRACT TRUNCATED AT 250 WORDS)
描述了一例具有恶性组织细胞增多症临床和组织学特征的B细胞淋巴瘤病例。一名57岁男性因横贯性脊髓病入住信州大学医院。入院前五个月,他注意到排尿障碍,并进展为尿路梗阻。接下来的一个月,他双腿出现双侧肌肉无力。几天后他无法站立,被送往当地医院。神经学检查发现,在所有感觉模式下,胸12水平以下均有感觉障碍,下肢明显无力和反射亢进。怀疑有脊髓肿瘤。然而,脊髓造影未显示异常。患者病情恶化,于1990年2月卧床不起。他被转至信州大学医院进行进一步评估。入院时,他营养不良,伴有发热、贫血、肝肿大和双侧胫前凹陷性水肿。未观察到淋巴结病。神经学检查显示胸12水平以下完全感觉丧失、痉挛性截瘫、腿部反射亢进和尿路梗阻。实验室检查结果显示血沉升高、C反应蛋白增加、全血细胞减少和低白蛋白血症。血清IgG、IgA、IgM、乳酸脱氢酶、碱性磷酸酶、谷丙转氨酶和总胆红素水平升高。脑脊液和脊髓MRI成像正常。在外周血和抽取的骨髓中观察到非典型组织细胞增殖并伴有明显的红细胞吞噬现象,这是恶性组织细胞增多症的特征性病理表现。使用B细胞标志物单克隆抗体L-26对骨髓进行免疫酶染色,显示为B细胞淋巴瘤。(摘要截取自250字)