Castleman病伪装成腰骶神经纤维瘤,对利妥昔单抗有良好的反应

F. Binesh, M. Mortazavizadeh, R. N. Moghadam, S. Shahcheraghi
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引用次数: 0

摘要

Castleman氏病是一种罕见的淋巴细胞增生性疾病。其病因尚不清楚。Castleman病很少累及脊柱。作者报告了一名50岁的男子,他从2.5年前开始接受马鞍麻醉和腰痛。CT扫描显示椎管S1-S2处有髓外肿块,未累及骨。MRI信号与神经纤维瘤信号相似,行穿刺活检。组织学检查证实为Castleman病,透明血管型。他接受了利妥昔单抗治疗,疼痛得到了显著缓解。虽然罕见,但在鉴别诊断髓外肿块时应考虑Castleman病。
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Castleman Disease masquerading as the lumbosacral neurofibroma with excellent response to rituximab
Castleman's disease is an uncommon, lymphoproliferative disease. Its etiology is unknown. Spine involvement is very scant in Castleman's disease. The authors report on the case of a 50 year-old man who referred with saddle anesthesia and low back pain from 2.5 years ago. A CT scan showed an extra medullary mass at S1-S2 level of the spinal canal without bone involvement. The signal specs on MRI were resembling to signal of neurofibroma .The patient underwent needle biopsy. Histological examination confirmed the diagnosis of Castleman disease, hyaline-vascular type. He received rituximab and pain was dramatically relieved. Although rare, Castleman disease should be considered in the differential diagnosis of an extramedullary mass.
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