Antonijevic N, Radosevic-Radojkovic N, Colovic M, Jovanovic V, Rolovic Z
Institute of Haematology, Clinical Center of Serbia, Belgrade, Yugoslavia.
Leuk Lymphoma. 1996 May;21(5-6):505-7. doi: 10.3109/10428199609093451.
Simultaneous occurrence of localized plasmacytomas of both hands and feet has not been reported so far. Here we report a 40-year old female patient, who had at presentation pain and deformity. Of hands and feet, with numerous cystic lytic lesions of phalangeal, metacarpal and metatarsal bones, detected by X-rays. The biopsy of the affected bone showed moderately differentiated plasmacytoma of lambda light chain type (lambda-LC). Serum and urine biochemical analysis revealed the existence of lambda LC monoclonal component. The patient was treated by local radiotherapy and subsequent systemic chemotherapy, which consisted of 3 cycles of the M-2 protocol and 7 cycles of melphalan-prednisone. Five years after the diagnosis, the absence of plasmacytoma was confirmed by puncture biopsy of the left hand phalanx. Monoclonal protein in serum and urine was not detected.
双手和双脚同时发生局限性浆细胞瘤的情况迄今尚未见报道。在此,我们报告一名40岁女性患者,其初诊时出现疼痛和畸形。双手和双脚的X线检查发现指骨、掌骨和跖骨有大量囊性溶骨性病变。受累骨骼的活检显示为λ轻链型(lambda-LC)中度分化浆细胞瘤。血清和尿液生化分析显示存在λ LC单克隆成分。该患者接受了局部放疗及随后的全身化疗,全身化疗包括3个周期的M-2方案和7个周期的美法仑-泼尼松治疗。诊断后5年,通过左手手指穿刺活检证实无浆细胞瘤。血清和尿液中未检测到单克隆蛋白。