Cohen A M, Mittelman M, Gal R, Halperin M, Djaldetti M
Hematology Unit, Golda Medical Center, Petah-Tikva, Israel.
Leuk Lymphoma. 1994 Dec;16(1-2):183-7. doi: 10.3109/10428199409114157.
A case of chronic myelomonocytic leukemia (CMML) associated with primary amyloidosis (AL) is presented. Hepatosplenomegaly, macroglossia, and xanthelasma were the major physical findings. Laboratory tests showed macrocytic anemia, thrombocytopenia, monocytosis and a bi-clonal gammopathy. Early monocytes and monoblasts were noted in the bone marrow aspiration biopsy. Cytogenetic evaluation showed a clonal deletion of chromosome 21 long arm (21q-). Amyloid was present in the liver, tongue and xanthelasma. In addition, the patient was noted to have osteosclerosis of the lower extremities. Treatment with prednisone and colchicine resulted in a subjective response. The unusual association of CMML, and primary amyloidosis is discussed.
本文报告一例慢性粒单核细胞白血病(CMML)合并原发性淀粉样变性(AL)的病例。肝脾肿大、巨舌症和睑黄瘤是主要的体格检查发现。实验室检查显示大细胞性贫血、血小板减少、单核细胞增多症和双克隆丙种球蛋白病。骨髓穿刺活检发现早期单核细胞和原单核细胞。细胞遗传学评估显示21号染色体长臂克隆性缺失(21q-)。肝脏、舌头和睑黄瘤中存在淀粉样物质。此外,该患者还被发现有下肢骨硬化。泼尼松和秋水仙碱治疗产生了主观反应。本文讨论了CMML与原发性淀粉样变性的不寻常关联。