Tsujimura T, Kishino B I, Itatani H, Aozasa K, Matsumoto K
Department of Pathology, Sumitomo Hospital, Osaka, Japan.
Acta Pathol Jpn. 1988 Oct;38(10):1337-44. doi: 10.1111/j.1440-1827.1988.tb02284.x.
A case of plasma cell dyscrasia with polyneuropathy and endocrine disorder is reported. Clinically, polycythemia vera, gynecomastia, pigmentation of the skin, hepatosplenomegaly, renal enlargement and severe polyneuropathy in the lower extremities were recognized. The peculiarity of this case was polycythemia vera that had been present for several years before manifestation of the clinical symptoms. Microscopically, retroperitoneal lymph nodes showed angio-follicular lymphoid hyperplasia and plasma cell infiltration in the interfollicular region. By means of the avidin-biotin-peroxidase complex method, plasma cells were positive for lambda light chain, IgA and IgG. Severe segmental demyelination and slight axonal atrophy were found in a sural nerve biopsy.
报告了一例伴有多发性神经病和内分泌紊乱的浆细胞发育异常病例。临床上,发现有真性红细胞增多症、男子女性型乳房、皮肤色素沉着、肝脾肿大、肾肿大以及严重的下肢多发性神经病。该病例的特点是在临床症状出现前数年就已存在真性红细胞增多症。显微镜下,腹膜后淋巴结显示血管滤泡性淋巴组织增生以及滤泡间区域的浆细胞浸润。通过抗生物素蛋白-生物素-过氧化物酶复合物法,浆细胞对λ轻链、IgA和IgG呈阳性反应。在腓肠神经活检中发现严重的节段性脱髓鞘和轻微的轴索萎缩。