Brouet J C, Seligmann M, Danon F, Belpomme D, Fine J M
Arch Intern Med. 1979 Jun;139(6):672-4. doi: 10.1001/archinte.139.6.672.
We report two cases of mu-heavy-chain disease. Both patients were affected with a lymphoproliferative disease that shared several suggestive features with the previously reported cases of mu-chain disease: the presence of vacuolated plasma cells in bone marrow, a small amount of alpha 2 moving abnormal mu-chain protein, and urinary kappa Bence Jones protein in one case.
我们报告了两例μ重链病。两名患者均患有淋巴增殖性疾病，该疾病与先前报道的μ链病病例有几个相似的特征：骨髓中存在空泡化浆细胞，一例存在少量α2移动异常的μ链蛋白，以及尿κ本周蛋白。
