Joshi K, Shrinivasa R, Shankar S K
Postgrad Med J. 1978 Oct;54(636):672-5. doi: 10.1136/pgmj.54.636.672.
A case of immunoblastic lymphadenopathy has been presented which had the characteristic clinical and histological features. The patient did not respond to chemotherapy and succumbed to the disease. Instead of the usual polyclonal gammopathy associated with this condition, he showed a fall in IgM levels, IgG and IgA being within normal limits. The significance of the latter finding is not known.
本文报告了一例具有典型临床和组织学特征的免疫母细胞性淋巴结病病例。该患者对化疗无反应,最终死于该病。与这种情况通常相关的多克隆丙种球蛋白病并未出现,相反,他的IgM水平下降,IgG和IgA在正常范围内。后一发现的意义尚不清楚。