Gaba A R, Stein R S, Sweet D L, Variakojis D
Am J Clin Pathol. 1978 Jan;69(1):86-90. doi: 10.1093/ajcp/69.1.86.
A patient with retroperitoneal and axillary lymphadenopathy and splenomegaly was demonstrated histologically to have the hyaline vascular type of giant lymph node hyperplasia, with plasma cell infiltrates in each region. The abdominal lesions were not surgically resectable and did not respond to radiotherapy. The clinical findings included polyclonal gammopathy, high cold agglutinin titers, neuropathy, and bilateral papilledema. All of these abnormalities have persisted three years since the initial diagnosis.
一名患有腹膜后和腋窝淋巴结病以及脾肿大的患者经组织学证实患有透明血管型巨大淋巴结增生，每个区域均有浆细胞浸润。腹部病变无法通过手术切除，对放疗也无反应。临床症状包括多克隆丙种球蛋白病、高冷凝集素滴度、神经病变和双侧视乳头水肿。自初次诊断以来，所有这些异常情况已持续三年。
