Multicentric giant lymph node hyperplasia.
Multicentric giant lymph node hyperplasia.
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多中心巨大淋巴结增生。
DOI：
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发表时间：
1978
影响因子：
3.5
通讯作者：
D. Variakojis
中科院分区：
文献类型：
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作者：
A. Gaba;R. Stein;D. Sweet;D. Variakojis
1例腹膜后和腋窝淋巴结肿大和脾肿大的患者，组织学检查显示透明血管型巨大淋巴结增生，每个区域均有浆细胞浸润。腹部病变不能手术切除，放疗无效。临床表现包括多克隆丙种球蛋白病、高冷凝集素滴度、神经病变和双侧视神经乳头水肿。所有这些异常自最初诊断以来持续了三年。
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.