Abdel-Reheim F A, Koss W, Rappaport E S, Arber D A
Department of Pathology, Scott and White Clinic, Temple, TX 76508, USA.
Arch Pathol Lab Med. 1996 Jan;120(1):91-6.
Coexistence of Hodgkin's disease and giant lymph node hyperplasia (Castleman's disease) is well documented in the literature. We present a unique case in which the original lymph node biopsy revealed interfollicular Hodgkin's disease (CD15+, CD30+, CD45-, Reed-Sternberg cells) with coexistent histologic features of the plasma-cell variant of Castleman's disease. The patient experienced a long-term remission following combined chemotherapy and radiation therapy. He presented at 18 years and again at 22 years later with clinical, hematologic, and histologic features of a multicentric plasma-cell variant of Castleman's disease without evidence of Hodgkin's disease. This unique case report further strengthens the association of Castleman's disease and Hodgkin's lymphoma. Two pathogenetic mechanisms for this association have been suggested: (1) secretion of interleukin-6 by Hodgkin's Reed-Sternberg cells and histiocytes, and (2) manifestation of an abnormal immune state associated with Hodgkin's disease. These two mechanisms may, indeed, be related.
霍奇金病与巨大淋巴结增生症(卡斯尔曼病)并存的情况在文献中有充分记载。我们报告一例独特病例,最初的淋巴结活检显示滤泡间霍奇金病(CD15 +、CD30 +、CD45 -,里德 - 斯腾伯格细胞),同时伴有卡斯尔曼病浆细胞变异型的组织学特征。该患者在接受联合化疗和放疗后长期缓解。他18岁时发病,22年后再次出现多中心性浆细胞变异型卡斯尔曼病的临床、血液学和组织学特征,未发现霍奇金病证据。这一独特病例报告进一步强化了卡斯尔曼病与霍奇金淋巴瘤之间的关联。对于这种关联提出了两种发病机制:(1)霍奇金里德 - 斯腾伯格细胞和组织细胞分泌白细胞介素 - 6,(2)与霍奇金病相关的异常免疫状态的表现。这两种机制可能确实相关。