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伴有巨大淋巴结病的窦性组织细胞增生症:泰国报道的首例三例病例

Sinus histiocytosis with massive lymphadenopathy: the first three cases reported in Thailand.

作者信息

Suvatte V, Mahasandana C, Tanphaichitr V S, Sukpanichnant S

机构信息

Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

Asian Pac J Allergy Immunol. 1990 Dec;8(2):127-32.

PMID:2091658
Abstract

Three cases of sinus histiocytosis with massive lymphadenopathy are reported in Thai children and is probably a first report in Thailand. They were clinically characterized by bilateral massive cervical lymphadenopathy. Other lymph node groups were also involved but no extranodal manifestations could be detected. Leukocytosis with neutrophilia, hypergammaglobulinemia and polyclonal gammopathy were common features. The characteristic histopathologic findings in the involved lymph nodes included pericapsular fibrosis, markedly dilatation of subcapsular and medullary sinuses which were filled with numerous histiocytes showing active phagocytosis of lymphocytes and lymphoplasmacytoid proliferation in paracortical strands and medullary cord. The disease characteristically has a benign protracted clinical course, and does not respond to either irradiation or chemotherapy. The etiology and pathogenesis of this disorder are unknown. The possible pathologic mechanisms include an abnormal response to a specific infectious process and an immune deficiency status.

摘要

本文报告了3例泰国儿童的窦性组织细胞增多症伴巨大淋巴结病,这可能是泰国的首例报告。其临床特征为双侧巨大颈部淋巴结病。其他淋巴结组也有累及,但未发现结外表现。白细胞增多伴中性粒细胞增多、高球蛋白血症和多克隆丙种球蛋白病是常见特征。受累淋巴结的特征性组织病理学表现包括包膜周围纤维化、包膜下和髓窦明显扩张,窦内充满大量组织细胞,这些组织细胞表现出对淋巴细胞的活跃吞噬作用,以及副皮质索和髓索中的淋巴浆细胞样增生。该疾病的特征是临床病程良性且迁延,对放疗或化疗均无反应。这种疾病的病因和发病机制尚不清楚。可能的病理机制包括对特定感染过程的异常反应和免疫缺陷状态。

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