Histiocytic necrotizing lymphadenitis without granulocytic infiltration.

S Pileri, M Kikuchi, D Helbron, K Lennert
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引用次数: 105

Abstract

Twenty-seven cases of an unusual necrotizing lymphadenitis previously described only in Japan are reported as occurring in West Germany (23 cases), Iran (1 case), Italy (1 case), Korea (1 case) and Spain (1 case). The lesion frequently develops in the cervical lymph nodes of young women. It is characterized by infiltration of the cortex and/or paracortex by large collections of proliferating histiocytes and is devoid of granulocytes. Complete or, more often, incomplete necrosis of lymphoid tissue is seen in all cases. In cases with incomplete necrosis, the histiocytes are interspersed with pyknotic cells and nuclear debris. Based on the histological findings, the term "histiocytic necrotizing lymphadenitis without granulocytic infiltration" is proposed. Lesions to be considered in a differential diagnosis are malignant histiocytic neoplasms and necrotizing lymphadenitis with granulocytic infiltration, which is seen in lupus erythematosus and bacterial infections. The aetiology of histiocytic necrotizing lymphadenitis without granulocytic infiltration is still unclear. Some clinical and histological features indicate the possibility of an underlying viral infection.

无粒细胞浸润的组织细胞坏死性淋巴结炎。
以前仅在日本报道的27例不寻常的坏死性淋巴结炎报告发生在西德(23例)、伊朗(1例)、意大利(1例)、韩国(1例)和西班牙(1例)。这种病变常发生在年轻女性的颈部淋巴结。其特征是大量增殖组织细胞浸润皮质和/或副皮质,缺乏粒细胞。所有病例均可见淋巴组织完全坏死或更常见的不完全坏死。在不完全坏死的情况下,组织细胞中散布着固缩细胞和核碎片。根据组织学结果,提出“无粒细胞浸润的组织细胞坏死性淋巴结炎”。在鉴别诊断中应考虑的病变是恶性组织细胞肿瘤和粒细胞浸润的坏死性淋巴结炎,可见于红斑狼疮和细菌感染。无粒细胞浸润的组织细胞坏死性淋巴结炎的病因尚不清楚。一些临床和组织学特征提示潜在病毒感染的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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