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无粒细胞浸润的组织细胞性坏死性淋巴结炎

Histiocytic necrotizing lymphadenitis without granulocytic infiltration.

作者信息

Pileri S, Kikuchi M, Helbron D, Lennert K

出版信息

Virchows Arch A Pathol Anat Histol. 1982;395(3):257-71. doi: 10.1007/BF00429352.

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.

摘要

据报道,此前仅在日本有描述的一种不寻常的坏死性淋巴结炎,在西德出现了23例,伊朗、意大利、韩国和西班牙各出现1例。该病变常发生于年轻女性的颈部淋巴结。其特征为大量增生的组织细胞浸润皮质和/或副皮质,且无粒细胞。所有病例均可见淋巴组织完全或更常见的不完全坏死。在不完全坏死的病例中,组织细胞间散布着固缩细胞和核碎片。基于组织学发现,提出了“无粒细胞浸润的组织细胞性坏死性淋巴结炎”这一术语。鉴别诊断时需考虑的病变有恶性组织细胞肿瘤和有粒细胞浸润的坏死性淋巴结炎,后者可见于红斑狼疮和细菌感染。无粒细胞浸润的组织细胞性坏死性淋巴结炎的病因仍不清楚。一些临床和组织学特征表明可能存在潜在的病毒感染。

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