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肉芽肿性淋巴结炎

Granulomatous lymphadenitis.

作者信息

Asano Shigeyuki

机构信息

Department of Pathology, Iwaki Kyoritsu General Hospital, Iwaki, Japan.

出版信息

J Clin Exp Hematop. 2012;52(1):1-16. doi: 10.3960/jslrt.52.1.

Abstract

In this review, representative types of granulomatous lymphadenitis (GLA) are described. GLA can be classified as noninfectious GLA and infectious GLA. Noninfectious GLA includes sarcoidosis and sarcoid-like reaction. The cause of sarcoidosis remains unknown, but it has good prognosis. Sarcoid-like reaction, which is considered to be a biological defense mechanism, is observed in regional lymph nodes with many underlying diseases. Infectious GLA can be classified as suppurative lymphadenitis (LA) and nonsuppurative LA. Suppurative LA generally shows follicular hyperplasia and sinus histiocytosis in the early phase. In tularemia and cat scratch disease, monocytoid B lymphocytes (MBLs) with T cells and macrophages contribute to the formation of granuloma. However, none of the epithelioid cell granulomas of Yersinia LA contains MBLs like in cat scratch disease. In addition, almost all have a central abscess in granulomas induced by Gram-negative bacteria. In terms of the lymph nodes, tularemia and cat scratch disease are apt to affect the axillary and cervical regions while Yersinia LA affects the mesenteric lymph node. Nonsuppurative LA includes tuberculosis and BCG-histiocytosis. These are induced by delayed allergic reaction of M. tuberculosis. Tuberculosis LA mainly appears in the cervical lymph node. Organisms are histologically detected by Ziehl-Neelsen staining in the necrotic area. Toxoplasmosis is also a nonsuppurative protozoan infection (Toxoplasma gondii). In toxoplasma LA, MBLs can also be seen, but round and organized, well-formed granulomas are not found in this disease. Furthermore, necrosis is not induced and there are no accompanying neutrophils, eosinophils and fibrosis. GLA described above is associated with characteristic histological findings. An accurate pathological diagnosis using the above findings can lead to precise treatment.

摘要

在本综述中,描述了肉芽肿性淋巴结炎(GLA)的代表性类型。GLA可分为非感染性GLA和感染性GLA。非感染性GLA包括结节病和结节病样反应。结节病的病因尚不清楚,但预后良好。结节病样反应被认为是一种生物防御机制,在许多潜在疾病的区域淋巴结中可见。感染性GLA可分为化脓性淋巴结炎(LA)和非化脓性LA。化脓性LA在早期通常表现为滤泡增生和窦组织细胞增生。在兔热病和猫抓病中,单核细胞样B淋巴细胞(MBL)与T细胞和巨噬细胞共同促进肉芽肿的形成。然而,耶尔森菌LA的上皮样细胞肉芽肿均不含有像猫抓病那样的MBL。此外,几乎所有由革兰氏阴性菌引起的肉芽肿都有中央脓肿。就淋巴结而言,兔热病和猫抓病易累及腋窝和颈部区域,而耶尔森菌LA累及肠系膜淋巴结。非化脓性LA包括结核病和卡介苗组织细胞增生症。这些由结核分枝杆菌的迟发性过敏反应引起。结核性LA主要出现在颈部淋巴结。通过齐-尼氏染色在坏死区域组织学检测到病原体。弓形虫病也是一种非化脓性原生动物感染(刚地弓形虫)。在弓形虫性LA中也可见MBL,但在该病中未发现圆形且有组织的、结构良好的肉芽肿。此外,不诱导坏死,也没有伴随的中性粒细胞、嗜酸性粒细胞和纤维化。上述GLA与特征性组织学表现相关。利用上述发现进行准确的病理诊断可实现精准治疗。

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