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木村病的淋巴结病。

Lymphadenopathy of Kimura's disease.

作者信息

Hui P K, Chan J K, Ng C S, Kung I T, Gwi E

机构信息

Clinical Pathology Unit, Kwong Wah Hospital, Hong Kong.

出版信息

Am J Surg Pathol. 1989 Mar;13(3):177-86. doi: 10.1097/00000478-198903000-00001.

Abstract

Kimura's disease is an important category of reactive lymphadenopathy in the Oriental population. The enlarged nodes are mostly located in the head and neck region. Salient pathological changes include florid germinal centers, Warthin-Finkeldey type polykaryocytes, vascularization of germinal centers, increased postcapillary venules in the paracortex, eosinophilic infiltration, and sclerosis. The pathology of Kimura's disease is quite different from that of angiolymphoid hyperplasia with eosinophilia (epithelioid hemangioma). Immunoperoxidase studies show IgE reticular networks in germinal centers. Nondegranulated surface IgE-positive mast cells are present in the paracortex. The authors propose that Kimura's disease represents an aberrant immune reaction to an as yet unknown stimulus. Although the individual histological features are nonspecific, the constellation of features is highly characteristic of Kimura's disease. Since lymphadenopathy can herald involvement of other tissues and the prognosis is excellent, accurate diagnosis of this disease in lymph node biopsies may spare the patients unnecessary radical surgery.

摘要

木村病是东方人群中一种重要的反应性淋巴结病类型。肿大的淋巴结大多位于头颈部区域。显著的病理变化包括丰富的生发中心、华氏巨细胞、生发中心血管化、副皮质区毛细血管后微静脉增多、嗜酸性粒细胞浸润和硬化。木村病的病理与嗜酸性粒细胞增多性血管淋巴样增生(上皮样血管瘤)有很大不同。免疫过氧化物酶研究显示生发中心有IgE网状网络。副皮质区存在非脱颗粒表面IgE阳性肥大细胞。作者提出木村病代表对一种尚未明确的刺激的异常免疫反应。尽管单个组织学特征不具特异性,但这些特征的组合对木村病具有高度特征性。由于淋巴结病可能预示其他组织受累且预后良好,在淋巴结活检中准确诊断此病可使患者避免不必要的根治性手术。

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