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组织细胞坏死性淋巴结炎(菊池病):9例临床病理研究

Histiocytic necrotizing lymphadenitis (Kikuchi's disease) a clinicopathologic study of 9 cases.

作者信息

Chan J K, Saw D

出版信息

Pathology. 1986 Jan;18(1):22-8. doi: 10.3109/00313028609090823.

Abstract

The clinicopathological features of histiocytic necrotizing lymphadenitis in 9 patients are described. This disease occurs predominantly in the second and third decades of life, and in our series, is slightly more common in males. The commonest presentation is lymph node enlargement. Fever is also common, and was the mode of presentation in two patients. Laboratory investigations are non-contributory, with only an occasional case showing leucopenia or a raised erythrocyte sedimentation rate. The disease is self-limiting in all patients. The characteristic histological feature is the presence of pale nodules in the paracortex, consisting of a mixture of activated lymphoid cells, histiocytes and karyorrhectic debris. Granulocytes are strikingly absent.

摘要

本文描述了9例组织细胞坏死性淋巴结炎的临床病理特征。该病主要发生于20至30岁年龄段,在我们的病例系列中,男性略为多见。最常见的表现是淋巴结肿大。发热也很常见,有2例患者以此为首发症状。实验室检查无诊断意义,仅偶尔有病例显示白细胞减少或红细胞沉降率升高。所有患者的病情均为自限性。其特征性组织学表现为副皮质区出现淡染结节,由活化的淋巴细胞、组织细胞和核碎裂碎片混合而成。显著缺乏粒细胞。

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