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颈部坏死性淋巴结炎(菊池病)。

Necrotizing lymphadenitis of the neck (Kikuchi's disease).

作者信息

Hussein A, Hellquist H B

机构信息

Department of Pathology, Medical Center Hospital, Orebro, Sweden.

出版信息

APMIS. 1994 Aug;102(8):633-7. doi: 10.1111/j.1699-0463.1994.tb05213.x.

Abstract

Kikuchi's histiocytic necrotizing lymphadenitis is a benign condition originally described in the Japanese literature in 1972. We here describe the clinicopathological features, including fine needle aspirate and bone marrow biopsy, of a case of Kikuchki's disease, which to our knowledge is the first reported from a Scandinavian country. The histopathological features of the enlarged lymph nodes were documented by multiple small necrotic foci showing karyorrhectic debris and haemorrhage. The necrotic foci were surrounded by a mantle of large histiocytic-like cells with vesicular nuclei and clear cytoplasm. The nodal architecture was almost completely effaced and the node infiltrated by a mixture of lymphoid cells of variable size. Neutrophils, eosinophils, and plasma cells were very few. The fine needle aspirate biopsy showed a mixture of small dark lymphocytes, larger activated lymphocytes, and many histiocytes. The bone marrow biopsy showed normal haematopoiesis but some large cells with phagocytosed leukocytes, i.e. similar to haemophagocytosis. Kikuchi's disease has a predilection for lymph nodes in the neck of young women, and is usually self-limited and subsides in 1 to 4 months. The patient described in this report received no treatment. Within 5 weeks the fever subsided and the lymph nodes diminished in size. One year later the patient is well and free of disease. We emphasize the benign nature of Kikuchi's disease, and that SLE and malignant lymphoma are the majori differential diagnoses.

摘要

菊池氏组织细胞性坏死性淋巴结炎是一种良性疾病,最初于1972年在日本文献中被描述。我们在此描述一例菊池氏病的临床病理特征,包括细针穿刺抽吸活检和骨髓活检,据我们所知,这是斯堪的纳维亚国家首次报道的病例。肿大淋巴结的组织病理学特征表现为多个小坏死灶,可见核碎裂碎片和出血。坏死灶被一层大的组织细胞样细胞所包绕,这些细胞具有泡状核和清亮的胞质。淋巴结结构几乎完全被破坏,淋巴结内浸润有大小不一的淋巴细胞混合成分。中性粒细胞、嗜酸性粒细胞和浆细胞极少。细针穿刺抽吸活检显示有小的深色淋巴细胞、较大的活化淋巴细胞和许多组织细胞混合存在。骨髓活检显示造血正常,但有一些吞噬白细胞的大细胞,即类似于噬血细胞现象。菊池氏病好发于年轻女性颈部淋巴结,通常为自限性,1至4个月内消退。本报告中描述的患者未接受治疗。5周内发热消退,淋巴结缩小。一年后患者情况良好,无疾病迹象。我们强调菊池氏病的良性本质,以及系统性红斑狼疮和恶性淋巴瘤是主要的鉴别诊断疾病。

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