Adhikari R C
Department of Pathology, Tribhuvan University Teaching Hospital, Maharajgunj, Kathmandu, Nepal.
J Nepal Health Res Counc. 2014 May-Aug;12(27):119-23.
Kikuchi-Fujimoto disease is an acute onset febrile illness of unknown etiology, predominantly affecting young women with predilection for cervical lymphadenopathy.
The study included 13 cases of Kikuchi-Fujimoto disease with both fine needle aspiration cytology and excisional biopsy of lymph node available and data & slides were retrieved from the department of Pathology, Tribhuvan University Teaching Hospital and Om Hospital & Research Centre Pvt. Ltd., Kathmandu, Nepal from August 2009 to July 2013.
The mean age of the patients was 27.6 years with a range of 17 to 38 years. Twelve of 13 patients had cervical lymphadenopathy. Cytomorphological features included cellularity, karyorrhectic debris, crescentichistiocytes, necrosis and cellular polymorphism. Histologically, Lymph nodes showed partially effaced architecture by paracortical pale foci with karyorrhectic debris. These foci were composed of phagocytic & non-phagocytic histiocytes, plasmacytoid monocytes, immunoblasts and lymphocytes.
Kikuchi-Fujimoto disease, in most cases, can be diagnosed cytologically on the basis of identification of karyorrhectic debris and crescentic macrophages with reactive background.
菊池-藤本病是一种病因不明的急性发热性疾病,主要影响年轻女性,以颈部淋巴结病为特征。
该研究纳入了13例菊池-藤本病患者,这些患者均有细针穿刺细胞学检查及淋巴结切除活检资料,数据及切片于2009年8月至2013年7月从尼泊尔加德满都的特里布万大学教学医院病理科以及奥姆医院及研究中心私人有限公司获取。
患者的平均年龄为27.6岁,年龄范围为17至38岁。13例患者中有12例出现颈部淋巴结病。细胞形态学特征包括细胞丰富度、核碎裂碎片、新月形组织细胞、坏死及细胞多形性。组织学上,淋巴结显示副皮质苍白病灶导致结构部分消失,并伴有核碎裂碎片。这些病灶由吞噬性和非吞噬性组织细胞、浆细胞样单核细胞、免疫母细胞和淋巴细胞组成。
在大多数情况下,菊池-藤本病可根据核碎裂碎片和具有反应性背景的新月形巨噬细胞的识别在细胞学上作出诊断。