Lorand-Metze I, Vassallo J, Mori S
Department of Internal Medicine, School of Medicine, State University of Campinas, Sâo Paulo, Brazil.
Pathol Int. 1994 Jul;44(7):548-50. doi: 10.1111/j.1440-1827.1994.tb02606.x.
Histiocytic necrotizing lymphadenitis is rare outside Japan, including Brazil, despite the many Japanese immigrants and descendants who live there. The authors describe the case of a 32 year old white female, who presented with cervical lymph node enlargement and severe anemia. Histological findings of the lymph node were typical for Kikuchi's disease. Bone marrow showed hyperplasia of normoblasts, suggesting hemolysis, but a Coombs' test was negative. The patient had a spontaneous resolution of all symptoms and has remained asymptomatic for 3 years. Especially where this disease is rarely reported, it is important to recognize it, in order to avoid a misdiagnosis of malignant lymphoma.
组织细胞性坏死性淋巴结炎在日本以外的地区较为罕见,包括巴西,尽管那里有许多日本移民及其后裔。作者描述了一名32岁白人女性的病例,该患者出现颈部淋巴结肿大和严重贫血。淋巴结的组织学检查结果符合菊池病。骨髓显示正成红细胞增生,提示溶血,但库姆斯试验为阴性。患者所有症状均自发缓解,且3年来一直无症状。特别是在这种疾病很少报道的地区,认识到它很重要,以避免误诊为恶性淋巴瘤。