Ria L, Mussardo V, D'Ambrosio E, De Filippo C, Matteo T, Potì R
Divisione di Medicina interna, Ospedale S. Cuore di Gesù, Gallipoli.
Recenti Prog Med. 1991 May;82(5):278-81.
We describe a case of necrotizing histiocytic lymphadenitis or Kikuchi and Fujimoto disease, a rare lymphadenopathy of unknown etiology usually striking young women. It was formerly described in Japan, and subsequently in other countries and in Italy as an anatomo-clinical entity. The disease has a favourable prognosis, therefore it has to be considered differently from other lymphadenopathies with severe prognosis whose anatomo-pathological differential features were analyzed by the authors. The case here observed differs from other cases described in literature because of the presence of a perilymphadenitic component.
我们描述了一例坏死性组织细胞性淋巴结炎，即菊池和藤本病，这是一种病因不明的罕见淋巴结病，通常侵袭年轻女性。该病最初在日本被描述，随后在其他国家以及意大利被作为一种解剖临床实体进行描述。该疾病预后良好，因此必须与其他预后严重的淋巴结病区别看待，作者对后者的解剖病理鉴别特征进行了分析。此处观察到的病例与文献中描述的其他病例不同，因为存在淋巴结周围炎成分。
