Canadas Sónia, Fernandes Rita, Santos Mónica, Vera-Cruz Ana, Moreira Ana Teresa
Medicine Department, Internal Medicine Service, Hospital Sousa Martins, Guarda, Portugal.
Hematology Service, Centro Hospitalar Tondela-Viseu, Viseu, Portugal.
Eur J Case Rep Intern Med. 2020 Mar 10;7(4):001516. doi: 10.12890/2020_001516. eCollection 2020.
Kikuchi-Fujimoto disease (KFD) is a rare, benign and usually self-limiting disorder that more often affects young women, which is characterized by cervical lymphadenopathy and fever. Clinical presentation may be indistinguishable from other diseases, and its inclusion in the differential diagnosis of lymphoproliferative, infective and autoimmune diseases is essential. An association with systemic lupus erythematosus is acknowledged. We present 2 different cases of 2 young women with KFD; the first case highlights the classic diagnostic features of this rare entity, and the second, the findings when KFD occurs in association with systemic lupus erythematosus.
Fever and cervical lymphadenopathy presenting in a young woman are the main features of KFD.A timely excisional lymph node biopsy is of the utmost importance in establishing a correct diagnosis and in the management of this condition.In most patients with KFD the course of the disease is benign and self-limiting; however, when associated with other conditions (mainly systemic lupus erythematosus) it can follow a more severe evolution.
菊池-藤本病(KFD)是一种罕见的、良性且通常自限性的疾病,更常影响年轻女性,其特征为颈部淋巴结病和发热。临床表现可能与其他疾病难以区分,将其纳入淋巴增殖性、感染性和自身免疫性疾病的鉴别诊断至关重要。已确认其与系统性红斑狼疮有关联。我们展示了2例年轻女性患KFD的不同病例;第一例突出了这种罕见疾病的典型诊断特征,第二例则展示了KFD与系统性红斑狼疮同时发生时的表现。
年轻女性出现发热和颈部淋巴结病是KFD的主要特征。及时进行切除性淋巴结活检对于正确诊断和处理这种疾病至关重要。在大多数KFD患者中,疾病进程是良性且自限性的;然而,当与其他疾病(主要是系统性红斑狼疮)相关时,病情可能会更严重。