Kikuchi-Fujimoto Disease Associated with Hashimoto's Thyroiditis: A Case Report.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
International Medical Case Reports Journal Pub Date : 2026-09-12 eCollection Date: 2026-01-01 DOI:10.2147/IMCRJ.S640058
Hala Alibrahim, Mohammad Yaman Haidar, Modar Doyya, Diana Yousef Saleem, Qutayba Abdullah, Zain Al Ibrahim
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引用次数: 0

Abstract

Background: Kikuchi-Fujimoto disease (KFD) is a rare, benign, and self-limiting disorder characterized primarily by cervical lymphadenopathy and fever. Although the disease has been reported worldwide, it is more frequently observed in young women of Asian descent. The etiology of this disease remains unclear. Kikuchi-Fujimoto disease has been reported in association with several autoimmune disorders. Its coexistence with Hashimoto's thyroiditis is rarely described in the literature.

Objective: To present a case of KFD associated with Hashimoto's thyroiditis and highlight the importance of considering this diagnosis in patients with autoimmune disorders.

Case presentation: A 37-year-old woman with a known history of Hashimoto's thyroiditis who presented with rapidly enlarging cervical lymphadenopathy. Laboratory investigations, Ultrasonography, and Excisional lymph node biopsy were performed.

Results: Laboratory tests revealed mild anemia, elevated ESR, and positive anti-TPO antibodies. Ultrasound showed multiple hypoechoic cervical lymph nodes. Biopsy confirmed KFD with characteristic histopathological features. The patient improved spontaneously without specific treatment.

Conclusions and significance: This case underscores the importance of including KFD in the differential diagnosis of cervical lymphadenopathy, particularly in young women with autoimmune diseases. Clinicians should be aware of this rare association to avoid misdiagnosis and unnecessary interventions.

菊池-藤本病合并桥本甲状腺炎1例报告。
背景:菊chi-藤本病(KFD)是一种罕见的、良性的、自限性疾病,主要表现为颈部淋巴结病变和发热。虽然该病在世界各地都有报道,但在亚洲裔年轻女性中更为常见。这种疾病的病因尚不清楚。据报道,菊池-藤本病与几种自身免疫性疾病有关。它与桥本甲状腺炎的共存在文献中很少被描述。目的:介绍一例KFD合并桥本甲状腺炎的病例,并强调在自身免疫性疾病患者中考虑这种诊断的重要性。病例介绍:一名37岁女性,有桥本甲状腺炎病史,表现为颈部淋巴结肿大。进行了实验室检查、超声检查和切除淋巴结活检。结果:实验室检查显示轻度贫血,ESR升高,抗tpo抗体阳性。超声显示颈部多发低回声淋巴结。活检证实KFD具有特征性的组织病理学特征。病人未经特殊治疗自行好转。结论和意义:本病例强调了将KFD纳入宫颈淋巴结病鉴别诊断的重要性,特别是在患有自身免疫性疾病的年轻女性中。临床医生应该意识到这种罕见的关联,以避免误诊和不必要的干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Medical Case Reports Journal
International Medical Case Reports Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
1.40
自引率
0.00%
发文量
135
审稿时长
16 weeks
期刊介绍: International Medical Case Reports Journal is an international, peer-reviewed, open access, online journal publishing original case reports from all medical specialties. Submissions should not normally exceed 3,000 words or 4 published pages including figures, diagrams and references. As of 1st April 2019, the International Medical Case Reports Journal will no longer consider meta-analyses for publication.
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