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ArticleInternational medical case reports journal2026

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

Hala Alibrahim, Mohammad Yaman Haidar, Modar Doyya, Diana Yousef Saleem, Qutayba Abdullah, Zain Al Ibrahim

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Article in International medical case reports journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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6 authors.

Hala AlibrahimDepartment of Otolaryngology - Head and Neck Surgery, Al-Mouwasat University Hospital, Faculty of Medicine, Damascus University, Damascus, Syria.ORCID 0009-0003-5558-5309
Mohammad Yaman HaidarFaculty of Medicine, Damascus University, Damascus, Syria.
Modar DoyyaDepartment of Otolaryngology - Head and Neck Surgery, Al-Mouwasat University Hospital, Faculty of Medicine, Damascus University, Damascus, Syria.ORCID 0009-0007-9330-2030
Diana Yousef SaleemDepartment of Otolaryngology - Head and Neck Surgery, Al-Mouwasat University Hospital, Faculty of Medicine, Damascus University, Damascus, Syria.
Qutayba AbdullahGeneral Surgery Department, Faculty of Medicine, Damascus University, Damascus, Syria.
Zain Al IbrahimDepartment of Pathology, Al-Mouwasat University Hospital, Faculty of Medicine, Damascus University, Damascus, Syria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Hashimoto DiseaseHistiocytic Necrotizing LymphadenitisAdultBiopsyDiagnosis, DifferentialFemaleHumansLymphadenopathyLymph NodesUltrasonographycase reporthashimoto’s thyroiditishistiocytic necrotizing lymphadenitiskikuchi–Fujimotolymphadenopathy

Identifiers

PMID42751348
PMCPMC13580652

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