Wijethilake Esha, Ranaweera Yamuna, Eleperuma Dilan Dharshana, Mujahieth M I, Edirisinghe Kamali
Internal Medicine, National Hospital of Sri Lanka, Colombo, LKA.
Otolaryngology - Head and Neck Surgery, National Hospital of Sri Lanka, Colombo, LKA.
Cureus. 2024 Dec 12;16(12):e75588. doi: 10.7759/cureus.75588. eCollection 2024 Dec.
Kikuchi-Fujimoto disease is a rare systemic illness commonly affecting young females with a higher tendency to occur in the Asian population. Clinical presentation varies with most patients presenting with fever and cervical lymphadenopathy. The patient discussed in this case report presented to a tertiary care hospital in Sri Lanka with a fever for two weeks and palpable cervical lymphadenopathy. She was extensively evaluated as a case of pyrexia of unknown origin and failed to detect any significant abnormality except pancytopenia, which is a rarely associated hematological manifestation. The diagnosis was confirmed by cervical lymph node excision biopsy, which showed typical features to suggest Kikuchi disease. She was treated accordingly with steroids, resulting in a complete resolution of symptoms. This is a rare clinical entity that may give rise to diagnostic difficulty due to its rarity as well as the uncommon associations with pancytopenia. Further, though Kikuchi disease is commonly self-limiting, it may mimic many sinister pathologies, which warrant their exclusion.
菊池-藤本病是一种罕见的全身性疾病,常见于年轻女性,在亚洲人群中发病倾向较高。临床表现各异,大多数患者表现为发热和颈部淋巴结肿大。本病例报告中讨论的患者因发热两周且可触及颈部淋巴结肿大,前往斯里兰卡的一家三级医院就诊。她作为不明原因发热的病例接受了广泛评估,除全血细胞减少外未发现任何明显异常,全血细胞减少是一种罕见的血液学表现。通过颈部淋巴结切除活检确诊,活检显示出提示菊池病的典型特征。她接受了相应的类固醇治疗,症状完全缓解。这是一种罕见的临床病症,由于其罕见性以及与全血细胞减少的不常见关联,可能导致诊断困难。此外,尽管菊池病通常为自限性,但它可能模仿许多严重疾病,因此需要排除这些疾病。