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发热伴全血细胞减少:菊池病的一种罕见表现

Pyrexia With Pancytopenia: An Uncommon Presentation of Kikuchi Disease.

作者信息

Wijethilake Esha, Ranaweera Yamuna, Eleperuma Dilan Dharshana, Mujahieth M I, Edirisinghe Kamali

机构信息

Internal Medicine, National Hospital of Sri Lanka, Colombo, LKA.

Otolaryngology - Head and Neck Surgery, National Hospital of Sri Lanka, Colombo, LKA.

出版信息

Cureus. 2024 Dec 12;16(12):e75588. doi: 10.7759/cureus.75588. eCollection 2024 Dec.

DOI:10.7759/cureus.75588
PMID:39803088
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11724740/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b5/11724740/87ca974ab67c/cureus-0016-00000075588-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b5/11724740/db4db491697b/cureus-0016-00000075588-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b5/11724740/cf60f0e2d5c4/cureus-0016-00000075588-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b5/11724740/87ca974ab67c/cureus-0016-00000075588-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b5/11724740/db4db491697b/cureus-0016-00000075588-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b5/11724740/cf60f0e2d5c4/cureus-0016-00000075588-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b5/11724740/87ca974ab67c/cureus-0016-00000075588-i03.jpg

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本文引用的文献

1
Kikuchi-Fujimoto disease, a rare benign disease with atypical histomorphology: more than meets the eye.菊池-藤本病,一种具有非典型组织形态学的罕见良性疾病:不只是表面所见。
Pathology. 2024 Apr;56(3):382-390. doi: 10.1016/j.pathol.2023.10.017. Epub 2024 Jan 6.
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Blood cell and marrow changes in patients with Kikuchi disease.菊池病患者的血细胞和骨髓变化
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Am J Case Rep. 2021 Nov 21;22:e933377. doi: 10.12659/AJCR.933377.
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Case Rep Med. 2020 Jan 5;2020:4385286. doi: 10.1155/2020/4385286. eCollection 2020.
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BMC Oral Health. 2019 Oct 21;19(1):223. doi: 10.1186/s12903-019-0920-4.
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Int Med Case Rep J. 2016 Jun 29;9:163-7. doi: 10.2147/IMCRJ.S106396. eCollection 2016.
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Turk J Haematol. 2012 Mar;29(1):80-1. doi: 10.5505/tjh.2012.98360. Epub 2012 Mar 5.
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Singapore Med J. 2010 Jan;51(1):e18-21.
9
Management of Kikuchi's disease using glucocorticoid.使用糖皮质激素治疗菊池病。
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