Journals / Adnan Menderes Üniversitesi Tıp Fakültesi Dergisi / 2009 / Cilt: 10 - Sayı: 1

Kikuchi fujimoto disease: A case report

Kikuchi fujimoto hastalığı: Olgu sunumu

Pages
33–35
Publication Date
2022-10-10
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

It is most common in Asia but has been described worldwide.We present a 20 years old man with complaints of cervical lymphadenopathy and fever, whom diagnosed as Kikuchi-Fujimoto disease with excisional lymph node biopsy and pathological inspection.HNL disease is one of the rarest causes of benign lymphadenopathy .This disease,whose etiology is not know ,is commonly misdiagnosed as lymphoma.This self-limiting disease should be kept in mind in differential diagnosis of benign lymphadenopathies.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Kikuchi-Fujimoto disease or Histiocytic necrotizing lymphadenitis (HNL) is a self-limited disorder characterized by necrotizing cervical lymphadenopathy in especially women (with a mean age of 30 years).
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Key Findings & Data:The disease usually resolves within 1-3 months.
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Conclusion & Impact:It is most common in Asia but has been described worldwide.We present a 20 years old man with complaints of cervical lymphadenopathy and fever, whom diagnosed as Kikuchi-Fujimoto disease with excisional lymph node biopsy and pathological inspection.HNL disease is one of the rarest causes of benign lymphadenopathy .This disease,whose etiology is not know ,is commonly misdiagnosed as lymphoma.This self-limiting disease should be kept in mind in differential diagnosis of benign lymphadenopathies.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Kikuchi-Fujimoto disease or Histiocytic necrotizing lymphadenitis (HNL) is a self-limited disorder characterized by necrotizing cervical lymphadenopathy in especially women (with a mean age of 30 years). It presents with fever, chills, myalgias, arthralgias, splenomegaly, and skin rashes. The disease usually resolves within 1-3 months. It is most common in Asia but has been described worldwide.We present a 20 years old man with complaints of cervical lymphadenopathy and fever, whom diagnosed as Kikuchi-Fujimoto disease with excisional lymph node biopsy and pathological inspection.HNL disease is one of the rarest causes of benign lymphadenopathy .This disease,whose etiology is not know ,is commonly misdiagnosed as lymphoma.This self-limiting disease should be kept in mind in differential diagnosis of benign lymphadenopathies.

Özet

Kikuchi-Fujimoto hastalığı veya histiyositik nekrotizan lenfadenit (HNL) özellikle ortalama 30 yaş civarındaki bayanlarda görülen kendiliğinden sınırlanan, nekrotizan servikal lenfadenopati ile karakterize bir hastalıktır. Ateş, titreme, kas ve eklem ağrısı, splenomegali ve deride döküntüleri kliniğe eşlik edebilir. Hastalık bir-üç ay içinde kendiliğinden düzelir. Asya’da daha yaygın olmakla beraber bütün dünyada görülebilir.Yirmi yaşında, servikal lenfadenopati ve ateş şikayeti olan, eksizyonel lenf nodu biyopsisinde ve patolojik değerlendirilmesinde HNL tanısı konulan bir erkek hasta sunuldu.HNL hastalığı benin lenfadenopatinin nadir nedenlerinden biridir. Benign, etyolojisi bilinmeyen bu hastalık yaygın olarak lenfoma yanlış tanısını alır. Kendiliğinden sınırlanan bu klinik tablo benign lenfadenopatilerin ayırıcı tanısında gözardı edilmemelidir.

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Cite This Article

ÇERMİK, H., EYİGÜN, C. P., GÜL, H. C., DEMİRBAŞ, Ş., COŞKUN, Ö. (2022). Kikuchi fujimoto disease: A case report. Adnan Menderes Üniversitesi Tıp Fakültesi Dergisi, Cilt: 10 - Sayı: 1, 33–35. https://ajindex.com/articles/428976

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