Journals / Fırat Üniversitesi Sağlık Bilimleri Tıp Dergisi / 2017 / Cilt: 31 - Sayı: 1

A Very Rare Entity at the Differential Diagnosis of Lymphoma ''Kikuchi-Fujimoto Disease'': Case Report

Lenfoma Ayırıcı Tanısında Ender Bir Antite ''Kikuchi- Fujimoto Hastalığı'': Olgu Sunumu

Pages
51–53
Publication Date
2022-10-18
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

In that case report; a young adult woman with Lymphoma-like sypmtoms, who was consulted to our clinic with pre-diagnosis of Lymphoma, was then diagnosed as Kikuchi-Fujimoto Disease after our examinations and healed spontaneously in a three months period, was presented.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Kikuchi-Fujimoto Disease is a rare condition which should not be forgotten at the differential diganosis of neck masses.
📊
Key Findings & Data:Etiology is not clear yet and it heals completely in 1-4 months by limiting itself.
💡
Conclusion & Impact:In that case report; a young adult woman with Lymphoma-like sypmtoms, who was consulted to our clinic with pre-diagnosis of Lymphoma, was then diagnosed as Kikuchi-Fujimoto Disease after our examinations and healed spontaneously in a three months period, was presented.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Kikuchi-Fujimoto Disease is a rare condition which should not be forgotten at the differential diganosis of neck masses. That disease which is also called as ''histiocytic necrotizing lymphadenitis'' is frequently observed at young adult females and most of the patients apply to the physician with Lymphoma-like symptoms and this is the reason why it is often mixed up with Lymphoma. Etiology is not clear yet and it heals completely in 1-4 months by limiting itself. On account of this, supportive treatment is almost all the time adequate for these patients. In that case report; a young adult woman with Lymphoma-like sypmtoms, who was consulted to our clinic with pre-diagnosis of Lymphoma, was then diagnosed as Kikuchi-Fujimoto Disease after our examinations and healed spontaneously in a three months period, was presented.

Özet

Kikuchi-Fujimoto Hastalığı boyun kitlelerinin ayırıcı tanısında unutulmaması gereken, nadir görülen bir hastalıktır. Nekrotizan histiositik lenfadenit olarak da isimlendirilen bu hastalık sıklıkla genç erişkin kadınlarda görülür ve lenfoma benzeri klinik tabloyla hastalar hekime başvurur bu yüzdendir ki en çok lenfomayla karışır. Etiyolojisi net olarak bilinmemektedir ve hastalık kendini sınırlayarak 1- 4 ay içinde tamamen iyileşir. Bundan dolayı destekleyici tedavi hemen her zaman yeterli olmaktadır. Bu vaka takdiminde lenfoma benzeri kliniği olan ve lenfoma ön tanısıyla merkezimize sevk edilen, yapılan tetkikler sonucunda Kikuchi-Fujimoto Hastalığı tanısı konulan ve üç aylık bir süreçte kendiliğinden tamamen iyileşen genç erişkin bir bayan hasta sunuldu.

🔖

Cite This Article

DURGUT, O., ŞAHİN, M. S. (2022). A Very Rare Entity at the Differential Diagnosis of Lymphoma ''Kikuchi-Fujimoto Disease'': Case Report. Fırat Üniversitesi Sağlık Bilimleri Tıp Dergisi, Cilt: 31 - Sayı: 1, 51–53. https://ajindex.com/articles/514562

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (15)

  1. Thongsuksai P, Kayasut K. Histiocytic necrotizing lymphadenitis (Kikuchi's disease): Clinicopathologic characteristics of 23 cases and literature review. J Med Assoc Thai 1999; 82: 812-818
  2. Bosch X, Guilabert A. Kikuchi-Fujimoto disease. Orphanet J Rare Dis 2006; 1: 18-20
  3. Kikuchi M. Lymadenitis showing focal reticulum cell hyperplasia with nuclear debris and phagocytes: A clinicopathological study. Acta Hematol Jpn 1972; 35: 379- 380
  4. Fujimoto Y, Kozimo Y, Yamaguchi K. Cervical subacute necrotizing lymphadenitis: A new clinicopathologic entity. Naika 1972; 20: 20-27
  5. Lorenzo AH, Amat CG, de la Victoria LOM, et al. Histiocytic necrotizing lymphadenitis: Kikuchi-Fujimoto disease. Apropos of 6 cases. An Med Interna 1999; 16: 301-304
  6. Eisner MD, Amory J, Mullaney B, et al. Necrotizing lymphadenitis associated with systemic lupus erythematosus. Semin Arthritis Rheum 1996; 26: 477-482
  7. George TI, Jones CD, Zehnder JL, et al. Lack of human herpesvirus 8 and Epstein-Barr virus in Kikuchi's histiocytic necrotizing lymphadenitis. Hum Pathol 2003; 34: 130-135
  8. Bhat NA, Hock YL, Turner NO, Das Gupta AR. Kikuchi's disease of the neck (histiocytic necrotizing lymphadenitis). J Laryngol Otol 1998; 112: 898-900
  9. Yen A, Fearneyhough P, Raimer SS, Hudnall SD. EBV associated Kikuchi's histiocytic necrotizing lymphadenitis with cutaneous manifestations. J Am Acad Dermatol 1997; 36: 342-346
  10. Bosch X, Guilabert A, Miquel R, Campo E. Enigmatic Kikuchi-Fujimoto disease: A comprehensive review. Am J Clin Pathol 2004; 122: 141-152
  11. Charalabopoulos K, Charalabopoulos A, Papadapoulou CH, Papalimneou V. Giardia lamblia intestinalis: A new pathogen with possible link to Kikuchi-Fujimoto disease. An additional element in the disease jigsaw. Int J Clin Pract 2004; 58: 1180-1183
  12. Spies J, Foucar K, Thompson CT, LeBoit PE. The histopathology of cutaneus lesions of Kikuchi's disease (necrotizing lymphadenitis): A report of five cases. Am J Surg Pathol 1999; 23: 104-107
  13. Menasce LP, Banerjee SS, Edmondson D, Harris M. Histiocytic necrotizing lymphadenitis (Kikuchi-Fujimoto disease): Continuing dignostic difficulties. Histopathology 1998; 33: 248-254
  14. Wustenberg EG, Theissig F, Offergeld C, Huttenbrink KB. Necrotizing lymphadenitis (KikuchiFujimoto disease) as a rare cause of cervical lymphadenitis. Diagnosis and differential diagnosis. Laryngorhinootologie 2000; 79: 935
  15. Pileri AS, Pileri A, Yasukawa K, et al. The Karma of Kikuchi's disease