Table of Contents    
CASE REPORT
 
Kikuchi's disease: A case report from south India
Sudhakar MK1, Sathyamurthy P2, Indhumathi E3, Amarabalan Rajendran4, Bavya Vivek5
1Professor, Department of Medicine, Sri Ramachandra University, Chennai, Tamilnadu, India.
2Assistant Professor, Department of Medicine, Sri Ramachandra University, Chennai, Tamilnadu, India.
3Associate Professor, Department of Medicine, Sri Ramachandra University, Chennai, Tamilnadu, India.
4Medical Officer, Department of Endocrinology Diabetes & Metabolism, Sri Ramachandra University, Chennai, Tamilnadu, India.
5Post Graduate student, Department of Medicine, Sri Ramachandra University, Chennai, Tamilnadu, India.

doi:10.5348/ijcri-2011-02-20-CR-4

Address correspondence to:
Dr. Amarabalan Rajendran
No.99, Madam Street
Pillayar palayam, Kanchipuram
Tamilnadu - 631501, INDIA.
Ph: +919940412624
Email: amarabalan@gmail.com

[HTML Full Text]   [PDF Full Text]

How to cite this article:
Sudhakar M K, Sathyamurthy P, Indhumathi E, Rajendran A, Vivek B. Kikuchi's disease: A case report from south India. International Journal of Case Reports and Images 2011;2(2):15-18.


Abstract

Introduction: Kikuchi-Fujimoto disease (KFD), or histiocytic necrotizing lymphadenitis, is a rare benign, self-limiting cervical lymphadenitis of unknown etiology. It predominantly affects young women and can closely mimic infective and immunological disorders.
Case Report: We report a 25 yr old female who presented with fever, polyarthritis and cervical lymphadenopathy. She had multiple enlarged cervical nodes. Examination of other systems was normal. Laboratory investigations were also normal. Fine needle aspiration cytology of the cervical node showed features suggestive of reactive lymphadenitis and the patient was started on oral antibiotics. Since the patient did not respond, lymph node biopsy was done and the histological features suggested the diagnosis of Kikuchi's disease. Immunohistochemistry confirmed the diagnosis. The Patient was treated symptomatically and complete remission occurred in few weeks.
Conclusion: Although the incidence of Kikuchi-Fujimoto disease is rare, clinicians should be aware of this condition as early recognition of the disease will minimize potentially harmful and unnecessary evaluations and treatments.

Key Words: Kikuchi-Fujimoto disease, Histiocytic Necrotizing Lymphadenitis, Systemic Lupus Erythematosus, Immunohistochemistry, Karyorrhexis

[HTML Full Text]  [PDF Full Text]

Author Contributions:
Sudhakar M K - Conception and design, Analysis and interpretation of data, Critical revision of the article, Final approval of the version to be published
Sathyamurthy P - Acquisition of data, Drafting the article, Final approval of the version to be published
Indhumathi E - Acquisition of data, Drafting the article, Final approval of the version to be published
Amarabalan Rajendran - Analysis and interpretation of data, Drafting the article, Critical revision of the article, Final approval of the version to be published
Bavya Vivek - Acquisition of data, Drafting the article, Final approval of the version to be published
Guarantor of submission:
The corresponding author is the guarantor of submission.
Source of support:
None
Conflict of interest:
The author(s) declare no conflict of interests.
Copyright:
© Amarabalan Rajendran et. al. 2011; This article is distributed the terms of Creative Commons Attribution License which permits unrestricted use, distribution and reproduction in any means provided the original authors and original publisher are properly credited. (Please see Copyright Policy for more information.)