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Indian J Dermatol. 2016 May-Jun;61(3):348. doi: 10.4103/0019-5154.182465.

Kikuchi-Fujimoto Disease, the Masquerading Menace: A Rare Case Report.

Indian journal of dermatology

Rohit Kataria, Pankaj Rao, Dilip Kachhawa, Vinod K Jain, Rajat K Tuteja, Manish Vijayvargiya

Affiliations

  1. Department of Dermatology and Venereology, Dr. S.N. Medical College, Jodhpur, Rajasthan, India.
  2. Department of Medicine, Dr. S.N. Medical College, Jodhpur, Rajasthan, India.
  3. Unipath Labs, Near SMS Hospital, Jaipur, Rajasthan, India.

PMID: 27293275 PMCID: PMC4885208 DOI: 10.4103/0019-5154.182465

Abstract

Kikuchi-Fujimoto disease (KFD) or histiocytic necrotizing lymphadenitis is a rare, benign, self-limiting disease with unknown etiology characterized by regional lymphadenopathy. A 30-year-old female presented with fever, weakness, multiple joint pain, oral ulcers, erythematous facial rashes, hemorrhagic crusting on both lips, and cervical lymphadenopathy of 2-month duration. Clinically, the disease was mimicking systemic lupus erythematosus, but immunofluorescence was negative for it. Lymph node biopsy suggested a diagnosis of KFD.

Keywords: Histopathology; Kikuchi-Fujimoto disease; lymphoma; maculopapular skin lesions; systemic lupus erythematosus

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