| Literature DB >> 23204033 |
Agata M Bogusz1, Parul Bhargava.
Abstract
Kikuchi-Fujimoto disease (KFD), a histiocytic necrotizing lymphadenitis (HNL), characteristically presents as cervical lymphadenopathy in young Asian women. Most resolve spontaneously with rare recurrences described. We report a patient with biopsy-proven recurrence of KFD-like HNL after almost 8 years and analyze 65 additional published cases with recurrences. While those with recurrences similarly affect young (average age = 27 years), Asian (80%) women (76%), 73% had multiple sites of involvement and 32% of those tested had underlying autoimmune conditions. Our case is unusual with respect to the following: (a) Age: 50 years, the oldest among the reported patients with recurrences. (b) Race: African descent, with only 3 others reported with recurrent HNL. Of these 4 cases, 2 had underlying autoimmunity. (c) Underlying condition: Her clinical and laboratory features were best felt to represent Sjögren's syndrome (SjS). Only 2 other cases of SjS-associated HNL have been reported; in 2 recently reported cases SjS developed subsequently.Entities:
Keywords: Kikuchi; Sjögren; lupus adenitis; recurrent Kikuchi–Fujimoto disease; recurrent histiocytic necrotizing lymphadenitis; relapsed Kikuchi–Fujimoto; relapsed histiocytic necrotizing lymphadenitis
Mesh:
Year: 2012 PMID: 23204033 DOI: 10.1177/1066896912467369
Source DB: PubMed Journal: Int J Surg Pathol ISSN: 1066-8969 Impact factor: 1.271