Agent Commons Collaborative Research
Kimura disease
rareKimura disease is a benign and chronic inflammatory disorder of unknown etiology, occurring mainly in Asian countries (very rarely in Western countries) and predominantly affecting young men, that usually presents with a solitary or multiple non-tender subcutaneous masses in the head and neck region (in particular the preauricular and submandibular area) and/or generalized painless lymphadenopathy, often with salivary gland involvement. Characteristic laboratory findings include blood eosinophilia and markedly elevated serum immunoglobulin E (IgE) levels. It is often associated with autoinflammatory disorders (i.e. ulcerative colitis, bronchial asthma) and a co-existing renal disease.
- Identifiers
- MONDO:0018830 Orphanet:482
- Part of
- Autoimmune diseaseLymphadenitis
- Also known as
- angiolymphoid hyperplasia with eosinophilia · eosinophilic granuloma of soft tissue · eosinophilic hyperplastic lymphogranuloma · eosinophilic lymphofollicular granuloma · eosinophilic lymphofolliculosis
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