| Literature DB >> 8358129 |
T Murakami1, J Kato, K Kogawa, N Watanabe, S Sakamaki, Y Kohgo, K Hamabe, N Ishiyama, H Enokihara, Y Niitsu.
Abstract
A case of episodic angioedema and eosinophilia syndrome is reported. An 18-year-old male suffered from monthly episodes of angioedema, pruritic papules, weight gain, and fever for twelve years. During the episodes, peripheral eosinophils and serum levels of interleukin (IL)-5, an eosinophil proliferating cytokine were elevated. Extensive evaluations disclosed neither visceral involvement nor evidence of parasitic infections, collagen diseases, or neoplastic disorders. Corticosteroid treatment brought about a dramatic clinical improvement concomitant with decrement of eosinophils and serum IL-5 was observed. These observations suggest that IL-5 may be a causative factor for this pathological state.Entities:
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Year: 1993 PMID: 8358129 DOI: 10.2169/internalmedicine.32.343
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271