Abstract
Kimura’s disease is a rare, benign, slow-growing chronic inflammatory swelling with a predilection for the head and neck region and almost always with peripheral blood eosinophilia and elevated serum IgE levels. Here, we report a 14-year-old male patient with left-sided cheek swelling. It was painless swelling situated anterior to left ear, of 1 year duration, without any other symptoms. Routine investigations were inconclusive. Excision biopsy revealed the diagnosis of Kimura’s disease.
References
Messina TMD, Armstrong WB, Pena F et al (1998) Kimura’s disease two case reports and a literature review. Ann Otol Rhinol Laryngol 107(12):1066–1071
Altman DA, Griner JM, Lowe L (1995) Angiolymphoid hyperplasia with Eosinophilia and nephrotic syndrome. Cutis 56:334–336
Takahashi N, Kondo K, Aoyagi J (1997) Acute myocardial infarction associated with hypereosinophilic syndrome in a young man. Jpn Circ J 61:803–806
Hirakawa Y, Koyanagi S, Matsumoto T et al (1989) A case of variant angina associated with Eosinophilia. Am J Med 87:472–474
Rothenberg ME (1998) Eosinophilia. N Engl J Med 338:1592–1600
Day TA, Abreo F, Hoajsoe DK et al (1995) Treatment of kimura’s disease: a therauptic enigma. Otolaryngol Head Neck Surg 112:333–337
Sato S, Kawashima H, Kuboshima S et al (2006) Combined treatment of steroids and Cyclosporin in Kimura’s disease. Pediatrics 118(3):921–923
Itami J, Arimizu N, Miyoshi T, Ogata H, Miura K (1989) Radiation therapy in Kimura’s disease. Acta Oncol 28(4):511–514
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Biradar, A., Patil, A.V., Kotennavar, M.S. et al. Kimura’s Disease: A Case Report. Indian J Surg 75 (Suppl 1), 430–431 (2013). https://doi.org/10.1007/s12262-012-0750-y
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DOI: https://doi.org/10.1007/s12262-012-0750-y