Kimura's Disease: A Rare Cause of Postauricular Swelling

Main Article Content

Suman Kumar Das
Mukesh Kumar Singh
Indranath Kundu
Swapan Kumar Ghosh

Abstract

Introduction


Kimura’s Disease is a chronic inflammatory disorder of lymph node which is very rare in Indian population.


Case Report


A 15 year old boy with multiple postauricular swelling for 18 months presenting in OPD and diagnosed having eosinophilia. Then excision biopsy was taken, which indicates Kimura’s Disease. Patient was treated with high dose of corticosteroid.


Conclusion


Kimura’s disease, though rare should be kept in mind for treating a patient with lymphadenopathy with eosinophilia or high IgE level, because it can spare the patient unnecessary invasive procedure.

Article Details

How to Cite
1.
Das SK, Singh MK, Kundu I, Ghosh SK. Kimura’s Disease: A Rare Cause of Postauricular Swelling. BJOHNS [Internet]. 2017Apr.30 [cited 2024May17];25(1):59-61. Available from: https://bjohns.in/journal3/index.php/bjohns/article/view/113
Section
Case report
Author Biographies

Suman Kumar Das, R. G. Kar medical college and hospital

ENT and Head Neck Surgery

Junior Resident (PGT)

Mukesh Kumar Singh

ENT and Head Neck Surgery

RMO cum clinical tutor

Indranath Kundu

ENT and Head Neck Surgery

Professor

Swapan Kumar Ghosh

ENT and Head Neck Surgery

Assistant Proffesor

References

Viswanatha B. Kimura’s Disease in children: A 9 years’ prospective study. Int. J Pediatric Otorhinolaryngol. 2007; 71:1521-5

Kimura T, Yoshimura S, Ishikawa E. On the unusual granulation combined with hyperplastic changes of lymphatic tissue. Trans Soc Patho Jpn. 1948; 37:179-80

Motoi M, Norie Y, A Kagi T. Kimura’s Disease: clinical, histological and immunohistochemical studies. Acta Med Okayama. 1992; 46: 449-55

Som PM, Biller NF. Kimura’s Disease involving parotid gland and cervical nodes: CT scan and MRI findings. J Comput Assist. Omogz. 1992; 16:320-2

Atar S, Oberman AS, Flatou E et al. Recurrent nephrotic syndrome associated with Kimura’s Disease in a young non-oriental male. Nephron 1994; 68: 259-61

Wierenga EA, Backx B, Snoek M et al. relative contributions of human type 1 and 2 T-helper cell derived eosinophilotrophic cytokines to development of eosinophilia. Blood 1993;82: 1471-9

Motoi M, Horie Y, A Kagi T. Kimura’s Disease: Clinical, histological and immunohistochemical studies. Acta Med Okayama. 1992; 46: 449-55

Chong WS, Thomas A, Goh CL. Kimura’s Disease and Angiolymphoid Hyperplasia with Eosinophilia: Two disease entities in the same patient: Case report and review of the literature. Int. J Dermatol. 2006; 45: 139-45

Maleki D, Sayyah A, Rahimi-Rad MN et al. Kimura’s Disease with eosinophilicpanniculitis treated with cyclosporine: A case report. Allergy Asthma Clin Immunol. 2010; 6: 5

Gumbs MA, Pai NB, Sraiya RJ et al. Kimura’s Disease: A case report and literature review. J SurgOncol 1999; 70:190-3

Day TA, Abreo F, Aarstad RF et al. Treatment of Kimura’s Disease: A therapeutic enigma. Otolaryngology Head Neck surgery 1995; 112: 333-7

Itami J, Miyoshi T, Ogata N et al. Radiation therapy in Kimura’s Disease. Acta Oncol. 1989; 82: 549-55

Li TJ, Chen XM, Wang SZ et al. Kimura’s disease: A clinicopathologic study of 54 Chinese patients. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1996; 82:549-55.

Most read articles by the same author(s)