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Kimura’s Disease – An Unusual Presentation
INTRODUCTION: Kimura’s disease is a rare chronic inflammatory disease of unknown etiology, presenting as painless subcutaneous nodules with lymphadenopathy and peripheral eosinophilia, mainly disturbing the head and neck region. It mainly affects Asian males in their 2(nd) to 4(th) decade of life. O...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930849/ https://www.ncbi.nlm.nih.gov/pubmed/27429955 |
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author | Banerjee, Praveer Kumar Jain, Abhineet D, Manjunath |
author_facet | Banerjee, Praveer Kumar Jain, Abhineet D, Manjunath |
author_sort | Banerjee, Praveer Kumar |
collection | PubMed |
description | INTRODUCTION: Kimura’s disease is a rare chronic inflammatory disease of unknown etiology, presenting as painless subcutaneous nodules with lymphadenopathy and peripheral eosinophilia, mainly disturbing the head and neck region. It mainly affects Asian males in their 2(nd) to 4(th) decade of life. One such case of Kimura’s disease, which is uncommon in Indian natives, is reported. CASE REPORT: A male patient presented with an insidious onset of a progressive painless disfiguring swelling over his nose since four years, which was associated with nasal obstruction and post aural swelling with a history of an inconclusive incisional biopsy. Clinical examination showed a bilobed subcutaneous swelling present over the nose and a collapsed nasal valve area on anterior rhinoscopy. FNAC was non-diagnostic and CT scan showed a mildly enhancing mass lesion over the external nose. Complete surgical excision was performed. Diagnosis was confirmed upon postoperative histopathology. During his 2nd week follow up, the patient had a small nasal recurrence, which was treated medically with oral steroids, cetirizine, and pentoxyphylline for 4 weeks. The patient was disease free for 6 months. CONCLUSION: Kimura’s disease, although difficult to diagnosis clinically, should be considered in the differential diagnosis of patients who have a primary lymphadenopathy with eosinophilia with or without subcutaneous nodules. It should be investigated accordingly as the disease has an indolent course and good prognosis. |
format | Online Article Text |
id | pubmed-4930849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-49308492016-07-15 Kimura’s Disease – An Unusual Presentation Banerjee, Praveer Kumar Jain, Abhineet D, Manjunath Iran J Otorhinolaryngol Case Report INTRODUCTION: Kimura’s disease is a rare chronic inflammatory disease of unknown etiology, presenting as painless subcutaneous nodules with lymphadenopathy and peripheral eosinophilia, mainly disturbing the head and neck region. It mainly affects Asian males in their 2(nd) to 4(th) decade of life. One such case of Kimura’s disease, which is uncommon in Indian natives, is reported. CASE REPORT: A male patient presented with an insidious onset of a progressive painless disfiguring swelling over his nose since four years, which was associated with nasal obstruction and post aural swelling with a history of an inconclusive incisional biopsy. Clinical examination showed a bilobed subcutaneous swelling present over the nose and a collapsed nasal valve area on anterior rhinoscopy. FNAC was non-diagnostic and CT scan showed a mildly enhancing mass lesion over the external nose. Complete surgical excision was performed. Diagnosis was confirmed upon postoperative histopathology. During his 2nd week follow up, the patient had a small nasal recurrence, which was treated medically with oral steroids, cetirizine, and pentoxyphylline for 4 weeks. The patient was disease free for 6 months. CONCLUSION: Kimura’s disease, although difficult to diagnosis clinically, should be considered in the differential diagnosis of patients who have a primary lymphadenopathy with eosinophilia with or without subcutaneous nodules. It should be investigated accordingly as the disease has an indolent course and good prognosis. Mashhad University of Medical Sciences 2016-05 /pmc/articles/PMC4930849/ /pubmed/27429955 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Banerjee, Praveer Kumar Jain, Abhineet D, Manjunath Kimura’s Disease – An Unusual Presentation |
title | Kimura’s Disease – An Unusual Presentation |
title_full | Kimura’s Disease – An Unusual Presentation |
title_fullStr | Kimura’s Disease – An Unusual Presentation |
title_full_unstemmed | Kimura’s Disease – An Unusual Presentation |
title_short | Kimura’s Disease – An Unusual Presentation |
title_sort | kimura’s disease – an unusual presentation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930849/ https://www.ncbi.nlm.nih.gov/pubmed/27429955 |
work_keys_str_mv | AT banerjeepraveerkumar kimurasdiseaseanunusualpresentation AT jainabhineet kimurasdiseaseanunusualpresentation AT dmanjunath kimurasdiseaseanunusualpresentation |