Kimura disease: A rare cause of cervical lymphadenopathy and a diagnostic challenge

Kimura disease (KD) is a rare chronic inflammatory disorder characterized by multiple painless solitary head and neck lymphadenopathy often accompanied by peripheral eosinophilia and elevated serum IgE levels. Initially, the lesion was described in 1937 as a neoplasm (Kimm and Szeto) and first coine...

Full description

Saved in:
Bibliographic Details
Main Authors: Virendra Kumar Goyal, Jagdish Vishnoi, Ruhi Dak, Shokat Ali Bohra, Gunjan Sharma
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-12-01
Series:Indian Journal of Allergy Asthma and Immunology
Subjects:
Online Access:https://journals.lww.com/ijaa/fulltext/2024/38020/kimura_disease__a_rare_cause_of_cervical.7.aspx
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1841526832527048704
author Virendra Kumar Goyal
Jagdish Vishnoi
Ruhi Dak
Shokat Ali Bohra
Gunjan Sharma
author_facet Virendra Kumar Goyal
Jagdish Vishnoi
Ruhi Dak
Shokat Ali Bohra
Gunjan Sharma
author_sort Virendra Kumar Goyal
collection DOAJ
description Kimura disease (KD) is a rare chronic inflammatory disorder characterized by multiple painless solitary head and neck lymphadenopathy often accompanied by peripheral eosinophilia and elevated serum IgE levels. Initially, the lesion was described in 1937 as a neoplasm (Kimm and Szeto) and first coined by Kimura, a Japanese scientist. Now it is well documented that it is a benign condition with unknown etiology. An allergic reaction and an alteration of the immune system remains one of the pathophysiological bases. Persistent antigenic stimulation following arthropod bites and parasitic or candida infection are also suspected. KD is a quite rare condition, affected Caucasians are very rare. It is found almost exclusively in Asian males in their 2nd to 4th decade of life (70–80%). There are only few cases of KD reported from Indian subcontinent. We present a case series of three patients of Kimura disease, presenting with painless cervical and parotid lymphadenopathy. All three patients underwent lymph node fine needle aspiration cytology (FNAC) showing no evidence of malignancy. This case series highlights the very rare yet important cause of cervical lymphadenopathy in young patients. Cervical lymphadenopathy can be misleading if not evaluated by histopathology and serum IgE levels.
format Article
id doaj-art-d3b6fe9634a84385a06055bccfbc8d36
institution Kabale University
issn 0972-6691
2320-4745
language English
publishDate 2024-12-01
publisher Wolters Kluwer Medknow Publications
record_format Article
series Indian Journal of Allergy Asthma and Immunology
spelling doaj-art-d3b6fe9634a84385a06055bccfbc8d362025-01-16T10:25:25ZengWolters Kluwer Medknow PublicationsIndian Journal of Allergy Asthma and Immunology0972-66912320-47452024-12-01382849010.4103/ijaai.ijaai_28_24Kimura disease: A rare cause of cervical lymphadenopathy and a diagnostic challengeVirendra Kumar GoyalJagdish VishnoiRuhi DakShokat Ali BohraGunjan SharmaKimura disease (KD) is a rare chronic inflammatory disorder characterized by multiple painless solitary head and neck lymphadenopathy often accompanied by peripheral eosinophilia and elevated serum IgE levels. Initially, the lesion was described in 1937 as a neoplasm (Kimm and Szeto) and first coined by Kimura, a Japanese scientist. Now it is well documented that it is a benign condition with unknown etiology. An allergic reaction and an alteration of the immune system remains one of the pathophysiological bases. Persistent antigenic stimulation following arthropod bites and parasitic or candida infection are also suspected. KD is a quite rare condition, affected Caucasians are very rare. It is found almost exclusively in Asian males in their 2nd to 4th decade of life (70–80%). There are only few cases of KD reported from Indian subcontinent. We present a case series of three patients of Kimura disease, presenting with painless cervical and parotid lymphadenopathy. All three patients underwent lymph node fine needle aspiration cytology (FNAC) showing no evidence of malignancy. This case series highlights the very rare yet important cause of cervical lymphadenopathy in young patients. Cervical lymphadenopathy can be misleading if not evaluated by histopathology and serum IgE levels.https://journals.lww.com/ijaa/fulltext/2024/38020/kimura_disease__a_rare_cause_of_cervical.7.aspxangiolymphoid hyperplasia with eosinophiliakimura diseaselymphadenopathyneck swellingserum immunoglobulin e
spellingShingle Virendra Kumar Goyal
Jagdish Vishnoi
Ruhi Dak
Shokat Ali Bohra
Gunjan Sharma
Kimura disease: A rare cause of cervical lymphadenopathy and a diagnostic challenge
Indian Journal of Allergy Asthma and Immunology
angiolymphoid hyperplasia with eosinophilia
kimura disease
lymphadenopathy
neck swelling
serum immunoglobulin e
title Kimura disease: A rare cause of cervical lymphadenopathy and a diagnostic challenge
title_full Kimura disease: A rare cause of cervical lymphadenopathy and a diagnostic challenge
title_fullStr Kimura disease: A rare cause of cervical lymphadenopathy and a diagnostic challenge
title_full_unstemmed Kimura disease: A rare cause of cervical lymphadenopathy and a diagnostic challenge
title_short Kimura disease: A rare cause of cervical lymphadenopathy and a diagnostic challenge
title_sort kimura disease a rare cause of cervical lymphadenopathy and a diagnostic challenge
topic angiolymphoid hyperplasia with eosinophilia
kimura disease
lymphadenopathy
neck swelling
serum immunoglobulin e
url https://journals.lww.com/ijaa/fulltext/2024/38020/kimura_disease__a_rare_cause_of_cervical.7.aspx
work_keys_str_mv AT virendrakumargoyal kimuradiseaseararecauseofcervicallymphadenopathyandadiagnosticchallenge
AT jagdishvishnoi kimuradiseaseararecauseofcervicallymphadenopathyandadiagnosticchallenge
AT ruhidak kimuradiseaseararecauseofcervicallymphadenopathyandadiagnosticchallenge
AT shokatalibohra kimuradiseaseararecauseofcervicallymphadenopathyandadiagnosticchallenge
AT gunjansharma kimuradiseaseararecauseofcervicallymphadenopathyandadiagnosticchallenge