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Kimura's disease embedding radial artery: A very rare presentation
Komal Sawaimul, Banyameen Iqbal1, Tushar Kambale
1Department of Pathology, Dr. Dnyandeo Yashwantrao Patil Medical College and Research Center, Pimpri, Pune, Maharashtra, India.
Journal of Cancer Research and Therapeutics
|February 17, 2016
Summary
Kimura's disease (KD) is a rare, benign condition often affecting young to middle-aged Asian males, typically in the head and neck. While usually self-limiting, it can mimic tumors and rarely involves peripheral vasculature.
Area of Science:
- Pathology
- Immunology
- Dermatology
Background:
- Kimura's disease (KD) was initially described in 1937 as eosinophilic hyperplastic lymphogranuloma.
- The condition was later named by Kimura et al. in 1948.
Observation:
- KD commonly presents as a painless, persistent lesion.
- It most frequently affects the head and neck region.
- The disease predominantly occurs in young and middle-aged Asian males.
Findings:
- Kimura's disease is characterized as a reactive, self-limiting condition.
- While typically localized, rare cases involving peripheral vasculature have been documented.
- The lesions can mimic neoplastic growth, necessitating careful diagnosis.
Implications:
- Understanding the epidemiology and clinical presentation of KD is crucial for accurate diagnosis.
- Distinguishing KD from neoplasms is essential for appropriate patient management.
- Further research into the pathogenesis and rare vascular involvements of KD may improve treatment strategies.
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