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Case Reports
. 2019 Apr;92(2):195-199.
doi: 10.15386/cjmed-1030. Epub 2019 Apr 25.

Kimura disease: case report and brief review of literature

Affiliations
Case Reports

Kimura disease: case report and brief review of literature

Harshi Dhingra et al. Med Pharm Rep. 2019 Apr.

Abstract

Kimura disease is a rare chronic inflammatory disorder of unknown cause, primarily seen in young Asian males. The disease is characterized by painless subcutaneous swelling, blood and tissue eosinophilia and raised IgE levels. Early diagnosis of Kimura's disease may spare the patient from unnecessary invasive diagnostic procedure. We describe a case of Kimura disease in a 14-year old male presenting with left submandibular swelling and also provide a brief review of the literature.

Keywords: IgE; Kimura disease; eosinophilia.

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Figures

Figure 1
Figure 1
Polymorphous population of lymphoid cells with eosinophils (MGG stain, 40X).
Figure 2
Figure 2
Gross image of the homogenous grey white cut surface of the lymph node.
Figure 3
Figure 3
Hyperplastic follicles with germinal centers (H&E stain, 10X).
Figure 4
Figure 4
Germinal center infiltrated by eosinophils and histiocytes (H&E, 40X).
Figure 5
Figure 5
Prominent eosinophilic infiltrate with microabscess formation (H&E stain, 10X).
Figure 6
Figure 6
Endothelial cell proliferation with lumen containing RBCs in the medulla (H&E stain, 40X).

References

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    1. Tseng CF, Lin HC, Huang SC, Su YC. Kimura’s disease presenting as bilateral parotid masses. Eur Arch of Otorhinolaryngol. 2005;262:8–10. - PubMed
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