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.
“…Kimura disease is a rare chronic inflammatory disease of unknown origin, first described by Kimura et al in 1948 1 . To date, there have only been 200 reported incidences of Kimura disease globally, 2 and only 1 reported case of Kimura Disease of the Breast in 2016 3 . Kimura disease predominantly occurs in Asian male populations, with incidence peaking around the second and third decade of life 4,5 …”
Section: Discussionmentioning
confidence: 99%
“…Patients commonly present with a palpable unilateral lump in their head and neck region including the salivary glands, but other regions including the axilla, groin, and arm have also been reported 2,4 . About 10 to 60% of patients with Kimura disease suffer from concurrent nephrotic syndrome, 5 with biopsies showing a membranous glomerulonephritis and mesangial proliferation, eosinophilic interstitial infiltrates, and some podocytic foot process effacement 9…”
“…Kimura disease is a rare chronic inflammatory disease of unknown origin, first described by Kimura et al in 1948 1 . To date, there have only been 200 reported incidences of Kimura disease globally, 2 and only 1 reported case of Kimura Disease of the Breast in 2016 3 . Kimura disease predominantly occurs in Asian male populations, with incidence peaking around the second and third decade of life 4,5 …”
Section: Discussionmentioning
confidence: 99%
“…Patients commonly present with a palpable unilateral lump in their head and neck region including the salivary glands, but other regions including the axilla, groin, and arm have also been reported 2,4 . About 10 to 60% of patients with Kimura disease suffer from concurrent nephrotic syndrome, 5 with biopsies showing a membranous glomerulonephritis and mesangial proliferation, eosinophilic interstitial infiltrates, and some podocytic foot process effacement 9…”
“…It is often accompanied by peripheral eosinophilia and markedly elevated serum IgE levels. 10 Although eosinophilia and increased IgE, tumors necrosis factor-alpha, interleukin IL-4, IL 5, IL-13, and mast cell levels in peripheral blood, as well as in the lesion, were observed in these patients, no specific antigens have been identified. 11 It has been proposed that autoimmunity, allergy, neoplasm's, and parasite infestation are possible risk factors.…”
<p>Kimura’s disease (KD) is a rare chronic inflammatory disorder of unknown etiology, primarily seen in young Asian males. In India, only 200 cases have been reported worldwide since its histopathological diagnosis. The disease is characterized by painless subcutaneous swelling in head & neck region, blood and tissue eosinophilia and raised Immunoglobulin E (IgE) levels. A systematic multidisciplinary approach is mandatory to rule out the other common causes of post auricular lymphadenopathy. The diagnosis of KD can be difficult and misleading and patients with this disease are often evaluated using avoidable procedures by just not being aware of KD. Here, we present a case of a 20 year old male who presented with nodular swellings in the bilateral post auricular region. The diagnosis of KD was done based on characteristic histopathologic finding in conjunction with peripheral eosinophilia.</p>
“…Some authors were able to diagnose Kimura’s disease on FNAC [ 13 ], whereas others have reported the swellings as lymphadenitis or malignancies [ 14 , 15 ]. The characteristic features of Kimura’s disease on FNAC are the presence of significant numbers of eosinophils in a background of lymphoid cells, with fragments of collagenous tissue, endothelial cells and occasional polykaryocytes [ 14 , 15 ].…”
Kimura’s disease is a rare chronic inflammatory disorder of unknown etiology which typically presents with subcutaneous nodules in the head and neck region and is frequently associated with regional lymphadenopathy or salivary gland enlargement. Peripheral blood eosinophilia and elevated serum immunoglobulin E levels are constant features of the disease. We present herein a 31-year-old male patient who presented with chronic neck lymphadenopathy. Kimura’s disease was diagnosed on fine needle aspiration cytology, the patient initially decided not to have further intervention. He presented 6 years later with lymphadenopathy and was treated with surgery. The diagnosis of Kimura’s disease was confirmed on histopathology. This patient had the disease for 6 years and did not have the typical features of peripheral eosinophilia and raise serum IgE level.
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