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Unilateral Intraparotid Swelling: A Case Report of Kimura’s Disease and Review of Differential DiagnosisDOI: 10.1155/2013/795921 Abstract: An interesting case of Kimura's disease was described in the 42-year-old patient manifesting itself as a unilateral parotid swelling, albeit the disease usually affects both parotid glands. Furthermore, first pathohistological finding was not suggestive of the disease, revealing only fatty tissue, but on the repeated biopsy together with CT the correct diagnosis was established. It should be emphasized that Kimura's disease has to be taken into account while making differential diagnosis in parotid gland swellings, especially in people of Oriental origin. 1. Introduction Kimura’s disease is an uncommon finding which was first described in 1937 as a reactive, self-limiting, painless, persistent, indolent lesion mimicking neoplasm, and being of unknown etiology. Usually it is seen in young and middle-aged men (male?:?female = 3.5?:?1) [1]. So far, more than 60 cases with oral involvement have been reported in the literature. Primarily it affects the tissue of lymph nodes. Usually, within face and neck area, it represents itself rarely as a parotid swelling (intraparotid or paraparotid lymph nodes are in fact affected) more frequently bilateral, but also unilateral together with few cases described where palate and cheek with eyelid were involved [2, 3]. Also, a case of a patient with Kimura’s disease manifesting itself as a lymphadenopathy and painful oral ulcerations was reported [4]. The common finding is also within subcutaneous tissues and lymph nodes. It can represent itself either as a single or multiple lesions, with the latter being less frequent. Other lymph nodes of the face and neck area can be affected, as well as distant subcutaneous lymph nodes either as a solitary or multiple lesions. Histopathologically, the disease is characterized with hyperplasia of the lymphoid tissue with well-developed lymphoid follicles, marked lymphocyte (eosinophil) infiltration, proliferation of thin-walled capillary venules, and varying degrees of fibrosis [1]. 2. Case Report A woman, 42 years old, presented with swelling of the left parotid gland at the Department of Oral Biology and Pathology, School of Dentistry, Brisbane, Australia. The parotid nodule was painless and firm (Figure 1). OPG finding was normal and she was sent to ENT for parotid gland biopsy. Her blood test showed eosinophilia and elevated IgE levels. First histopathological finding showed only fatty tissue, then patient was sent to CT scan where mass involving parotid gland was seen (Figure 2). Again biopsy of the parotid gland was performed and this time histopathological finding revealed
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