Faras Fatemah, Abo-Alhassan Fawaz, Al-Sebeih Khalid, Bastaki Jassem
Department of ENT, Sabah and Zain Hospital, Ministry of Health, 40188 Mishref, Kuwait.
Department of Surgery, Al-Adan Hospital, Ministry of Health, 40188 Mishref, Kuwait.
Case Rep Surg. 2014;2014:648607. doi: 10.1155/2014/648607. Epub 2014 Nov 24.
Kimura disease is a rare, benign, chronic inflammatory swelling of the subcutaneous tissue, lymph nodes, and glandular tissue. Characteristic features of the disease include, but not limited to, painless subcutaneous head and neck swelling, blood and tissue eosinophilia, and markedly elevated immunoglobulin E (IgE) levels. Herein, we report a rare case of Kimura disease manifesting as synchronous bilateral parotid swelling of 12 years duration in a 33-year-old Middle-Eastern man. To our knowledge only few cases have been reported in the literature involving bilateral parotid glands, and this is the first case to be reported in the Middle East.
木村病是一种罕见的、良性的、慢性炎症性疾病,可累及皮下组织、淋巴结和腺组织。该疾病的特征包括但不限于无痛性头颈部皮下肿胀、血液和组织嗜酸性粒细胞增多以及免疫球蛋白E(IgE)水平显著升高。在此,我们报告一例罕见的木村病病例,该病例表现为一名33岁中东男性双侧腮腺同步肿胀达12年之久。据我们所知,文献中仅报道了少数累及双侧腮腺的病例,而这是中东地区报道的首例此类病例。