Lee Dong Hoon, Kim Ga-Eon, Yang Eunmi, Yoon Tae Mi, Lee Joon Kyoo, Lim Sang Chul
Department of Otolaryngology-Head and Neck Surgery Department of Pathology Department of Pediatrics, Chonnam National University Medical School and Chonnam National University Hwasun Hospital, Hwasun, South Korea.
Medicine (Baltimore). 2017 Dec;96(48):e8990. doi: 10.1097/MD.0000000000008990.
Kimura disease is a rare benign, chronic inflammatory disorder that typically presents with slowly enlarging, nontender, subcutaneous swellings in the head and neck region. The occurrence of Kimura disease in the oral cavity is extremely rare.
A 16-year-old boy presented with a complaint of a right painless buccal mass of 3 years' duration.
The patient had been diagnosed with nephrotic syndrome and treated with corticosteroid at the age of 5 years.
We report an extremely rare case of Kimura disease of the buccal region in a 16-year-old boy with nephrotic syndrome.
We controlled Kimura disease and nephrotic syndrome in this patient by using a combination of surgical resection of the buccal mass and systemic steroid therapy.
木村病是一种罕见的良性慢性炎症性疾病,通常表现为头颈部区域缓慢增大、无压痛的皮下肿物。木村病发生于口腔极为罕见。
一名16岁男孩主诉右侧颊部无痛性肿物,病程3年。
该患者5岁时被诊断为肾病综合征并接受糖皮质激素治疗。
我们报告了一例极为罕见的16岁肾病综合征男孩颊部木村病病例。
我们通过联合手术切除颊部肿物及全身类固醇治疗,控制了该患者的木村病和肾病综合征。