Department of Radiology, Sunway Medical Centre, Kuala Lumpur, Malaysia.
Department of Radiology, Hospital Sultanah Nora Ismail, Johor, Malaysia.
Curr Med Imaging. 2022;18(4):436-439. doi: 10.2174/1573405617666211029163214.
Kimura disease is a rare inflammatory condition classically manifested as painless subcutaneous nodules in the head and neck region and associated with regional cervical lymphadenopathy and salivary gland involvement.
The purpose of this report is to illustrate the diagnostic difficulty due to its rarity and non-specific clinical presentation.
We present a case of Kimura disease with bilateral eyelid swelling, parotid involvement, and cervical lymphadenopathy in a young boy. Computed Tomography (CT) showed ill- defined enhancing masses in both upper eyelids with lacrimal gland infiltration, multiple nodular lesions in both parotid glands, and bilateral enlargement of cervical nodes. After several multidisciplinary discussions and trials of medications, Kimura's disease was finally confirmed by histology examination.
In conclusion, a rare disease such as Kimura must be considered earlier if the patient is not responding to the treatment.
木村病是一种罕见的炎症性疾病,典型表现为头颈部无痛性皮下结节,并伴有区域性颈部淋巴结病和唾液腺受累。
本报告的目的是说明由于其罕见性和非特异性临床表现而导致的诊断困难。
我们报告了一例年轻男性双侧眼睑肿胀、腮腺受累和颈部淋巴结病的木村病病例。计算机断层扫描(CT)显示双侧上眼睑有边界不清的增强肿块,伴有泪腺浸润,双侧腮腺有多发性结节病变,双侧颈部淋巴结肿大。经过多次多学科讨论和药物试验,最终通过组织学检查确诊为木村病。
总之,如果患者对治疗没有反应,应更早考虑罕见疾病,如木村病。