KIMURA’S DISEASE IN AN ASIAN MALE: A VERY RARE CAUSE OF LYMPHADENOPATHY

V. Goyal, Ruhi Dak, Vibhas Mohan Sood
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Abstract

The present case study highlights  Kimura’s Disease in an Asian Male. Kimura disease (KD) is a rare chronic inflammatory disorder of unknown etiology. It usually presents as subcutaneous mass in the head and neck region and is frequently associated with regional lymphadenopathy or salivary gland involvement. A study done at Dept of Internal Medicine ,American Institute Of Medical sciences, GBH general hospital, Udaipur, Rajasthan, India. A case report of a 13 year old male, admitted to GBH general Hospital on 1st January, 2023 with chief complains of swelling (painless) Left side of the  face below eye since 4 months and swelling under Rt. lobe of the ear since 3 months.On radiological examination, Kimura’s disease mimics other chronic and malignant diseases such as tuberculosis or lymphoma. This is an important study since it is a rare case and further research should be done in this area for further management and prompt diagnosis of such rare causes of upper body lymphadenopathy(frequently confused with malignancy),unless histopathology is clearly demonstrated.
一名亚洲男性的木村氏病:一种非常罕见的淋巴结病
本案例研究强调了一名亚洲男性的木村病。木村病是一种罕见的慢性炎症性疾病,病因不明。它通常表现为头颈部皮下肿块,常伴有局部淋巴结病或涎腺受累。这项研究是在印度拉贾斯坦邦乌代普尔GBH综合医院美国医学研究所内科部完成的。一例13岁男性患者,于2023年1月1日在GBH总医院住院,主诉为眼下左侧面部肿胀(无痛)4个月,耳垂下肿胀3个月。在放射学检查中,木村氏病类似于其他慢性和恶性疾病,如肺结核或淋巴瘤。这是一项重要的研究,因为它是一个罕见的病例,应该在该领域进行进一步的研究,以进一步管理和及时诊断这种罕见的上半身淋巴结病(经常与恶性肿瘤混淆),除非组织病理学得到明确证明。
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