首页> 外文期刊>Journal of International Medical Research >Prominent gallbladder enlargement: Kawasaki disease or other congenital or acquired gallbladder disease? A case report
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Prominent gallbladder enlargement: Kawasaki disease or other congenital or acquired gallbladder disease? A case report

机译:显着的胆囊扩大:川崎疾病或其他先天性或胆囊疾病? 案例报告

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Kawasaki disease (KD) is a common systemic vasculitis in childhood that can result in damage to multiple body systems. However, prominent gallbladder (GB) enlargement in the acute stage is especially rare. A 5-year-old boy was admitted to the hospital with an 8-day history of a cervical mass, 7-day history of fever, and 5-day history of abdominal pain and rash. The child was diagnosed with KD. After treatment with high-dose intravenous immunoglobulin therapy (2 g/kg), all clinical manifestations were relieved except the abdominal pain. Enhanced computed tomography showed distinct enlargement of the GB, and a congenital choledochal cyst was strongly suspected. After high-dose glucocorticoid treatment, his obviously enlarged GB returned to normal size in the subacute phase. No abnormality was found during 2 years of follow-up. Prominent GB enlargement may emerge in the acute stage of KD. The enlarged GB can return to normal size within the subacute stage by standard treatment for KD. Proper diagnosis, thorough differential diagnosis, and active anti-inflammatory treatment of KD are crucial to avoid surgery.
机译:川崎病(KD)是儿童时期常见的全身血管炎,可能导致多个身体系统损坏。然而,急性阶段的显着胆囊(GB)放大尤其罕见。一个5岁的男孩被医院录取了医院,宫颈肿块,7天发烧历史和5天的腹痛和皮疹病史。孩子被诊断为KD。在用高剂量静脉内免疫球蛋白疗法治疗(2g / kg)后,除腹痛外,所有临床表现都松弛。增强的计算断层摄影显示出GB的明显扩大,并强烈怀疑先天性胆总管囊肿。在高剂量糖皮质激素治疗后,他明显扩大的GB在亚急性期恢复到正常尺寸。在2年后没有发现异常。突出的GB扩大可能在KD的急性阶段出现。扩大的GB可以通过标准治疗KD返回亚急性阶段内的正常尺寸。适当的诊断,彻底的鉴别诊断和KD的抗炎治疗至关重要,避免手术。

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