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作 者:郭凤霞 张慧琴 熊淑芬 李洁 李丽 GUO Fengxia;ZHANG Huiqin;XIONG Shufen;LI Jie;LI Li(Mudanjiang Medical University,Mudanjiang 157011;Hongqi Hospital Affiliated to Mudanjiang Medical University,Mudanjiang 157011,China)
机构地区:[1]牡丹江医学院,黑龙江牡丹江157011 [2]牡丹江医学院附属红旗医院,黑龙江牡丹江157011
出 处:《临床医学研究与实践》2021年第29期4-6,共3页Clinical Research and Practice
基 金:2018年度黑龙江省省属高等学校基本科研业务费科研项目(No.2018-KYYWF-MY-0069)。
摘 要:分析本院接收的1例前期误诊为胆石症的遗传性球形细胞增多症(HS)的病例资料。患者因“胆囊结石伴胆囊炎”行胆囊切除术后,双下肢无力进行性加重,小便呈红茶色,大便成白色陶土样变,半年内体重下降约5 kg,诊断为HS,随访6个月,目前病情稳定。The clinical data of a case of hereditary spherocytosis(HS)misdiagnosed as cholelithiasis admitted in our hospital was analyzed.The patient was diagnosed as HS after cholecystectomy for"cholecystolithiasis with cholecystitis",the weakness of both lower limbs was aggravated,the urine was red brown,the stool became white clay-like,and the weight decreased by about 5 kg within half a year.He was followed up for 6 months,the patient's condition is stable at present.
关 键 词:遗传性球形细胞增多症 胆结石 误诊
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