实用肝脏病杂志
實用肝髒病雜誌
실용간장병잡지
JOURNAL OF CLINICAL HEPATOLOGY
2015年
5期
486-490
,共5页
陈韬%叶昊%方文敏%吴亮%黄元成
陳韜%葉昊%方文敏%吳亮%黃元成
진도%협호%방문민%오량%황원성
肝豆状核变性%黄疸%临床特征%鉴别诊断
肝豆狀覈變性%黃疸%臨床特徵%鑒彆診斷
간두상핵변성%황달%림상특정%감별진단
Wilson’s Disease%Hyperbilirubinemia%Clinical features%Differential diagnosis
目的:观察肝豆状核变性(WD)伴黄疸患者的临床特征,探讨肝豆状核变性黄疸患者临床鉴别诊断的侧重点。方法回顾性分析52例以“黄疸待查”初次入院的WD患者的临床资料,包括临床表现和常规实验室指标的变化。采用序列分析法检测全血基因组8、12、13、16外显子的突变情况。结果本研究纳入WD患者24例和慢性乙型肝炎重度患者28例。WD患者发病中位年龄(33.2岁)显著低于乙型肝炎(41.8岁,P=0.049),WD患者自起病至明确诊断的中位时间(8.2月)显著长于乙型肝炎(1月,P<0.001);WD患者24 h尿铜水平(919.83±1017.15μg)显著高于乙型肝炎(204.79±191.85μg,P<0.001);WD患者血清γ-谷氨酰转肽酶水平(175.74±245.99 U/L)显著高于乙型肝炎(133.44±115.95 U/L,P=0.004),且与24 h尿铜水平呈正相关(r=0.552,P=0.012);24例WD患者全部,而仅4例乙型肝炎患者可检出ATP7B突变。结论肝豆状核变性伴黄疸患者除可利用血清铜、铜蓝蛋白检测进行筛选性诊断外,24 h尿铜检测为重要的鉴别诊断指标,而血清γ-谷氨酰转肽酶可能是该病潜在的诊断指标。
目的:觀察肝豆狀覈變性(WD)伴黃疸患者的臨床特徵,探討肝豆狀覈變性黃疸患者臨床鑒彆診斷的側重點。方法迴顧性分析52例以“黃疸待查”初次入院的WD患者的臨床資料,包括臨床錶現和常規實驗室指標的變化。採用序列分析法檢測全血基因組8、12、13、16外顯子的突變情況。結果本研究納入WD患者24例和慢性乙型肝炎重度患者28例。WD患者髮病中位年齡(33.2歲)顯著低于乙型肝炎(41.8歲,P=0.049),WD患者自起病至明確診斷的中位時間(8.2月)顯著長于乙型肝炎(1月,P<0.001);WD患者24 h尿銅水平(919.83±1017.15μg)顯著高于乙型肝炎(204.79±191.85μg,P<0.001);WD患者血清γ-穀氨酰轉肽酶水平(175.74±245.99 U/L)顯著高于乙型肝炎(133.44±115.95 U/L,P=0.004),且與24 h尿銅水平呈正相關(r=0.552,P=0.012);24例WD患者全部,而僅4例乙型肝炎患者可檢齣ATP7B突變。結論肝豆狀覈變性伴黃疸患者除可利用血清銅、銅藍蛋白檢測進行篩選性診斷外,24 h尿銅檢測為重要的鑒彆診斷指標,而血清γ-穀氨酰轉肽酶可能是該病潛在的診斷指標。
목적:관찰간두상핵변성(WD)반황달환자적림상특정,탐토간두상핵변성황달환자림상감별진단적측중점。방법회고성분석52례이“황달대사”초차입원적WD환자적림상자료,포괄림상표현화상규실험실지표적변화。채용서렬분석법검측전혈기인조8、12、13、16외현자적돌변정황。결과본연구납입WD환자24례화만성을형간염중도환자28례。WD환자발병중위년령(33.2세)현저저우을형간염(41.8세,P=0.049),WD환자자기병지명학진단적중위시간(8.2월)현저장우을형간염(1월,P<0.001);WD환자24 h뇨동수평(919.83±1017.15μg)현저고우을형간염(204.79±191.85μg,P<0.001);WD환자혈청γ-곡안선전태매수평(175.74±245.99 U/L)현저고우을형간염(133.44±115.95 U/L,P=0.004),차여24 h뇨동수평정정상관(r=0.552,P=0.012);24례WD환자전부,이부4례을형간염환자가검출ATP7B돌변。결론간두상핵변성반황달환자제가이용혈청동、동람단백검측진행사선성진단외,24 h뇨동검측위중요적감별진단지표,이혈청γ-곡안선전태매가능시해병잠재적진단지표。
Objective To explore the clinical features of patients with Wilson’s disease and hyperbiliru-binemia. Method Twenty-four patients with Wilson’s disease and twenty-eight with chronic hepatitis B of severe degree were included in this study. The manifestation and routine laboratory tests were collected. The peripheral blood ATP7B gene mutations in exon 8,12,13 and 16 were analyzed by direct sequencing. Results The pa-tients with WD had the features of significantly younger (33.2 vs. 41.8 yr old,P=0.049),longer delay diagnosis time (8.2 vs. 1 month,P<0.001) as compared to patients with hepatitis B;the total urine copper in 24 hours was significantly elevated [(919.83±1017.15)μg vs. (204.79±191.85)μg,P<0.001];the patients with WD had signifi-cantly higher serum glutamyltranspeptidase level [(175.74±245.99) U/L] as compared with in patients with hepati-tis B[(133.44±115.95) U/L,P=0.004],which had a positive correlation with 24 hours total urine copper drainage (r=0.552,P=0.012);all the patients with WD were positive for ATP7B mutation,while only 4 patients with hep-atitis B positive. Conclusion Serum copper and ceruloplasmin levels may be useful for screening patients with WD and jaundice,and the 24 hour urine copper excretion is an important index for differential diagnosis from se-vere chronic hepatitis B.