中华普通外科杂志
中華普通外科雜誌
중화보통외과잡지
CHINESE JOURNAL OF GENERAL SURGERY
2010年
2期
119-121
,共3页
高志刚%熊启星%冯志刚%钭金法%王金湖%黄寿奖%钱云忠
高誌剛%熊啟星%馮誌剛%鈄金法%王金湖%黃壽獎%錢雲忠
고지강%웅계성%풍지강%두금법%왕금호%황수장%전운충
黄疸%阻塞性%腹腔镜检查%胆道闭锁%婴儿
黃疸%阻塞性%腹腔鏡檢查%膽道閉鎖%嬰兒
황달%조새성%복강경검사%담도폐쇄%영인
Jaundice,obstruction%Laparoscopy%Biliary atresia%Infant
目的 探讨腹腔镜胆道探查对婴儿阻塞性黄疸的诊断和治疗价值.方法 对56例经内科保守治疗2周血清胆红素水平无明显下降的阻塞性黄疸婴儿进行胆道探查及胆道造影,并对诊断明确的非先天性胆道闭锁患儿予以胆道冲洗.结果 本组56例婴儿经腹腔镜胆道探查及胆道造影后均明确诊断,其中浓缩胆栓综合征12例(21%),胆管发育不良4例(7%),胆道闭锁40例(72%).16例非先天性胆道闭锁患儿经胆囊造瘘、胆道冲洗后病情好转,黄疸消退,随访6~42个月,均恢复良好无复发.结论 利用腹腔镜早期干预阻塞性黄疸患儿可以对疾病进行早期的诊断和治疗,具有较高的临床实用价值.对浓缩胆栓综合征及先天性胆管发育不良患儿,可以在镜下造影明确诊断后行胆囊造瘘及胆道冲洗,以减轻胆汁淤积对肝脏的进一步损害;对胆道闭锁患儿可以争取到早期手术的时机.
目的 探討腹腔鏡膽道探查對嬰兒阻塞性黃疸的診斷和治療價值.方法 對56例經內科保守治療2週血清膽紅素水平無明顯下降的阻塞性黃疸嬰兒進行膽道探查及膽道造影,併對診斷明確的非先天性膽道閉鎖患兒予以膽道遲洗.結果 本組56例嬰兒經腹腔鏡膽道探查及膽道造影後均明確診斷,其中濃縮膽栓綜閤徵12例(21%),膽管髮育不良4例(7%),膽道閉鎖40例(72%).16例非先天性膽道閉鎖患兒經膽囊造瘺、膽道遲洗後病情好轉,黃疸消退,隨訪6~42箇月,均恢複良好無複髮.結論 利用腹腔鏡早期榦預阻塞性黃疸患兒可以對疾病進行早期的診斷和治療,具有較高的臨床實用價值.對濃縮膽栓綜閤徵及先天性膽管髮育不良患兒,可以在鏡下造影明確診斷後行膽囊造瘺及膽道遲洗,以減輕膽汁淤積對肝髒的進一步損害;對膽道閉鎖患兒可以爭取到早期手術的時機.
목적 탐토복강경담도탐사대영인조새성황달적진단화치료개치.방법 대56례경내과보수치료2주혈청담홍소수평무명현하강적조새성황달영인진행담도탐사급담도조영,병대진단명학적비선천성담도폐쇄환인여이담도충세.결과 본조56례영인경복강경담도탐사급담도조영후균명학진단,기중농축담전종합정12례(21%),담관발육불량4례(7%),담도폐쇄40례(72%).16례비선천성담도폐쇄환인경담낭조루、담도충세후병정호전,황달소퇴,수방6~42개월,균회복량호무복발.결론 이용복강경조기간예조새성황달환인가이대질병진행조기적진단화치료,구유교고적림상실용개치.대농축담전종합정급선천성담관발육불량환인,가이재경하조영명학진단후행담낭조루급담도충세,이감경담즙어적대간장적진일보손해;대담도폐쇄환인가이쟁취도조기수술적시궤.
Objective To explore the value of early laparoscopic intervention in infant cholestatic jaundice.Method 56 cholestatic jaundiced infants underwent early laparoscopic biliary tract exploration and cholangiography after two weeks of regular conservative treatments,which failed to decrease bilirubin level significantly.The non-congenital biliary atresia patients with definite preoperative diagnosis received bitiary tract irrigation.Results Correct diagnosis was established in all those 56 patients by laparoscopic procedures.Among those,12 cases were diagnosed as cholestatic syndrome(21%) ,4 cases were diagnosed as congenital bile duct dysplasia(7%),40 cases were diagnosed as biliary atresia(72%).16 cases who were diagnosed as non-congenital biliary atresia recovered after laparoscopic cholecystostomy and biliary tract irrigation.All infants were followed-up for 6 months to 42 months,they were all in good condition and there were no symptom recurrence.Conclusion Early laparoscopic intervention in infant with cholestatic jaundice helps to establish early diagnosis and early correct treatment.For cholestatic syndrome and congenital bile duct dysplasia patients,cholecystostomy and biliary tract irrigation reduces cholestasisinduced liver damage.For biliary atresia patients,this procedure offers an early operation opportunity.