中华外科杂志
中華外科雜誌
중화외과잡지
CHINESE JOURNAL OF SURGERY
2013年
9期
788-791
,共4页
邓小耿%唐晶%伍耀豪%Maharjan Aumir%张杰%周嘉嘉%曾乐祥%邱荣林
鄧小耿%唐晶%伍耀豪%Maharjan Aumir%張傑%週嘉嘉%曾樂祥%邱榮林
산소경%당정%오요호%Maharjan Aumir%장걸%주가가%증악상%구영림
腹腔镜检查%脾切除术%脾大%儿童%血液病
腹腔鏡檢查%脾切除術%脾大%兒童%血液病
복강경검사%비절제술%비대%인동%혈액병
Laparoscopy%Splenectomy%Splenomegaly%Child%Hematologic diseases
目的 总结改良的腹腔镜辅助下巨脾切除术治疗儿童血液病的经验和特点.方法 回顾性分析2007年3月至2011年12月30例行腹腔镜巨脾切除术的血液病患儿的临床资料.其中男性18例,女性12例;年龄2~14岁.原发病包括地中海贫血17例、遗传性球形红细胞增多症4例、原发性血小板减少性紫癜9例.采用改良的腹腔镜辅助下巨脾切除术:双重夹闭脾动脉暂不切断,分离完毕、脾血充分回流后,再将脾脏完全游离.记录患者手术及并发症情况,术后1周复查血红蛋白及血小板计数.结果 26例顺利完成手术;中转开腹4例,其中2例特发性血小板减少性紫癜因接受激素治疗后过于肥胖而致术中暴露差,1例β型地中海贫血因合并肝重度肿大致腹腔内操作不便,1例为脾栓塞术后因脾周粘连严重术中分离时出血量较多.手术时间110 ~ 130 min,平均120 min.术中出血量35 ~ 100 ml,平均45 ml.患儿术后恢复顺利,平均住院时间5 d.与术前相比,术后1周患者血红蛋白及血小板计数明显改善.结论 改良腹腔镜巨脾切除术使许多过去认为难以实施的伴巨脾的血液病患儿的腹腔镜手术成为了可能.
目的 總結改良的腹腔鏡輔助下巨脾切除術治療兒童血液病的經驗和特點.方法 迴顧性分析2007年3月至2011年12月30例行腹腔鏡巨脾切除術的血液病患兒的臨床資料.其中男性18例,女性12例;年齡2~14歲.原髮病包括地中海貧血17例、遺傳性毬形紅細胞增多癥4例、原髮性血小闆減少性紫癜9例.採用改良的腹腔鏡輔助下巨脾切除術:雙重夾閉脾動脈暫不切斷,分離完畢、脾血充分迴流後,再將脾髒完全遊離.記錄患者手術及併髮癥情況,術後1週複查血紅蛋白及血小闆計數.結果 26例順利完成手術;中轉開腹4例,其中2例特髮性血小闆減少性紫癜因接受激素治療後過于肥胖而緻術中暴露差,1例β型地中海貧血因閤併肝重度腫大緻腹腔內操作不便,1例為脾栓塞術後因脾週粘連嚴重術中分離時齣血量較多.手術時間110 ~ 130 min,平均120 min.術中齣血量35 ~ 100 ml,平均45 ml.患兒術後恢複順利,平均住院時間5 d.與術前相比,術後1週患者血紅蛋白及血小闆計數明顯改善.結論 改良腹腔鏡巨脾切除術使許多過去認為難以實施的伴巨脾的血液病患兒的腹腔鏡手術成為瞭可能.
목적 총결개량적복강경보조하거비절제술치료인동혈액병적경험화특점.방법 회고성분석2007년3월지2011년12월30례행복강경거비절제술적혈액병환인적림상자료.기중남성18례,녀성12례;년령2~14세.원발병포괄지중해빈혈17례、유전성구형홍세포증다증4례、원발성혈소판감소성자전9례.채용개량적복강경보조하거비절제술:쌍중협폐비동맥잠불절단,분리완필、비혈충분회류후,재장비장완전유리.기록환자수술급병발증정황,술후1주복사혈홍단백급혈소판계수.결과 26례순리완성수술;중전개복4례,기중2례특발성혈소판감소성자전인접수격소치료후과우비반이치술중폭로차,1례β형지중해빈혈인합병간중도종대치복강내조작불편,1례위비전새술후인비주점련엄중술중분리시출혈량교다.수술시간110 ~ 130 min,평균120 min.술중출혈량35 ~ 100 ml,평균45 ml.환인술후회복순리,평균주원시간5 d.여술전상비,술후1주환자혈홍단백급혈소판계수명현개선.결론 개량복강경거비절제술사허다과거인위난이실시적반거비적혈액병환인적복강경수술성위료가능.
Objective To summarize the experience and characteristics of the modified laparoscopic splenectomy for massive splenomegaly in the treatment of children with hematologic disease.Methods The clinical data of 30 cases of laparoscopic splenectomy for massive splenomegaly of children with hematologic disease from March 2007 to December 2011 was analyzed retrospectively.There were 18 male and 12 female patients,aging from 2 to 14 vears.Primary disease included mediterranean anemia (17 cases),hereditary spherocytosis (4 cases) and idiopathic thrombocytopenic purpura (ITP,9 cases).Dissection started with cutting off the gastrosplenic ligaments and lesser sac to fully reveal the splenic hilum,the splenic artery was clamped twice with 10 mm tiatanum clamp.When most of blood stored in the spleen back to heart through the veins and the splenic volume had already decreased,the splenic vein was ligated with 10 mm titanium clip and cut with ligsure and splenic pedicle separated.The Surgery and complication were recorded.For 1 week after surgery,the hemoglobin and platelet counts were reviewed.Results Twenty-six cases were performed successfully,and 4 cases were converted to open procedure.Of the 4 cases,2 cases was obesity because of idiopathic thrombocytopenic purpura,1 case was β thalassaemia combined severe liver enlargement,and 1 case was after partial splenic embolization.In cases of laparoscopic splenectomy,operation time was 110 to 130 minutes,with an average of 120 minutes,and blood loss during operation was 35 to 180 ml,with an average of 45 ml.Compared with pre-operation,the hemoglobin of mediterranean anemia and hereditary spherocytosis patients were (92 ± 8) g/L,and blood platelet count of ITP patients was (127 ±20) × 109/L,and they increased obviously at 1 week after operation (t =4.175 and 8.253,both P =0.000).Conclusion The modified surgical method make the laparoscopic splenectomy for massive splenomegaly in many children with hematologic diseases possible,which was thought to be impossible in the past.