中华普通外科杂志
中華普通外科雜誌
중화보통외과잡지
CHINESE JOURNAL OF GENERAL SURGERY
2010年
12期
959-962
,共4页
李培坤%耿小平%赵义军%赵红川%刘付宝%王国斌%张志功
李培坤%耿小平%趙義軍%趙紅川%劉付寶%王國斌%張誌功
리배곤%경소평%조의군%조홍천%류부보%왕국빈%장지공
肝肿瘤%肝切除术%诊断%治疗
肝腫瘤%肝切除術%診斷%治療
간종류%간절제술%진단%치료
Liver neoplasms%Hepatectomy%Diagnosis%Therapy
目的 探讨肝脏罕见肿瘤的诊断和治疗方法.方法 回顾性分析我院2005年5月至2010年1月收治的25例肝脏罕见肿瘤患者的临床病理资料.结果 25例患者中肝局灶性结节性增生6例,肝血管平滑肌瘤、肝门部神经鞘瘤、肝左叶动脉瘤、肝胆管囊腺瘤、肝错构瘤、肝胆管绒毛状腺瘤、肝弥漫性大B细胞淋巴瘤各1例,肝血管平滑肌脂肪瘤2例,肝原发间质瘤2例,肝母细胞瘤5例,肝胚胎性肉瘤3例;术前行B超检查24例,CT检查22例,MRI检查6例,仅有3例(16.7%)检查和术后病理结果一致.术前诊断和术后病理符合5例(20%).25例均行手术切除治疗,包括半肝切除术7例,肝叶切除术7例,肝段切除术9例,肿瘤局部挖除2例.肝脏良性、低度恶性肿瘤及1例弥漫性大B细胞淋巴瘤术后无复发,5例恶性肿瘤随访中3例术后复发行再次手术切除,术后随访无复发;另2例死亡,平均术后生存期4个月.结论肝脏罕见肿瘤影像学诊断率低,手术切除是主要的治疗手段,对能切除的复发性肿瘤性病变应争取再次手术切除.
目的 探討肝髒罕見腫瘤的診斷和治療方法.方法 迴顧性分析我院2005年5月至2010年1月收治的25例肝髒罕見腫瘤患者的臨床病理資料.結果 25例患者中肝跼竈性結節性增生6例,肝血管平滑肌瘤、肝門部神經鞘瘤、肝左葉動脈瘤、肝膽管囊腺瘤、肝錯構瘤、肝膽管絨毛狀腺瘤、肝瀰漫性大B細胞淋巴瘤各1例,肝血管平滑肌脂肪瘤2例,肝原髮間質瘤2例,肝母細胞瘤5例,肝胚胎性肉瘤3例;術前行B超檢查24例,CT檢查22例,MRI檢查6例,僅有3例(16.7%)檢查和術後病理結果一緻.術前診斷和術後病理符閤5例(20%).25例均行手術切除治療,包括半肝切除術7例,肝葉切除術7例,肝段切除術9例,腫瘤跼部挖除2例.肝髒良性、低度噁性腫瘤及1例瀰漫性大B細胞淋巴瘤術後無複髮,5例噁性腫瘤隨訪中3例術後複髮行再次手術切除,術後隨訪無複髮;另2例死亡,平均術後生存期4箇月.結論肝髒罕見腫瘤影像學診斷率低,手術切除是主要的治療手段,對能切除的複髮性腫瘤性病變應爭取再次手術切除.
목적 탐토간장한견종류적진단화치료방법.방법 회고성분석아원2005년5월지2010년1월수치적25례간장한견종류환자적림상병리자료.결과 25례환자중간국조성결절성증생6례,간혈관평활기류、간문부신경초류、간좌협동맥류、간담관낭선류、간착구류、간담관융모상선류、간미만성대B세포림파류각1례,간혈관평활기지방류2례,간원발간질류2례,간모세포류5례,간배태성육류3례;술전행B초검사24례,CT검사22례,MRI검사6례,부유3례(16.7%)검사화술후병리결과일치.술전진단화술후병리부합5례(20%).25례균행수술절제치료,포괄반간절제술7례,간협절제술7례,간단절제술9례,종류국부알제2례.간장량성、저도악성종류급1례미만성대B세포림파류술후무복발,5례악성종류수방중3례술후복발행재차수술절제,술후수방무복발;령2례사망,평균술후생존기4개월.결론간장한견종류영상학진단솔저,수술절제시주요적치료수단,대능절제적복발성종류성병변응쟁취재차수술절제.
Objective To sum up our experience on the diagnosis and treatment of rare hepatic tumors. Methods The data of 25 patients with rare liver tumors admitted in our hospital from May 2005 to January 2010 were analyzed retrospectively. Results The final pathologic diagnosis of focal nodular hyperplasia was made in 6 cases, and the diagnosis of vascular leiomyoma, hilar neurilemoma, intrahepatic aneurysm, biliary cystadenoma, hepatic hamartoma, biliary villous adenoma, and hepatic diffuse large B-cell lymphoma was established in one each case, respectively. The diagnosis of angiomyolipoma in 2patients, primary liver gastroimestinal stromal tumor in 2 patients, hepatoblastoma in 5 patients and liver undifferentiated sarcoma in 3 patients was established. Preoperative ultrasonography, CT and MRI were performed in 24, 22 and 6 patients respectively. Preoperative tentative diagnosis was finally confirmed by pathology in only 3 (16.7%) cases, all by CT report. Preoperative diagnosis was consistent with postoperative pathology in 5 patients (20%); All patients underwent liver resection including hemihepatectomy in 7 patients, hepatic lobectomy in 7 patients, segmentectomy in 9 patients and tumor enucleation in 2 patients; There was no recurrence after resection of benign, low malignant tumors and hepatic diffuse large B-cell lymphoma; Postoperative follow-up was made for all the 5 cases of malignant tumours, and there was recurrence in 3 cases. These 3 eases underwent second resection and there were no recurrences after reoperation. The two recurrent patients died with a mean survival of 4 months.Conclusions The preoperative correct imaging diagnostic rate for rare hepatic tumors is low. Surgery is the most effective therapy and reoperation should always be attempted for tumor recurrence in order to prolong survival.