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β地中海贫血患者腹腔镜胆囊切除术的独特特征。

Unique features of laparoscopic cholecystectomy in Beta thalassemia patients.

作者信息

Katz Ran, Goldfarb Ada, Muggia Michael, Gimmon Zvi

机构信息

Departments of General Surgery, Hadassah Medical Center, Hebrew University, Ein Kerem, Jerusalem, Israel.

出版信息

Surg Laparosc Endosc Percutan Tech. 2003 Oct;13(5):318-21. doi: 10.1097/00129689-200310000-00006.

Abstract

Beta Thalassemia patients suffer from a high incidence of gallstones as well as systemic complications of iron overload. We performed laparoscopic cholecystectomy in 8 beta thalassemia patients and describe their specific features. Diagnosis was based on patients' clinical presentation and sonography. Trocars were readjusted due to the hepatomegaly. No intraoperative cholangiograms were performed. Follow-up included clinical assessment and abdominal sonography. All procedures were completed laparoscopically. Pigment cirrhosis and fibrosis around the cystic duct were noted in all patients. No biliary injury occurred. Post operatively, 4 patients suffered fluid leakage through the trocar site, treated conservatively. No major cardiopulmonary complications occurred. During a mean follow-up time of 65 months, all patients are symptom free and without evidence of biliary lithiasis. Thalassemia patients are difficult and often high-risk patients. Improvement in anesthesia and monitoring enables better management of these patients. Laparoscopic cholecystectomy should be advised in carefully selected thalassemia patients.

摘要

β地中海贫血患者胆结石发病率高,且存在铁过载的全身并发症。我们对8例β地中海贫血患者实施了腹腔镜胆囊切除术,并描述了其特殊情况。诊断基于患者的临床表现及超声检查。因肝肿大对套管针进行了重新调整。未进行术中胆管造影。随访包括临床评估及腹部超声检查。所有手术均通过腹腔镜完成。所有患者均发现胆囊管周围有色素性肝硬化及纤维化。未发生胆管损伤。术后,4例患者出现套管针穿刺部位漏液,经保守治疗。未发生重大心肺并发症。在平均65个月的随访期内,所有患者均无症状,且无胆石症迹象。地中海贫血患者手术难度大,且往往是高危患者。麻醉和监测的改善有助于更好地管理这些患者。对于精心挑选的地中海贫血患者,建议实施腹腔镜胆囊切除术。

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