Katz Ran, Goldfarb Ada, Muggia Michael, Gimmon Zvi
Departments of General Surgery, Hadassah Medical Center, Hebrew University, Ein Kerem, Jerusalem, Israel.
Surg Laparosc Endosc Percutan Tech. 2003 Oct;13(5):318-21. doi: 10.1097/00129689-200310000-00006.
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.
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。