Ordóñez-Samaniego Robert, Puga-Tejada Miguel
Hospital Básico Arenillas. Arenillas, Ecuador.
Rev Gastroenterol Peru. 2016 Oct-Dec;36(4):357-362.
Gallbladder agenesis is a rare disease, which its symptomatology emulates biliary pathology. It is presented between 0.007 to 0.027% of those patients in whom a cholecystectomy is performed. After it, its evolution is asymptomatic. We present the case of a 19 years old female patient with clinical presentationof cholelithiasis. Ultrasound reveals scleroatrophic vesicle. Elective cholecystectomy was performed,but the gallbladder was not found. The patient presented an asymptomatic evolution in the postoperative period and in the annual follow-up. In addition, we performed a case review from clinical case reports obtained from Medline. Fourteen patients were included in the review of cases, compared to another five studied in a series of cases. There was no significant difference between the two groups. Gallbladder agenesis usually happens between 40 and 64 years, with pain in the upper right quadrant and ultrasound diagnosis of cholelithiasis. It is unlikely to reach a preoperative diagnosis. If it is intervened, it is preferable to limit to laparoscopic examination. The following evolution will be asymptomatic, althoughthe cause of it is not known yet.
胆囊缺如是一种罕见疾病,其症状与胆道疾病相似。在接受胆囊切除术的患者中,其发生率为0.007%至0.027%。术后,病情发展通常无症状。我们报告一例19岁女性患者,临床表现为胆石症。超声检查显示胆囊萎缩硬化。遂行择期胆囊切除术,但未发现胆囊。该患者术后及年度随访期间均无任何症状。此外,我们对从医学文献数据库(Medline)获取的临床病例报告进行了病例回顾。病例回顾纳入了14例患者,与另一组系列研究中的5例患者进行比较。两组之间无显著差异。胆囊缺如通常发生在40至64岁之间,表现为右上腹疼痛,超声诊断为胆石症。术前诊断不太可能实现。如果进行干预,最好仅限于腹腔镜检查。尽管其病因尚不清楚,但后续病情发展将无症状。