Lugo-Vicente H L
JSLS. 1997 Jan-Mar;1(1):61-4.
The purpose of this study was to describe clinico-pathological characteristics in a group of children with motility disorders of the gallbladder and correlate the findings with cases receiving surgical treatment for gallstone during the same period.
Retrospective chart analysis of all cholecystectomies from January, 1990 to June, 1995. Analysis of demographics, symptoms and duration, associated illnesses, diagnostic studies, pathological stratification, length of stay, complications, follow-up and patient satisfaction. Statistical comparison of clinical variables between gallstone and dyskinesia patients was analyzed using chi-square, and analysis of variance (ANOVA).
Twelve children (14%) of 85 underwent laparoscopic cholecystectomy during a 66-month period for gallbladder dyskinesia. Their mean age was 14 +/- 3 years (range 7 to 18). Ten patients were female and two were males for a 5:1 ratio. Classic biliary symptoms (RUQ abdominal pain and FFI) predominated for a mean of 48 weeks. A predisposing factor was previous family history of gallstones in five cases (42%). The diagnosis was obtained after gallbladder non-visualization in one child and low ejection fractions after CCK stimulated hepatobiliary scan studies in the remainder. Mean ejection fraction was 16.8%. Ten cases (83%) had mild to moderate chronic cholecystitis, and two children had unremarkable pathologic changes. These changes correlated with the mean duration of symptoms, not with ejection fraction volumes. After a mean follow-up of 17 months, 11 children are free of symptoms, and one continues with intermittent diarrhea. Comparison between calculous and dyskinesia patients showed that biliary dyskinesia children suffer more dyspepsia, undergo more diagnostic studies and have a significant family history of gallstones.
Gallbladder dyskinesia (GD) is a motility disorder causing symptoms similar to those of gallstones, although the clinical picture is more protracted. Diagnosis is confirmed using CCK stimulated hepatobiliary scan ejection fractions after thorough diagnostic work-up for other gastrointestinal causes. Laparoscopic cholecystectomy is the treatment of choice. Most children present with mild to moderate changes of chronic cholecystitis depending on duration of symptoms. Clinical improvement is seen in most cases after surgery.
本研究旨在描述一组胆囊动力障碍患儿的临床病理特征,并将研究结果与同期接受胆囊结石手术治疗的病例进行对比。
对1990年1月至1995年6月期间所有胆囊切除术病例进行回顾性病历分析。分析人口统计学资料、症状及持续时间、相关疾病、诊断性检查、病理分层、住院时间、并发症、随访情况及患者满意度。采用卡方检验和方差分析对胆囊结石患者与运动障碍患者的临床变量进行统计学比较。
在66个月的时间里,85例患儿中有12例(14%)因胆囊运动障碍接受了腹腔镜胆囊切除术。他们的平均年龄为14±3岁(范围7至18岁)。女性患者10例,男性患者2例,男女比例为5:1。典型的胆系症状(右上腹疼痛和脂肪泻)平均持续48周。5例(42%)患者有胆结石家族史这一诱发因素。1例患儿经胆囊不显影确诊,其余患儿经胆囊收缩素刺激肝胆扫描检查后胆囊排空分数较低确诊。平均排空分数为16.8%。10例(83%)患儿有轻至中度慢性胆囊炎,2例患儿病理改变不明显。这些改变与症状的平均持续时间相关,而非与排空分数相关。平均随访17个月后,11例患儿无症状,1例仍有间歇性腹泻。结石性胆囊炎患者与运动障碍患者的比较显示,胆囊运动障碍患儿消化不良症状更多,接受的诊断性检查更多,且有明显的胆结石家族史。
胆囊运动障碍(GD)是一种动力障碍性疾病,其症状与胆结石相似,尽管临床表现更为迁延。在对其他胃肠道病因进行全面诊断评估后,通过胆囊收缩素刺激肝胆扫描的排空分数来确诊。腹腔镜胆囊切除术是首选治疗方法。大多数患儿根据症状持续时间表现为轻至中度慢性胆囊炎改变。大多数病例术后临床症状改善。