Clinical Features and Outcomes of Gallbladder Polyps in Children.

Orxan Ferzeliyev, Berna Oğuz, Tutku Soyer, Özlem Boybey Türer, Mithat Haliloglu, Feridun Cahit Tanyel
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Abstract

Background: Gallbladder polyps are rare lesions protruding into the gallbladder lumen with variable clinical presentation. No standard treatment algorithm has been developed for pediatric gallbladders, and the malignant potential of the gallbladder is not clear in children. Therefore, a retrospective study was performed to evaluate the clinical features and treatment options of gallbladder polyps in children.

Methods: Between 2014 and 2020, children diagnosed with gallbladder polyps were evaluated for age, gender, clinical features, results of follow-up with ultrasound findings, and treatment options retrospectively.

Results: The records of 15 patients with a mean age of 13.2 years (2-20 years) were included. The male: female ratio was 7 : 8. Gallbladder polyps was detected incidentally in 73.3% (n = 11) of the patients. Four (20%) of the patients were symptomatic (26.7%) and complained about abdominal pain. Laboratory tests were normal except in 3 patients who showed slightly increased liver function tests. Two of the patients had 3 polyps on admission. The polyps were 2-10 mm in size. The size of the polyp increased in 5 patients (33.3%) and disappeared in 4 patients (26.6%) in follow-up ultrasound examinations. Five of the patients underwent cholecystectomy and 1 of them was scheduled for surgery. Five of the asymptomatic patients who have polyps less than 10 mm in size are still on follow-up. In patients with cholecystectomy, the histopathology of gallbladders revealed cholesterol polyps (n = 2) and hyperplastic polyps (n = 2). One of the patients with cholecystectomy showed no polyps in histopathological evaluation.

Conclusion: Despite the lack of a standardized algorithm, our data suggested that multiple polyps, polyps with increased in size or greater than 10 mm, and the presence of symptoms might require cholecystectomy in children. Asymptomatic patients with small-sized polyps can be identified using ultrasound, and the polyps may disappear during the subsequent follow-up.

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儿童胆囊息肉的临床特点及预后。
背景:胆囊息肉是一种罕见的突出于胆囊腔内的病变,临床表现多变。目前还没有针对儿童胆囊的标准治疗方法,儿童胆囊的恶性潜能也不清楚。因此,我们对儿童胆囊息肉的临床特点和治疗方案进行回顾性研究。方法:回顾性分析2014 - 2020年诊断为胆囊息肉患儿的年龄、性别、临床特征、超声随访结果及治疗方案。结果:纳入15例患者,平均年龄13.2岁(2 ~ 20岁)。男女比例为7:8。胆囊息肉的检出率为73.3% (n = 11)。4例(20%)患者有症状(26.7%),主诉腹痛。实验室检查除3例患者肝功能轻度增高外均正常。其中2例患者入院时有3个息肉。息肉大小为2- 10mm。随访超声检查息肉大小增大5例(33.3%),消失4例(26.6%)。5例患者行胆囊切除术,其中1例计划手术。5例息肉小于10mm的无症状患者仍在随访中。胆囊切除术患者的胆囊组织病理学检查显示胆固醇息肉(n = 2)和增生性息肉(n = 2)。1例胆囊切除术患者的组织病理学检查未发现息肉。结论:尽管缺乏标准化的算法,但我们的数据表明,儿童多发息肉、息肉大小增大或大于10mm以及出现症状可能需要胆囊切除术。无症状的小息肉患者可以通过超声识别,在后续随访中息肉可能消失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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