Giant simple biliary cyst in a 2-year-old child: a case report

IF 0.2 Q4 PEDIATRICS
Ashagre Gebremichael Ganta , Wintana Tesfaye Desta
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Abstract

Introduction

Simple biliary cysts are exceptionally rare in pediatric patients and seldom manifest as giant hepatic masses. Their clinical and radiological overlap with malignant tumors poses diagnostic challenges, potentially leading to unnecessary aggressive interventions.

Case presentation

A 2-year-old female presented with progressive abdominal distension and recurrent pneumonias. Physical examination revealed a protuberant abdomen with visible venous collaterals. Liver span was 18 cm by percussion, with no splenomegaly. Laboratory findings included a hemoglobin level of 10.8 g/dL. Tumor markers (AFP and β-hCG) were within normal limits. X-ray studies demonstrated bilateral elevated hemidiaphragm and right basal consolidation. Abdominal ultrasound found a large anechoic lesion (18 × 15 × 12 cm) with internal septations and posterior acoustic enhancement, replacing the right hepatic lobe, with no Doppler flow, and compression of the inferior vena cava. Contrast-enhanced computerized tomography (CT) revealed a hypodense mass with peripheral rim enhancement and absence of centripetal filling, alongside right renal displacement, gastric compression, and diaphragmatic elevation. The patient was taken to the operating room for an exploratory laparotomy. Through a supraumbilical transverse incision extended on the midline below the umbilicus, the mass was entirely delivered. Anatomical resection of segments IV A and B was performed, including the mass, which weighted 6.5 kg. The postoperative course was uneventful apart from a self-limiting biliary leak managed conservatively. Histopathological analysis confirmed a simple biliary cyst with no evidence of malignancy. The patient had a complete resolution of respiratory symptoms and showed no recurrence at six months of follow-up.

Conclusion

Simple biliary cysts, although rare, must be considered in the differential diagnosis of giant hepatic cystic masses in children. Complete surgical excision is the treatment of choice.
2岁儿童巨大单纯性胆道囊肿1例
单纯性胆道囊肿在儿科患者中极为罕见,很少表现为巨大的肝脏肿块。它们与恶性肿瘤的临床和放射学重叠构成诊断挑战,可能导致不必要的积极干预。病例表现:一名2岁女性,表现为进行性腹胀和复发性肺炎。体格检查显示腹部隆起,可见静脉侧支。肝跨18 cm,未见脾肿大。实验室检查结果包括血红蛋白水平10.8 g/dL。肿瘤标志物(AFP、β-hCG)均在正常范围内。x线检查显示双侧横膈膜升高和右侧基底实变。腹部超声示大无回声病灶(18 × 15 × 12 cm),内隔,后侧声增强,取代右肝叶,无多普勒血流,下腔静脉受压。计算机断层扫描(CT)显示低密度肿块,外周边缘增强,无向心充盈,伴右侧肾脏移位,胃受压,膈抬高。病人被带到手术室进行剖腹探查术。通过在脐下中线延伸的脐上横向切口,将肿块完全娩出。解剖切除IV节A节和B节,包括重6.5 kg的肿块。术后除了保守处理的自限性胆道泄漏外,一切顺利。组织病理学分析证实为单纯性胆道囊肿,无恶性肿瘤迹象。患者呼吸道症状完全消失,随访6个月无复发。结论单纯性胆道囊肿虽罕见,但在儿童巨大肝囊性肿物鉴别诊断中应予以重视。完全的手术切除是治疗的选择。
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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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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