Appendiceal hydatid cyst in a 5-year-old child: A case report

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Abstract

Introduction

Hydatidosis is the formation of cysts caused by the parasitic infection of Echinococcus granulosus. This disease predominantly affects the liver and lungs. The involvement of other organs is quite rare.

Case presentation

A 5-year-old Iranian boy presented with abdominal pain, anorexia, and hepatomegaly. The pain had been present for about 1 year. He had developed low-grade fever during the previous two months. On physical exam he had abdominal distention and a palpable mass on the right lower quadrant. Basic blood work revealed leukocytosis and eosinophilia. An abdominal ultrasound revealed a 5 × 6 × 8 cm cystic lesion in the pelvis, and two cystic lesions located in the right lobe of the liver. A computerized tomography (CT) scan of the abdomen confirmed the findings. CT of the chest and brain ruled out further cystic lesions. The patient had a positive Indirect hemagglutination assay (IHA), confirming the diagnosis of hydatidosis. A regimen of an albendazole was initiated. He was taken to the operating room for the resection of all cysts. The hepatic cysts were drained and re-filled with hypertonic saline solution, which was left in place for several minutes. Next, the hypertonic solution was drained and all hepatic cysts removed. We turned our attention to the pelvic cyst. It had a thick wall and was indistinguishable from the surrounding tissues. After dissecting it we found that it was arising from the wall of the appendix. We surrounded it with gauze embedded in hypertonic solution and resected the majority of it, leaving a small aspect of the external layer that was densely adherent to the bowel. He recovered well from the operation, remained on albendazole for 6 months, and has had no recurrences this far.

Conclusion

Appendiceal hydatid cysts should be included in the differential diagnosis of patients with hydatid disease and pelvic cysts.
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一名 5 岁儿童的阑尾水瘤囊肿:病例报告
导言棘球蚴病是由棘球蚴寄生感染引起的囊肿形成。这种疾病主要影响肝脏和肺部,其他器官受累的情况非常罕见。病例介绍 一名 5 岁的伊朗男孩因腹痛、厌食和肝肿大就诊。疼痛已持续了约 1 年。此前两个月,他曾出现低烧。体格检查时,他腹部胀痛,右下腹可触及肿块。基础血液检查显示白细胞增多和嗜酸性粒细胞增多。腹部超声波检查显示,盆腔内有一个 5 × 6 × 8 厘米的囊性病变,肝脏右叶有两个囊性病变。腹部计算机断层扫描(CT)证实了这一结果。胸部和脑部CT排除了其他囊性病变。患者的间接血凝试验(IHA)呈阳性,确诊为包虫病。患者开始接受阿苯达唑治疗。他被送进手术室,切除了所有囊肿。肝囊肿被引流出来,重新注入高渗盐水,并在原位停留数分钟。然后,排出高渗溶液,切除所有肝囊肿。我们将注意力转向盆腔囊肿。该囊肿壁很厚,与周围组织无法区分。解剖后我们发现,它是从阑尾壁上长出来的。我们用浸泡在高渗溶液中的纱布将其包围,并切除了大部分,只留下一小部分与肠道紧密粘连的外层。结论阑尾包虫囊肿应纳入包虫病和盆腔囊肿患者的鉴别诊断中。
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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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