Giant splenic mesothelial cyst in a child: A case report

Saad Andaloussi , Omar Dalero , Abdelkrim Haita , Jinane Kharmoum , Zakarya Alami Hassani , Aziz Elmadi
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Abstract

Introduction

Splenic mesothelial cysts are rare, accounting for a small fraction of primary non-parasitic splenic cysts. They often present as incidental findings but can become symptomatic when they reach a significant size.

Case presentation

An 8-year-old girl presented with a 30-day history of progressive left upper quadrant abdominal pain. Physical exam revealed a firm, tender mass in the left upper quadrant. Laboratory tests including complete white count and inflammatory markers were all within normal limits. Hydatid serology was normal. Abdominal ultrasonography (US) revealed splenomegaly with a large hypoechoic cystic lesion arising from the spleen without Doppler flow. Contrast-enhanced computed tomography scan of the abdomen and pelvis confirmed the splenomegaly and a large unilocular cystic lesion measuring 15 × 10 × 14 cm, occupying nearly the entire splenic parenchyma, displacing adjacent organs. No internal enhancement, solid components, or calcifications were observed. Preoperative vaccinations were administered. Due to the size of the cyst and the persistence of pain, the patient was taken to the operating room for a laparoscopic exploration. We found minimal residual splenic tissue around the large cyst, so we proceeded with a total splenectomy after aspirating the cyst. The histopathology analysis was consistent with a mesothelial cyst. The postoperative course was uneventful. The patient was enrolled in a structured vaccination program and remains asymptomatic with no complications at two years of follow-up.

Conclusion

For symptomatic giant splenic cysts involving the splenic hilum, laparoscopic total splenectomy remains a safe and effective option when spleen-preserving alternatives are anatomically unfeasible.
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一名儿童的巨大脾间皮细胞囊肿:病例报告
脾间皮囊肿是罕见的,只占原发性非寄生性脾囊肿的一小部分。它们通常表现为偶然发现,但当它们达到显着大小时可能成为症状。病例介绍:一名8岁女孩以30天进行性左上腹腹痛病史就诊。体格检查显示左上腹有一个坚硬、压痛的肿块。实验室检查包括全白细胞计数和炎症标志物均在正常范围内。包虫血清学正常。腹部超声检查(US)显示脾肿大,无多普勒血流显示脾有大的低回声囊性病变。腹部和骨盆ct增强扫描证实脾肿大,并有一个大的单眼囊性病变,大小为15 × 10 × 14 cm,几乎占据了整个脾实质,取代了邻近的器官。未观察到内部强化、固体成分或钙化。术前接种疫苗。由于囊肿的大小和持续疼痛,患者被带到手术室进行腹腔镜探查。我们在大囊肿周围发现了少量残余脾组织,因此我们在抽吸囊肿后进行了全脾切除术。组织病理学分析与间皮囊肿一致。术后过程平淡无奇。患者参加了一项有组织的疫苗接种计划,在两年的随访中仍无症状,无并发症。结论对于累及脾门的有症状的巨大脾囊肿,在脾保留术在解剖学上不可行的情况下,腹腔镜脾全切除术是一种安全有效的选择。
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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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