先天性胃畸形青少年的间皮囊肿:病例报告

IF 0.2 Q4 PEDIATRICS
Jamie E. Anderson , Aqiba Bokhari , Eric Diaz , Minna Wieck , Payam Saadai
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引用次数: 0

摘要

导言良性间皮细胞囊肿非常罕见,据我们所知,目前还没有关于有胃螺裂病史的患者患有良性间皮细胞囊肿的病例报道。病例介绍一名15岁的女孩因背痛和腹胀到急诊科就诊,她小时候曾患有复杂性胃螺裂并接受过多次手术。就诊时,她发热,但基本血检结果在正常范围内。包括腹部超声波、腹部计算机断层扫描和腹部磁共振成像在内的影像学检查显示,她的腹部盆腔有一个 31×21×11 厘米的囊性病变,病变来源不明。甲胎蛋白、CA 125、CA 19-9、β HCG、癌胚抗原、抑制素 A/B、乳酸脱氢酶等肿瘤标志物均正常。用针抽取了液体样本。采集到琥珀色液体,其中大部分为巨噬细胞(72%)。放置了一根辫子导管,引流出 2500 毫升黄色/棕色透明液体。她带着引流管被送回家,原计划进行选择性囊肿切除术,但几天后她因肠梗阻来到医院。她接受了广泛的腹腔镜粘连溶解术、引流管移除术和囊肿壁部分切除术。病理分析结果与良性间皮囊肿一致。没有放置新的引流管。手术后她恢复良好。随访 3 个月后,她的情况良好,超声检查显示囊肿没有复发。结论良性间皮细胞囊肿虽然罕见,但应作为腹部大囊肿患者的鉴别诊断,尤其是有腹部手术史的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mesothelial Cyst in a Teenager born with Gastroschisis: A case report

Introduction

Benign mesothelial cysts are rare, and to our knowledge there are no reported cases of benign mesothelial cysts in patients with a history of gastroschisis.

Case presentation

A 15-year-old girl with a history of complicated gastroschisis and multiple operations as a child presented to the emergency department with back pain and abdominal bloating that worsened over the course of a year. At the time of presentation, she was febrile, but her basic blood tests were within normal limits. Imaging studies including an abdominal ultrasound, a computed tomography of the abdomen, and a magnetic resonance imagining of the abdomen demonstrated a 31× 21 × 11cm cystic abdominopelvic lesion, the origin of which was unclear. Tumor markers including alpha fetoprotein, CA 125, CA 19–9, beta HCG, carcinoembryonic antigen, inhibin A/B, and lactate dehydrogenase were normal. The fluid was sampled by needle aspiration. Amber fluid with mostly macrophages (72 %) and was obtained. A pigtail catheter was placed, and 2500 ml of clear yellow/brown fluid were drained. She was sent home with the drain and was scheduled for an elective cyst excision but presented to the hospital with a bowel obstruction a few days later. She underwent an extensive laparoscopic lysis of adhesions, drain removal, and partial excision of the cyst wall. The pathology analysis was consistent with a benign mesothelial cyst. No new drains were placed. She recovered well from the operation. At 3 months of follow up she is doing well and has no recurrence of the cyst by ultrasound. She will continue to be monitored with periodic ultrasounds.

Conclusion

While rare, benign mesothelial cysts should be on the differential diagnosis of patients with large abdominal cysts, particularly if they have a history of prior abdominal operations.

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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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