Three-dimensional modelling and printing for preoperative planning in the resection of an ischiorectal epithelioid sarcoma: a case report

IF 0.2 Q4 PEDIATRICS
Rachel J. Livergant , Trevor D. Hamilton , Daniel G. Rosenbaum , Sima Zakani , John Jacob , Shahrzad Joharifard
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Abstract

Introduction

Epithelioid sarcomas are rare malignant mesenchymal tumours, accounting for approximately 3–4 % of pediatric soft-tissue sarcomas, and present unique surgical challenges due to their infiltrative nature and proximity to critical anatomical structures. While three-dimensional modelling has emerged as a valuable adjunct in preoperative planning for complex tumours, its use in pediatric soft-tissue sarcomas is rare, with no described cases involving epithelioid sarcomas.

Case presentation

A 13-year-old girl presented with a year-long history of perineal pain and a palpable mass. Imaging revealed a tumour involving the rectum and external sphincter, abutting the posterior vaginal wall. Biopsy confirmed epithelioid sarcoma and staging showed indeterminate pulmonary nodules. She underwent neoadjuvant chemoradiotherapy. Two surgical options were considered: abdominoperineal resection with hysterectomy or vaginal preservation with increased risk of residual disease. A three-dimensional model with 2cm margins was created to aid decision-making. After multidisciplinary review and model consultation, the patient opted for vaginal preservation. She underwent abdominoperineal resection with VRAM flap reconstruction. Final pathology confirmed negative margins. Nearly three years later, she developed a pancreatic tail metastasis and progressive pulmonary lesions, which were treated with distal pancreatectomy, splenectomy, radiotherapy, and cryoablation. Additional metastases in the stomach, scalp, retroperitoneum, and flank are being managed with palliative radiotherapy.

Conclusion

Three-dimensional printed models can be helpful in the preoperative planning for the resection of tumours of the ischiorectal region.
三维建模和打印用于坐骨直肠上皮样肉瘤切除术的术前规划:1例报告
上皮样肉瘤是一种罕见的恶性间充质肿瘤,约占小儿软组织肉瘤的3 - 4%,由于其浸润性和靠近关键解剖结构,给手术带来了独特的挑战。虽然三维建模在复杂肿瘤的术前规划中已经成为一种有价值的辅助手段,但它在小儿软组织肉瘤中的应用很少见,没有涉及上皮样肉瘤的病例。病例介绍:一名13岁的女孩,因会阴疼痛和可触及的肿块长达一年。影像显示肿瘤累及直肠及外括约肌,紧靠阴道后壁。活检证实为上皮样肉瘤,分期不确定为肺结节。她接受了新辅助放化疗。考虑了两种手术选择:腹部会阴切除合并子宫切除术或阴道保留,但会增加残留疾病的风险。为了帮助决策,他们创建了一个边缘为2厘米的三维模型。经过多学科回顾和模型咨询,患者选择阴道保留。她接受了腹部会阴切除术和VRAM皮瓣重建。最终病理证实阴性边缘。近三年后,她出现胰腺尾部转移和进行性肺部病变,并接受远端胰腺切除术、脾切除术、放疗和冷冻消融治疗。胃、头皮、腹膜后和腹部的其他转移灶正在接受姑息性放疗。结论三维打印模型有助于坐骨直肠肿瘤切除术的术前规划。
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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