Emre Senol, Karagoz Ayse, Hakalmaz Ali Ekber, Ocak Suheyla, Ucar Ayse Kalyoncu, Kepil Nuray, Kendigelen Pinar, Tutuncu Cigdem, Kurugoglu Sebuh, Senyuz Osman Faruk
Department of Pediatric Surgery, Istanbul University-Cerrahpasa, Cerrahpasa School of Medicine, Istanbul, Turkey.
Department of Pediatric Hematology and Oncology, Istanbul University-Cerrahpasa, Cerrahpasa School of Medicine, Istanbul, Turkey.
Pediatr Surg Int. 2025 Jun 25;41(1):193. doi: 10.1007/s00383-025-06101-y.
Undifferentiated embryonal sarcoma of the liver (UESL) presents significant diagnostic and therapeutic challenges due to its rarity and unpredictable clinical course. This study emphasizes the importance of individualized, case-based assessment by highlighting the distinctive preoperative, intraoperative, and postoperative challenges encountered in pediatric UESL patients.
We performed a retrospective review of nine pediatric patients treated for UESL at our institution from 2012 to 2022. We systematically evaluated clinical presentations, radiological assessments, surgical techniques, perioperative findings, treatment protocols, and follow-up outcomes.
Each patient presented unique diagnostic and therapeutic challenges at various management stages. Preoperatively, overlapping radiologic and immunohistochemical features led to diagnostic uncertainty; notably, weak β-catenin positivity and low AFP levels initially resulted in misdiagnosis and incorrect treatment protocol application in one case. Significant intraoperative events included unexpected pulmonary embolism, while another patient developed posterior reversible encephalopathy syndrome (PRES) immediately preoperatively, delaying surgical intervention. Excluding one patient who experienced an unexplained sudden death on postoperative day 5, no other major surgical complications (such as hemorrhage, infection, bile leakage, biliary complications, or sepsis) were recorded. At a median follow-up of 7.2 years (range: 13 months to 12 years), five patients remained disease-free, one patient continued with intermittent chemotherapy, two patients succumbed to progressive metastatic recurrence, and one patient died postoperatively on day 5 due to an unexplained event.
UESL requires individualized, case-based evaluation and multidisciplinary collaboration. Each patient may present unique diagnostic, surgical, and postoperative management challenges. Awareness of potential complications and the unpredictable nature of UESL highlights the importance of centralized, multidisciplinary care to optimize clinical outcomes.
肝未分化胚胎性肉瘤(UESL)因其罕见性和不可预测的临床病程,在诊断和治疗上面临重大挑战。本研究通过强调小儿UESL患者术前、术中和术后遇到的独特挑战,凸显了个体化、基于病例评估的重要性。
我们对2012年至2022年在我院接受UESL治疗的9例小儿患者进行了回顾性研究。我们系统评估了临床表现、影像学评估、手术技术、围手术期发现、治疗方案及随访结果。
每位患者在不同管理阶段都呈现出独特的诊断和治疗挑战。术前,影像学和免疫组化特征重叠导致诊断不确定;值得注意的是,一例患者因β-连环蛋白弱阳性和甲胎蛋白水平低,最初导致误诊并错误应用治疗方案。术中重大事件包括意外肺栓塞,而另一例患者在术前即刻出现后部可逆性脑病综合征(PRES),延迟了手术干预。除一名患者术后第5天原因不明突然死亡外,未记录到其他重大手术并发症(如出血、感染、胆漏、胆道并发症或脓毒症)。中位随访7.2年(范围:13个月至12年),5例患者无疾病生存,1例患者继续接受间歇化疗,2例患者因进行性转移复发死亡,1例患者术后第5天因不明原因事件死亡。
UESL需要个体化、基于病例的评估以及多学科协作。每位患者可能面临独特的诊断、手术及术后管理挑战。认识到潜在并发症及UESL的不可预测性,凸显了集中多学科护理对优化临床结局的重要性。