Successful treatment with decompressive laparotomy for abdominal compartment syndrome induced by asparaginase-associated pancreatitis in a pediatric patient with acute lymphoblastic leukemia: a case report.

IF 1.5 4区 医学 Q2 PEDIATRICS
Translational pediatrics Pub Date : 2025-05-30 Epub Date: 2025-05-26 DOI:10.21037/tp-24-440
Huiwen Zhang, Weifeng Lu
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引用次数: 0

Abstract

Background: Asparaginase (ASP) has significantly improved the complete remission rate and long-term event-free survival in children with acute lymphoblastic leukemia (ALL). Asparaginase-associated pancreatitis (AAP) is a potentially toxic side effect of ASP, which may even lead to fatal abdominal compartment syndrome (ACS) in extreme cases. Currently, there is no consensus on the indications for decompressive laparotomy (DL), including when to initiate it, what criteria to use for decision-making, or how to perform the procedure. Moreover, available research data remain limited.

Case description: We present a case of a 2-year-old boy with ALL who developed ACS, a fatal complication of severe acute pancreatitis (SAP) following treatment with pegaspargase (PEG-ASP). Massive transfusion stabilized his hemodynamics and intraluminal contents were evacuated, yet his symptoms progressed. Consequently, the patient underwent DL and continuous venovenous hemodiafiltration (CVVHDF) with ultrafiltration. Postoperative complications including enteroatmospheric fistulas and abdominal abscesses were gradually corrected by negative-pressure wound therapy (NPWT). The boy was discharged from the intensive care unit (ICU) on the 93rd day after hospital admission. During follow-up, the child's abdominal symptoms gradually improved, and bridging therapy with blinatumomab was administered.

Conclusions: In this case, a pediatric ALL patient developed life-threatening complications following PEG-ASP administration, which were ultimately successfully managed through multidisciplinary intervention. When pediatric hematology-oncology patients develop ACS, clinicians should carefully evaluate the oncological context and thoroughly assess the risks of surgical versus conservative management for this potentially fatal condition. Optimal timing of surgical intervention combined with advanced perioperative care is critical for achieving favorable outcomes. We strongly recommend conducting high-quality clinical research to establish evidence-based treatment guidelines.

小儿急性淋巴细胞白血病患者天冬酰胺酶相关性胰腺炎所致腹膜间室综合征的减压开腹成功治疗:1例报告。
背景:天冬酰胺酶(ASP)显著提高急性淋巴细胞白血病(ALL)患儿的完全缓解率和长期无事件生存率。天冬酰胺酶相关性胰腺炎(AAP)是ASP潜在的毒副作用,在极端情况下甚至可能导致致命的腹腔隔室综合征(ACS)。目前,对于剖腹减压术(DL)的适应症,包括何时开始,使用什么标准进行决策,或如何执行手术,还没有达成共识。此外,可用的研究数据仍然有限。病例描述:我们报告了一个2岁的ALL男孩,他在接受pegaspargase (PEG-ASP)治疗后发展为ACS,这是严重急性胰腺炎(SAP)的致命并发症。大量输血稳定了他的血流动力学,排出了腔内内容物,但他的症状仍在恶化。因此,患者接受了DL和持续静脉-静脉血液滤过(CVVHDF)和超滤。术后并发症,包括肠大气瘘和腹部脓肿逐渐纠正负压伤口治疗(NPWT)。该男孩在入院后第93天从重症监护病房(ICU)出院。随访期间,患儿腹部症状逐渐改善,给予blinatumumab桥接治疗。结论:在本病例中,一名儿科ALL患者在给药PEG-ASP后出现了危及生命的并发症,最终通过多学科干预成功控制。当儿童血液肿瘤患者发生ACS时,临床医生应仔细评估肿瘤背景,并彻底评估手术与保守治疗的风险。手术干预的最佳时机结合先进的围手术期护理是获得良好结果的关键。我们强烈建议开展高质量的临床研究,以建立循证治疗指南。
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
Translational pediatrics
Translational pediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
4.50
自引率
5.00%
发文量
108
期刊介绍: Information not localized
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