Pediatric Radiology, Medical University of Lublin, Lublin, Poland.
Laboratory of Genetic Diagnostics, Medical University of Lublin, Lublin, Poland.
Medicine (Baltimore). 2023 Sep 8;102(36):e34965. doi: 10.1097/MD.0000000000034965.
Acute lymphoblastic leukemia (ALL) represents approximately 1-quarter of all new cases of childhood cancer. Although overall survival following diagnosis has improved in recent years, the toxicity of chemotherapy remains a concern.
We describe an 11-year-old male patient diagnosed with T-cell precursor ALL who developed compounded complications during the induction phase of chemotherapy. Patient was hospitalized in the Department of Pediatric Hematology, Oncology, and Transplantology of the Medical University of Lublin, Poland. The patient's induction therapy was started according to the AIEOP-BFM ALL 2017 protocol IAp (International Collaborative Treatment Protocol for Children and Adolescents with Acute Lymphoblastic Leukemia).
Patient developed compounded complications such as cholecystitis, hepatotoxicity, pancreatitis and myelosuppression.
The patient was treated with leukapheresis, received a broad-spectrum antibiotic, potassium supplementation and hepatoprotective treatment and laparotomy cholecystectomy.
In the available literature, there is a limited amount of similar clinical cases with multiple complications in pediatric patients with ALL. Toxicities cause delays in the treatment of the underlying disease.
In children with acute lymphoblastic leukemia, there are side effects during the treatment such as cholecystitis and pancreatitis. Complications during treatment require a quick response and modification of disease management. Abdominal ultrasound performed before treatment makes it possible to observe the dynamics of lesions. Genetic mutation analysis could allow us to more precisely respond to the possible susceptibility to and appearance of complications after the use of a given chemotherapeutic agent.
急性淋巴细胞白血病(ALL)约占儿童癌症新发病例的四分之一。尽管近年来诊断后的总体生存率有所提高,但化疗的毒性仍然令人担忧。
我们描述了一位 11 岁男性患者,被诊断为 T 细胞前体 ALL,在化疗诱导期出现了复合并发症。患者在波兰卢布林医科大学儿科血液学、肿瘤学和移植学部住院。根据 AIEOP-BFM ALL 2017 IAp 方案(儿童和青少年急性淋巴细胞白血病国际协作治疗方案)开始了患者的诱导治疗。
患者出现了复合并发症,如胆囊炎、肝毒性、胰腺炎和骨髓抑制。
患者接受了白细胞分离术,接受了广谱抗生素、钾补充和保肝治疗,并进行了剖腹胆囊切除术。
在现有文献中,儿童 ALL 患者中存在多种并发症的类似临床病例数量有限。毒性会导致基础疾病治疗的延迟。
在急性淋巴细胞白血病患儿中,治疗过程中会出现胆囊炎和胰腺炎等副作用。治疗期间的并发症需要快速反应和调整疾病管理。在治疗前进行腹部超声检查可以观察到病变的动态。基因突变为我们提供了在使用特定化疗药物后可能出现并发症的易感性和出现的可能,从而让我们能够更精确地做出反应。