Cases of Patients Treated in Countries With Limited Resources and Discussed by Experts of the International CML Foundation (iCMLf)-Case No. 1: A Boy Presenting With Priapism and Loss of Vision.

IF 0.6 Q4 ONCOLOGY Case Reports in Oncological Medicine Pub Date : 2024-07-29 eCollection Date: 2024-01-01 DOI:10.1155/2024/5534445
Nirmalya Roy Moulik, Arlene Harriss-Buchan, Guiseppe Saglio, Nicola Evans, Meinolf Suttorp
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Abstract

Pediatric chronic myeloid leukemia (pCML) is a rare malignancy accounting for only 2%-3% of all childhood leukemias. Due to this rarity, familiarity with pCML is limited among most pediatric practitioners, including even pediatric hemato-oncologists. In low- and middle-income countries (LMICs), limited financial resources and limited data specific to pCML represent obstacles that healthcare providers must face in diagnosing and treating this rare condition in children. The International CML Foundation (iCMLf) is improving outcomes for people with CML in these countries where resources, diagnostics, and access to medicines may be limited (https://www.cml-foundation.org/lmic-programs.html). Virtual meetings with the purpose of teaching participating pediatricians from LMICs of defined geographical regions were organised by the iCMLf in 2023. At a virtual meeting of the South Asia region, the case of a 14-year-old Indian boy was presented diagnosed with CML in a chronic phase complicated by priapism and loss of vision in his left eye due to hyperleukocytosis. Key aspects of this case are discussed in-depth from the perspective of (i) a pediatric hemato-oncologist practicing in a high-income country, (ii) a pediatric hemato-oncologist practicing in a LMIC, (iii) an adult CML hematologist, and (iv) from the iCMLf in improving the care of children with CML worldwide. Thus by discussing a multifaceted complicated case of pCML in written form as well as pointing to the pediatric module of the iCMLf Knowledge Centre will hopefully contribute to minimize existing knowledge gaps in a rare pediatric malignancy.

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国际骨髓增生性白血病基金会 (iCMLf) 专家讨论的资源有限国家患者治疗病例 - 病例 1:一名出现尿崩症和视力丧失的男孩。
小儿慢性髓性白血病(pCML)是一种罕见的恶性肿瘤,仅占所有儿童白血病的 2%-3%。由于这种罕见性,大多数儿科医生,甚至包括儿科血液肿瘤专家,对 pCML 的了解都很有限。在中低收入国家(LMICs),有限的财政资源和针对 pCML 的有限数据是医疗服务提供者在诊断和治疗这种罕见儿童疾病时必须面对的障碍。国际骨髓增生性白血病基金会 (iCMLf) 正在改善这些国家骨髓增生性白血病患者的治疗效果,因为这些国家在资源、诊断和药物获取方面可能都很有限 (https://www.cml-foundation.org/lmic-programs.html)。2023 年,iCMLf 组织了虚拟会议,目的是向来自特定地理区域的低收入、中等收入和中等收入国家的儿科医生传授知识。在南亚地区的虚拟会议上,一名 14 岁的印度男孩被诊断为慢性骨髓增生性白血病(CML)慢性期并发症,由于白细胞过多,他的左眼出现视力丧失。我们从以下角度深入讨论了该病例的主要方面:(i) 在高收入国家执业的儿科血液肿瘤学家;(ii) 在低收入国家执业的儿科血液肿瘤学家;(iii) 成人 CML 血液学家;(iv) iCMLf 在改善全球儿童 CML 患者护理方面的作用。因此,通过书面形式讨论 pCML 的多方面复杂病例,并指出 iCMLf 知识中心的儿科模块,希望能有助于最大限度地缩小罕见儿科恶性肿瘤方面现有的知识差距。
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来源期刊
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发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
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