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Bilateral massive nephromegaly–A rare presentation of t-cell acute lymphoblastic leukemia

机译:双侧大量肾脏 - 稀有T细胞急性淋巴细胞白血病的罕见介绍

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IntroductionRenal infiltration by leukemia causing massive bilateral nephromegaly is an extremely rare presentation of T-cell acute lymphoblastic leukemia(T-ALL).Case report18-month-old female toddler presented with fever and progressive abdominal distension of 4–6 weeks duration. Imaging revealed bilateral massively enlarged kidneys with normal excretion. Peripheral blood counts and smear examination was unremarkable and immunophenotypic evaluation of marrow was consistent with T-ALL. Chest imaging was unremarkable. She was started on modified Indian Childhood Collaborative Leukemia Group (ICiCLe) ALL protocol. Even with the best anti-tumor lysis syndrome (TLS) prophylaxis the child required two sessions of hemodialysis. An end-induction morphological remission & end-consolidation negative minimal residual disease (MRD) could be achieved.ConclusionBilateral massive nephromegaly is an extremely rare presentation of T-ALL. This case emphasizes the unusual presentation, need for prompt remediation of TLS, and most importantly the use of early intensification with four drug anthracycline & dexamethasone-based therapy for the treatment of T-ALL in children.
机译:白血病引入造成巨大双侧肾脏的引入渗透是T细胞急性淋巴细胞白血病(T-All)的极其罕见的介绍.CASE报告18个月大的女性小孩,发烧和渐进腹胀4-6周的持续时间。成像揭示了双侧大规模扩大的肾脏具有正常排泄。外周血计数和涂片检查是不起眼的,对骨髓的免疫表型评估与T-全部相一致。胸部成像不起眼。她始于改良印度儿童协同白血病集团(冰柱)所有议定书。即使是最好的抗肿瘤裂解综合征(TLS)预防儿童也需要两次血液透析。结束归因形态缓解&结束终结负数最小残留疾病(MRD)可以实现。结论分子分子大规模肾脏,是T-全部的极其罕见的呈现。本例强调了不寻常的介绍,需要迅速修复TLS,最重要的是利用四种药物蒽环类&amp的早期增殖;基于地塞米松的治疗治疗儿童的T-all。

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