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Renal Presentation in Pediatric Acute Leukemia Report of 2 Cases

机译:小儿急性白血病的肾脏表现2例报道

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Renal enlargement at time of diagnosis of acute leukemia is very unusual. We here in report 2 pediatric cases of acute leukemia who had their renal affection as the first presenting symptom with no evidences of blast cells in blood smear and none of classical presentation of acute leukemia.The first case is a 4-year-old girl who presented with pallor and abdominal enlargement. Magnetic resonance imaging showed bilateral symmetrical homogenous enlarged kidneys suggestive of infiltration. Complete blood picture (CBC) revealed white blood count 11x10(9)/L, hemoglobin 8.7g/dL and platelet count 197x10(9)/L. Bone marrow aspiration was performed, and diagnosed precursor B-cell ALL was made. The child had an excellent response to modified CCG 1991 standard risk protocol of chemotherapy with sustained remission, but unfortunately relapsed 11 month after the end of therapy.The second child was 13-month old, presented with pallor, vomiting, abdominal enlargement, and oliguria 2 days before admission. Initial CBC showed bicytopenia, elevated blood urea, creatinine, and serum uric acid, while abdominal ultrasonography revealed bilateral renal enlargement. Bone marrow examination was done and showed 92% blast of biphenotypic nature. So, biphynotypic leukemia with bilateral renal enlargement and acute renal failure was subsequently diagnosed. The patients admitted to ICU and received supportive care and prednisolone. Renal function normalized and chemotherapy was started. The child achieved complete remission with marked reduction of kidney size but, unfortunately she died from sepsis in consolidation phase of therapy. This case demonstrates an unusual early renal enlargement in childhood acute leukemia.Renal involvement of acute leukemia should be considered in child presenting with unexplained bilateral renal enlargement with or without renal function abnormalities and bone marrow examination should be included in the workup.
机译:诊断急性白血病时肾脏增大非常罕见。我们在这里报告了2例急性白血病的儿科病例,他们的肾脏疾病为首发症状,没有血涂中有母细胞的迹象,也没有经典的急性白血病表现。第一例是一名4岁女孩,表现为苍白和腹部肿大。磁共振成像显示双侧对称的均匀肾脏增大,提示有浸润。全血图片(CBC)显示白细胞计数为11x10(9)/ L,血红蛋白为8.7g / dL,血小板计数为197x10(9)/ L。进行骨髓穿刺,并诊断出前体B细胞ALL。这名儿童对改良的CCG 1991标准化疗方案具有持续缓解的良好反应,但不幸的是在治疗结束后11个月复发了;第二名儿童13个月大,表现出苍白,呕吐,腹部增大和少尿入学前2天。最初的CBC表现为双细胞减少,血尿素,肌酐和血清尿酸升高,而腹部超声检查显示双侧肾脏增大。进行了骨髓检查,显示出92%的双表型自然原始细胞。因此,随后诊断出双侧肾增大和急性肾功能衰竭的双型白血病。患者入ICU并接受支持治疗和泼尼松龙。肾功能恢复正常并开始化疗。该孩子完全缓解,肾脏大小明显减少,但是不幸的是,她在巩固治疗期间死于败血症。该病例表明儿童急性白血病早期肾脏异常增大。患有原因不明的双侧肾脏增大伴肾功能异常或不伴肾功能异常的儿童应考虑急性白血病的肾脏受累,并应进行骨髓检查。

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