Cystic Partially Differentiated Nephroblastoma, A Hyperfavourable Variant of Nephroblatoma: A Case Report with Review of the Literature

B. Ojo, W. Yongo, C. Soo, I. Annongu, R. Vhriterhire, H. Mohammed, E. Ogwuche, O. Shorun, I. Ugwu, E. Umobong, B. Eke, D. Omeh, M. Ogiator, P. Abayol
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Abstract

Cystic partially differentiated nephroblastoma is a rare variant of Wilm’s tumor and it represents the hyperfavourable end of the Wilm’s spectrum affecting young children. We described the first documented case from the northern part of Nigeria. The index patient presented with left flank mass. He had unilateral nephrectomy and surgical pathology established its diagnosis. It is a lower risk but malignant tumor that comes as the differential diagnosis of pediatric cystic renal lesions and need to be differentiated from benign lesions such as cystic nephroma and mixed epithelial and stroma tumor of kidney. It should always be considered as a differential diagnosis of childhood abdominal mass with appropriate investigations and management since it is curable by nephrectomy alone.
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囊性部分分化肾母细胞瘤,肾母细胞瘤的一种恶性变异:1例报告并文献复习
囊性部分分化肾母细胞瘤是一种罕见的肾母细胞瘤,它代表了肾母细胞瘤谱系中影响幼儿的超有利端。我们描述了来自尼日利亚北部的第一例有记录的病例。首发患者表现为左侧肿块。他接受了单侧肾切除术,手术病理证实了其诊断。它是一种风险较低但恶性的肿瘤,是儿童囊性肾病变的鉴别诊断,需要与良性病变如囊性肾瘤、肾上皮和间质混合瘤鉴别。由于仅靠肾切除术即可治愈,因此应将其视为儿童腹部肿块的鉴别诊断,并进行适当的调查和治疗。
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