一例罕见的双侧囊性部分分化型肾母细胞瘤复发为双侧囊性威尔姆斯瘤。
A rare case of bilateral cystic partially differentiated nephroblastoma recurring as bilateral cystic Wilms tumour.
作者信息
Kurian Jujju Jacob, Ninan Pradeep Joseph
机构信息
Department of Paediatric Surgery, Christian Medical College, Vellore, Tamil Nadu, India.
出版信息
BMJ Case Rep. 2015 Apr 15;2015:bcr2015209771. doi: 10.1136/bcr-2015-209771.
Abstract
Childhood cystic partially differentiated nephroblastoma (CPDN) is an uncommon renal neoplasm. Bilateral CPDN or CPDN co-existing with a cystic nephroma/Wilms tumour is extremely rare. Treatment of CPDN is by complete surgical excision. Although local recurrences are uncommon, distant metastases have not been described. We present a case of bilateral CPDN that, after complete excision, recurred as bilateral cystic Wilms tumour. To the best of our knowledge, this is the first reported case in the literature where a bilateral CPDN has recurred as bilateral Wilms tumour.
摘要
儿童囊性部分分化型肾母细胞瘤（CPDN）是一种罕见的肾脏肿瘤。双侧CPDN或CPDN与囊性肾瘤/肾母细胞瘤并存极为罕见。CPDN的治疗方法是完整手术切除。虽然局部复发不常见，但尚未见远处转移的报道。我们报告一例双侧CPDN病例，在完整切除后复发为双侧囊性肾母细胞瘤。据我们所知，这是文献中首次报道的双侧CPDN复发为双侧肾母细胞瘤的病例。
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