ArticleTranslational andrology and urology2026
Surgical management and molecular diagnosis of pediatric cystic nephroma: a single-center case series with implications for
Article in Translational andrology and urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Pediatric cystic nephroma (pCN) is a rare renal neoplasm associated with Case Description: We retrospectively analyzed 5 patients with pCN treated between November 2020 and November 2024. Clinical data, imaging, surgical approaches (including robot-assisted laparoscopy), pathological findings, and genetic results were reviewed. The cohort comprised 3 males and 2 females, with a median age of 13 months (range, 7-86 months). Three patients were asymptomatic, with tumors detected incidentally during routine examinations (including one prenatal diagnosis at 6 months gestation); the remaining two presented with palpable abdominal masses. Radiological assessment confirmed multilocular cystic architecture in all cases. Surgical management was tailored to preoperative imaging characteristics and intraoperative findings, consisting of 2 open radical nephrectomies, 1 open partial nephrectomy, and 2 robot-assisted laparoscopic partial nephrectomies. Pathology confirmed pCN in all cases. Comprehensive genetic testing revealed paired germline and somatic Conclusions: pCN is a rare entity associated with
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