RESUMEN
Background: Renal ganglioneuroma is an extremely rare benign tumour that affects neural crest cells. Here we report a case of renal ganglioneuroma with nodal metastasis managed by surgical resection. Case report: A 38-year-old female presented with anorexia and early satiety. On examination, she had a palpable mass per abdomen. CT scan revealed a large heterogenous mass in retroperitoneum in right suprarenal region with enlarged retrocrural lymph nodes. She underwent right radical nephrectomy as the mass was inseparable from the right kidney. Postoperative period was uneventful. HPE revealed renal ganglioneuroma. Conclusion: Primary renal ganglioneuroma is difficrult to differentiate from other etroperitoneal lesions. Surgical resection is the most effective treatment.
RESUMEN
Objective To describe CT and MR apearance of retroperitoneal ganglioneuroma .Methods CT and MR findings ofretroperitoneal tumor in a patient with ganglioneuroma biopsy-proved were retrospectively analyzed,and a literature review was conducted. Results The mass was well-circumscribed,non-enhanced CT showed homogeneous low atenuation, and a punctate calcification was seeninside tumor.Contrast uptake was delayed.Progressive but incomplete enhancement was observed.On MRI,T_2WI showed a high signalintensity and T_1WI show a low signal intensity.Enhanced MR depicted the mild enhancment.Conclusion Retroperitoneal ganglioneuroma is a rare tumor which should nevertheless be included in differential diagnosis of retroperitoneal masses when presenting as a well-delimitedtumor with possible tendency to surroud or displace major blood vessels.Low density on non-enhanced CT,and delayed progressiveenhancement on CT and MRI.