A Rare Case Mimicking Collecting System Tumor: Antopol-Goldman Lesion

Journal Title: Üroonkoloji Bülteni - Year 2018, Vol 17, Issue 4

Abstract

Antopol-Goldman (AG) lesion is a benign condition characterized by flank pain, hematuria, and radiologically detected filling defect in the renal pelvis. It is clinically important because it is confused with renal parenchymal and collecting system tumors. In this case report, we present a 75-year-old male patient who was evaluated with the suspicion of renal pelvis tumor but was diagnosed with AG lesion and treated conservatively after excluding malignancy with radiology, endoscopy, and pathology. Our aim is to emphasize the importance of diagnostic flexible ureterorenoscopy before planning radical treatment in patients with hematuria, flank pain, and radiological signs of filling defect in the renal pelvis.

Authors and Affiliations

Kamil Gökhan Şeker, Emre Şam, Osman Özdemir, İsmail Yiğitbaşı, Ekrem Güner, Volkan Tuğcu

Keywords

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  • EP ID EP437631
  • DOI 10.4274/uob.1052
  • Views 118
  • Downloads 0

How To Cite

Kamil Gökhan Şeker, Emre Şam, Osman Özdemir, İsmail Yiğitbaşı, Ekrem Güner, Volkan Tuğcu (2018). A Rare Case Mimicking Collecting System Tumor: Antopol-Goldman Lesion. Üroonkoloji Bülteni, 17(4), 150-152. https://www.europub.co.uk/articles/-A-437631