Non-ischaemic priapism without trauma in a patient with relapsing Henoch-Schönlein purpura [0.03%]
一名复发性过敏性紫癜患者发生无创伤非缺血性阴茎异常勃起
Miguel Gil,José Cabrita Carneiro,Luís Campos Pinheiro
Miguel Gil
Non-ischaemic priapism is a rare subtype, almost always associated with trauma. We report the case of a 26-years-old male with significant medical history of relapsing Henoch-Schönlein purpura, who presented with a painless, persistent ere...
A rare case of scrotal vascular fibroblastoma with rapid growth: diagnostic challenges and pathological features [0.03%]
阴囊血管纤维瘤一例：迅速生长的诊断陷阱及病理特征
Yunfei Li,Zhuang Li,Junjie Zhu et al.
Yunfei Li et al.
Daniel I Sanford,Alexandra Lee,Shelby Smith et al.
Daniel I Sanford et al.
Testicular ischemia is a urologic emergency that is most commonly caused by testicular torsion, though other etiologies have been described. We present a patient who had two separate episodes of acute testicular ischemia followed by an even...
Identifiying the ideal point of injection in ICG-assisted lymphatic-sparing Palomo procedure: A case report [0.03%]
吲哚菁绿辅助下Palomo手术中理想的注射部位选择——一例报告
Giuseppe Autorino,Oana Sciboz,Oliver Sanchez et al.
Giuseppe Autorino et al.
We report a 13-year-old boy with varicocele, testicular hypotrophy, and recurrent torsion-detorsion episodes who underwent combined ICG-assisted lymphatic-sparing laparoscopic Palomo varicocelectomy and bilateral orchidopexy. Three ICG inje...
Adult retroperitoneal Ganglioneuroma: Case report of an incidental mass treated with robotic excision [0.03%]
成人腹膜后神经节细胞神经瘤的病例报告及机器人切除术治疗经验
Yazeid Alrefaey,Ibrahim Beshawri,Omar Shaikhomar et al.
Yazeid Alrefaey et al.
Retroperitoneal ganglioneuromas are rare, benign neural crest-derived tumors that typically occur in children and infrequently in adults. Their preoperative diagnosis is difficult due to nonspecific imaging findings, requiring histopatholog...
Atypical juxtaglomerular cell tumor in a young male with resistant hypertension and normal renin-aldosterone levels [0.03%]
一名年轻男性原发性顽固性高血压伴肾素-醛固酮正常的异位系膜细胞瘤病例报告
Mehdi Dadpour,Sara Besharati,Nima Saeedi et al.
Mehdi Dadpour et al.
Juxtaglomerular cell tumor (JGCT), or reninoma, is a rare renin-secreting renal neoplasm that typically presents with severe hypertension, hypokalemia, and elevated renin and aldosterone levels. We describe an atypical case of a 21-year-old...
Iatrogenic meatal obstruction after circumcision leading to acute renal failure: A case report [0.03%]
包皮环切术后医源性尿道口阻塞导致急性肾功能衰竭1例报告
Asma Jabloun,Fares Chaabouni,Malek Boughdir et al.
Asma Jabloun et al.
Circumcision is the most commonly performed surgical procedures in children, yet it is not without potential complications. We report the case of a 5-year-old boy who developed dysuria then complete anuria with acute renal failure following...
Penile mass with a past: Tertiary syphilis presenting as a penile gumma [0.03%]
既往史阳痿病：三期梅毒以阴茎树胶肿形式表现出来
Gabriel E Martin,Sharon Wang,Nolan S Maloney et al.
Gabriel E Martin et al.
A 46-year-old man presented with a rapidly growing, verrucous penile mass with bilateral inguinal lymphadenopathy, clinically consistent with locally advanced penile carcinoma. He had no history of sexually transmitted infections and negati...
Neovesicovaginal fistula due to a retained double-J stent in an ileal neobladder: surgical management and clinical considerations [0.03%]
存留双J支架引起的回肠新膀胱输尿管阴道瘘的手术治疗及临床思考
Lorena Vera Ubillús,Rocío Zavala Zavala,Segundo Gamboa Kcomt
Lorena Vera Ubillús
We report a neovesicovaginal fistula in a woman with an ileal neobladder after radical cystectomy, caused by prolonged retention of a double-J ureteral stent that became calcified. The patient presented with continuous urinary leakage and r...
Double trouble: A novel case report of synchronous bilateral renal cell carcinoma of differing histology [0.03%]
双重重症：不同组织学的同步双侧肾细胞癌的新病例报告
Andrew Shanholtzer,Sahith Kaki,Shane Daugherty et al.
Andrew Shanholtzer et al.
Renal cell carcinomas account for 2-3 % of all malignancies. In non-familial syndrome patients, another kidney tumor synchronous, antecedent, or subsequent to diagnosis of RCC is relatively rare. It is very rare for the kidney tumor to be m...