Intrarenal parapelvic cysts presenting as allograft dysfunction 10 years post-renal transplantation: a case report [0.03%]
移植后十年因肾功能障碍发现并报道肾内盂旁囊肿一例
Hyunwoong Harry Chae,Terri Ser,David Harriman et al.
Hyunwoong Harry Chae et al.
Parapelvic cysts (PPCs) are rare renal cysts that can masquerade as ureteric obstruction and hydronephrosis on imaging. We describe an atypical case of intrarenal PPCs in a renal allograft that presented 10 years post-transplantation with g...
A rare case of successful treatmeat of xanthogranulomatous prostatitis and literature reviews [0.03%]
Xanthogranulomatous前列腺炎的一例罕见成功治疗病例及文献复习
Yuli Zheng,Xiaoxuan Wang,Shanfang Tang
Yuli Zheng
Xanthogranulomatous prostatitis (XGP) is extremely rare, and its clinical symptoms or imaging findings are difficult to distinguish from those of prostate cancer. This patient presented clinically with severe urinary tract infection and uri...
Not all penile tumours are alike: A rare case of penile melanoma [0.03%]
并非所有的阴茎肿瘤都一样：一例罕见的阴茎黑色素瘤病例报告
Miguel Gil,José Cabrita Carneiro,Ana Meireles et al.
Miguel Gil et al.
Penile melanoma is a rare neoplasm with aggressive biological behaviour and a dismal prognosis. We report the case of a 65-year-old male with a pigmented nodular lesion on the glans. Histopathology confirmed the diagnosis of penile melanoma...
Jun Yang,Yuan-Yuan Zhu,Shao-Jun Li
Jun Yang
Xanthogranulomatous Prostatitis (XGP) is a rare benign inflammatory condition of the prostate. Patients typically present with lower urinary tract symptoms or elevated serum prostate-specific antigen (PSA) levels. Differentiating XGP from p...
Intra-abdominal seminoma in polyorchidism with ipsilateral vanishing testis syndrome: A rare case report [0.03%]
多睾症合并同侧睾丸消失征的腹腔内精原细胞瘤一例报告
Joshua David Bruinsma,Matthew Chau,Hugo C Temperley et al.
Joshua David Bruinsma et al.
Polyorchidism is a rare anomaly, often associated with cryptorchidism and risk of malignancy. Vanishing testis syndrome results from antenatal torsion with resorption. A 38-year-old male with prior orchiectomy for atrophic testis presented ...
Complete extrarenal migration of a double-J ureteral stent following ureteral stone management: A case report [0.03%]
双J尿管支架经非泌尿系统异位1例报告
Maachi Youssef,Elafari Amine,Bentaleb Youssef et al.
Maachi Youssef et al.
Ureteral stenting is widely used to relieve obstruction, but rare complications such as migration may occur. We report a 60-year-old woman with recurrent nephrolithiasis who presented with pyelonephritis due to a left ureteral stone. After ...
Scary varicocele secondary to gonadal vessel paraganglioma - A rare case report [0.03%]
罕见的阴囊血管副神经节瘤引起的阴囊静脉曲张病例报告
Aamir Bashir Raina,Sajad Ahmad Para,Ghulam Mustafa et al.
Aamir Bashir Raina et al.
Varicocele is the most common non-ductal surgically correctable pathology affecting the male reproductive potential. It is more common on left side. Solitary right side varicocele is infrequent and if identified, pathologies like renal tumo...
Unexpected complete resolution of intravesical inflammatory myofibroblastic tumor after immunotherapy for melanoma: A case report [0.03%]
免疫治疗黑色素瘤后膀胱炎性肌纤维母细胞肿瘤的意外完全缓解：病例报告
Michael Lesgart,Steven Leonard,Francesca Montanaro et al.
Michael Lesgart et al.
Inflammatory myofibroblastic tumors (IMT) are exceedingly rare, particularly when originating in the bladder. Complete surgical resection is the gold standard treatment for IMTs. We describe a case of IMT of the urinary bladder that achieve...
High-grade undifferentiated prostatic sarcoma with heterologous differentiation: A rare case report and literature review [0.03%]
高级别异质性分化前列腺肉瘤一例报告及文献复习
Abenezer Bogale Abera,Lijalem Mekonnen Geremew,Hailemaryam Shiferaw et al.
Abenezer Bogale Abera et al.
Primary prostatic sarcomas are extremely rare, accounting for less than 0.1 % of prostatic malignancies. They arise from mesenchymal stromal cells and exhibit aggressive behavior. We report a 45-year-old man with progressive lower urinary t...
Low-grade non-muscle-invasive urothelial carcinoma of the bladder in a 16-year-old boy with UGT1A1 polymorphism and Gilbert's syndrome: A case report [0.03%]
UGT1A1基因多态性和吉莱尔氏症患者16岁男孩低级别非肌层浸润性膀胱尿路上皮癌一例报告
Madhavan N,Balabhaskar H,Nirmal Kp et al.
Madhavan N et al.
Bladder cancer in the pediatric and adolescent population is exceedingly rare.Genetic susceptibility factors, including polymorphisms in phase II detoxifying enzymes, may play a role in early tumorigenesis. We report the case of a 16-year-o...