IJU Case ReportsPub Date : 2026-07-14eCollection Date: 2026-07-01DOI: 10.1002/iju5.70230
Teppei Takeshima
{"title":"Editorial Comment to Varicocelectomy Restores Spermatogenesis in Fontan-Associated Varicocele: A Two-Case Series.","authors":"Teppei Takeshima","doi":"10.1002/iju5.70230","DOIUrl":"10.1002/iju5.70230","url":null,"abstract":"","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":"e70230"},"PeriodicalIF":0.5,"publicationDate":"2026-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13368696/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148457713","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Selective Tumor-to-Tumor Metastasis of the LCNEC Component of a Combined Lung Carcinoma to Clear Cell Renal Cell Carcinoma Despite a Concurrent Meningioma.","authors":"Nakanori Fujii, Yoshinobu Hoshii, Koichiro Hiyoshi, Takanori Tokunaga, Kosuke Shimizu, Keita Kobayashi, Hiroshi Hirata, Koji Shiraishi","doi":"10.1002/iju5.70225","DOIUrl":"10.1002/iju5.70225","url":null,"abstract":"<p><strong>Introduction: </strong>Tumor-to-tumor metastasis is a rare pathological phenomenon. We report an extremely rare case in which the large cell neuroendocrine carcinoma (LCNEC) component of a combined lung carcinoma selectively metastasized to clear cell renal cell carcinoma (RCC) despite the presence of a concurrent meningioma.</p><p><strong>Case presentation: </strong>A 65-year-old man with recurrent meningioma was incidentally found to have a right lung nodule and a left renal mass. The lung tumor was diagnosed as combined LCNEC and adenocarcinoma. Partial nephrectomy revealed clear cell RCC containing a discrete metastatic focus. Hematoxylin and eosin staining showed no definitive adenocarcinoma features, whereas immunohistochemistry demonstrated CD56 and synaptophysin positivity, strongly suggesting metastasis from the LCNEC component.</p><p><strong>Conclusion: </strong>This highly selective tumor-to-tumor metastasis pattern is extremely rare, and to our knowledge, this is the first report describing selective LCNEC metastasis to RCC while sparing a synchronous meningioma.</p>","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":"e70225"},"PeriodicalIF":0.5,"publicationDate":"2026-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13364402/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148438820","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Successful Treatment of Primary Mediastinal Seminoma With Radiotherapy Following Chemotherapy Under a Bloodless Treatment Policy Based on Patient's Religious Sentiments.","authors":"Eisuke Fujii, Yoshiyuki Yamamoto, Kentaro Takezawa, Koji Hatano, Yoichi Kakuta, Atsunari Kawashima, Norio Nonomura, Taigo Kato","doi":"10.1002/iju5.70215","DOIUrl":"10.1002/iju5.70215","url":null,"abstract":"<p><strong>Introduction: </strong>Primary mediastinal seminoma is rare with a favorable prognosis when appropriately treated, and surgical resection after chemotherapy is the standard treatment. However, refusal of blood transfusion for religious reasons can limit curative surgical management.</p><p><strong>Case presentation: </strong>A 47-year-old Jehovah's Witness man was found to have a 10.8-cm anterior mediastinal tumor. Biopsy confirmed seminoma. As the patient refused transfusion, definitive chemotherapy followed by radiotherapy was selected. Three cycles of chemotherapy (etoposide, ifosfamide, and cisplatin) resulted in 44% tumor reduction and partial response. Intensity-modulated radiotherapy of the residual tumor (36 Gy in 20 fractions) achieved complete response, maintained for 11 months without recurrence or late toxicity.</p><p><strong>Conclusion: </strong>Sequential chemotherapy followed by consolidative radiotherapy appeared to be a safe and effective option for primary mediastinal germ cell tumor in the short term when surgical resection was not feasible for religious reasons.</p>","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":"e70215"},"PeriodicalIF":0.5,"publicationDate":"2026-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13364509/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148450344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
IJU Case ReportsPub Date : 2026-07-13eCollection Date: 2026-07-01DOI: 10.1002/iju5.70224
Yamato Numata, Go Kimura, Jun Akatsuka, Hikaru Mikami, Kotaro Obayashi, Yuki Endo, Hayato Takeda, Yuka Toyama, Ryuji Ohashi, Yukihiro Kondo
{"title":"Meaningful Radiographic and Metabolic Response to Enzalutamide Plus Radium-223 Therapy in Metastatic Castration-Resistant Prostate Cancer With PSA-Discordant Progression: A Case Report.","authors":"Yamato Numata, Go Kimura, Jun Akatsuka, Hikaru Mikami, Kotaro Obayashi, Yuki Endo, Hayato Takeda, Yuka Toyama, Ryuji Ohashi, Yukihiro Kondo","doi":"10.1002/iju5.70224","DOIUrl":"10.1002/iju5.70224","url":null,"abstract":"<p><strong>Introduction: </strong>The combination of enzalutamide and radium-223 has demonstrated clinical efficacy in metastatic castration-resistant prostate cancer; however, real-world evidence remains limited, particularly with PSA-discordant progression.</p><p><strong>Case presentation: </strong>A 74-year-old man with high-risk localized prostate cancer was treated with androgen deprivation therapy followed by definitive external beam radiotherapy. Eight months later, the disease progressed radiographically with extensive bone, nodal, and solitary liver metastases, while prostate-specific antigen levels remained persistently low, consistent with prostate-specific antigen-discordant progression. Bone turnover markers and disease activity markers were markedly elevated. Combination therapy with enzalutamide and radium-223 was initiated, and six cycles of radium-223 were completed. Following treatment, skeletal disease activity and bone turnover markers improved markedly. Apart from grade 3 anemia requiring transfusion, no severe adverse events occurred.</p><p><strong>Conclusion: </strong>This case suggests that enzalutamide combined with radium-223 may provide clinical benefit in metastatic castration-resistant prostate cancer with PSA-discordant progression.</p>","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":"e70224"},"PeriodicalIF":0.5,"publicationDate":"2026-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13364506/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148450361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A Hybrid Retroperitoneal-Transperitoneal Approach for Robot-Assisted Radical Nephrectomy: A Technical Report of Two Cases.","authors":"Takayuki Ohzeki, Yuto Mitsuhashi, Lan Inoki, Tsuyoshi Morita, Taiji Hayashi, Tsukasa Nishioka, Saizo Fujimoto, Kazutoshi Fujita","doi":"10.1002/iju5.70226","DOIUrl":"10.1002/iju5.70226","url":null,"abstract":"<p><strong>Introduction: </strong>Robot-assisted radical nephrectomy (RARN) can be performed using either transperitoneal or retroperitoneal approaches; however, each has inherent limitations, particularly in cases with complex hilar anatomy or post-systemic therapy fibrosis.</p><p><strong>Case presentation: </strong>Hybrid RARN was performed in two patients with renal cell carcinoma, including one who had received systemic therapy. The procedure consisted of initial retroperitoneal dissection with secure control of the renal hilum, followed by a transperitoneal nephrectomy with an expanded field. This sequential approach enabled reliable vascular control and sufficient working space for tumor resection. Perioperative outcomes were comparable to conventional RARN.</p><p><strong>Conclusion: </strong>This hybrid approach may enhance surgical flexibility and safety.</p>","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":"e70226"},"PeriodicalIF":0.5,"publicationDate":"2026-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13357014/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148438870","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A Rare Case of Suspected Immune-Related Encephalopathy Following Pembrolizumab Plus Lenvatinib Therapy for Renal Cell Carcinoma.","authors":"Yuina Nagao, Kyotaro Fukuta, Yuichiro Atagi, Keisuke Ozaki, Takeshi Nakashima, Kenta Sato, Ryoichi Nakanishi, Hirofumi Izaki, Junya Furukawa","doi":"10.1002/iju5.70227","DOIUrl":"10.1002/iju5.70227","url":null,"abstract":"<p><strong>Introduction: </strong>Immune-related encephalopathy is a rare neurological adverse event associated with immune checkpoint inhibitors. Neuroimaging and cerebrospinal fluid findings are often unremarkable, making the diagnosis challenging.</p><p><strong>Case presentation: </strong>A 70-year-old man with advanced clear cell renal cell carcinoma (RCC) was considered unresectable because of suspected adjacent organ invasion and high surgical risk. Therefore, pembrolizumab plus lenvatinib therapy was initiated, but 6 days later, he developed confusion, speech difficulty, and gait disturbance. Blood tests, whole-body computed tomography (CT), contrast-enhanced brain CT, contrast-enhanced brain magnetic resonance imaging (MRI), electroencephalography, and cerebrospinal fluid examination showed no significant abnormalities. After excluding other causes, grade 3 immune-related encephalopathy was suspected. Pembrolizumab and Lenvatinib were discontinued and high-dose corticosteroids were started, leading to subsequent neurological improvement without residual deficits.</p><p><strong>Conclusion: </strong>Immune-related encephalopathy may occur early after pembrolizumab therapy. Early recognition and prompt steroid treatment are essential for a favorable neurological recovery.</p>","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":"e70227"},"PeriodicalIF":0.5,"publicationDate":"2026-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13358212/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148438873","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Metastatic Testicular Germ Cell Tumor in a Patient With Neurofibromatosis Type 1: Treatment With Trametinib Based on <i>NF1</i> Gene Mutation.","authors":"Keita Goto, Toshiki Kijima, Yusuke Sato, Kousuke Watanabe, Hidenori Kage, Katsutoshi Oda, Tatsunori Shimoi, Kazuyuki Ishida, Haruki Kume, Takao Kamai","doi":"10.1002/iju5.70223","DOIUrl":"10.1002/iju5.70223","url":null,"abstract":"<p><strong>Introduction: </strong>Neurofibromatosis type 1 (NF1) is a genetic disorder that increases the risk of various tumors. However, its association with testicular germ cell tumors (GCTs) is rare. We report a case of metastatic GCT in an NF1 patient treated with precision medicine.</p><p><strong>Case presentation: </strong>A 40-year-old male with NF1 presented with a left testicular non-seminomatous GCT and lung metastases. The tumor showed progressive disease after chemotherapy (VIP, TGP) and surgical removal of metastases. Comprehensive genomic profiling (CGP) test found a pathogenic <i>NF1</i> frameshift mutation (p.Q514fs*43). Based on this finding, the patient received the MEK inhibitor trametinib under patient-proposed healthcare services (BELIEVE Trial). Treatment resulted in normalization of serum alpha-fetoprotein (AFP) for 6 months before the tumor eventually progressed. The patient died at 39 months after diagnosis.</p><p><strong>Conclusion: </strong>This is the first report of trametinib for a metastatic GCT with an <i>NF1</i> mutation, suggesting a possible but limited treatment effect.</p><p><strong>Trial registration: </strong>The prospective trial of patient-proposed healthcare services with multiple targeted agents based on the results of gene profiling by multigene panel test (BELIEVE), NCCH1901/jRCTs031190104.</p>","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":"e70223"},"PeriodicalIF":0.5,"publicationDate":"2026-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13349590/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148426427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Acquired Autoimmune Factor XIII Deficiency as a Novel Immune-Related Adverse Event of Combined Ipilimumab and Nivolumab Therapy for Renal Cell Carcinoma: A Case Report.","authors":"Shigeyasu Tetsushi, Koura Mikifumi, Ootsubo Satoshi, Hasegawa Shuji, Tatsugami Katsunori","doi":"10.1002/iju5.70207","DOIUrl":"10.1002/iju5.70207","url":null,"abstract":"<p><strong>Introduction: </strong>Combination therapy with immune checkpoint inhibitors (ICIs) has become the standard pharmacological treatment for renal cell carcinoma; however, careful attention must be paid to immune-related adverse events (irAEs). We report a rare case of acquired autoimmune factor XIII deficiency following ipilimumab plus nivolumab therapy.</p><p><strong>Case presentation: </strong>A 75-year-old woman who had previously undergone nephrectomy for left renal cell carcinoma developed pancreatic and pulmonary metastases and was started on combination immunotherapy. Six months after treatment initiation, she presented with bleeding symptoms. Laboratory testing revealed anti-factor XIII autoantibodies, confirming a diagnosis of acquired autoimmune factor XIII deficiency.</p><p><strong>Conclusion: </strong>To our knowledge, few reports have described this condition as an irAE. Nonetheless, other irAE-related acquired coagulation factor deficiencies-such as factor V deficiency and acquired hemophilia A-have been reported. These precedents suggest a high likelihood that the current case represents a novel manifestation of irAE.</p>","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":"e70207"},"PeriodicalIF":0.5,"publicationDate":"2026-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13345983/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148426461","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A Case of Bladder Paraganglioma With Negative Photodynamic Diagnosis Completely Resected by Staged En Bloc Transurethral Resection.","authors":"Shu Gozu, Yasukazu Nakanishi, Gaku Okumura, Erika Ikezoe, Naoki Imasato, Kohei Hirose, Madoka Kataoka, Shugo Yajima, Hitoshi Masuda","doi":"10.1002/iju5.70220","DOIUrl":"10.1002/iju5.70220","url":null,"abstract":"<p><strong>Introduction: </strong>Bladder paraganglioma can be challenging to distinguish from nonpapillary bladder cancer. Here, we report a case of nonfunctional bladder paraganglioma treated with photodynamic diagnosis-assisted en bloc transurethral resection of the bladder tumor.</p><p><strong>Case presentation: </strong>A 78-year-old man was incidentally diagnosed with a bladder tumor on imaging. Radiological and cystoscopic findings suggested bladder paraganglioma or nonpapillary urothelial carcinoma. The patient underwent en bloc transurethral resection of the bladder tumor with photodynamic diagnosis using 5-aminolevulinic acid. No fluorescence enhancement was observed during photodynamic diagnosis. Histopathological examination revealed nonfunctional bladder paraganglioma. A second-look en bloc transurethral resection with photodynamic diagnosis confirmed the absence of a residual tumor.</p><p><strong>Conclusion: </strong>This case highlights the diagnostic pitfalls of nonfunctional bladder paraganglioma presenting as a photodynamic diagnosis-negative bladder tumor and suggests that en bloc transurethral resection may be an effective organ-preserving approach in selected cases.</p>","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":"e70220"},"PeriodicalIF":0.5,"publicationDate":"2026-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13331875/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148392442","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Two Cases of Bilateral Ureteral Metastases From Prostate Cancer Initially Presenting With Postrenal Acute Kidney Injury","authors":"Hiroshi Ushida, Ryo Ikari, Hiromu Tokuchi, Yumi Manabe","doi":"10.1002/iju5.70222","DOIUrl":"10.1002/iju5.70222","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Introduction</h3>\u0000 \u0000 <p>Although prostate-specific antigen (PSA) screening has facilitated early detection of prostate cancer, approximately 5% of patients still present with distant metastases at diagnosis. Ureteral metastasis from prostate cancer is extremely rare.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Case Presentation</h3>\u0000 \u0000 <p>We report two cases of clinically diagnosed bilateral ureteral metastases in which postrenal acute kidney injury caused by bilateral hydronephrosis preceded the diagnosis of prostate cancer. Histopathological confirmation by ureteroscopic biopsy was not possible in either case. However, marked improvement in ureteral obstruction following initiation of androgen deprivation therapy supported the diagnosis.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Bilateral ureteral metastases from prostate cancer may present with acute kidney injury, and therapeutic response to androgen deprivation therapy may provide an important diagnostic clue when pathological confirmation is difficult.</p>\u0000 </section>\u0000 </div>","PeriodicalId":52909,"journal":{"name":"IJU Case Reports","volume":"9 4","pages":""},"PeriodicalIF":0.5,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13320363/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148370869","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}