Case Reports in Urology最新文献

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Nivolumab and Ipilimumab Combination Immunotherapy for Patients with Metastatic Collecting Duct Carcinoma. 纳武单抗和伊匹单抗联合免疫治疗转移性集管癌。
Case Reports in Urology Pub Date : 2021-07-02 eCollection Date: 2021-01-01 DOI: 10.1155/2021/9936330
Tetsuya Danno, Shohei Iwata, Fusako Niimi, Sachi Honda, Haruka Okada, Takeshi Azuma
{"title":"Nivolumab and Ipilimumab Combination Immunotherapy for Patients with Metastatic Collecting Duct Carcinoma.","authors":"Tetsuya Danno,&nbsp;Shohei Iwata,&nbsp;Fusako Niimi,&nbsp;Sachi Honda,&nbsp;Haruka Okada,&nbsp;Takeshi Azuma","doi":"10.1155/2021/9936330","DOIUrl":"https://doi.org/10.1155/2021/9936330","url":null,"abstract":"<p><p>Collecting duct carcinoma (CDC) is a rare, extremely aggressive form of renal cancer. Recently, immune checkpoint inhibitors (ICI), anti-programmed death-1 (PD-1) antibody, and anti-cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) antibody were approved for use against metastatic renal cell carcinoma. We herein described two cases of metastatic renal collecting duct carcinoma treated with a combination immunotherapy consisting of nivolumab and ipilimumab. In the first case, which included a bone metastasis, the best response achieved was stable disease (SD) for one year. In the second case, which was accompanied by a lung metastasis, the best response achieved was a partial response. The outcome of these cases suggested that the combination of nivolumab and ipilimumab is effective against renal collecting duct carcinoma.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270715/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39221740","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}
引用次数: 6
Clear Cell Adenocarcinoma of the Ureter Similar to Clear Cell Renal Cell Carcinoma Histology. 输尿管透明细胞腺癌与肾透明细胞癌相似。
Case Reports in Urology Pub Date : 2021-05-28 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5599014
Kazuhiro Watanabe, Go Hasegawa, Yohei Ikeda, Noboru Hara, Tsutomu Nishiyama
{"title":"Clear Cell Adenocarcinoma of the Ureter Similar to Clear Cell Renal Cell Carcinoma Histology.","authors":"Kazuhiro Watanabe,&nbsp;Go Hasegawa,&nbsp;Yohei Ikeda,&nbsp;Noboru Hara,&nbsp;Tsutomu Nishiyama","doi":"10.1155/2021/5599014","DOIUrl":"https://doi.org/10.1155/2021/5599014","url":null,"abstract":"<p><p>A 70-year-old woman was referred to our hospital with gross hematuria and diagnosed with right invasive ureteral cancer and bladder urothelial carcinoma in situ. Intravesical BCG therapy and neoadjuvant chemotherapy with carboplatin and gemcitabine were performed at the same time. Subsequently, laparoscopic right nephroureterectomy was performed. Urothelial carcinoma in situ persisted; however, most of the tumor was clear cell carcinoma. The clear cell carcinoma lesion had clear cytoplasm with round nuclei and visible nucleoli in an insular arrangement as is the case with clear cell renal cell carcinoma. No transitional lesion between clear cell adenocarcinoma and urothelial carcinoma was presented. The clear cell carcinoma lesion was GATA3 negative and HNF4<i>α</i> positive; however, the urothelial cancer lesion was GATA3 positive and HNF4<i>α</i> negative. Clear cell carcinoma was diagnosed as clear cell adenocarcinoma similar to clear cell renal cell carcinoma histology.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178004/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39238884","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}
引用次数: 0
The Management of Primary Hyperaldosteronism in a Poor Technology Environment. 低技术环境下原发性高醛固酮增多症的治疗。
Case Reports in Urology Pub Date : 2021-05-10 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6672052
Jean Sossa, Dedjinnin Josue Georges Avakoudjo, Dodji Magloire Ines Yevi, Lionelle Fanou, Gilles Natchagande, Michel Michael Agounkpe, Fred Hodonou, Yao Felicien Hounto, Felix Atadokpede
{"title":"The Management of Primary Hyperaldosteronism in a Poor Technology Environment.","authors":"Jean Sossa,&nbsp;Dedjinnin Josue Georges Avakoudjo,&nbsp;Dodji Magloire Ines Yevi,&nbsp;Lionelle Fanou,&nbsp;Gilles Natchagande,&nbsp;Michel Michael Agounkpe,&nbsp;Fred Hodonou,&nbsp;Yao Felicien Hounto,&nbsp;Felix Atadokpede","doi":"10.1155/2021/6672052","DOIUrl":"https://doi.org/10.1155/2021/6672052","url":null,"abstract":"<p><p>We report a case of Conn's adenoma in a 35-year-old female successfully managed in a poor hospital technology environment.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131141/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39034970","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}
引用次数: 0
Utilizing Colpocleisis to Repair a Vesicovaginal Fistula in a Cervical Cancer Patient with History of Pelvic Radiation: A Case Report and Literature Review. 应用阴道冲洗术修复盆腔放射史宫颈癌患者膀胱阴道瘘:1例报告并文献复习。
Case Reports in Urology Pub Date : 2021-05-05 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8865146
Ahmad Dahman, Daniel McClelland, Stanley Zaslau, Valerie Galvan Turner, Omar Duenas, Robert Shapiro
{"title":"Utilizing Colpocleisis to Repair a Vesicovaginal Fistula in a Cervical Cancer Patient with History of Pelvic Radiation: A Case Report and Literature Review.","authors":"Ahmad Dahman,&nbsp;Daniel McClelland,&nbsp;Stanley Zaslau,&nbsp;Valerie Galvan Turner,&nbsp;Omar Duenas,&nbsp;Robert Shapiro","doi":"10.1155/2021/8865146","DOIUrl":"https://doi.org/10.1155/2021/8865146","url":null,"abstract":"<p><strong>Background: </strong>Vesicovaginal fistula is a rare and distressing urological condition. It is especially prevalent in developing countries with the predominant etiology secondary to obstructed labor. Radiation therapy in female patients with cervical cancer is a risk factor for vesicovaginal fistula formation in the United States. <i>Case Presentation</i>. A 53-year-old woman with a history of cervical cancer and radiation presented with continuous urinary incontinence. Following diagnostic vaginoscopy, a 1 cm vesicovaginal fistula was diagnosed at the vaginal apex. The patient elected for surgical repair. She subsequently underwent successful transvaginal fistula closure using colpocleisis to optimally address the systemic factors of poor wound healing associated with irradiated tissue. Because of the adjacent tissue having been compromised by pelvic radiation, we opted to use a biologic graft made of human cadaveric pericardial tissue (CPT) instead of a native tissue flap to provide additional support for the fistula repair.</p><p><strong>Conclusion: </strong>A transvaginal approach for surgical repair of vesicovaginal fistula can be successful in patients with a prior history of pelvic radiation. Transvaginal colpocleisis is a viable option to augment vesicovaginal fistula repair for patients with significant comorbidities when sexual intercourse is no longer desired.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8118741/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39019204","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}
引用次数: 3
Asynchronous Bilateral Ureteric-Arterial Fistula: Diagnosis and Treatment. 非同步双侧输尿管-动脉瘘的诊断与治疗。
Case Reports in Urology Pub Date : 2021-05-03 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5590432
Pietro Pepe, Letterio D'Arrigo, Domenico Patane', Ludovica Pepe, Giuseppe Candiano, Michele Pennisi
{"title":"Asynchronous Bilateral Ureteric-Arterial Fistula: Diagnosis and Treatment.","authors":"Pietro Pepe,&nbsp;Letterio D'Arrigo,&nbsp;Domenico Patane',&nbsp;Ludovica Pepe,&nbsp;Giuseppe Candiano,&nbsp;Michele Pennisi","doi":"10.1155/2021/5590432","DOIUrl":"https://doi.org/10.1155/2021/5590432","url":null,"abstract":"<p><p>A 48-year-old woman submitted to anterior exenteration plus ileal-cutaneous conduit for metastatic cervical cancer during the change of the ureteral stent showed massive bleeding in the left ureter. A selective intra-arterial angiography showed a fistula between the ureter and the left common iliac artery that the interventional radiologist quickly repaired by inserting a vascular endoprosthesis. Six months later, gross hematuria secondary to right ureter-iliac fistula occurred again and a second endoprosthesis was inserted. Asynchronous bilateral ureteric stent-related vascular fistula is an uncommon scenario, but it should be suspected in the presence of hematuria following ureteral stent replacement.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110400/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38996886","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}
引用次数: 1
Leptomeningeal Carcinomatosis in Urothelial Carcinoma of the Urinary Bladder: A Report of a Patient with a Fulminant Course Who Died of Cancer after Definitive Therapies. 尿路上皮性膀胱癌的轻脑膜癌:一名患者在经过明确的治疗后死于癌症的暴发性病程。
Case Reports in Urology Pub Date : 2021-04-30 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5543939
Masayuki Tomioka, Makoto Kawase, Daiki Kato, Manabu Takai, Koji Iinuma, Kengo Horie, Keita Nakane, Natsuko Suzui, Tatsuhiko Miyazaki, Takuya Koie
{"title":"Leptomeningeal Carcinomatosis in Urothelial Carcinoma of the Urinary Bladder: A Report of a Patient with a Fulminant Course Who Died of Cancer after Definitive Therapies.","authors":"Masayuki Tomioka,&nbsp;Makoto Kawase,&nbsp;Daiki Kato,&nbsp;Manabu Takai,&nbsp;Koji Iinuma,&nbsp;Kengo Horie,&nbsp;Keita Nakane,&nbsp;Natsuko Suzui,&nbsp;Tatsuhiko Miyazaki,&nbsp;Takuya Koie","doi":"10.1155/2021/5543939","DOIUrl":"https://doi.org/10.1155/2021/5543939","url":null,"abstract":"<p><p>A 45-year-old Japanese man visited a community hospital with the chief complaint of asymptomatic macrohematuria. He was diagnosed with muscle-invasive bladder cancer (MIBC), and he received intra-arterial chemotherapy followed by radiation therapy at another institution. Twenty-eight months after chemoradiotherapy, magnetic resonance imaging (MRI) revealed MIBC recurrence. After neoadjuvant chemotherapy, robot-assisted radical cystectomy was performed. Pathological examination indicated high-grade urothelial carcinoma with lymphovascular invasion, a positive surgical margin, and skip lesions of cancer cells in the perivesical adipose tissue. Three months after surgery, he was brought to our hospital in an ambulance with the chief complaint of rotatory vertigo and was speaking inarticulately. Head and whole spine MRI revealed meningeal metastasis along both the vestibulocochlear nerves and cauda equina. Analysis of the cerebrospinal fluid revealed malignant cells. The patient was diagnosed with leptomeningeal carcinomatosis originating from the MIBC. He received whole-brain radiotherapy followed by the administration of pembrolizumab. Unfortunately, the patient's condition quickly deteriorated, and he died of cancer 4 months after surgery.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8105107/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38998743","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}
引用次数: 2
Rare Associations with Posterior Urethral Valves. 尿道后瓣膜的罕见关联。
Case Reports in Urology Pub Date : 2021-04-26 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6647692
Ahmed Osama Mohamed, Bala Eradi, Anthony Owen, Ashok Rajimwale
{"title":"Rare Associations with Posterior Urethral Valves.","authors":"Ahmed Osama Mohamed, Bala Eradi, Anthony Owen, Ashok Rajimwale","doi":"10.1155/2021/6647692","DOIUrl":"10.1155/2021/6647692","url":null,"abstract":"<p><p>Posterior urethral valves are a common cause of congenital bladder outlet obstruction. Known associations include cardiac malformations and gastrointestinal abnormalities. In this case series, we report on two cases of PUV associated with anorectal malformations along with a case of PUV in monochorionic diamniotic twins. We explore the difficulty in achieving a diagnosis and the final management. The association of posterior urethral valves in a patient with anorectal malformation should be suspected in case of associated oligohydramnios or oliguria postnatally. There should be a high index of suspicion in twin pregnancy even if only one of the twins is suspected of bladder outlet obstruction.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096564/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38988986","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}
引用次数: 0
Complaint of Testicular Discomfort in Patient with Esophageal Adenocarcinoma. 食管癌患者睾丸不适的主诉。
Case Reports in Urology Pub Date : 2021-04-19 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6692578
Kevin Krughoff, Alan Schned, Bing Ren, Vernon M Pais
{"title":"Complaint of Testicular Discomfort in Patient with Esophageal Adenocarcinoma.","authors":"Kevin Krughoff,&nbsp;Alan Schned,&nbsp;Bing Ren,&nbsp;Vernon M Pais","doi":"10.1155/2021/6692578","DOIUrl":"https://doi.org/10.1155/2021/6692578","url":null,"abstract":"<p><p>We report a case of esophageal cancer with solitary metastasis to the testicle in a 71-year-old man. The tumor was picked up on physical exam following new onset complaints of pain and swelling. While most testicular masses in older men are due to lymphoma, this case highlights the need to consider metastatic disease as a source of new symptoms in patients with a recent cancer diagnosis.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-04-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079193/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38910581","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}
引用次数: 2
Rare Case of Multiple Perirenal, Extra-Adrenal Myelolipoma: Case Report, Current Management Options, and Literature Review. 罕见多发性肾周、肾上腺外骨髓瘤:病例报告、当前治疗方案及文献回顾。
Case Reports in Urology Pub Date : 2021-04-13 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6614641
Goran Benko, Andrina Kopjar, Marin Plantak, Danijel Cvetko, Vicko Glunčić, Anita Lukić
{"title":"Rare Case of Multiple Perirenal, Extra-Adrenal Myelolipoma: Case Report, Current Management Options, and Literature Review.","authors":"Goran Benko,&nbsp;Andrina Kopjar,&nbsp;Marin Plantak,&nbsp;Danijel Cvetko,&nbsp;Vicko Glunčić,&nbsp;Anita Lukić","doi":"10.1155/2021/6614641","DOIUrl":"https://doi.org/10.1155/2021/6614641","url":null,"abstract":"Extra-adrenal myelolipomas are rare, asymptomatic entities, although large tumors may cause local symptoms or hemorrhage. When these lesions occur outside the adrenals in the retroperitoneum, they are radiographically easily confused with both primary and secondary retroperitoneal tumors, which tend to be aggressive. Although myelolipomas are benign and can be managed conservatively, if malignancy is suspected, a surgical procedure is an option. We report a case of a 68-year-old patient with multiple perirenal extra-adrenal myelolipomas. Initial abdominal ultrasound reviled an inhomogeneous mass surrounding the left kidney. Subsequent CT examination of the abdomen showed four separate, extrarenal, well-circumscribed, round-shaped, fat-containing retroperitoneal tumors. Given the significant size of the masses, that compressed major abdominal vessels and the suspicion of liposarcoma, a surgical excision of the lesions was performed. The tumors were easily separated, all surrounding structures were spared, and they were removed completely. Histologically, all masses consisted of hematopoietic and mature fat tissue and the final diagnosis was extra-adrenal myelolipoma. The patient was released from the hospital 7th day after surgery in good condition and at his baseline. Since myelolipomas are, by definition, nonfunctional benign tumors, there was no need for further follow-up. The radiological evaluation and fine needle biopsy are usually sufficient to establish the diagnosis, but in some cases of well-differentiated liposarcoma, the differentiation between myelolipoma and liposarcoma can be challenging. Therefore, considering that myelolipomas and liposarcomas have opposite prognoses, which affects the surgeon's decision on the extent of surgical procedure and further treatment, we also emphasize the importance of intraoperative assessment of the tumor, both by the surgeon and by intraoperative pathology consultation.","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8057894/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38873995","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}
引用次数: 1
An Intratumoral Aneurysm and an Extrarenal Synchronous Cystic Tumour in a Case of a Renal Cell Carcinoma. 肾细胞癌一例瘤内动脉瘤和肾外同步囊性肿瘤。
Case Reports in Urology Pub Date : 2021-04-06 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8878429
Supun De Silva, Lalani De Silva, Susantha De Silva, Priyani Amarathunga
{"title":"An Intratumoral Aneurysm and an Extrarenal Synchronous Cystic Tumour in a Case of a Renal Cell Carcinoma.","authors":"Supun De Silva,&nbsp;Lalani De Silva,&nbsp;Susantha De Silva,&nbsp;Priyani Amarathunga","doi":"10.1155/2021/8878429","DOIUrl":"https://doi.org/10.1155/2021/8878429","url":null,"abstract":"<p><strong>Background: </strong>Renal cell carcinoma is a heterogeneous group of malignant tumors originating from the kidney. We report a case of a renal cell carcinoma with two very rare associates, i.e., a large intratumoral aneurysm and a synchronous extrarenal cystic tumor outside the main tumor. <i>Case Presentation</i>. A 31-year-old woman, who presented with painless hematuria and loin pain, was diagnosed to have a large renal mass measuring 15 × 9 × 8.5 cm with an intralesional arterial aneurysm measuring 4.5 × 3.5 cm on radiological examination. During surgery, a separate cystic tumor measuring 5 × 4.5 × 4 cm with distinct vascular supply was noted anteromedial to the kidney, in addition to the renal mass. The histology of the main tumor was compatible with t(6:11) type microphthalmia-associated transcription factor (MiT) family translocation RCC. The aneurysm was of venous origin histologically, and a radiologically demonstrable arteriovenous fistula was recognized retrospectively. The extrarenal cyst has also showed similar histology to that of main tumor and had no evidence of a degenerated lymph node. <i>Discussion</i>. Although few cases were reported with various vascular anomalies associated with a renal tumor, this is the first ever case to find an arteriovenous fistula with a secondary venous aneurysm located inside a malignant renal mass. Similarly, no solid RCC is reported to present with an extrarenal malignant cystic nodule. The prognostic and oncological significance of the extrarenal malignant cyst is unclear. Both of these extraordinary features of this case were not properly identified on preoperative imaging. Reviewing the preoperative imaging when pathology reports are available helps to overcome difficulties in making the final diagnosis of complex cases.</p><p><strong>Conclusion: </strong>RCCs can house vascular anomalies like arteriovenous fistula and venous aneurysms and can exist with concomitant extrarenal malignant cystic nodules.</p>","PeriodicalId":30323,"journal":{"name":"Case Reports in Urology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-04-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8046523/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38814433","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}
引用次数: 0
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