Journal of Case Reports and Images in Urology最新文献

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Pulmonary alveolar microlithiasis with calcifications in the seminal vesicles and prostate causing infertility: A case report 肺泡微石症伴精囊和前列腺钙化导致不育:病例报告
Journal of Case Reports and Images in Urology Pub Date : 2024-08-08 DOI: 10.5348/100045z15nr2024cr
Nezha Reguig, Mohamed Anouar Messaoudi, Wafae Omari, Mohammed Aharmim, Mouna Soualhi, Rachida Zahraoui
{"title":"Pulmonary alveolar microlithiasis with calcifications in the seminal vesicles and prostate causing infertility: A case report","authors":"Nezha Reguig, Mohamed Anouar Messaoudi, Wafae Omari, Mohammed Aharmim, Mouna Soualhi, Rachida Zahraoui","doi":"10.5348/100045z15nr2024cr","DOIUrl":"https://doi.org/10.5348/100045z15nr2024cr","url":null,"abstract":"\u0000 Introduction: Pulmonary alveolar microlithiasis (PAM) is a rare hereditary disease caused by the mutation of the SLC34A2 gene, characterized by the deposition of calcium phosphate microliths throughout the alveolar spaces. Calcifications have also been reported in other organs such as the genitalia of male patients and can be associated with infertility cases. Our case report is the first Moroccan case reported in the literature of a male with PAM and infertility.\u0000\u0000 Case Report: We present a case of a 47-year-old male patient (Moroccan, North African) presented with complaints of persistent grade I dyspnea for the last six years. He also claimed primary infertility of 20 years since marriage, PAM was diagnosed based on the typical appearance of the chest and pelvic high resolution computed tomography (HRCT). The infertility was due to distal obstruction of the seminal tract by small calcifications similar to pulmonary microliths. Low dose inhaled corticosteroids/long-acting beta2-agonists (ICS-LABA) was started as a treatment of symptoms with good control of symptoms.\u0000\u0000 Conclusion: Pulmonary alveolar microlithiasis is a rare autosomal recessive disorder not easily described because of its rarity worldwide, its clinical course, and its evolution. Its association with infertility may be more common than is currently known, suggests the need to make a particularly close examination of the chest X-ray in some cases of male infertility.\u0000","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"58 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141928915","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Renal artery embolization in a case of renal cell carcinoma with intractable hematuria with acute myocardial infarction 肾细胞癌伴顽固性血尿和急性心肌梗死病例中的肾动脉栓塞术
Journal of Case Reports and Images in Urology Pub Date : 2024-07-03 DOI: 10.5348/100044z15ls2024cr
Laxmi Kant Sharma, Madhu Sudan Agrawal, Naveen Kumar, Anurag Yadav, Dilip Mishra, Gaurav Sharma
{"title":"Renal artery embolization in a case of renal cell carcinoma with intractable hematuria with acute myocardial infarction","authors":"Laxmi Kant Sharma, Madhu Sudan Agrawal, Naveen Kumar, Anurag Yadav, Dilip Mishra, Gaurav Sharma","doi":"10.5348/100044z15ls2024cr","DOIUrl":"https://doi.org/10.5348/100044z15ls2024cr","url":null,"abstract":"\u0000 Introduction: Renal artery embolization is a valuable treatment option for various renal tumors, both malignant and benign. The indications for this procedure include preoperative arterial embolization of large and vascular renal cell carcinoma to reduce intraoperative hemorrhagic complications, management of malignant renal tumors in patients who are not suitable candidates for surgery, treatment of symptomatic hematuria and palliative care for metastatic renal cancer.\u0000\u0000 Case Report: In this case report, we present the case of a 56-year-old female with a known history of hypertension and cerebrovascular accident, who presented with complaints of hematuria and urinary retention. A diagnosis of left renal mass suggestive of renal cell carcinoma was made. The patient was planned for left radical nephrectomy and advised to discontinue aspirin for a week. However, on the morning of surgery, she experienced acute myocardial infarction and had to be hospitalized in intensive cardiac care. Aspirin was restarted, leading to recurrent severe hematuria. The patient underwent renal artery embolization, which successfully controlled the hematuria. Following cardiac stabilization, radical nephrectomy was performed three months later. The surgery and post-operative period were uneventful.\u0000\u0000 Conclusion: This case study demonstrates the use of renal artery embolization as an effective modality for controlling hematuria, and temporizing management in a case of renal cell carcinoma where surgery was not immediately feasible due to a medical emergency.\u0000","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"152 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141681683","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Paraganglioma in paratesticular: A rare case report 睾丸旁副神经节瘤:罕见病例报告
Journal of Case Reports and Images in Urology Pub Date : 2024-04-05 DOI: 10.5348/100043z15aa2024cr
Ahmed Mousa Almuhanna, Basim Alghorairy, Turki H Alessawi, Sara Sameer Albagshi, Abdulrahman Alhazeem, Hussain M AlModhi
{"title":"Paraganglioma in paratesticular: A rare case report","authors":"Ahmed Mousa Almuhanna, Basim Alghorairy, Turki H Alessawi, Sara Sameer Albagshi, Abdulrahman Alhazeem, Hussain M AlModhi","doi":"10.5348/100043z15aa2024cr","DOIUrl":"https://doi.org/10.5348/100043z15aa2024cr","url":null,"abstract":"\u0000 Paraganglioma at a paratesticular location is extremely rare. We report a 58-year-old Saudi male presented with two years history of right painless scrotal mass. On physical examination the scrotum revealed a right-sided non-tender mass not attached to right testis. Normal tumor markers of testicular tumor. Ultrasonography revealed a well-defined, homogeneous, hyperechoic lesion measuring approximately 2 cm in the right extratesticular region. Magnetic resonance imaging (MRI) with intravenous (IV) gadolinium contrast for abdominal and pelvis showed right extratesticular soft tissue mass not separable from the spermatic cord and there was no distant metastasis. The patient underwent exploratory excision of the mass with preservation of cord and testis. Histopathology showed paratesticular paraganglioma.\u0000","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"17 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140738984","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Septic shock secondary to xanthogranulomatous pyelonephritis: A case report and literature review 黄疽性肾盂肾炎继发的脓毒性休克:病例报告和文献综述
Journal of Case Reports and Images in Urology Pub Date : 2024-03-27 DOI: 10.5348/100042z15cj2024cr
Cesar Alberto Lopez Jaime, Armando Alonso Morales, Carlos Tadeo Perzabal Avilez, Francisco Netzahualc Hernandez Garza
{"title":"Septic shock secondary to xanthogranulomatous pyelonephritis: A case report and literature review","authors":"Cesar Alberto Lopez Jaime, Armando Alonso Morales, Carlos Tadeo Perzabal Avilez, Francisco Netzahualc Hernandez Garza","doi":"10.5348/100042z15cj2024cr","DOIUrl":"https://doi.org/10.5348/100042z15cj2024cr","url":null,"abstract":"\u0000 Introduction: Xanthogranulomatous pyelonephritis is described by histopathology as a destruction of the renal parenchyma and replaced by a chronic infiltrate of lipid-laden macrophages. It is known that patients with xanthogranulomatous pyelonephritis have a high rate of perioperative and postoperative morbimortality; however, there are few case reports on this entity.\u0000\u0000 Case Report: A 35-year-old woman attended the emergency department due to the presence of pain in the left flank, accompanied by an altered state of consciousness and respiratory distress. The study protocol started, identifying a significant increase in the left kidney, the presence of a central staghorn stone, dilated minor calices, and clinically with septic shock. The clinical conditions improved by adding intravenous fluids, vasoactive amines, red blood cells concentrates, and broad-spectrum antibiotics. Subsequently, a left nephrectomy was performed. On the following days, the septic shock gradually resolved, leading to the patient’s discharge. Eventually, histopathology report was reviewed, confirming a xanthogranulomatous pyelonephritis.\u0000\u0000 Conclusion: When a xanthogranulomatous pyelonephritis clinical suspicion is found, it is considered a surgical emergency. Furthermore, if proper management is not given immediately, there is a high risk of complications and death. However, the current statistics in Mexico have not been updated to contrast these data.\u0000","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"40 17","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140373875","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Which came first? An association between Fournier’s gangrene and a presentation of priapism 哪个先出现?福尼尔坏疽与前列腺增生之间的联系
Journal of Case Reports and Images in Urology Pub Date : 2024-02-15 DOI: 10.5348/100041z15js2024cr
Jordan Sarver, Remington Farley, Alexander Tapper
{"title":"Which came first? An association between Fournier’s gangrene and a presentation of priapism","authors":"Jordan Sarver, Remington Farley, Alexander Tapper","doi":"10.5348/100041z15js2024cr","DOIUrl":"https://doi.org/10.5348/100041z15js2024cr","url":null,"abstract":"\u0000 Introduction: Fournier’s gangrene and priapism are two urological emergencies that have a similar goal of prompt surgical evaluation.\u0000\u0000 Case Report: A 62-year-old male was presented for perineal pain along with a rigid phallus. He was found to have a necrotizing infection of his suprapubic region, scrotum, phallus, and corporal bodies associated with a presentation of priapism.\u0000\u0000 Conclusion: Prior case studies have reported isolated Fournier’s gangrene to the penile shaft, corpora of the penis, and even more unique in the penile corpora with an associated diagnosis of priapism. Here we present one of the only known cases of Fournier’s gangrene associated with a presentation of priapism.\u0000","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"41 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139775132","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Which came first? An association between Fournier’s gangrene and a presentation of priapism 哪个先出现?福尼尔坏疽与前列腺增生之间的联系
Journal of Case Reports and Images in Urology Pub Date : 2024-02-15 DOI: 10.5348/100041z15js2024cr
Jordan Sarver, Remington Farley, Alexander Tapper
{"title":"Which came first? An association between Fournier’s gangrene and a presentation of priapism","authors":"Jordan Sarver, Remington Farley, Alexander Tapper","doi":"10.5348/100041z15js2024cr","DOIUrl":"https://doi.org/10.5348/100041z15js2024cr","url":null,"abstract":"\u0000 Introduction: Fournier’s gangrene and priapism are two urological emergencies that have a similar goal of prompt surgical evaluation.\u0000\u0000 Case Report: A 62-year-old male was presented for perineal pain along with a rigid phallus. He was found to have a necrotizing infection of his suprapubic region, scrotum, phallus, and corporal bodies associated with a presentation of priapism.\u0000\u0000 Conclusion: Prior case studies have reported isolated Fournier’s gangrene to the penile shaft, corpora of the penis, and even more unique in the penile corpora with an associated diagnosis of priapism. Here we present one of the only known cases of Fournier’s gangrene associated with a presentation of priapism.\u0000","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"251 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139834966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Congenital unilateral absence of the vas deferens 先天性单侧输精管缺失
Journal of Case Reports and Images in Urology Pub Date : 2024-02-13 DOI: 10.5348/100040z15wo2024cr
Winston Owens, Jonathan Hakim
{"title":"Congenital unilateral absence of the vas deferens","authors":"Winston Owens, Jonathan Hakim","doi":"10.5348/100040z15wo2024cr","DOIUrl":"https://doi.org/10.5348/100040z15wo2024cr","url":null,"abstract":"\u0000 Introduction: A 65-year-old male with a known history of unilateral renal agenesis was found to have concurrent absence of the vas deferens ipsilaterally.\u0000\u0000 Case Report: The patient presented with organic erectile dysfunction and wanted to proceed with surgical management. Routine pre-operative evaluation confirmed history of a left solitary kidney, and physical exam revealed absence of the right vas deferens. Previous imaging confirmed right renal agenesis, and with subsequent absence of the right vas deferens noted on physical exam, this confirmed embryological arrest as the cause of the anatomic abnormality.\u0000\u0000 Conclusion: Congenital unilateral absence of the vas deferens (CUAVD) is an uncommon finding that is largely found during infertility evaluations and vasectomy consults. It is important to understand genetic components and embryological origins of CUAVD to appropriately evaluate patients for additional defects.\u0000","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"72 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139780345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Congenital unilateral absence of the vas deferens 先天性单侧输精管缺失
Journal of Case Reports and Images in Urology Pub Date : 2024-02-13 DOI: 10.5348/100040z15wo2024cr
Winston Owens, Jonathan Hakim
{"title":"Congenital unilateral absence of the vas deferens","authors":"Winston Owens, Jonathan Hakim","doi":"10.5348/100040z15wo2024cr","DOIUrl":"https://doi.org/10.5348/100040z15wo2024cr","url":null,"abstract":"\u0000 Introduction: A 65-year-old male with a known history of unilateral renal agenesis was found to have concurrent absence of the vas deferens ipsilaterally.\u0000\u0000 Case Report: The patient presented with organic erectile dysfunction and wanted to proceed with surgical management. Routine pre-operative evaluation confirmed history of a left solitary kidney, and physical exam revealed absence of the right vas deferens. Previous imaging confirmed right renal agenesis, and with subsequent absence of the right vas deferens noted on physical exam, this confirmed embryological arrest as the cause of the anatomic abnormality.\u0000\u0000 Conclusion: Congenital unilateral absence of the vas deferens (CUAVD) is an uncommon finding that is largely found during infertility evaluations and vasectomy consults. It is important to understand genetic components and embryological origins of CUAVD to appropriately evaluate patients for additional defects.\u0000","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"104 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139840283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Incidental discovery of seminoma after simple orchiectomy in transgender individuals: A case series 变性人单纯睾丸切除术后意外发现精索瘤:病例系列
Journal of Case Reports and Images in Urology Pub Date : 2023-12-08 DOI: 10.5348/100038z15tt2023cs
Telisha Tausinga, Liem Snyder, Jonathon Mahlow, Cori Agarwal, James M Hotaling, Benjamin J McCormick
{"title":"Incidental discovery of seminoma after simple orchiectomy in transgender individuals: A case series","authors":"Telisha Tausinga, Liem Snyder, Jonathon Mahlow, Cori Agarwal, James M Hotaling, Benjamin J McCormick","doi":"10.5348/100038z15tt2023cs","DOIUrl":"https://doi.org/10.5348/100038z15tt2023cs","url":null,"abstract":"\u0000 Introduction: Seminoma is a common malignancy reported in young, cisgender men. However, there is sparse literature describing cases of seminoma in the transgender and gender diverse patient population.\u0000\u0000 Case Series: We present two cases of seminoma incidentally discovered after simple bilateral orchiectomy performed as part of genital gender affirming surgery. In both instances, patients had not reported any testicular firmness or abnormality prior to surgery. After a thorough literature review, only two other such cases have been reported. Herein, we discuss our two cases and their implications for surgical management of suspected testicular malignancy intraoperatively, a methodical inspection of testicles removed during gender affirming surgery and providing affirming care when navigating discussions of genitalia with transgender and gender diverse patients.\u0000\u0000 Conclusion: Testicular malignancy such as seminoma may be found incidentally when transgender and gender diverse patients undergo genital gender affirming surgery. Thus, special attention is required to identify suspicious exam findings, adjust surgical techniques as indicated, and properly examine surgical specimens. As there is a significant paucity of literature surrounding testicular malignancies in the transgender and gender diverse patient population, it is crucial to continue to investigate how to provide affirming care in these situations.\u0000","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"52 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138588156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Complete left ureter replacement using appendiceal interposition 利用阑尾插管完成左输尿管置换术
Journal of Case Reports and Images in Urology Pub Date : 2023-11-24 DOI: 10.5348/100037z15mg2023cr
Marion Ghenassia, Jean Baptiste Bedel, Louis Surlemont, Christian Pfister, Lucie Vangheluwe
{"title":"Complete left ureter replacement using appendiceal interposition","authors":"Marion Ghenassia, Jean Baptiste Bedel, Louis Surlemont, Christian Pfister, Lucie Vangheluwe","doi":"10.5348/100037z15mg2023cr","DOIUrl":"https://doi.org/10.5348/100037z15mg2023cr","url":null,"abstract":"Introduction: Emergency ureteral replacement for large defect, especially in dilapidated abdominal cancer surgery remains an important surgical challenge. Several methods have been described. Here we aimed to present the complete left ureter replacement using appendix interposition, after a large resection of a rectosigmoid mass invading both ureter and iliac artery. Case Report: A 64-year-old male patient diagnosed of a rectosigmoid hinge lesion invading the ureter and iliac artery. He underwent a large tumor resection. The left ureter was cut during the surgery below the renal pelvis with a loss of substance of more than 12 cm. The procedure involved replacement of the ureter by appendix interposition, with wire drainage by transvesicoparietal catheter and a bladder catheter. Neither ureterohydronephrosis nor urinary fistula was observed at the 2-month follow-up computed tomography. Conclusion: In our experience, appendiceal interposition in extensive left ureteral defect is a feasible and safe surgical option.","PeriodicalId":400698,"journal":{"name":"Journal of Case Reports and Images in Urology","volume":"92 8","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139239099","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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