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A Peculiar Cause of Shock: Analysing Two Clinical Cases 休克的特殊原因:分析两个临床病例
Pub Date : 2023-12-02 DOI: 10.1155/2023/8901383
João Oliveira, Alberto Costa-Silva, L. Vale, D. Costa, Rui Almeida-Pinto, C. Martins-Silva, T. Antunes-Lopes, João Silva
Introduction Pheochromocytoma is a rare neoplasia arising from the adrenal medulla that secretes catecholamines. Those afflicted by this condition can present a wide range of symptoms. One of the most common is paroxysmic hypertension. Interestingly, although rare, some patients present with shock. We describe two cases of pheochromocytoma in which the initial presentation was shock. Case 1. 49 year-old woman, with a history of resistant hypertension, presented to the emergency department with thoracic pain and fever. EKG, echocardiogram (ECC), and myocardial necrosis markers were compatible with Takotsubo syndrome (TS). CT demonstrated a staghorn calculus, hydronephrosis, and signs compatible with xanthogranulomatous pyelonephritis in the right kidney. Additionally, and incidentally, it revealed a 60 mm nodule on the right adrenal gland. Piperacillin/tazobactam was started immediately, and the patient was submitted to urgent upper urinary tract drainage. This procedure was complicated by a cardiorespiratory arrest that was treated with adrenaline administration. The patient was admitted to the ICU due to multifactorial shock and started alpha and, posteriorly, beta blockage. Biochemical adrenal incidentaloma endocrinologic study was negative (under hemodialysis). Multiorgan failure progressively improved. After 2 weeks, the patient was submitted to a laparoscopic transperitoneal right adrenalectomy. No complications were reported. Histological analysis revealed a pheochromocytoma. Case 2. 28-year-old woman presented to the emergency department with headaches and nausea. Vitals were compatible with shock. CT revealed an incidental 72 mm mass on the right adrenal. EKG, ECC, and myocardial necrosis markers were compatible with TS. The patient was started on alpha and, posteriorly, beta blockage. Adrenal incidentaloma endocrinological study demonstrated high urinary catecholamines. Right transperitoneal adrenalectomy was performed. No complications were noted. Histological analysis revealed a pheochromocytoma. Conclusion Pheochromocytoma can present with complex, enigmatic, and rare clinical pictures. Clinicians should be wary of the possibility of this diagnosis when managing adrenal masses.
嗜铬细胞瘤是一种罕见的肿瘤,起源于分泌儿茶酚胺的肾上腺髓质。患有这种疾病的人可能会出现各种各样的症状。其中最常见的是阵发性高血压。有趣的是,虽然罕见,但有些患者会出现休克。我们描述了两例嗜铬细胞瘤,其中最初的表现是休克。案例1。49岁女性,有顽固性高血压病史,因胸痛和发热到急诊科就诊。心电图、超声心动图(ECC)和心肌坏死标志物与Takotsubo综合征(TS)一致。CT显示右肾鹿角状结石、肾积水及黄色肉芽肿性肾盂肾炎征象。另外,顺便一提,在右肾上腺上发现了一个60毫米的结节。立即开始使用哌拉西林/他唑巴坦,患者被提交紧急上尿路引流。这一过程因心肺骤停而变得复杂,并给予肾上腺素治疗。患者因多因素休克而入住ICU,并开始α和后β阻塞。生化肾上腺偶发瘤内分泌学研究阴性(血液透析下)。多器官功能衰竭逐渐改善。2周后,患者接受腹腔镜经腹膜右肾上腺切除术。无并发症报道。组织学分析显示为嗜铬细胞瘤。例2。28岁女性因头痛和恶心到急诊室就诊。生命体征与休克相符。CT显示右肾上腺偶发72毫米肿块。心电图、ECC和心肌坏死标志物与TS一致。患者开始进行α阻滞,随后进行β阻滞。肾上腺偶发瘤内分泌学研究显示尿儿茶酚胺含量高。行右侧经腹膜肾上腺切除术。无并发症。组织学分析显示为嗜铬细胞瘤。结论嗜铬细胞瘤临床表现复杂、难解、罕见。临床医生在处理肾上腺肿块时应警惕这种诊断的可能性。
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引用次数: 0
Prune Belly Syndrome in a Female Newborn following In Vitro Fertilization-Induced Pregnancy: A Case Report and Literature Review. 体外受精诱导妊娠后女性新生儿妊娠脐综合征:病例报告和文献综述。
Pub Date : 2023-11-29 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5521590
Ibraheem M Alkhawaldeh, Jaber H Jaradat, Mohammad Al-Jafari, Abdulqadir J Nashwan, Samer Irshaid Alrahamneh

Prune belly syndrome (PBS) is a rare congenital anomaly characterized by a triad of abdominal flaccidity, varying degrees of urinary system involvement, and cryptorchidism. The exact cause of PBS is unknown. Clinical symptoms can range from stillbirth to significant renal and respiratory abnormalities to almost normal children. Treatment typically involves surgical repair of the abdominal wall defect and urinary tract abnormalities, early orchiopexy, and supportive management of related problems. We report the first case of a female newborn with PBS following in vitro fertilization-induced pregnancy with a comprehensive systematic review of all relevant cases.

槑肚综合征(PBS)是一种罕见的先天性畸形,以腹部松弛、泌尿系统不同程度受累和隐睾三联症为特征。PBS 的确切病因尚不清楚。临床症状从死胎、明显的肾脏和呼吸系统异常到几乎正常的儿童都有。治疗通常包括手术修复腹壁缺损和泌尿道异常、早期睾丸切除术以及相关问题的支持性治疗。我们报告了首例体外受精诱导妊娠后患有 PBS 的女性新生儿病例,并对所有相关病例进行了全面系统的回顾。
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引用次数: 0
Male Genital Mutilation in the Name of Ritual Circumcision: A Case Report and Literature Review. 以仪式包皮环切术为名切割男性生殖器:一例报告及文献复习。
Pub Date : 2023-10-07 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9935247
Latif Dar, Alhareth Baarimah, Saeed Alshehrani, Alhassan Alasiri, Mohammad Alassiri, Saleh Al-Ghamdi

Unlike female genital mutilation, the alteration of male genitals has not received much attention. Circumcision is the most common and oldest surgical procedure being performed. When performed by surgeons or well-trained personal the procedure is safe, but most of the times it is being performed by untrained people with no or little medical background. This has led to many complications. Total skin loss is an uncommon but serious complication. There is an ongoing debate regarding the management of this complication. Here, we present a case of total penile skin loss which had resulted from penile mutilation in the name of ritual circumcision.

与切割女性生殖器不同,男性生殖器的改变没有受到太多关注。包皮环切术是最常见和最古老的外科手术。当由外科医生或训练有素的个人进行手术时,手术是安全的,但大多数时候是由没有或几乎没有医学背景的未经训练的人进行的。这导致了许多复杂情况。皮肤完全脱落是一种罕见但严重的并发症。关于这种复杂情况的管理,目前正在进行辩论。在这里,我们提出了一个完全的阴茎皮肤损失的案例,这是由于以仪式包皮环切的名义切割阴茎造成的。
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引用次数: 0
Unusual Location of Residual Mass in an Uncorrected Undescended Testis with Germ Cell Tumor. 未矫正未发现睾丸生殖细胞肿瘤残留肿块的异常位置。
Pub Date : 2023-10-03 eCollection Date: 2023-01-01 DOI: 10.1155/2023/6626799
Navid Masoumi, Mostafa Farajpour, Atoosa Gharib

Intra-abdominal cancer in an adult with undescended testis (UDT) is rare owing to widespread screening and management during childhood. Here, we present a 33-year-old gentleman with a complaint of abdominal pain and pelvic mass which appeared to be an uncorrected UDT with cancerous degeneration. Additional evaluation revealed a suspicious mass in the retrovesical space which remained after chemotherapy. Histologic evaluation after resection of this mass indicated cancer spread of testicular origin behind the bladder.

由于儿童时期广泛的筛查和治疗,患有睾丸下发(UDT)的成年人的术中癌症是罕见的。在这里,我们介绍一位33岁的先生,他主诉腹痛和骨盆肿块,这似乎是一个未经矫正的UDT,伴有癌变。进一步评估显示,化疗后膀胱后间隙有可疑肿块。切除该肿块后的组织学评估表明,癌症起源于睾丸,在膀胱后扩散。
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引用次数: 0
First Two Cases of Conservative Treatment for Extreme Proximal Penile Fracture of the Corpora Cavernosa. 阴茎海绵体近端极端骨折保守治疗的头两个病例。
Pub Date : 2023-06-10 eCollection Date: 2023-01-01 DOI: 10.1155/2023/5706109
Alicia Blondeau, Aurélie Grandmougin, Clément Larose, Charles Mazeaud

Penile fracture is a urological emergency, and surgery is usually recommended to prevent complications. However, proximal locations are scarce and not well investigated. We present two rare penile fractures involving the proximal corpora cavernosa with an original conservative strategy to manage this clinical presentation. Twenty-five- and thirty-eight-year-old men with no previous medical history were admitted to the emergency room for penile trauma during sexual intercourse a few months apart. Both presented with "butterfly pattern" ecchymosis with a palpable hematoma on the perineum. They had no hematuria or voiding dysfunction. Ultrasound found a hematoma and a tear of the proximal corpus cavernosum for the younger one. Then, an MRI confirmed a longitudinal fracture of the right corpus cavernosum for the first patient and left for the second, without urethral injury. In agreement with the patients facing this atypical presentation, we proposed a conservative treatment with analgesics, monitoring, and advice to stop sexual activity for three weeks. After six weeks and four weeks, respectively, we performed a clinical evaluation and a second MRI that found no residual tear or hematoma. The IIEF-5 questionnaire was 24/25 and 25/25. The patients were clinically symptom-free at 8 and 11 months of follow-up. Extreme proximal fracture of the corpus cavernosum can be managed conservatively in selected situations. MRI is useful for decision-making by confirming the diagnosis and location to avoid surgery.

阴茎骨折是泌尿科急症,通常建议采用手术治疗以预防并发症。然而,近端位置的骨折很少见,而且研究也不深入。我们介绍了两例罕见的阴茎骨折,均涉及阴茎海绵体近端,并采用独创的保守策略来处理这一临床表现。25岁和38岁的男性无病史,因性交时阴茎外伤被送入急诊室,时间相隔数月。两人都出现了 "蝴蝶状 "瘀斑,会阴部可触及血肿。他们没有血尿或排尿功能障碍。超声波检查发现血肿,年轻患者的海绵体近端撕裂。然后,核磁共振检查证实,第一名患者的右侧海绵体纵向骨折,第二名患者的左侧海绵体纵向骨折,但没有尿道损伤。针对患者的这种非典型表现,我们建议采取保守治疗,使用镇痛剂,进行监测,并建议患者在三周内停止性生活。六周和四周后,我们分别进行了临床评估和第二次核磁共振成像检查,均未发现残余撕裂或血肿。IIEF-5调查问卷分别为24/25和25/25。随访8个月和11个月时,患者均无临床症状。在某些情况下,海绵体近端极端骨折可以采取保守治疗。核磁共振成像有助于通过确诊和确定位置做出决策,从而避免手术。
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引用次数: 0
Robot-Assisted Removal of a Partially Intravesical Intrauterine Device (IUD) and Large Bladder Stone. 机器人辅助移除部分膀胱内节育器(IUD)和大膀胱结石。
Pub Date : 2023-01-27 eCollection Date: 2023-01-01 DOI: 10.1155/2023/8074689
Cassandra Heaney, Paul Lee, Andrew Winer

An intrauterine device (IUD) is a highly effective and widely utilized option for long-acting reversible contraception. IUDs are generally well-tolerated with a low rate of serious complications. Perforation of an IUD through the uterine wall and into the urinary bladder is a rare event that may be asymptomatic. The approach for surgical removal primarily depends on the location of the device. We present a case report of a 41-year-old woman who was found to have a partially intravesical IUD and associated 2.4 cm bladder calculus. Removal of the intravesical IUD and stone was achieved with cystoscopy, cystolitholapaxy, and robot-assisted laparoscopic cystotomy.

宫内节育器(IUD)是一种高效且广泛使用的长效可逆避孕方法。宫内节育器通常耐受性良好,严重并发症发生率较低。宫内节育器穿过子宫壁进入膀胱是一种罕见的无症状事件。手术切除的方法主要取决于器械的位置。我们报告了一名41岁女性的病例报告,她被发现有部分膀胱内宫内节育器和相关的2.4 cm膀胱结石。通过膀胱镜检查、膀胱取石术和机器人辅助腹腔镜膀胱切开术去除膀胱内宫内节育器和结石。
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引用次数: 0
Drug-Induced Urinary Stone of Atazanavir Incidentally Found in an Asymptomatic Patient: A Case Report. 偶然在无症状患者中发现阿扎那韦药物性尿路结石一例报告。
Pub Date : 2023-01-01 DOI: 10.1155/2023/4890711
Maëlle Plawecki, Marie Bistoquet, Pierre-Edouard Grillet, Nicolas Abdo, Jean-Sébastien Souweine, Jean-Paul Cristol

A HIV-infected female treated with a combination of emtricitabine/elvitegravir/tenofovir since 2017 presented an acute renal failure during her hospitalization for a SARS-CoV2 pneumonia. A computed tomography demonstrated left ureterohydronephrosis and ureteral stone. Fragments extracted by ureteroscopy showed a calculus composed of atazanavir and calcium oxalate. The patient's medical history showed atazanavir intake during ten years and then discontinued in 2017. This case report emphasizes that drug-induced urolithiasis should be considered when renal function declines, even far from discontinuation of atazanavir and without clinical signs of renal colitis. Moreover, identification of risk factors should alert to the possibility of drug-induced nephrolithiasis.

一名自2017年以来接受恩曲他滨/艾韦替诺福韦/替诺福韦联合治疗的艾滋病毒感染女性在因SARS-CoV2肺炎住院期间出现急性肾衰竭。电脑断层显示左侧输尿管积水及输尿管结石。输尿管镜检查显示结石由阿扎那韦和草酸钙组成。患者的病史显示,10年来服用阿扎那韦,然后于2017年停药。本病例报告强调,当肾功能下降时应考虑药物性尿石症,即使没有停用阿扎那韦,也没有肾性结肠炎的临床症状。此外,危险因素的识别应警惕药物性肾结石的可能性。
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引用次数: 0
Solitary Abdominal Wall Lymph Node Recurrence in Prostate Cancer Patient with Dramatic Prostate-Specific Antigen Decrease following Metastasectomy. 前列腺癌转移切除术后前列腺特异性抗原显著降低的孤立腹壁淋巴结复发。
Pub Date : 2023-01-01 DOI: 10.1155/2023/7301284
Andrew Williams, Amr A Elbakry, Tyler Trump, Ion Prisneac, Matthew Smolkin, David Zekan, Mohamad W Salkini

Prostate cancer patients routinely undergo surveillance for recurrence using prostate-specific antigen (PSA). While PSA's benefit in screening is controversial, its use for detecting recurrence in patients with history of prostate cancer is pivotal. Rising PSAs with the newly advanced prostate-specific membrane antigen positron emission tomography (PSMA PET) can help localize the location of recurrences for better excision and management. Here, we present a 55-year-old with prostate cancer, with initially undetectable postprostatectomy PSA levels, who later presented with a PSA of 3.47 ng/mL. PSMA PET showed isolated uptake in an abdominal wall mass. Pelvic lymphadenectomy and abdominal wall mass excision were performed, confirming a single metastasis in an abdominal wall lymph node. Metastasectomy led to a dramatic drop in PSA to 0.10 ng/mL both postoperatively and on long-term follow-up. Our case illustrates the potential benefit of metastasis-directed therapy in delayed oligometastasis following definitive management of prostate cancer.

前列腺癌患者常规接受前列腺特异性抗原(PSA)监测复发。虽然PSA在筛查中的益处存在争议,但其用于检测前列腺癌病史患者的复发是至关重要的。psa与最新的前列腺特异性膜抗原正电子发射断层扫描(PSMA PET)一起上升,可以帮助定位复发部位,以便更好地切除和治疗。在这里,我们报告了一位55岁的前列腺癌患者,前列腺切除术后PSA水平最初无法检测到,后来PSA为3.47 ng/mL。PSMA PET显示腹壁肿块孤立摄取。行盆腔淋巴结切除术和腹壁肿块切除术,证实腹壁淋巴结有单一转移。在术后和长期随访中,转移瘤切除术导致PSA急剧下降至0.10 ng/mL。我们的病例说明了转移导向治疗在前列腺癌最终治疗后延迟性少转移的潜在益处。
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引用次数: 0
Priapism in a Child from Homocystinuria from Methylenetetrahydrofolate Reductase MTHFR (C677T) Mutation. 亚甲基四氢叶酸还原酶(MTHFR) (C677T)突变致同型半胱氨酸尿患儿阴茎勃起症
Pub Date : 2023-01-01 DOI: 10.1155/2023/2263341
Ameer Kakaje, Ammar Fadel, Osama Hosam Aldeen, Othman Hamdan

Priapism is a prolonged involuntary erection that can have severe complications if left untreated. Ischaemic priapism is very rare in children and requires urgent intervention to prevent permanent erectile dysfunction and penile shortening. It can be caused by ischaemia in sickle cell anaemia, leukaemia, trauma, drugs, or idiopathy. Homocystinuria is a rare autosomal recessive disorder that can cause hyperhomocysteinemia and hypercoagulability. Very few reports suggested that priapism can be caused by hyperhomocysteinemia, and they were in adults. However, we present the first of such a case to the best of our knowledge of a prepubescent child who only had the MTHFR (C677T) mutation that causes homocystinuria and had ischaemic priapism. A nine-year-old Syrian Arab boy was presented with priapism that lasted for a few hours. Blood tests show normal blood count, film, and haemoglobin electrophoresis. However, prothrombin time, partial thromboplastin time, homocysteine level, and C-reactive protein were elevated. Other coagulation tests were within the normal range. Doppler ultrasonography found decreased cavernous blood flow, and warm 0.9% saline lavage of the cavernosa was indicated and successfully treated the priapism. Genetic testing for the homozygous MTHFR (C677T) mutation was later confirmed, and warfarin was indicated. In conclusion, homocystinuria is very rare in priapism, and this is the first case to report this phenomenon in a child. Ultrasonography in low-income countries is an essential tool that helps identify a wide variety of medical conditions such as priapism and can be successfully managed by aspiration with warm saline.

阴茎勃起是一种长时间的不自主勃起,如果不及时治疗,可能会产生严重的并发症。缺血性阴茎勃起是非常罕见的儿童,需要紧急干预,以防止永久性勃起功能障碍和阴茎缩短。它可由镰状细胞性贫血、白血病、创伤、药物或自发性贫血引起。同型半胱氨酸尿是一种罕见的常染色体隐性遗传病,可引起高同型半胱氨酸血症和高凝性。很少有报告表明,高同型半胱氨酸血症可引起阴茎勃起障碍,而且是在成人中。然而,据我们所知,我们报告了首例这样的病例:一个只有MTHFR (C677T)突变导致同型半胱氨酸尿的青春期前儿童,并患有缺血性阴茎勃起。一名9岁的叙利亚阿拉伯男孩出现了持续几个小时的阴茎勃起。血液检查显示血球计数、膜和血红蛋白电泳正常。然而,凝血酶原时间、部分凝血活酶时间、同型半胱氨酸水平和c反应蛋白升高。其他凝血检查均在正常范围内。多普勒超声检查发现海绵体血流减少,提示海绵体温盐水灌洗,成功治疗了阴茎勃起。后来证实纯合子MTHFR (C677T)突变的基因检测,并指示使用华法林。总之,同型半胱氨酸尿在阴茎勃起症中是非常罕见的,这是第一例在儿童中报告这种现象。在低收入国家,超声检查是一种必不可少的工具,有助于识别各种医疗状况,如阴茎勃起,并可通过温盐水吸吸成功处理。
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引用次数: 0
Progressive Ureteropelvic Junction Obstruction and Renal Function Deterioration in Adult, Even in a Short Period of Time. 成人进行性肾盂输尿管连接处梗阻和肾功能恶化,即使在短时间内。
Pub Date : 2023-01-01 DOI: 10.1155/2023/6855975
Abbas Basiri, Behzad Narouie, Saeed Reza Ghanbarizadeh, Hamidreza Rouientan, Mohadese Ahmadzade

Introduction: The ureteropelvic junction obstruction is more common in children; however, it can also affect adults. The management of this condition has shifted toward a nonoperative approach with serial ultrasonography and renography. Case Presentation. The ureteropelvic junction obstruction imaging with significant renal function deterioration in an adult patient is described in this report. Laparoscopic exploration revealed aberrant vessels that compress the ureteropelvic junction against the lower pole of the kidney.

Conclusion: It is important to consider that some of the ureteropelvic junction obstruction cases can get worse even in a short period of time.

导读:肾盂输尿管连接处梗阻多见于儿童;然而,它也会影响成年人。这种情况的治疗已经转向非手术方法,通过连续超声检查和肾造影。案例演示。肾盂输尿管连接处梗阻成像与显著肾功能恶化的成人患者在此报告中进行了描述。腹腔镜检查发现异常血管压迫肾盂输尿管连接处,压迫肾的下极。结论:部分肾盂输尿管连接处梗阻可在短时间内恶化,应予以重视。
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引用次数: 0
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Case Reports in Urology
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