x
Filter:
Filters applied
- Molecular Biophysics
- Case ReportsRemove Case Reports filter
- LetterRemove Letter filter
Publication Date
Please choose a date range between 2021 and 2021.
Author
- Cain, Mark P2
- Cheng, Julie W2
- Ahn, Jennifer J1
- Alhalabi, Feras1
- Anderson, Jamie E1
- Arenas-Gallo, Camilo1
- Baboudjian, Michael1
- Baker, Zoë1
- Basourakos, Spyridon P1
- Bayne, Christopher E1
- Boissier, Romain1
- Braga, Luis H1
- Carmel, Maude E1
- Carpenter, Christina P1
- Chang, Andy Y1
- Chavez, Jacqueline A1
- Chertman, Willy1
- Christie, Alana L1
- Clarke, Jacob A1
- Deledalle, Francois-Xavier1
- DeMarco, Romano T1
- Diaz, Parris1
- Efimenko, Iakov1
- Falzarano, Sara M1
- Fuentes, Jorge L1
Molecular Biophysics
21 Results
- Letters to the editor
We Must Stop Misusing the Term Prostatitis
UrologyVol. 161p158–159Published online: December 11, 2021- Jeannette M. Potts
Cited in Scopus: 0Chief complaints and referrals continue to include the word “prostatitis.” A recent PubMed search revealed the persistence of “CP/CPPS” (Chronic Prostatitis/Chronic Pelvic Pain), whether mood, semen quality, weather or brain functional connectivity were being correlated, and whether the interventions employed acupuncture, psychotherapy or low intensity shockwave therapy. - Pediatric Case Reports
Bladder Cancer in a Long-term Survivor of the Prune Belly Syndrome
UrologyVol. 161p93–95Published online: December 6, 2021- Fuki Kondo
- Fumi Matsumoto
- Shinta Suenaga
- Futoshi Matsui
- Koji Yazawa
- Akira Nagahara
- and others
Cited in Scopus: 0Prune belly syndrome (PBS) is a rare but morbid complexity of congenital anomalies that consists of abdominal wall defect, bilateral cryptorchidism, and urinary tract dilation. With the recent advances in perinatal care, the life expectancy of patients with PBS has improved. Although renal and sexual outcomes are frequently discussed in the literature, little is known about urinary tract malignancies in adulthood. Herein, we present a case of advanced bladder cancer in a 38-year-old man with PBS. - Pediatric Case Reports
Ovotesticular Disorder Mimicking Acute Spermatic Cord Torsion
UrologyVol. 161p96–99Published online: November 28, 2021- Eric Midenberg
- Christopher E. Bayne
- Sara M. Falzarano
- Romano T. DeMarco
Cited in Scopus: 0Ovotesticular disorder is a rare form of sexual development in which a patient may have one ovary and one testis, or more commonly a gonad or gonads containing both ovarian and testicular tissue. Patients with this condition typically present in infancy with ambiguous genitalia. Delayed presentations of clinically symptomatic, older patients with normal external genitalia are extremely rare. We present a case of a 14-year-old male with normal external genitalia who presented with symptoms and signs consistent with spermatic cord torsion but found to have ovotesticular disorder on evaluation. - Letters to the editor
Author Reply
UrologyVol. 160p229–230Published online: November 26, 2021- Jacqueline A. Chavez
- Jorge L. Fuentes
- Alana L. Christie
- Feras Alhalabi
- Maude E. Carmel
- Gary E. Lemack
- and others
Cited in Scopus: 0It seems that their comments are generally in agreement with our viewpoints. “However, these two papers failed to report the incorrect diagnosis of SUI, and urine accumulates in the diverticulum and flows out after pressurization, which is mistaken for SUI.” The authors insist here on the challenge of diagnosing true SUI when a diverticulum is present, a condition called pseudo-incontinence, which corresponds to the emptying of the fluid content of the diverticulum pocket during stress efforts. This was discussed in several sections of our manuscript and is the main reason why we generally omit urodynamic testing in these women. - Pediatric Case Reports
Persistent Anhydramnios and Lower Urinary Tract Obstruction in a Patient With a Vesicoamniotic Shunt
UrologyVol. 165p319–321Published online: November 26, 2021- Arthi Hannallah
- Zoë Baker
- Andy Y. Chang
- Joan S. Ko
Cited in Scopus: 0Persistent anhydramnios after placement of a vesicoamniotic shunt is a rare but potentially serious concern in a patient in utero. We present the case a male fetus who at 32-week gestation had bilateral hydroureteronephrosis, a distended bladder, and anhydramnios. A vesicoamniotic shunt was placed, but the anhydramnios persisted. Postnatally, the child was found to have a migrated shunt, left grade V vesicoureteral reflux and posterior urethral valves. He underwent a posterior urethral valves ablation and removal of the migrated shunt. - Pediatric Case Reports
Bedside Intervention for Neonatal Hydrometrocolpos and Imperforate Hymen
UrologyVol. 160p191–194Published online: November 24, 2021- Lauren N. Nicassio
- Julie W. Cheng
- Mark P. Cain
Cited in Scopus: 0Low complexity cases of neonatal hydrometrocolpos from imperforate hymen are typically treated with hymenotomy or hymenectomy. Although this is commonly performed in the operating room, bedside management is also safe and effective. We present a case of prenatally diagnosed, simple hydrometrocolpos treated via bedside hymenotomy on the first day of life. The patient received periprocedural antibiotics prior to the procedure and had full resolution of hydrometrocolpos without any complication or need for further intervention. - Letters to the Editor
Stress Urinary Incontinence After Urethral Diverticulum Repair Without Concomitant Anti-Incontinence Procedure
UrologyVol. 160p229Published online: November 20, 2021- Yazheng Sun
- Bo Peng
- Jie Wu
- Qinglong Li
Cited in Scopus: 0Recently, we read the report of Chavez et al1 who demonstrated that post-urethral diverticulum (UD) repair, the rate of persistent stress urinary incontinence (SUI) was present in 14 of 31 (45%) cases, and de novo SUI occurred in 4 of 30 (13%) cases. It is controversial to perform SUI and UD surgeries simultaneously, and this paper provides new evidence about this topic. At the same time, Greiman et al demonstrated that the resolution of SUI in simultaneous surgery is 83% and the resolution is 53% in UD surgery alone. - Letters to the editor
Author Reply
UrologyVol. 160p231Published online: November 14, 2021- Lindsey N. Wright
- James Hotaling
- Alexander W. Pastuszak
Cited in Scopus: 0Thank you for your response to our article “Erectile Dysfunction and Treatment: An Analysis of Associated Chronic Health Conditions.” Your letter-to-the-editor makes thoughtful additions regarding the complexities many young men encounter in seeking healthcare. Your point on the cultural implications that impact young men when seeking preventative measures is especially noteworthy. As medicine begins to utilize telemedicine more often, it may provide a unique opportunity for young men to establish meaningful long-term rapport with providers. - Pediatric Case Reports
Nephron-Sparing Approach For Familial Bilateral Synchronous Wilms Tumors
UrologyVol. 160p199–202Published online: November 6, 2021- Victoria Turnbull
- Harkanwal Randhawa
- Yuding Wang
- Melissa McGrath
- Luis H. Braga
Cited in Scopus: 0Wilms tumors are the most common renal malignancy of childhood, often presenting as asymptomatic abdominal masses. These tumors can occur either in a unilateral or bilateral fashion, with bilateral tumors more commonly associated with various genetic syndromes and familial inheritance with some known loci. Bilateral tumors present challenges with regards to balancing oncologic control with renal function. Here, we present an unusual case of a young female patient diagnosed with bilateral Wilms tumors on the background of a strong family history and unknown genetic loci. - Letters to the Editor
“Erectile Dysfunction and Treatment: An Analysis of Associated Chronic Health Conditions”
UrologyVol. 160p230–231Published online: November 2, 2021- Erin Jesse
- Wade Muncey
- Nannan Thirumavalavan
Cited in Scopus: 0The article entitled “Erectile Dysfunction and Treatment: An Analysis of Associated Chronic Health Conditions” by Lindsey Wright et al. recently published online ahead of print in Urology 2021 Aug 21; S0090-4295(21)00782-2. highlights one of the many reasons why “Men's Health” is in need of a reformation. - Letter
Author Reply to Letter to the Editor
UrologyVol. 159p257–258Published online: October 30, 2021- Romain Boissier
- Francois-Xavier Deledalle
- Michael Baboudjian
- Eric Lechevallier
Cited in Scopus: 0We thank Kokayi et al for their interest in our study on the feasibility and outcomes of active surveillance (AS) in renal oncocytoma recently published in Urology.1 We also read with great interest their results on the growth and renal function dynamics of renal oncocytomas in patients on AS.2 It is a great satisfaction to see that our institutions share common research topics in addition to similar conclusions. - Pediatric Case Reports
Congenital Giant Megaureter in a 16-Year-Old Female Presenting With Abdominal Pain: A Case Report and Review of Literature
UrologyVol. 159p210–213Published online: October 30, 2021- Jacob A. Clarke
- Vatche Melkonian
- Tim Phillips
- Christian Saliba
- Shin Miyata
- Jose Greenspon
Cited in Scopus: 0We describe a case of congenital giant megaureter in a 16-year-old female. She presented with a 5-day history of abdominal distention, right flank pain and tenderness. Right pyelonephritis was suspected. Computerized tomography showed a large cystic abdominal mass with no appreciably functioning left kidney causing secondary compression of the contralateral right ureter. A left upper nephroureterectomy was performed, draining over 3.5 L of fluid. Our experience suggests that congenital giant megaureter should be considered in the differential for pediatric patients presenting with a cystic abdominal mass. - Letters to the Editor
Letter to the Editor-Active Surveillance for Biopsy Proven Renal Oncocytomas: Outcomes and Feasibility
UrologyVol. 159p257Published online: October 23, 2021- Adio Kokayi
- Hannah Warren
- Maxine Tran
Cited in Scopus: 0We welcome this contribution to the growing body of evidence demonstrating the safety of active surveillance (AS) for biopsy-proven renal oncocytomas. The low median growth rate of 2.4 mm/y reported in this work is in keeping with our own series1 and that of others,2,3 in which no patient has developed metastases or disease-related mortality during median follow up of 29-34 months. - Genomics Case Report
Whole Exome Sequencing Identifies a Rare Mutation in NACAD as a Possible Cause of COVID Orchitis in Brothers
UrologyVol. 159p83–86Published online: October 19, 2021- Rohit Reddy
- Iakov Efimenko
- Willy Chertman
- Taylor Kohn
- Parris Diaz
- Deepa Seetharam
- and others
Cited in Scopus: 2COVID orchitis (testicular pain) is reported in 10-15% of men with long COVID. We identified 2 siblings with COVID orchitis and hypothesized that genetic mutations are associated with susceptibility. Blood samples from 5 COVID-19 (+) men, three of whom had orchitis were evaluated by whole-exome-sequencing. A rare deletion on chromosome 7 was found in NACAD among the 3 men with orchitis. Interestingly, circulating ACE2 levels was decreased in men with COVID orchitis. This pilot study generated the hypothesis that men who develop COVID orchitis could have underlying genetic variants and altered levels in circulating ACE2 that may increase their risk. - Pediatric Case Reports
Pediatric Penile Non-Involuting Congenital Hemangioma With an Associated Pyogenic Granuloma: Surgical Management of a Rare Vascular Anomaly
UrologyVol. 158p197–199Published online: October 1, 2021- Miyad Movassaghi
- JuneK Wu
- Christina P. Carpenter
Cited in Scopus: 0Vascular anomalies include both tumors and malformations. Infantile hemangiomas are the most common benign vascular tumor of infancy that proliferate after birth and eventually involute. By contrast, congenital hemangiomas are formed at birth and are categorized into three groups: rapidly involuting, partially-involuting, and non-involuting congenital hemangiomas (NICH). NICH do not regress and grow with age. Pyogenic granulomas, another acquired vascular tumor, develop over vascular lesions and cause bleeding. - Pediatric Case Reports
Misdiagnosis of Congenital Posterior Urethroperineal Fistula and Comparison With Urethral Duplications and Rectourethral Fistula
UrologyVol. 158p193–196Published online: October 1, 2021- Julie W. Cheng
- Jennifer J. Ahn
- Mark P. Cain
- Jamie E. Anderson
- Caitlin A. Smith
- Samuel E. Rice-Townsend
Cited in Scopus: 0Congenital posterior urethroperineal fistula (CUPF) is a urothelium-lined tract between the posterior urethra and perineum. This condition is rare and has been proposed to be a urethral duplication variant. A case of CUPF that was misdiagnosed and surgically treated as a rectourethral fistula is presented. The clinical presentation, diagnosis, and treatment of CUPF are discussed and compared with those of Y-type urethral duplications and H-type rectourethral fistulas. - Pediatric Case Reports
Fluorescent Guided Lymph Node Harvest in Laparoscopic Wilms Nephroureterectomy
UrologyVol. 158p189–192Published online: October 1, 2021- Max J. Pachl
Cited in Scopus: 3Lymph node harvest is an integral part of Wilms tumor surgery with both SIOP and COG protocols asking for more than 6 lymph nodes to best evaluate for nodal spread and a subsequent need for intensification of treatment. The majority of studies show that in both open and minimally invasive resections the median number of nodes removed is 4. Indocyanine green and near infrared fluorescence may be the key to solving this problem. In adult gynaecology, colorectal and breast cancers, ICG is used to identify sentinel nodes and facilitate nodal retrieval. - Letters to the Editor
Re: Dudith Pierre-Victor, Howard L. Parnes, Gerald L. Andriole, et al. Prostate Cancer Incidence and Mortality Following a Negative Biopsy in a Population Undergoing PSA Screening. Urology 2021 Jun 26;S0090-4295(21)00539-2
UrologyVol. 156p324Published online: August 2, 2021- Patrick Lewicki
- Camilo Arenas-Gallo
- Spyridon P. Basourakos
- Bashir Al Hussein Al Awamlh
- Siv Venkat
- Douglas S. Scherr
- and others
Cited in Scopus: 0We read with great interest the recent work of Pierre-Victor et al on prostate cancer incidence and mortality in the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial.1 We previously reported, in 2017, on a similar cohort from this trial.2 We studied men in the screening arm who screened positive (via prostate-specific antigen or digital rectal exam) during the first year of the trial, and whose linked biopsy was negative. We found a similar mortality rate after a median follow-up of 12.9 years of 1.1% (vs 1.2% in the present study). - Letter
Author Reply
UrologyVol. 155p214Published online: July 16, 2021- Kathleen Kieran
Cited in Scopus: 0Dear Dr Kaufman: - Letters to the Editor
Letter to the Editor re: Gender Differences in Authorship in Urology: A Five-year Review of Publications in Five High-impact Journals
UrologyVol. 155p214Published online: July 14, 2021- Melissa R Kaufman
Cited in Scopus: 0Appreciate the contribution by Whitley et al. 1 which provides valuable perspective on female authorship in urology journals. However, there is a significant error in Table 1 listing the impact factor for the journals evaluated. The impact factor for The Journal of Urology is listed as 2.114 while the correct number for 2019 is 5.925. - Letters to the Editor
Letter-to-the-Editor ReplyReply to letter ‘Re: ‘Is Stone-Free Status After Surgical Intervention for Kidney Stones Associated with Better Health-Related Quality of Life? - A Multicenter Study from the North American Stone Quality of Life Consortium’ by Senol Tonyali (10.1016/j.urology.2020.12.044)
UrologyVol. 154e21Published online: January 22, 2021- Necole M. Streeper
- Kristina L. Penniston
Cited in Scopus: 0We thank you for your interest in our recent article evaluating patients’ HRQOL and stone-free status following kidney stone surgery. We are pleased with the dialogue our findings are generating and hope this propels the emphasis of HRQOL as an important measurement of treatment success. We acknowledge the limitations of retrospective cross-sectional studies, such as ours. Despite this, we hope our study serves as a guide for future studies.