AN UNUSUAL CASE OF LARGE PENILE URETHRAL CALCULUS WITH URETHROCUTANEOUS FISTULA IN AN ELDERLY MAN.

2021 ◽  
pp. 75-76
Author(s):  
Santosh Patil ◽  
Vinay S Kundargi ◽  
Basavesh S Patil ◽  
Abhijit Samal

Impacted penile urethral calculus complicated with urethrocutaneous stula is a rare condition. Such calculi can form as a result of urethral strictures, meatal stenosis, urethral diverticulum, and migration of stones from the proximal urinary tract. A 65 year old male presented to our emergency department with complaints of fever and urinary dribbling since 2-3 weeks and obstructive lower urinary tract symptoms since 6 months. He showed features of sepsis and a palpable bladder on examination. Xray KUB and penile USG was suggestive of a 2x1.5cm distal penile urethral calculus. In this paper we present our approach to such case.

2019 ◽  
Vol 101 (6) ◽  
pp. e139-e141
Author(s):  
S Chen ◽  
X Su ◽  
M Jiang ◽  
H Mi

Urethral diverticulum is a condition where the urethra or the periurethral glands push into the connective tissue layers that surround it. Patients of urethral diverticulum present with nonspecific symptoms such as incontinence, urinary frequency and urgency, and pain during sexual intercourse and urination. The incidence of this condition is low. We report a case of giant anterior urethra stones combined with a diverticulum with no lower urinary tract symptoms. We believe that this case is extremely rare, and the process of diagnosis and treatment is of great significance in clinical practice.


2011 ◽  
Vol 2011 ◽  
pp. 1-2 ◽  
Author(s):  
Sadat Haider Quoraishi ◽  
Faisal Khan ◽  
Dler Besarani ◽  
Krishna Patil

We present the case of a 13-year-old boy with a congenital anterior urethral diverticulum. This is a rare condition in males which can lead to obstructive lower urinary tract symptoms and urosepsis. Diagnosis is by urethroscopy and radiological imaging. Surgical treatment can be open or endoscopic. Long-term followup is required to check for reoccurrence of the obstruction.


2013 ◽  
Vol 7 (6) ◽  
pp. 421-424 ◽  
Author(s):  
David A Manson-Bahr ◽  
Rajiv Swamy ◽  
Jim M Adshead

Benign vesica melanosis (BVM) is a rare condition with only 15 reported cases in the literature (Table 1). There is limited understanding of its aetiology. Here we present a four-year follow-up of a case of BVM in a 53-year-old Caucasian male presenting with lower urinary tract symptoms.


Author(s):  
Rohit Juneja ◽  
L Manjunath ◽  
H S Veerendra ◽  
Ananth S Mathad

AbstractAnterior urethral valves (AUVs) are rare congenital anomalies causing lower urinary tract obstruction in children. Although they are referred to as valves, these obstructive structures often occur in the form of a diverticulum. Congenital anterior urethral diverticulum (CAUD) is an uncommon/rare entity in children which can lead to obstructive lower urinary tract symptoms and urosepsis. Over the past 20 years, more than 260 cases have been reported. However, most cases are diagnosed on prenatal ultrasonography (USG) in early life if patients present with bilateral hydronephrosis and/or azotemia. Diagnosis is by ureteroscopy and radiological imaging. Surgical treatment can be open or endoscopic. Here, we report a new case of CAUD and discuss its clinical presentation, diagnosis, and management. A brief review of the literature is also presented.


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