Segmental partial thrombosis of the corpora cavernosa: Case report and diagnostic/therapeutic algorithm

2021 ◽  
Author(s):  
Fabián Claudio Militello ◽  
Alejo Aredez ◽  
Emilia Yarade ◽  
Maximiliano Pérez
Keyword(s):  
Case Report ◽  
Corpora Cavernosa ◽  
Therapeutic Algorithm ◽  
Partial Thrombosis

Congenital megalourethra: a case report of an isolated delayed presentation

2016 ◽  
Vol 28 (1) ◽  
pp. 115-117
Author(s):  
Anurag Puri ◽  
Dilip Kumar Pal
Keyword(s):  
Case Report ◽  
Corpus Spongiosum ◽  
Delayed Presentation ◽  
Mechanical Obstruction ◽  
Anterior Urethra ◽  
Corpora Cavernosa ◽  
Congenital Megalourethra

Abstract Megalourethra is a diffuse dilatation of the anterior urethra due to lack of corpus spongiosum with or without corpora cavernosa; it usually presents as a dilatation of that part of the urethra. The absence of these structures causes a ballooning of the urethra despite there being no mechanical obstruction. A 7-year-old boy presented with the complaints of weak stream, ballooning of the penis before and during voiding urine and post voiding dribbling. After examination and micturating urethrogram, he was diagnosed as having megalourethra, which was then corrected using reduction urethroplasty. These days megalourethra is diagnosed with prenatal ultrasonogram. This was a case of isolated delayed presentation of megalourethra without any associated anomaly.

scholarly journals Prelaminated Gracilis Flap with Buccal Mucosal Graft for Salvage of Devastated Urethra

2015 ◽  
Vol 2015 ◽  
pp. 1-5
Author(s):  
Dmitriy Nikolavsky
Keyword(s):  
Case Report ◽  
Penetrating Trauma ◽  
Gracilis Muscle ◽  
Dorsal Plate ◽  
Local Tissue ◽  
Corpora Cavernosa ◽  
Buccal Mucosa Graft ◽  
Buccal Mucosal Graft ◽  
Novel Variation

In patients with devastated bulbous urethra, that is, bulbar necrosis, failed fasciocutaneous repairs and “watering can perineum” repair options are limited by paucity of reliable local tissue suitable for reconstruction. In this case report we demonstrate a novel variation of a two-stage technique for reconstruction of a devastated bulbous urethra in a 57-year-old male who suffered penetrating trauma to his previously reconstructed urethra. Because of extensive loss of local tissue from the prior reconstruction and subsequent trauma and infection a 2-stage technique with use of gracilis was employed. This technique involved creation of two independently vascularized urethral hemi-plates prelaminated with buccal mucosa graft (BMG). In the first stage the dorsal plate was created by quilting buccal graft onto corpora cavernosa to create a temporary augmented perineal urethrostomy. In the same stage the future ventral neourethral plate was created by grafting another BMG onto the exposed distal gracilis muscle. Eight weeks later the two prelaminated plates were anastomosed by tunneling the gracilis-BMG composite into the perineum. At 8-month follow-up patient has normal voiding and continence. To our knowledge this is the first report of reconstructing an entire segment of devastated urethra in such a manner.

Congenital Abnormality of Corpora Cavernosa and Erectile Dysfunction: A Case Report

1993 ◽  
Vol 149 (5 Part 1) ◽  
pp. 1135-1136 ◽  
Author(s):  
Claudio Teloken ◽  
Wilson F.S. Busato ◽  
Joao Fidelis J. Νeto ◽  
Antonio Hartmann ◽  
Jorge Winckler ◽  
...  
Keyword(s):  
Erectile Dysfunction ◽  
Case Report ◽  
Congenital Abnormality ◽  
Corpora Cavernosa

An unusual congenital scrotal lymphatic malformation with absent corpora cavernosa: a case report

2008 ◽  
Vol 43 (9) ◽  
pp. 1729-1731 ◽  
Author(s):  
Avinash V. Joshi ◽  
Rahul K. Gupta ◽  
Hemanshi Shah ◽  
Sandesh Parelkar ◽  
Abhaya Gupta ◽  
...  
Keyword(s):  
Case Report ◽  
Lymphatic Malformation ◽  
Corpora Cavernosa

Neurofibroma of the penis: Case report

1997 ◽  
Vol 64 (4) ◽  
pp. 458-460
Author(s):  
M. De Marco ◽  
N. Angileri ◽  
M. Ferrera ◽  
G. Di Natale ◽  
G. Galfano
Keyword(s):  
Case Report ◽  
Sexual Activity ◽  
Clinical Picture ◽  
Negative Impact ◽  
Sexual Life ◽  
Sexual Relations ◽  
Corpora Cavernosa ◽  
Von Recklinghausen's Neurofibromatosis ◽  
Operation Results ◽  
Von Recklinghausen’S Neurofibromatosis

– The reported case concerns an unusual localisation of “Royal Tumour” connected with von Recklinghausen's neurofibromatosis. Surgery was necessary because of the increasing difficulty of the patient in having sexual relations due to the progressive swelling of the penile neoformation. The typical clinical picture, the integrity of the corpora cavernosa and the negative impact of the neoformation on the patient's sexual life all indicated the necessity for operation. Results were satisfactory both surgically and functionally/aesthetically and the patient regained normal sexual activity.

scholarly journals Penile fracture with bilateral corporeal rupture and complete urethral disruption: case report and literature review

2013 ◽  
Vol 5 (2) ◽  
pp. 23
Author(s):  
Nathan A. Hoag ◽  
Kiara Hennessey ◽  
Alan So
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Erectile Function ◽  
Surgical Repair ◽  
Review Of The Literature ◽  
Penile Fracture ◽  
Rare Injury ◽  
Surgical Exploration ◽  
Corpora Cavernosa

Penile fracture is a rare injury most commonly sustained duringsexual intercourse. We report the case of a 35-year-old man whopresented with bilateral rupture of the corpora cavernosa andcomplete disruption of the urethra. A review of the literature onpenile fracture is also presented. Urgent surgical exploration wasperformed and the injuries repaired primarily. In follow-up, thepatient reported satisfactory erectile function. This case highlightsthe importance of early surgical repair and evaluation for concomitanturethral injuries in cases of penile fracture.

scholarly journals Concealed epispadias: a rare anomaly - case report and review

2019 ◽  
Vol 6 (8) ◽  
pp. 2979
Author(s):  
Vivek Parameswara Sarma
Keyword(s):  
Case Report ◽  
Clinical Signs ◽  
Male Child ◽  
Corpora Cavernosa ◽  
Good Outcome ◽  
Rare Anomaly ◽  
Surgical Options

Epispadias with an intact prepuce (Concealed Epispadias) is an uncommon anomaly. The specific clinical signs in this situation are broad, spade-like glans with a dorsally directed preputial opening, gap between the corpora cavernosa may be palpable, dorsal chordee and abnormalities of the penile raphae. We report the case of a 3 year old male child with Concealed Epispadias who underwent a modified Cantwell-Ransley operation with good outcome. The relevant anatomy, embryology and surgical options are reviewed.

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