Infected Congenital Urethral Diverticulum Manifested as a Scrotal Mass in an Adult Male: Case Report and Review of the Literature

2008 ◽  
Vol 81 (2) ◽  
pp. 234-237 ◽  
Author(s):  
Tommaso Cai ◽  
Andrea Gavazzi ◽  
Enrico Sarti ◽  
Umberto Farina ◽  
Franco Melone ◽  
...  
Keyword(s):  
Case Report ◽  
Adult Male ◽  
Urethral Diverticulum ◽  
Review Of The Literature ◽  
Scrotal Mass

A giant urethral diverticulum presenting as a scrotal mass in an adult male

2001 ◽  
Vol 83 (4) ◽  
pp. 522-523 ◽  
Author(s):  
De Filippo ◽  
Kurzrock ◽  
Stein ◽  
Skinner
Keyword(s):  
Adult Male ◽  
Urethral Diverticulum ◽  
Scrotal Mass

scholarly journals A persistent urethral diverticulum in pregnancy: Case report and review of the literature

2020 ◽  
Vol 26 ◽  
pp. e00189
Author(s):  
Katherine Artis ◽  
Kanapathippillai Sivanesan ◽  
Mayooran Veerasingham
Keyword(s):  
Case Report ◽  
Urethral Diverticulum ◽  
Review Of The Literature ◽  
In Pregnancy

Intrascrotal Lipoblastoma With a Complex Karyotype: A Case Report and Review of the Literature

2004 ◽  
Vol 128 (7) ◽  
pp. 797-800 ◽  
Author(s):  
Gino R. Somers ◽  
Ikuko Teshima ◽  
Ahmed Nasr ◽  
Anthony Cook ◽  
Antoine E. Khoury ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Adipose Tissue ◽  
Case Report ◽  
Young Children ◽  
Head And Neck ◽  
Cytogenetic Analysis ◽  
Chromosome 12 ◽  
Complex Karyotype ◽  
Review Of The Literature ◽  
Scrotal Mass

Abstract Lipoblastoma is a tumor of adipose tissue that usually occurs in young children. Most lipoblastomas occur on the extremities, trunk, and head and neck, and most have rearrangements of the 8q region. We describe a lipoblastoma in a 12-month-old boy who presented with a rapidly enlarging scrotal mass. Electron microscopy revealed features consistent with immature adipocytes, and cytogenetic analysis revealed the following karyotype: 57,XY,+4,+6,+7,der(8)t(8;12) (q22;q13), +der(8)t(8;12) (q22;q13), +9,+10,+12,−16,+17,+der(18)t(8;18)(q22;q23),+19,+20. Interestingly, the breakpoint on chromosome 12 (q13) is the same as that seen in lipoblastomas. To our knowledge, this is the first reported case of such a complex karyotype in lipoblastoma and adds to the expanding list of karyotypic abnormalities seen in such tumors.

scholarly journals Absence of the celiac trunk and trifurcation of the common hepatic artery: a case report

2016 ◽  
Vol 15 (3) ◽  
pp. 259-262
Author(s):  
Satheesha Nayak Badagabettu ◽  
Ashwini Aithal Padur ◽  
Naveen Kumar ◽  
Deepthinath Reghunathan
Keyword(s):  
Case Report ◽  
Hepatic Artery ◽  
Rare Variant ◽  
Adult Male ◽  
Celiac Trunk ◽  
Anatomical Variations ◽  
Common Hepatic Artery ◽  
Review Of The Literature ◽  
Male Cadaver ◽  
The Common

Abstract Anatomical variations of the celiac trunk and its branches are particularly important from a surgical perspective due to their relationships with surrounding structures. We report here a particularly rare variant involving absence of the celiac trunk in association with trifurcation of the common hepatic artery. These variations were found in an adult male cadaver. We perform a review of the literature and discuss the clinical and embryological significance of these variations. Recognition of celiac trunk and hepatic artery variations is of utmost importance to surgeons and radiologists because multiple variations can lead to undue complications.

Symptomatic Müllerian cyst in the retroperitoneum of an adult male: Case report and review of the literature

2019 ◽  
Vol 4 (2) ◽  
pp. 53
Author(s):  
MusliuAdetola Tolani ◽  
Ahmad Bello ◽  
Muhammed Ahmed ◽  
HussainiYusuf Maitama
Keyword(s):  
Case Report ◽  
Adult Male ◽  
Review Of The Literature

scholarly journals Congenital Anterior Urethral Diverticulum in a Male Teenager: A Case Report and Review of the Literature

2011 ◽  
Vol 2011 ◽  
pp. 1-2 ◽  
Author(s):  
Sadat Haider Quoraishi ◽  
Faisal Khan ◽  
Dler Besarani ◽  
Krishna Patil
Keyword(s):  
Case Report ◽  
Lower Urinary Tract ◽  
Rare Condition ◽  
Urethral Diverticulum ◽  
Radiological Imaging ◽  
Review Of The Literature ◽  
Urinary Tract Symptoms ◽  
Anterior Urethral Diverticulum ◽  
Lower Urinary

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.

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