Combined Laparoscopically Assisted and Anterior Sagittal Anorectoplasty for Imperforate Anus with Rectobulbar Urethral Fistula: A Case Report

Videoscopy ◽  
2014 ◽  
Vol 24 (6) ◽  
Author(s):  
Tetsuya Ishimaru ◽  
Masahiko Sugiyama ◽  
Mari Arai ◽  
Jun Fujishiro ◽  
Chizue Uotani ◽  
...  
Keyword(s):  
Case Report ◽  
Imperforate Anus ◽  
Urethral Fistula ◽  
Anterior Sagittal Anorectoplasty

scholarly journals Urethral calculi with a urethral fistula: a case report and review of the literature

2017 ◽  
Vol 10 (1) ◽  
Author(s):  
Mingqiang Zeng ◽  
Fanchang Zeng ◽  
Zhao Wang ◽  
Ruizhi Xue ◽  
Liang Huang ◽  
...  
Keyword(s):  
Case Report ◽  
Review Of The Literature ◽  
Urethral Fistula

scholarly journals A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report

2014 ◽  
Vol 12 (2) ◽  
pp. 234-236
Author(s):  
Kleiton Gabriel Ribeiro Yamaçake ◽  
Amilcar Martins Giron ◽  
Uenis Tannuri ◽  
Miguel Srougi
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Imperforate Anus ◽  
Rare Case ◽  
Coloanal Anastomosis ◽  
Histopathological Examination ◽  
Congenital Clubfoot ◽  
Anorectal Anomaly ◽  
Male Neonate ◽  
Nonpalpable Testis

A full-term male neonate with anorectal anomaly and external perineal anomalies was referred to our service. Physical examination showed an epithelized perineal mass with cutaneous orifices, which had urine fistulization, hipotrofic perineal musculature, bilateral congenital clubfoot, hipospadic urethra, criptorquidy bilateral with nonpalpable testis and imperforate anus. A colostomy was constructed immediately after birth. The child underwent excision of perineal mass, bilateral orchidopexy, Duplay neourethroplasty and coloanal anastomosis at 3 months of age. The histopathological examination of the perineal mass revealed a hamartoma.

scholarly journals Imperforate anus in symmetrical conjoined live twins

2016 ◽  
Vol 10 (4) ◽  
Author(s):  
Hassan Mahmood Tabassum ◽  
Muhammad Anwar Chaudhry ◽  
Saeed Akhtar Malik
Keyword(s):  
Case Report ◽  
Imperforate Anus ◽  
Sagittal Plane ◽  
Symmetrical Body

This is a case report of newly born twins. The live twins were with two separate heads and a symmetrical body, conjoined in a sagittal plane. Their thorax and abdomen were broader then singleton normal. Spines were separate in cervical regions but gradually approached each other and completely fused at sacrum. Single perineum had an imperforate anus.

scholarly journals Congenital Urethral Fistula: A Case Report and Literature Review

2020 ◽  
Vol 2020 ◽  
pp. 1-4
Author(s):  
Aamer Alghamlas ◽  
Frédéric Auber ◽  
Yann Chaussy
Keyword(s):  
Case Report ◽  
Surgical Technique ◽  
Literature Review ◽  
Rare Condition ◽  
Postoperative Results ◽  
Ventral Aspect ◽  
Urethral Fistula ◽  
Abnormal Opening

Male congenital urethral fistula is an extremely rare condition. It is characterized by an abnormal opening of the ventral aspect of the penis. We report the case of a 1-month-old boy with congenital urethral fistula. We will describe the surgical technique, postoperative results, and literature review.

Hypertension Associated with Crossed Renal Ectopia in an Infant

PEDIATRICS ◽  
1971 ◽  
Vol 48 (3) ◽  
pp. 454-457
Author(s):  
David T. Mininberg ◽  
Stephanie Roze ◽  
H. J. Yoon ◽  
Marylin Pearl
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Imperforate Anus ◽  
Male Infant ◽  
Age Group ◽  
Renal Ectopia ◽  
Type Iii ◽  
Group A ◽  
Crossed Renal Ectopia ◽  
Spontaneous Delivery

Hypertension is not found commonly in infants under 1 year of age. Renovascular type of hypertension is extremely rare in this age group. A 3-month-old male infant is presented who developed hypertension secondary to the unilateral anomaly of crossed renal ectopia. This was associated with two other developmental anomalies, imperforate anus Type III-B and rectourethral fistula. The hypertension was treated successfully by surgery. Case Report A male infant, the full-term product of a 34-year-old G6P4A1 mother, was born by normal spontaneous delivery, weighing 5 pounds 8½ ounces. Physical examination was entirely normal except for the presence of an imperforate anus which subsequently proved to be Type III-B.

scholarly journals Traumatic posterior urethral fistula to hip joint following gunshot injury: a case report

2009 ◽  
Vol 3 (1) ◽  
Author(s):  
Ahmad Rezaee ◽  
Behzad Narouie ◽  
Rahim Haji-Rajabi ◽  
Mohammad Ghasemi-rad ◽  
Abdolsamad Shikhzadeh
Keyword(s):  
Case Report ◽  
Hip Joint ◽  
Gunshot Injury ◽  
Urethral Fistula

Dorsal urethral fistula: case report and review of literature

Urology ◽  
2004 ◽  
Vol 63 (1) ◽  
pp. 175-176 ◽  
Author(s):  
Tagore M. Grandhi ◽  
Odhran Shelley ◽  
Arup K. Ray ◽  
John R. McGregor
Keyword(s):  
Case Report ◽  
Review Of Literature ◽  
Urethral Fistula

scholarly journals Sacral nerve stimulation in the treatment of bowel dysfunction from imperforate anus: A case report

2016 ◽  
Vol 24 ◽  
pp. 115-118 ◽  
Author(s):  
Saleh M. Eftaiha ◽  
George Melich ◽  
Ajit Pai ◽  
Slawomir J. Marecik ◽  
Leela M. Prasad ◽  
...  
Keyword(s):  
Case Report ◽  
Nerve Stimulation ◽  
Imperforate Anus ◽  
Sacral Nerve Stimulation ◽  
Bowel Dysfunction ◽  
Sacral Nerve

scholarly journals VP11.19: Imperforate anus diagnosis at first trimester ultrasound: a case report

2021 ◽  
Vol 58 (S1) ◽  
pp. 142-142
Author(s):  
E. Becker ◽  
V. Schneider Müller ◽  
E.V. Cunha Filho
Keyword(s):  
Case Report ◽  
Imperforate Anus ◽  
First Trimester ◽  
First Trimester Ultrasound
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