The Surgical Management of Imperforate Anus

1955 ◽  
Vol 35 (5) ◽  
pp. 1251-1257 ◽  
Author(s):  
Jonathan E. Rhoads ◽  
C. Everett Koop
Keyword(s):  
Surgical Management ◽  
Imperforate Anus

Vaginal anomalies and atresia associated with imperforate anus: Diagnosis and surgical management

2015 ◽  
Vol 50 (3) ◽  
pp. 431-437 ◽  
Author(s):  
Kartikey A. Pandya ◽  
Hiroyuki Koga ◽  
Manabu Okawada ◽  
Arnold G. Coran ◽  
Atsuyuki Yamataka ◽  
...  
Keyword(s):  
Surgical Management ◽  
Imperforate Anus

Procedure for Prolapsed Hemorrhoids for Treatment of Rectal Mucosa Prolapse following Anorectoplasty for Imperforate Anus

2008 ◽  
Vol 74 (5) ◽  
pp. 443-446
Author(s):  
Jose D. Amortegui ◽  
Julio A. Solla
Keyword(s):  
Pelvic Floor ◽  
Surgical Management ◽  
Imperforate Anus ◽  
Rectal Mucosa ◽  
Mucosal Prolapse ◽  
Pelvic Floor Reconstruction ◽  
Rectal Mucosal Prolapse ◽  
Internal Hemorrhoids ◽  
History Of

Surgical management of imperforate anus and rectal mucosal prolapse has evolved significantly over the last two decades. The procedure for prolapsed hemorrhoids (PPH) is now widely used primarily for rectal mucosal prolapse and internal hemorrhoids. We describe the use of PPH in the management of symptomatic rectal mucosal prolapse in a 39-year-old man with a history of a high imperforate anus and pelvic floor reconstruction. At 4-year follow up, the prolapse has not recurred and the preoperative symptoms have resolved. To the best of our knowledge, this is the first report on the use of a PPH in the management of rectal mucosal prolapse in a patient with these characteristics.

scholarly journals Surgical Management of Congenital Rectovaginal Fistula and Type III Atresia Ani in an Umbalachery Calf

2018 ◽  
Vol 14 (1) ◽  
Author(s):  
R. Uma Rani ◽  
P. Tamilmahan
Keyword(s):  
Congenital Anomaly ◽  
Surgical Management ◽  
Imperforate Anus ◽  
Rectovaginal Fistula ◽  
Present Report ◽  
Dorsal Wall ◽  
Type Iii

Congenital rectovaginal fistula is characterised by the communication between the dorsal wall of the vagina and the ventral portion of the rectum, so that the vulva functions as a common opening to the urogenital and gastrointestinal tracts (Shakoor et al., 2012). Type III Atresia Ani is a congenital anomaly in which imperforate anus combined with the blind rectal pouch which is more than 1 cm away from the anal dimple (Vianna and Tobias, 2005). The present report records a case of congenital rectovaginal fistula and type III Atresia Ani in an Umbalacheri calf and its successful surgical management.

Immediate and long-term results of surgical management of low imperforate anus in girls

1998 ◽  
Vol 33 (2) ◽  
pp. 198-203 ◽  
Author(s):  
Patrick J Javid ◽  
Douglas C Barnhart ◽  
Ronald B Hirschl ◽  
Arnold G Coran ◽  
Carroll M Harmon
Keyword(s):  
Surgical Management ◽  
Imperforate Anus ◽  
Long Term Results ◽  
Low Imperforate Anus

scholarly journals Surgical management of complete penile duplication accompanied by multiple anomalies

2014 ◽  
Vol 8 (9-10) ◽  
pp. 741 ◽  
Author(s):  
Irfan Karaca ◽  
Erdal TURK ◽  
A. Basak Ucan ◽  
Derya Yayla ◽  
Gulcin Itirli ◽  
...  
Keyword(s):  
Surgical Management ◽  
Imperforate Anus ◽  
Congenital Anomalies ◽  
Symphysis Pubis ◽  
Rectal Duplication

Diphallus (penile duplication) is very rare and seen once every 5.5 million births. It can be isolated, but is usually accompanied by other congenital anomalies. Previous studies have reported many concurrent anomalies, such as bladder extrophy, cloacal extrophy, duplicated bladder, scrotal abnormalities, hypospadias, separated symphysis pubis, intestinal anomalies and imperforate anus; no penile duplication case accompanied by omphalocele has been reported. We present the surgical management of a patient with multiple anomalies, including complete penile duplication, hypogastric omphalocele and extrophic rectal duplication.

Surgical Management of Patients With 22q11.2 Deletion Syndrome

2019 ◽  
Vol 4 (5) ◽  
pp. 857-869
Author(s):  
Oksana A. Jackson ◽  
Alison E. Kaye
Keyword(s):  
Surgical Management ◽  
Preoperative Evaluation ◽  
Preoperative Assessment ◽  
22Q11.2 Deletion Syndrome ◽  
Deletion Syndrome ◽  
22Q11.2 Deletion ◽  
Surgical Decision ◽  
Obstructive Sleep ◽  
Spine Abnormalities ◽  
Speech Assessment

Purpose The purpose of this tutorial was to describe the surgical management of palate-related abnormalities associated with 22q11.2 deletion syndrome. Craniofacial differences in 22q11.2 deletion syndrome may include overt or occult clefting of the palate and/or lip along with oropharyngeal variances that may lead to velopharyngeal dysfunction. This chapter will describe these circumstances, including incidence, diagnosis, and indications for surgical intervention. Speech assessment and imaging of the velopharyngeal system will be discussed as it relates to preoperative evaluation and surgical decision making. Important for patients with 22q11.2 deletion syndrome is appropriate preoperative screening to assess for internal carotid artery positioning, cervical spine abnormalities, and obstructive sleep apnea. Timing of surgery as well as different techniques, common complications, and outcomes will also be discussed. Conclusion Management of velopharyngeal dysfunction in patients with 22q11.2 deletion syndrome is challenging and requires thoughtful preoperative assessment and planning as well as a careful surgical technique.

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