PEDIATRICS Vol. 62 No. 4 October 1978, pp. 584-587
This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Malangoni, M. A.
Right arrow Articles by Kleiman, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Malangoni, M. A.
Right arrow Articles by Kleiman, M.

Congenital Rectal Stenosis: A Sign of a Presacral Pathologic Condition

Mark A. Malangoni M.D.1, Jay L. Grosfeld M.D.1, Thomas V.N. Ballantine M.D.1, and Martin Kleiman M.D.1

1 Section of Pediatric Surgery, Department of Surgery, and the Department of Pediatrics, Indiana; University Scihool of Medicine, and the James Whitcomb Riley Hospital for Children, indianapolis

Congenital rectal stenosis may be detected in the newborn during the initial physical examination. Failure of conservative therapy (dilatation) should alert the physician to the presence of an associated pathologic condition in the presacral space. Presacral teratoma, anterior sacral meningocele, or bony anomalies may be the underlying extrinsic causes of congenital rectal stenosis. Prompt recognition and appropriate operative management directed at the presacral lesion will relieve obstructive symptoms and minimize morbidity.

Submitted on December 19, 1977
Accepted on February 10, 1978




This article has been cited by other articles:


Home page
J. Med. Genet.Home page
S. A. Lynch, Y. Wang, T Strachan, J. Burn, and S. Lindsay
Autosomal dominant sacral agenesis: Currarino syndrome
J. Med. Genet., August 1, 2000; 37(8): 561 - 566.
[Abstract] [Full Text]


Home page
Behav ModifHome page
F. F. L. Boon and N. N. Singh
A Model for the Treatment of Encopresis
Behav Modif, July 1, 1991; 15(3): 355 - 371.
[Abstract]


Home page
Arch SurgHome page
F. Moazam and J. L. Talbert
Congenital Anorectal Malformations: Harbingers of Sacrococcygeal Teratomas
Arch Surg, July 1, 1985; 120(7): 856 - 859.
[Abstract] [PDF]