Literature DB >> 10415302

A case of incomplete Currarino triad with malignant transformation.

B Tander1, D Baskin, M Bulut.   

Abstract

A case of an incomplete Currarino triad is reported. The baby underwent an emergency laparotomy due to a life-threatening intestinal obstruction caused by severe rectal stenosis. During the posterosagittal anorectoplasty (PSARP), a presacral teratoma was identified and resected. The tumor recurred three times; she initially responded to chemotherapy, but nonetheless died at the age of 4 years. In cases with evidence of anorectal stenosis, a presacral mass should be suspected. PSARP is the best choice of treatment for both the anorectal anomaly and excision of the presacral mass. The presacral region should be followed up closely for recurrence of the tumor.

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Year:  1999        PMID: 10415302     DOI: 10.1007/s003830050615

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  3 in total

1.  Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome.

Authors:  In-Suk Kim; Soo-Young Oh; Suk-Joo Choi; Jong-Hwa Kim; Kwan Hyun Park; Hyun-Kyung Park; Jong-Won Kim; Chang-Seok Ki
Journal:  J Hum Genet       Date:  2007-07-06       Impact factor: 3.172

Review 2.  Long-term functional outcomes in children with Currarino syndrome.

Authors:  Atsushi Yoshida; Kiki Maoate; Russell Blakelock; Stephen Robertson; Spencer Beasley
Journal:  Pediatr Surg Int       Date:  2010-05-15       Impact factor: 1.827

3.  Atypical presentation of currarino syndrome: A case report.

Authors:  Paul Hage; Cedric Kseib; Carmen Adem; Camil J Chouairy; Reva Matta
Journal:  Int J Surg Case Rep       Date:  2019-03-18
  3 in total

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