CC BY 4.0 · European J Pediatr Surg Rep. 2020; 08(01): e71-e74
DOI: 10.1055/s-0040-1715182
Case Report

Colorectal Hamartoma Presenting As a Perineal Mass in a Boy with Proximal Hypospadias

Katja P. Wolffenbuttel
1   Department of Urology and Pediatric Urology, Erasmus MC Sophia, Rotterdam, The Netherlands
,
Cornelius E. J. Sloots
2   Department of Pediatric Surgery, Erasmus MC Sophia, Rotterdam, The Netherlands
› Author Affiliations

Abstract

Congenital perineal lesions are rare and can occur along with other birth defects such as anorectal malformations (ARMs) and urogenital anomalies. A colorectal hamartoma associated with a urogenital anomaly without ARM is extremely rare. We recently treated a newborn with posterior hypospadias and a solid perineal mass diagnosed as a colorectal hamartoma.



Publication History

Received: 06 April 2020

Accepted: 22 June 2020

Article published online:
18 September 2020

© .

Georg Thieme Verlag KG
Stuttgart · New York

 
  • References

  • 1 Shaul DB, Monforte HL, Levitt MA, Hong AR, Peña A. Surgical management of perineal masses in patients with anorectal malformations. J Pediatr Surg 2005; 40 (01) 188-191
  • 2 Sun J, Vongphet S, Zhang Z, Mo J. Perineal mass protrusion with rectal mucosa: a rectal duplication that underwent exstrophy. J Pediatr Surg 2011; 46 (08) e5-e8
  • 3 Liu SP, Yang JX, Cao DY, Lang JH. Congenital perineal mass with cervovaginal duplication: a case report and literature review. J Pediatr Adolesc Gynecol 2014; 27 (02) 102-103
  • 4 Gangopadhyay AN, Biswas SK, Khanna S. Exstrophy of the urorectal septum—report of two cases and embryological review. Pediatr Surg Int 1992; 7: 311-313
  • 5 Patiño Mayer J, Bettolli M. Alimentary tract duplications in newborns and children: diagnostic aspects and the role of laparoscopic treatment. World J Gastroenterol 2014; 20 (39) 14263-14271