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Volume 73, Issue 12, Pages 1613-1615 (December 2009)


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Sialodochostomy as treatment for imperforate submandibular duct: A systematic literature review and report of two cases

David E. Rosow, Robert F. Ward, Max M. AprilCorresponding Author Informationemail address

Received 26 January 2009; accepted 11 March 2009.

Summary 

Objective

To better understand the diagnosis, treatments, and outcomes of congenitally imperforate salivary ducts.

Methods

A systematic literature review was performed using the following terms: imperforate submandibular duct, imperforate Wharton's duct, congenital atresia submandibular duct, congenital atresia sublingual duct, and congenital ranula. Only papers focusing on congenital floor of mouth cysts arising from imperforate salivary ducts were included. Two additional patients from our own experience are also discussed.

Results

Seventeen papers published since 1950 met inclusion criteria. A total of 26 patients underwent therapy ranging from mere observation to complete excision of the cyst with the sublingual gland. Both of our 2 additional patients both underwent simple sialodochostomy (excision of the imperforate sublingual caruncle) with cyst decompression. For all 28 patients, there have been no reported recurrences, with mean follow-up of 24.8 months and median follow-up of 14.8 months.

Conclusions

Congenital floor of mouth cysts arising from imperforate salivary ducts are rare, but they may mimic the appearance of a ranula. Unlike ranulas, these cysts may be safely and effectively cured by simple sialodochostomy. To date, 26 other cases have been described in the literature, and nearly all have been successfully treated with simple incision or marsupialization without recurrence. Care should be taken to exclude ranula as a diagnosis, as incomplete excision may likely result in recurrence.

Department of Otorhinolaryngology, Weill Cornell Medical College, New York, NY, USA

Corresponding Author InformationCorresponding author at: 1305 York Ave., 5th Floor, New York, NY 10021, USA. Tel.: +1 646 962 2225; fax: +1 646 962 0100.

PII: S0165-5876(09)00131-1

doi:10.1016/j.ijporl.2009.03.007


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