Format

Send to

Choose Destination
Ophthal Plast Reconstr Surg. 2009 Jan-Feb;25(1):52-3. doi: 10.1097/IOP.0b013e318192ebc5.

Surgical treatment of familial dacryocystocele and lacrimal puncta agenesis.

Author information

1
Otolaryngology Department, Hospital de Fuenlabrada, Madrid, Spain. gplaza.hflr@salud.madrid.org

Abstract

Bilateral agenesis of the lacrimal puncta and enlargement of the nasolacrimal canal are rare anatomic variants. The authors present 2 familial cases: a 39-year-old woman with bilateral dacryocystocele and lacrimal puncta agenesis and her 46-year-old brother, who had a long history of epiphora and recurrent dacryocystitis, and also had bilateral lacrimal puncta agenesis and a left dacryocystocoele. The authors report the endoscopic, CT, and MRI findings, and describe the surgical treatments, by endoscopic dacryocystorhinostomy in the first case, and conjunctivodacryocystorhinostomy with Jones tube in the second case. At 24 months after surgery, both patients' symptoms were improved.

PMID:
19273928
DOI:
10.1097/IOP.0b013e318192ebc5
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Wolters Kluwer
Loading ...
Support Center