Monocanalicular Versus Bicanalicular Silicone Intubation for Nasolacrimal Duct Stenosis in Adults

2005 ◽  
Vol 21 (2) ◽  
pp. 142-147 ◽  
Author(s):  
Mohsen Bahmani Kashkouli ◽  
Roxanne C. Kempster ◽  
Gavin D. Galloway ◽  
Bijan Beigi
1994 ◽  
Vol 103 (2) ◽  
pp. 110-114 ◽  
Author(s):  
Franz Josef Steinkogler ◽  
Andreas Kuchar ◽  
Ernst Huber ◽  
Franz Karnel

The causes of nasolacrimal duct stenosis in adults can vary greatly. In general, the symptoms can also vary, but most cases share a tendency toward recurring inflammations in the prestenotic area. The treatment of these disorders is limited to either conservative therapy to control inflammation or surgically invasive measures. By using balloon catheters, usually applied in percutaneous transluminal coronary angioplasty (PTCA), dilation of the relative postsaccal stenosis can be performed under radiographic control. An exact diagnosis using various testing methods, including digital dacryocystography for detailed localization and documentation of any pathologic changes, is decisive to success. Only in cases of incomplete postsaccal stenosis is retrograde balloon dilation of the distal nasolacrimal duct indicated. A guide wire, designed for the PTCA balloon catheter set, is introduced via the canaliculus to the nasal cavity antegradely and caught with a thin hook and pulled from the naris, under visual control with an image converter. The balloon catheter is retrogradely threaded over the guide wire. The balloon is then placed at the site of the pathologic stenosis under radiographic control and dilated with high pressure. To ensure the permeability of the system, monocanalicular silicone intubation has to be performed immediately afterwards. This procedure has been performed successfully on 6 patients with a follow-up of 6 to 27 months. These initial results give rise to the hope that this minimally invasive, interdisciplinary technique represents a new alternative in the treatment of incomplete postsaccal lacrimal stenosis.


2014 ◽  
Vol 25 (3) ◽  
pp. 1009-1011 ◽  
Author(s):  
Dima Andalib ◽  
Reza Nabie ◽  
Leila Abbasi

2019 ◽  
Vol 33 (1) ◽  
pp. 95 ◽  
Author(s):  
Yeonji Jang ◽  
Namju Kim ◽  
Keun-Wook Lee ◽  
Ho-Kyung Choung ◽  
Sang In Khwarg

2016 ◽  
Vol 67 (2) ◽  
pp. 109-113
Author(s):  
Shigechika KOHASHI ◽  
Hideya ISAI ◽  
Tomotaka TOMIYAMA ◽  
Toshihiko NAKASHIMA ◽  
Makoto TAKEDA

2008 ◽  
Vol 22 (6) ◽  
pp. 629-634 ◽  
Author(s):  
Roee Landsberg ◽  
Oren Cavel ◽  
Yoram Segev ◽  
Avi Khafif ◽  
Dan M. Fliss

Background It is well documented that inverted papillomas (IP) have a localized attachment site. Still, instead of concentrating on the attachment site, endoscopic surgeons often perform an extended resection similar to the one achieved after external surgery. Objective Our objective was to evaluate an attachment-oriented endoscopic surgical strategy and to determine IP attachment diameter and location. Methods A prospective study was conducted. Thirty-three consecutive patients who underwent endoscopic IP excision (2001-2007) were enrolled. Thirty patients had adequate follow-up. Attachment diameters were measured in 25/33 patients. Surgery included debulking, identifying the precise mucosal attachment site, subperiosteal dissection and excision of the attachment, frozen section control, and resection/drilling of underlying bone. Results The mean measured attachment diameter (n = 25) was 8.4 ± 6 mm (range, 3-23 mm). Attachment locations included maxillary sinus (39%), ethmoid sinus (21%), nasal cavity (21%), frontal sinus (6%), sphenoid sinus (6%), lamina papyracea (3%), and cribriform plate (3%). The mean follow-up (n = 30) was 40 ± 21 months. Three patients had Krouse stage 1, 10 patients had stage 2, and 17 patients had stage 3. Nine patients had undergone previous surgeries. After attachment-oriented endoscopic surgery, three patients had persistent disease. Nasolacrimal duct stenosis was the only complication (n = 1). Conclusion Even advanced IP have small attachments. Their Identification facilitates efficacious resection with minimal morbidity.


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