Metachronous multiple esophageal squamous cell carcinomas and Lugol-voiding lesions after endoscopic mucosal resection

Endoscopy Volume 41 Issue 4 Page 304-309 published_at 2009
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Title ( eng )
Metachronous multiple esophageal squamous cell carcinomas and Lugol-voiding lesions after endoscopic mucosal resection
Creator
Urabe Yuji
Hiyama Tooru
Source Title
Endoscopy
Volume 41
Issue 4
Start Page 304
End Page 309
Abstract
Background and study aims: Endoscopic mucosal resection (EMR) has been applied to the treatment of superficial esophageal squamous cell carcinoma (SCC). The incidence and characteristics of metachronous multiple esophageal SCCs and Lugol-voiding lesions (LVLs) were investigated in a retrospective study in patients who had undergone EMR for superficial esophageal SCC. Patients and methods: 96 patients with esophageal SCC who had been treated by EMIR were followed up by endoscopy for 12 months or longer. Clinicopathologic parameters such as tumor size and location and presence of LVLs were examined. Results: 10 patients (10%) had synchronous multiple SCCs, and 12 (13%) developed metachronous multiple SCCs. The mean annual incidence of newly diagnosed tumor was 4.4%. The incidence of a speckled pattern of LVLs was 20/74 (27%) in patients with solitary SCC, 5/10 (50%) in synchronous multiple SCC, and 10/12 (83%) in metachronous multiple SCC. The incidence of the presence of speckled pattern of LVLs was significantly higher in patients with multiple SCCs than in those with solitary SCC (68% vs. 27%, P = 0.0004). Conclusions: Patients who have undergone EMR for esophageal SCC, especially those with metachronous multiple LVLs in the background mucosa, should undergo follow-up with close endoscopic observation using Lugol staining.
NDC
Medical sciences [ 490 ]
Language
eng
Resource Type journal article
Publisher
Georg Thieme Verlag KG
Date of Issued 2009
Rights
(c) Georg Thieme Verlag Stuttgart
The original publication is available at www.thieme-connect.com
Publish Type Author’s Original
Access Rights open access
Source Identifier
[ISSN] 0013-726X
[DOI] 10.1055/s-0029-1214477
[NCID] AA00635110
[DOI] http://dx.doi.org/10.1055/s-0029-1214477