Endoscopy 2013; 45(07): 585-588
DOI: 10.1055/s-0033-1344228
Innovations and brief communications
© Georg Thieme Verlag KG Stuttgart · New York

Microvascular caliber changes in intramucosal and submucosally invasive esophageal cancer

E. G. R. Santi
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Japan
,
H. Inoue
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Japan
,
H. Ikeda
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Japan
,
A. Yoshida
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Japan
,
M. Onimaru
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Japan
,
H. Sato
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Japan
,
R. Maselli
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Japan
,
B.-H. Hayee
2   King’s College Hospital NHS Foundation Trust, Department of Gastroenterology, London, United Kingdom
,
S.-E. Kudo
1   Digestive Disease Center, Showa University Northern Yokohama Hospital, Japan
› Author Affiliations
Further Information

Publication History

submitted 17 December 2012

accepted after revision 02 April 2013

Publication Date:
25 June 2013 (online)

Background and study aim: Intrapapillary capillary loops (IPCLs) show distinct pattern changes corresponding to tumor progression and depth of invasion, important for in vivo characterization of superficial squamous cell carcinoma (SCC). We examined the relation between invasion depth and histopathologic IPCL diameter.

Patients and methods: Prospectively, before lesion resection, magnification endoscopy and narrow band imaging were used to identify IPCL patterns of type V1 (corresponding to tumors limited to the mucosa; 10 patients) and type Vn (submucosally invading tumors; 10 patients). Post-resection, IPCL samples (type I [normal mucosa], n = 103; V1, n = 113; Vn, n = 100) were stained with hematoxylin & eosin, CD34, and desmin, and vessel diameter measured using light microscopy.

Results: Mean (standard deviation [SD]) histopathologic calibers of IPCLs of types I, V1, and Vn were significantly different, being 7.7 (2.8) µm, 21.9 (7.4) µm, and 65.2 (22.9) µm; type 1 vs. V1, P < 0.001; V1 vs. Vn, P < 0.001.

Conclusions: Magnification endoscopy observation of IPCLs allows in vivo discrimination between intramucosal and submucosally invasive cancer.