Narrow-banding images and structures of microvessels of colonic lesions.

BACKGROUND: Magnifying colonoscopy with NBI has been shown to be useful for the differential diagnosis of tumors. However, the relationship between findings on NBI magnification and the microvessel architecture of colorectal lesions remains to be clarified. AIMS: The aim of this study was to clarify the correlation between NBI findings and the microvascular architecture of colorectal lesions according to the depth of microvessels from the mucosal surface.
METHODS: A total of 22 colorectal lesions (11 tubular adenomas and 11 hyperplasia) obtained from 22 patients were studied. These lesions were analyzed microscopically on tissue specimens immunostained with CD34. Three-dimensional images were reconstructed from serial sections of tubular adenomas, hyperplasia, and normal mucosa.
RESULTS: Three-dimensional reconstructed images of tubular adenoma and normal mucosa to a depth of less than 150 μm from the mucosal surface showed similar structures to images obtained by NBI magnification. Microvessel diameter was significantly larger in tubular adenoma than in normal mucosa (P = 0.002) and hyperplasia (P = 0.034), and microvessel area was significantly larger in tubular adenoma than in normal mucosa (P < 0.001) and hyperplasia (P < 0.001) only in the superficial mucosal layer (to a depth of less than 150 μm).
CONCLUSIONS: TA was characterized by thicker microvessels and higher volume of microvessels than NM and HP. Compared with white light, NBI can more accurately depict the characteristics of microvessels because it uses light with short wavelengths, thereby contributing to high diagnostic capability.

Introduction

To reduce morbidity and mortality from colorectal cancer, colonoscopy is considered the method of choice for the detection and removal of colon neoplasms, especially adenomatous lesions and early cancers. Distinguishing colorectal neoplasms from non-neoplastic lesions is one of the main roles of colonoscopy.

Narrow-band imaging (NBI) is a newly developed imaging technique that uses special filters to narrow the bandwidth of light [1]. NBI systems allow visualization of microvessels and the surface structure of the mucosa. NBI in combination with magnifying endoscopy has been reported to be useful for the diagnosis of neoplasms arising in the esophagus, stomach, and oropharynx [2-5]. Several studies have shown that NBI with magnifying endoscopy (NBI magnification) is useful for differentiating hyperplastic from neoplastic lesions in the colon. Machida and others have reported that NBI is superior to conventional colonoscopy and equivalent to chromoendoscopy for differentiating hyperplastic from neoplastic polyps [6-18]. However, the relationship between findings on NBI magnification and the microvessel architecture of colorectal lesions and the reasons why NBI magnification is useful for differentiating hyperplastic from neoplastic polyps remain to be clarified.

In the present study, images obtained by NBI magnification were compared with computer-aided 3-dimensional reconstructed images. Three-dimensional visualization of the microvessel network according to the distance from mucosal surface is an effective tool for understanding the depth of microvessels visualized on NBI magnification. Next, we quantitatively analyzed three vascular variables (diameter, area, number) in hyperplasia (HP), tubular adenoma (TA), and normal mucosa (NM) according to the depth from the mucosal surface.

Materials and Methods

Patients

A total of 22 colorectal lesions from 22 patients were studied. All patients underwent colonoscopy at the Digestive Disease Center, Showa University Northern Yokohama Hospital. The subjects were 14 men and 8 women with a mean age of 56.7 years (range 35–79). All patients received a detailed explanation of the study protocol and gave written informed consent.

Colonoscopy Procedure and Lesions

All colonoscopic examinations were performed by experienced endoscopists in our center, using a magnifying videoendoscope (CF-H260AZI; Olympus, Tokyo, Japan) and a standard videoendoscopic system (LUCERA; Olympus) equipped with the standard optical filter (white light) and the NBI system. All lesions were examined by NBI magnification. NBI diagnoses were based on the Wada classification [15]. All lesions were examined by NBI magnification. NBI diagnoses were based on the Wada classification. All lesions were resected endoscopically and fixed in 10% buffered formalin for 12–48 h. Hematoxylin-eosin-stained sections were histopathologically examined by a single pathologist in our hospital. The histopathological diagnosis was established according to the World Health Organization criteria. The 22 lesions analyzed in this study were 11 HP lesions and 11 TA. NBI diagnosis and histopathological diagnosis were consistent in all lesions. All HP lesions were similar in color to the adjacent normal mucosa on NBI without magnification, and all had an unclear vessel network, even on NBI magnification. This corresponded to the faint pattern of the Wada classification. The mean size of TA was 5.3 ± 2.4 mm. All TA appeared brownish on NBI without magnification and had a regular meshwork of smooth microvessels on NBI magnification. This corresponded to the regular network pattern of the Wada classification. The mean size of HP was 7.3 ± 2.6 mm.

Microvessel Immunohistochemical Staining

All 22 lesions were examined immunohistochemically by CD34 staining of endothelial cells. The histopathological characteristics of the tumors were reviewed, and the most representative tumor block was selected for immunohistochemical analysis. Sections (4 μm thick) were cut from formalin-fixed and paraffin-embedded blocks of tumor tissue. Anti-CD34 monoclonal antibody (Nichirei, Tokyo, Japan) and the streptavidin–biotin method (Dako LSAB kit; Dako Japan, Kyoto, Japan) were used for immunohistochemical staining.

Three-Dimensional Reconstruction

For 3-dimensional reconstruction, we prepared 100 serial sections of NM (3.5 μm thick), HP (3.5 μm thick), and TA (5 μm thick) by CD34 immunostaining. The microscope images of serial sections were digitized and recorded. The outlines of the vessels were traced and registered for each section, and 3-dimensional reconstructed images were produced using a computer reconstruction program (TRI/3D SRF II; RATOC System Engineering, Tokyo, Japan) [19].

Microvessel Analysis

One section immunostained with CD34 was analyzed per lesion. The entire tumor section was first carefully scanned at ×100 (×10 ocular, ×10 objective) to find the most vascular areas (“hotspots”). These hotspots were identified as areas with the highest density of brown-stained CD34 cells [20, 21]. Any brown-stained endothelial cell or endothelial cell cluster that was clearly separated from the adjacent microvessels was considered a single countable vessel. Microscope images of magnified fields (×200) within hotspots were digitized and recorded. Images were captured using an optical microscope connected to a color video camera and saved on a disc as bmp files. Each digitized image corresponded to a microscope field measuring 500 μm2 (960 × 960 pixels).

To evaluate microvessels, we counted the numbers of microvessels, measured the diameters and areas of microvessels, and measured the distance from each vessel to the mucosal surface. The minor axis of each microvessel was defined as the diameter of the vessel. The vertical distance from the center of the vessel to the mucosal surface (mucosal surface-vessel distance) was determined by counting the number of pixels on digitized images. To measure the microvessel area, outlines of all vessels were traced and painted black with the use of Microsoft paint software (Microsoft, Redmond, WA, USA). Subsequently, image-processing software (NIH Scion Image Beta 4.0.3; Scion, http://www.scioncorp.com/) was used to measure the area of each vessel as follows: image conversion to gray scale, thresholding, scale setting, and area measurement [22]. For each section of HP, microvessels of the NM that were distant from the hyperplastic lesion were measured.

To evaluate the correlation between microvessel-related variables and mucosal surface–vessel distance, microvessels were divided into the following three groups according to the mucosal surface–vessel distance: upper layer (≤150 μm), middle layer (>150 to ≤300), and lower layer (>300 to ≤450). Three variables were analyzed in this study: microvessel diameter (MVD), the average diameter of all individual microvessels in each layer; microvessel area (MVA), the sum of the areas of all individual microvessels in each layer; and microvessel count (MVC), the sum of the number of all individual microvessels in a field. Data were evaluated by the Mann–Whitney test.

Results

Figure 1 shows a compilation of CD34-stained sections (first row), images on NBI magnification (second row), and 3-dimensional reconstructed images of microvessels (third and fourth rows) for NM, HP, and TA. Three-dimensional images were reconstructed for microvessels to depths of less than 450 μm and less than 150 μm from the mucosal surface.

Fig. 1

CD34-stained sections (first row), images on NBI magnification (second row), and 3-dimensional reconstruction of microvessels (third and fourth rows) in normal mucosa (NM), hyperplasia (HP), and tubular adenoma (TA). Three-dimensional images were reconstructed for microvessels to depths of less than 450 μm (third row) and less than 150 μm (fourth row) from the mucosal surface

Reconstructed images of TA and NM to a depth of less than 450 μm from the mucosal surface showed complicated structures because of many layers of microvessels. In contrast, reconstructed images of TA and NM to a depth of less than 150 μm from the mucosal surface showed structures similar to those on NBI magnification.

Three-dimensional reconstructed images of the microvessels of NM showed a regular honeycomb-like network, similar to the images obtained by NBI magnification. Microvascular networks surrounded the openings of mucosal glands. Three-dimensional reconstruction of HP showed the absence of microvascular networks. The microvasculature was fragmentary. NBI magnification of HP showed an unclear vascular pattern. Three-dimensional reconstruction of TA showed vascular networks similar to those present in NM. However, the networks around the mucosal glands were elongated. Similar to NM, 3-dimensional reconstructed images of TA were consistent with the images obtained by NBI magnification. In contrast, HP showed a different pattern from that obtained by NBI magnification in the upper layer.

Mean MVD values are summarized in Tables 1 and 2 and Fig. 2. In the upper layer, MVD differed significantly between NM and TA (P = 0.002) and between HP and TA (P = 0.034), but did not differ significantly between NM and HP. In contrast, there were no significant differences in MVD between NM, HP, or TA in the middle or lower layers. Mean MVD was slightly but not significantly higher in TA than in HP when microvessels in all layers were compared or when the upper and middle layers were compared.

Table 1

Relationship between microvessel diameter (MVD) and mucosal surface–vessel distance

	Average MVD (µm)
	Upper (≤150)a	Middle (>150 to ≤300)a	Lower (>300 to ≤450)a
Normal mucosa (NM)	7.4 ± 0.9	6.9 ± 1.5	8.8 ± 3.3
Hyperplasia (HP)	7.6 ± 2.1	10.1 ± 3.0	8.7 ± 1.8
Tubular adenoma (TA)	10.9 ± 3.4	8.3 ± 3.1	7.6 ± 1.3

Microvessel diameter was defined as the average diameter of all individual microvessels in each layer. MVD differed significantly between NM and TA (P = 0.002) and between HP and TA (P = 0.034) in the upper layer

aMicrovessels were divided into the following three groups according to mucosal surface–vessel distance: upper layer (≤150 μm), upper and middle layer (>0 to ≤300 μm), and all layers (>0 to ≤450 μm)

Table 2

Relationship between microvessel diameter (MVD) and mucosal surface–vessel distance

	Average MVD (µm)
	Upper (≤150)a	Upper + middle (>0 to ≤300)a	All (>0 to ≤450)a
Normal mucosa (NM)	7.4 ± 0.9	7.3 ± 1.1	7.6 ± 1.5
Hyperplasia (HP)	7.6 ± 2.1	8.8 ± 1.8	8.7 ± 1.5
Tubular adenoma (TA)	10.9 ± 3.4	10.3 ± 3.1	9.5 ± 2.4

Microvessel diameter was defined as the average diameter of all individual microvessels in each layer. MVD differed significantly between HP and TA in the upper layer (P = 0.034), but there were no significant differences in upper + middle (P = 0.289) layer or all layers (P = 0.762)

aMicrovessels were divided into the following three groups according to mucosal surface–vessel distance: upper layer (≤150 μm), upper and middle layer (>0 to ≤300 μm), and all layers (>0 to ≤450 μm)

Fig. 2

MVD, MVA, and MVC of NM, HP, and TA. MVD and MVA differed significantly between NM and TA and between HP and TA, but did not differ significantly between NM and HP in the upper layer. MVC differed significantly between NM and HP and between TA and HP in the upper layer. There were no significant differences in MVD, MVA, or MVC between NM, HP, or TA in the middle layer or lower layer. When microvessel analysis was done after combining the upper and middle layers (0–300 μm) or the upper, middle, and lower layers (0–450 μm), MVD differed significantly between HP and TA in the upper layer, but there were no significant differences in upper and middle layer (0–300 μm) or all layers (0–450 μm)

Mean MVA values are summarized in Tables 3 and 4 and Fig. 2. In the upper layer, MVA differed significantly between NM and TA (P < 0.001) as well as between HP and TA (P < 0.001), but did not differ significantly between NM and HP. There were no significant differences in MVA between NM, HP, or TA in the middle layer or lower layer.

Table 3

Relationship between microvessel area (MVA) and mucosal surface–vessel distance

	Average MVA (μm2)
	Upper (≤150)a	Middle (>150 to ≤300)a	Lower (>300 to ≤450)a
Normal mucosa (NM)	1,263 ± 364	757 ± 365	1,129 ± 808
Hyperplasia (HP)	1,031 ± 653	1,651 ± 637	911 ± 398
Tubular adenoma (TA)	3,782 ± 2,361	1,863 ± 1,626	845 ± 420

Microvessel area was defined as the sum of the areas of all individual microvessels in each layer. MVA differed significantly between NM and TA (P < 0.001), as well as between HP and TA (P < 0.001) in the upper layer

aMicrovessels were divided into the following three groups according to mucosal surface–vessel distance: upper layer (≤150 μm), upper and middle layer (>0 to ≤300 μm), and all layers (>0 to ≤450 μm)

Table 4

Relationship between microvessel area (MVA) and mucosal surface–vessel distance

	Average MVA (μm2)
	Upper (≤150)a	Upper + middle (>0 to ≤300)a	All (>0 to ≤450)a
Normal mucosa (NM)	1,263 ± 364	1,010 ± 339	1,050 ± 413
Hyperplasia (HP)	1,031 ± 653	1,288 ± 502	1,162 ± 405
Tubular adenoma (TA)	3,782 ± 2,361	2,823 ± 1,601	2,163 ± 1,102

MVA differed significantly between NM and TA (P < 0.001), as well as between HP and TA in the upper layer (P < 0.001), upper + middle layer (P = 0.008), and all layers (P = 0.034)

aMicrovessels were divided into the following three groups according to mucosal surface–vessel distance: upper layer (≤150 μm), upper and middle layer (>0 to ≤300 μm), and all layers (>0 to ≤450 μm)

Mean MVC values are summarized in Table 5 and Fig. 2. In the upper layer, MVC differed significantly between NM and HP (P = 0.04) and between HP and TA (P = 0.012), but did not differ between NM and TA. There were no significant differences in MVC between NM, HP, or TA in the middle layer or lower layer. MVC did not differ significantly between TA and HP in all layers or in the upper plus middle layers.

Table 5

Relationship between microvessel count (MVC) and mucosal surface-vessel distance

	Average MVC (no. of microvessels/mm2)
	Upper (≤150)a	Middle (>150 to ≤300)a	Lower (>300 to ≤450)a
Normal mucosa (NM)	157.3 ± 51.5	82.7 ± 32.0	84.0 ± 51.0
Hyperplasia (HP)	97.3 ± 62.3	118.7 ± 52.8	70.7 ± 31.6
Tubular adenoma (TA)	89.3 ± 40.5	174.7 ± 43.6	84.0 ± 56.6

Microvessel count was defined as the sum of the number of all individual microvessels in a field. MVC differed significantly between NM and HP (P = 0.04) and between HP and TA (P = 0.012) in the upper layer

aMicrovessels were divided into the following three groups according to mucosal surface–vessel distance: upper layer (≤150 μm), upper and middle layer (>0 to ≤300 μm), and all layers (>0 to ≤450 μm)

Discussion

NBI systems have two major characteristics. First, these systems use light with a wavelength of 415 μm, which is absorbed by hemoglobin, thereby enhancing the visualization of microvessels. Second, because NBI systems use light with short wavelengths the penetration depth is shallow. The structure of the superficial layer can therefore be visualized more clearly than that on imaging with the use of white light. Many studies have reported that NBI is useful for the diagnosis of colorectal lesions [9, 23, 24]. To our knowledge, however, no previous study has examined the relationship between NBI images and the microstructures of blood vessels according to the depth from the mucosal surface. A better understanding of this relationship may facilitate the diagnosis and evaluation of lesions.

First, three-dimensional images of TA, HP and NM were reconstructed for microvessels in this study. An important advantage of 3-dimensional reconstruction based on digitized images is that microvascular structures can be reconstructed from arbitrarily selected layers of lesions. This enables images obtained by NBI magnification to be compared with microvascular structure according to the distance from the mucosal surface. Reconstructed images of TA and NM to a depth of less than 150 μm were in accord with the images obtained by NBI magnification. On the other hand, reconstructed images to a depth of less than 450 μm were not consistent with NBI images because many layers of microvessels appeared to overlap in a complex fashion.

Although we could not accurately evaluate the depth of microvessels seen on NBI on the basis of 3-dimensional reconstructed images, these results suggested that NBI magnification can accurately depict superficial microvessels in mucosa located to a depth of around 150 μm.

When microvessel analysis was performed according to depth, MVD, MVA, and MVC were found to differ significantly among NM, HP, and TA only in the upper layer. When microvessel analysis was done after combining the upper and middle layers (0–300 μm) or the upper, middle, and lower layers (0–450 μm), mean MVD was slightly but not significantly higher in TA than in HP. Moreover, the statistical significance of the difference in MVA between TA and HP (i.e., MVA greater in TA than in HP) became stronger when only the most superficial layers were evaluated.

Several investigators have reported that the diameter of microvessels is larger in neoplastic lesions than in non-neoplastic lesions [9, 23–25]. Therefore, the fine microvascular architecture of TA is often evaluated by means of NBI magnification.

Our results were consistent with the findings of previous studies. In our study, MVD tended to be larger in TA than in HP in the more superficial layers. However, MVD differed significantly between TA and HP only in the upper layer. Because NBI uses light with shorter wavelengths than white light, it can more clearly depict microvessels in the superficial layer of the mucosa. One factor underlying the high diagnostic capability of NBI magnification is the fact that NBI can more accurately detect differences in MVD between TA and HP (i.e., MVD is larger for TA than HP) in the superficial layer, as compared with techniques using white light.

Several investigators have reported that TA lesions can be discriminated from non-neoplastic lesions on NBI because the surface of adenomas is darker brown than that of non-neoplastic lesions [11]. In our study, the MVA of microvessels differed significantly between TA and non-neoplastic lesions. The difference in MVA was particularly large in the superficial layer. MVA is thought to correlate with the volume of microvessels. TAs thus had more microvessels than non-neoplastic lesions in the superficial layer. This higher microvessel volume is considered responsible for the darker brown appearance of adenomas on NBI.

MVD and MVA differed significantly between TA and non-neoplastic lesions, whereas MVC did not. It is speculated that thicker and higher volumes of microvessels are important characteristics of TA.

Tanaka et al. [26] reported that some HP lesions had features similar to those of TA. In our study, some HP lesions had large MVD and MVA, as shown in Fig. 1. Such HP lesions may be difficult to distinguish from TA.

Our study had a limitation. We assessed microvessels to a depth of only 450 μm. However, 3-dimensional reconstructed images of microvessels to a depth of 150 μm were consistent with the images on NBI. Therefore, a depth down to 450 μm was considered a sufficient range for evaluating microvessels in the superficial layer of the mucosa.

In conclusion, our results suggest that TA is characterized by thicker microvessels and a higher volume of microvessels than HP and NM. This tendency was most clearly demonstrated in the superficial layer of the mucosa. Because NBI using light with shorter wavelengths than that of white light, it can more reliably detect the characteristics of microvessels, potentially contributing to higher diagnostic accuracy.