Confocal endoscopy
| Confocal endoscopy | |
|---|---|
 Insertion tip of an endoscope |
Confocal endoscopy, or confocal laser endomicroscopy (CLE), is a modern imaging technique that allows the examination of real-time microscopic and histological features inside the body. In the word "endomicroscopy", endo- means "within" and -skopein means "to view or observe". CLE, also known as "optical biopsy", can analyse histology and cytology features of a tissue which otherwise is only possible by tissue biopsy. Similar to confocal microscopy, the laser in CLE filtered by the pinhole excites the fluorescent dye through a beam splitter and objective lens. The fluorescent emission then follows similar paths into the detector. A pinhole is used to select emissions from the desired focal plane. Two categories of CLE exist, namely probe-based (pCLE) and the less common endoscopy-based endoscopy (eCLE).[1]
CLE can be intubated to study the gastrointestinal (GI) tract and accessory digestive organs with a fluorescent dye. A variety of diseases, including inflammatory bowel disease (IBD) and Barrett's oesophagus, can be diagnosed by the magnified and in-depth view in combination with traditional endoscopy.[2]
Significance
[edit]CLE can identify the lesions with a small depths of view under the tissue, in contrast to the surface level in conventional endoscopy.[3] It also allows clinicians to discriminate benign or malignant lesions through real-time histological diagnosis by revealing the properties of the lamina at a cellular level.[3][4]
An example is Whipple's disease.[5] Conventional endoscopy presents a whitish-patterned duodenal mucosa. CLE, in comparison, generates two images –– the superficial images show capillary leak in duodenal mucosa while the deep images show cells of duodenal mucosa, including goblet cells and foamy macrophages in lamina propria. Compared to histological examination of the same duodenal site after periodic acid-Schiff staining, CLE identifies similar patterns of goblet cells and foamy macrophages.[5]
Types
[edit]Two types of CLE have been invented, namely probe-based (pCLE) and endoscope-based CLE (eCLE).
Probe-based CLE
[edit]pCLE, developed by Mauna Kea Technologies, is a fibre bundle transit through the 2.8 mm working channel (the hollow hole) of the standard endoscope into the GI tract.[1] With a fixed plane of imaging, each fibre acts as a pinhole to filter unwanted noise. The frame rate lies between 9 and 12 images/second.[1]
| pCLE Products | Usage |
|---|---|
| GastroFlex | Upper GI |
| ConolFlex | Lower GI |
| CholangioFlex | Cholangiopancreatography |
| AQ-19 | Fine needle aspiration |
| Needle-based CLE | Endoscopic ultrasound needle (EUS) |
Endoscope-based CLE
[edit]eCLE, developed by Pentax, is a confocal microscopy fixed at the end of the endoscopic tube. The integrated machine of eCLE is larger than the pCLE in diameter, making GI tract endoscopic intubation more difficult. eCLE has ceased commercially due to the camera's inflexibility.[1]
Medical uses
[edit]
Oesophagus
[edit]CLE is effective in detecting premalignant, including Barrett's oesophagus, and malignant (cancerous) lesions in the upper GI tract.[3][6][7] The modifications of mucosa shown in histopathology as an index of malignancy can be identified under CLE, such as high-grade dysplasia. CLE can also be implemented to refer to the treatment of Barrett's oesophagus by measuring the lateral extent of neoplasia.[3][7]
The Miami classification is the most popular system in oesophageal CLE diagnosis.[6][8]
Stomach and duodenum
[edit]Similar to that of the oesophagus, CLE is able to detect early gastric cancer, as well as premalignant conditions, such as gastritis and intestinal metaplasia.[1][2][6] CLE can detect and distinguish the stomach pit patterns to identify the disease in accordance with the Miami classification, which was refined in 2016 to include both pit patterns and the architecture of blood vessels.[1][2][8][9] The refined classification allows clinicians to differentiate between neoplastic and non-neoplastic lesions.[9]
The presence of Helicobacter pylori can also be identified using CLE by viewing the morphological changes in tissues.[10][11]
Lower Gastrointestinal Tract
[edit]CLE reveals "soccer ball-like pattern" of narrower capillaries in malignant lymphomas; distorted architecture and fluorescein leakage from lumen in colonic adenocarcinoma; and blunt-shaped villi and crypts and increased intraepithelial lymphocytes in coeliac disease.[1][2][12]
CLE can be utilized to identify adenoma and neoplasia in colorectal polyps and lesions.[13][14] The Miami classification provides guidelines for clinicians to differentiate neoplastic and non-neoplastic lesions.[8]
Inflammatory Bowel Disease (IBD)
[edit]CLE can be used for the identification of IBD and its subtypes (Crohn's disease and ulcerative colitis) based on the observation on morphological characteristics, such as architectural distortion, lowered crypt density, crypt irregularity and an abnormally high density of epithelial gaps.[1][2][15] The prediction of IBD progression on non-inflamed epithelium is achievable, too, making way for a novel "treat-to-target" therapeutic approach.[1][2]
Pancreas
[edit]Incorporating an EUS, CLE can accurately diagnose pancreatic cystic lesions, including mucinous and non-mucinous lesions.[2][16] Special needles are used to collect fluid and cyst wall tissues for testing.[16] Pancreatic ductal adenocarcinoma (PDAC) can also be viewed by CLE.[4] Observing cystic lesions and PDAC, clinicians can identify early chronic pancreatitis and determine the malignancies of lesions.[4]
Biliary duct
[edit]Biliary stricture can be viewed by CLE.[1] The Miami and Paris classifications can be adapted to differentiate cancerous and inflammatory causes.[17]
Others
[edit]The discrimination of inflammation and malignant tumor in lung and the urinary system may be done by using CLE and this is currently under research.[10][18] Some usages such as oral and other head-and-neck cancer diagnosis have been proposed.[19][20]
Molecular imaging
[edit]
Antibodies of molecular targets are used to diagnose GI diseases by histology.[21][22] CLE captures the fluorescence produced by specific antibodies binding to vascular endothelial growth factor (VEGF). Comparing the significant difference in fluorescent strength, clinicians can differentiate normal and neoplastic tissue. Molecular imaging with antibodies may be applied to CLE as a diagnostic benchmark due to high correlation with ex vivo microscopy.[21]
The molecular imaging technique can be used in a similar manner in the examination of head and neck cancer using CLE, though the diagnostic targets may be different from those in the gastrointestinal tract.[20][23]
Mechanism
[edit]
Basic mechanism
[edit]The laser emitted by CLE through a pinhole is reflected by the beam splitter or a dichroic mirror and focused by an objective lens. The fluorescent dye in targeted tissue is excited and emits a specific wavelength. The emission from the focal plane of the tissue then is collected by the objective lens and the beam splitter. The laser is eventually filtered by a pinhole to reduce out-of-focus noise to enter the detector or photomultiplier tube.[1]
Topical dyes
[edit]Cresyl violet and acriflavine can be used as topical dyes. Cresyl violet is a common stain in histology used for light microscopy sections, especially brain sections. In CLE, it can enhance the viewing of the cytoplasm, yet it limits tissue penetration and does not show anything about vasculature. Acriflavine is an antiseptic and dye. In CLE, it can stain the nuclei of GI surface epithelial cells. It is however subjected to cytotoxic and mutagenic properties, in addition to common side effects of irritation.[1]
Intravenous dyes
[edit]
Fluorescein is the most popular IV dye for CLE. Fluorescein is an FDA-cleared dye that is used in ophthalmology clinics in routine as it appears green under cobalt blue light.[12] It is commonly applied topically to identify corneal diseases with slit lamp microscopes including corneal abrasion, ulcers, and infections; or intravenously to identify retinal diseases with angiography including macular degeneration and diabetic retinopathy. In CLE, it is usually administered intravenously immediately before the intubation of an endoscopic tube. The fluorescence is reported to be the most prominent from a few seconds to 8 minutes.[1] Fluorescein is slowly eliminated; thus the fluorescence slowly decays up to a minimal detectable level after 1 hour, giving a time window for clinicians to investigate.[1]
Recognition and optical flow algorithm
[edit]CLE's narrow field of vision makes it difficult for clinicians to identify the location and path of the probe, making it challenging to correspond the image obtained and the lesion location and direction. Research has proposed a crypt recognition algorithm, which predicts the pixel displacement by the moving angle and distance. By restoring the exploration path of CLE, clinicians can locate the sites of interest and improve diagnostic efficiency.[24]
Image quality assessment
[edit]Research has proposed a new assessment method for filtering images yielded from CLE. As CLE often encounters image distortions, the degradation of image quality and loss of image information, eventually increase the difficulty of accurate diagnosis.[25] A new image quality assessment (IQA) utilising Weber's Law and local descriptors assesses the quality and filters images with low diagnostic value.[25]
Limitations
[edit]
The variety of pathology conditions identifiable by CLE is limited.[3] The histological diagnosis is limited to cancerous lesions and inflammation where the number of specific diseases identifiable is not numerous. Moreover, it requires specific training to operate CLE and correctly interpret CLE images, which are rarely used skills by experts in endoscopy.[10][14] Owing to the narrow field of view, the applications of CLE might be restricted.[1] Computer-aided diagnosis with AI technology may be beneficial in diagnosing CLE images.[2]
Fluorescein is the only safe dye approved while cresyl violet and acriflavine are commonly used agents. The lack of choice of contrast agents may limit the application of CLE.[2] For instance, patients allergic to fluorescein should never undergo CLE that involves the use of this intravenous dye.[4]
The optical system consists of complex microscopic optical instruments, which are difficult to manufacture and assemble.[2] Therefore, the tool is expensive.[3]
CLE is mostly used in combination with other techniques instead of replacing conventional endoscopy with biopsy.[7] CLE can only serve as a complementary to the traditional biopsy. By sharing the same working channel, conventional biopsy and CLE can be done alternatively by single intubation.[2]
Adverse effects
[edit]
The allergic properties of fluorescein, the common intravenous fluorescent dye for CLE, is the major culprit for the mild adverse events.[13]
Intubation
[edit]CLE, similar to other diagnostic endoscopic techniques, may give rise to pancreatitis when used to examine the pancreas.[13][26] The likelihood for pancreatitis is especially high in needle-based CLE. The incidence can be minimized by shortening the inspection time and avoiding excessive needle movement within the pancreatic cyst wall.[13]
Fluorescein
[edit]
Mild side effects, which are rare, include[1]
- Nausea
- Vomiting with mild epigastric pain
- Rash at injection site
- Transient hypotension without shock
- Diffuse erythema
These effects are manageable unless patients have prior experiences of them.[1]
Cases of anaphylaxis are reported by ophthalmological uses of fluorescein. Prophylactic use of antihistamines can reduce the chances of allergic reactions or skin prick tests can identify the risk of allergic reactions.[1]
Acriflavine
[edit]Acriflavine, another contrast agent for CLE, is potentially carcinogenic to humans due to its known mutagenic ability. The dye is therefore not approved by the FDA.[13]
History
[edit]CLE is a modern, in vivo adaptation of confocal microscopy, the microscopic technique invented by Marvin Minsky in 1957.[10]
Since 2004, CLE has been used for observing histopathological changes in gastrointestinal tissues.[10]
See also
[edit]References
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