In Vivo and Ex Vivo Confocal Microscopy for Nail Diseases

Author(s):  
Diletta Fiorani ◽  
Jean Luc Perrot ◽  
Pietro Rubegni ◽  
Elisa Cinotti
2022 ◽  
Vol 11 (2) ◽  
pp. 393
Author(s):  
Alvin Wei Jun Teo ◽  
Hassan Mansoor ◽  
Nigel Sim ◽  
Molly Tzu-Yu Lin ◽  
Yu-Chi Liu

Keratoconus is the most common primary corneal ectasia characterized by progressive focal thinning. Patients experience increased irregular astigmatism, decreased visual acuity and corneal sensitivity. Corneal collagen crosslinking (CXL), a minimally invasive procedure, is effective in halting disease progression. Historically, keratoconus research was confined to ex vivo settings. In vivo confocal microscopy (IVCM) has been used to examine the corneal microstructure clinically. In this review, we discuss keratoconus cellular changes evaluated by IVCM before and after CXL. Cellular changes before CXL include decreased keratocyte and nerve densities, disorganized subbasal nerves with thickening, increased nerve tortuosity and shortened nerve fibre length. Repopulation of keratocytes occurs up to 1 year post procedure. IVCM also correlates corneal nerve status to functional corneal sensitivity. Immediately after CXL, there is reduced nerve density and keratocyte absence due to mechanical removal of the epithelium and CXL effect. Nerve regeneration begins after 1 month, with nerve fibre densities recovering to pre-operative levels between 6 months to 1 year and remains stable up to 5 years. Nerves remain tortuous and nerve densities are reduced. Corneal sensitivity is reduced immediately postoperatively but recovers with nerve regeneration. Our article provides comprehensive review on the use of IVCM imaging in keratoconus patients.


Pancreatology ◽  
2001 ◽  
Vol 1 (1) ◽  
pp. 48-57 ◽  
Author(s):  
Tobias Keck ◽  
Vanessa Campo-Ruiz ◽  
Andrew L. Warshaw ◽  
R. Rox Anderson ◽  
Carlos Fernández-del Castillo ◽  
...  

Cornea ◽  
2008 ◽  
Vol 27 (4) ◽  
pp. 439-445 ◽  
Author(s):  
Akira Kobayashi ◽  
Yasuhisa Ishibashi ◽  
Yosaburo Oikawa ◽  
Hideaki Yokogawa ◽  
Kazuhisa Sugiyama

2014 ◽  
Vol 92 ◽  
pp. 0-0
Author(s):  
M HAOUAS ◽  
C GUILLEMOT ◽  
D GRIVET ◽  
E CINOTTI ◽  
JL PERROT ◽  
...  

2020 ◽  
Vol 13 (11) ◽  
Author(s):  
Elisa Cinotti ◽  
Valerio Belgrano ◽  
Bruno Labeille ◽  
Damien Grivet ◽  
Catherine Douchet ◽  
...  

2006 ◽  
Vol 175 (1) ◽  
pp. 327-336 ◽  
Author(s):  
Vanessa Campo-Ruiz ◽  
Gregory Y. Lauwers ◽  
R. Rox Anderson ◽  
Emilio Delgado-Baeza ◽  
Salvador González

2021 ◽  
Author(s):  
Khuong Duy Mac ◽  
Muhammad Mohsin Qureshi ◽  
Myeongsu Na ◽  
Sunghoe Chang ◽  
Hyuk-Sang Kwon ◽  
...  

AbstractIn microscopic imaging of biological tissues, particularly real-time visualization of neuronal activities, rapid acquisition of volumetric images poses a prominent challenge. Typically, two-dimensional (2D) microscopy can be devised into an imaging system with 3D capability using any varifocal lens. Despite the conceptual simplicity, such an upgrade yet requires additional, complicated device components and suffers a reduced acquisition rate, which is critical to document neuronal dynamics properly. In this study, we implemented an electro-tunable lens (ETL) in the line-scan confocal microscopy, enabling the volumetric acquisition at the rate of 20 frames per second with the maximum volume of interest of 315 × 315 × 80 μm3. The axial extent of point-spread-function (PSF) was 17.6 ± 1.6 μm and 90.4 ± 2.1 μm with the ETL operating in either stationary or resonant mode, respectively, revealing significant depth elongation by the resonant mode ETL microscopy. We further demonstrated the utilities of the ETL system by volume imaging of cleared mouse brain ex vivo samples and in vivo brains. The current study foregrounds the successful application of resonant ETL for constructing a basis for a high-performance 3D line-scan confocal microscopy system, which will enhance our understanding of various dynamic biological processes.


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