500-MHz quantitative acoustic microscopy imaging of unstained fixed 6-µm thin sections from cancerous human lymph nodes

Author(s):  
Daniel Rohrbach ◽  
Emi Saegusa-Beecroft ◽  
Junji Machi ◽  
Ernest J. Feleppa ◽  
Jonathan Mamou
HYBRIDS ◽  
1992 ◽  
Vol 8 (3) ◽  
pp. 31-33
Author(s):  
Steven R. Martell ◽  
Thomas E. Adams

Author(s):  
F. Al-Bagdadi ◽  
C. Seger

Hemal lymph nodes occur in a wide range of animals including ruminants, primates, horses and man. It is generally believed that they are separate lymphatic organs capable of performing hemopoietic and immunologic functions. The plasma cells are the main source of antibody synthesis. They are formed when antigens enter B-lymphocytes and induce their transformation into plasma cells. The plasma cells release immunoglobulins (Russell's bodies) directly into adjacent tissues.Different reports expressed varied opinions on the significance and the fate of Russell bodies in plasma cells. Some of the opinions are that Russell bodies appear in pathological conditions. it is believed that the appearance of Russell's bodies in plasma cells is a cellular defect. They are also considered heterogenous in nature. This report shows that Russell bodies have appeared in plasma cell of healthy ovine hemal lymph nodes.Hemal lymph nodes were collected from different regions near the viscera of five native Louisiana sheep. Small slices of the nodes were fixed in 3% gluteraldehyde in phosphate buffer (pH 7.4), postfixed in 1% OSO4 and embedded in epon. Ultra-thin sections were examined with a Zeiss 10 electron microscope.


1994 ◽  
Vol 48 (7) ◽  
pp. 857-866 ◽  
Author(s):  
Hannah R. Morris ◽  
Clifford C. Hoyt ◽  
Patrick J. Treado

Acousto-optic tunable filters (AOTF) and liquid crystal tunable filters (LCTF) are evaluated for their suitability as fluorescence microscopy imaging spectrometers. AOTFs are solid-state birefringent crystals that provide an electronically tunable spectral notch passband in response to an applied acoustic field. LCTFs also provide a notch passband that can be controlled by incorporating liquid crystal waveplate retarders within a Lyot birefringent filter. In this paper, spectroscopic performance and imaging quality are contrasted by evaluation of model systems. Studies include transmission imaging of standard resolution targets, multispectral fluorescence emission imaging of tagged polystyrene microspheres, and immunofluorescence imaging of neurotransmitters within rat-brainstem thin sections. In addition, the first use of LCTFs for Raman microscopy is demonstrated. Raman microscopy is a noninvasive spectral imaging technique that can provide chemically significant image contrast complementary to fluorescence microscopy without the use of stains or tags.


2018 ◽  
Vol 26 (2) ◽  
pp. 141-148
Author(s):  
Mihaela Ignat ◽  
Veronique Lindner ◽  
Michel Vix ◽  
Jacques Marescaux ◽  
Didier Mutter

Background. Frozen section is the standard method to histologically distinguish parathyroid tissue from thyroid tissue during endocrine neck surgery. Frozen section can be time-consuming and costly. Its drawback is that it is to be performed only after the removal of a suspected pathological tissue. This study demonstrates the use of probe-based confocal laser endomicroscopy (pCLE) to confirm histology prior to tissue resection. Design. A prospective, single-institution, nonrandomized study was conducted. No sample size calculation was performed for this observational trial. The primary objective was the description of histological rendering of normal and pathological tissues through pCLE. Real-time in vivo fluorescence microscopy imaging was performed with the CystoFlex UHD probe after intravenous injection of 2.5 mL of 10% fluorescein sodium. Results. Eleven patients with hyperparathyroidism and thyroid conditions were included. A total of 104 videos showing thyroid, parathyroid, adipose tissue, muscle, laryngeal nerve, and lymph nodes were recorded. Videos were compared with visual information and pathological samples (when sampling was indicated). Thyroid tissue could be identified based on the presence of colloid follicles (intensely fluorescent area surrounded by a small ridge of low-fluorescence epithelial cells) including the pathognomonic aspect of resorption vacuole. Parathyroid tissue could be identified based on a regular, “diamond-shaped” capillary network encompassing parathyroid chief cells. Blinded reinterpretation of pCLE videos demonstrated an 89.3% sensitivity and a 90% specificity as compared with histology in tissue recognition. Conclusion. This pilot study describes representative renderings of intraoperative pCLE to nontraumatically differentiate thyroid, parathyroid, and lymph nodes before surgical removal.


2020 ◽  
Vol 11 ◽  
pp. 703-716
Author(s):  
Edgar Cruz Valeriano ◽  
José Juan Gervacio Arciniega ◽  
Christian Iván Enriquez Flores ◽  
Susana Meraz Dávila ◽  
Joel Moreno Palmerin ◽  
...  

In this work, a high-resolution atomic force acoustic microscopy imaging technique is developed in order to obtain the local indentation modulus at the nanoscale level. The technique uses a model that gives a qualitative relationship between a set of contact resonance frequencies and the indentation modulus. It is based on white-noise excitation of the tip–sample interaction and uses system theory for the extraction of the resonance modes. During conventional scanning, for each pixel, the tip–sample interaction is excited with a white-noise signal. Then, a fast Fourier transform is applied to the deflection signal that comes from the photodiodes of the atomic force microscopy (AFM) equipment. This approach allows for the measurement of several vibrational modes in a single step with high frequency resolution, with less computational cost and at a faster speed than other similar techniques. This technique is referred to as stochastic atomic force acoustic microscopy (S-AFAM), and the frequency shifts of the free resonance frequencies of an AFM cantilever are used to determine the mechanical properties of a material. S-AFAM is implemented and compared with a conventional technique (resonance tracking-atomic force acoustic microscopy, RT-AFAM). A sample of a graphite film on a glass substrate is analyzed. S-AFAM can be implemented in any AFM system due to its reduced instrumentation requirements compared to conventional techniques.


2016 ◽  
Vol 140 (4) ◽  
pp. 3187-3187
Author(s):  
Jonathan Mamou ◽  
Daniel Rohrbach ◽  
Emi Saegusa-Beecorft ◽  
Junji Machi

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