Background: Anticancer drugs for targeted molecular therapies have been applied to the treatment of lung cancer. Since the effects of medicine for adenocarcinoma (ADC) or squamous cell carcinoma (SQCC) differ, the ability to discriminate these lesions is important. In the present study, we examined whether ADC and SQCC could be distinguished using low-vacuum scanning electron microscopy (LVSEM) to examine cytopathological specimens.
Methods: Thirty-seven cases of bronchoscopic samples were retrospectively examined using LVSEM on the surface structures of the cancer cells.
Results: Among the Pap-stained slides, 81.1% of the cases could be distinguished: 96.2% of the ADC cases were distinguishable, and 45.5% of the SQCC cases were distinguishable. Among the significant findings for ADC using LVSEM, a spherical shape (73.1%), long filaments (65.4%), dense filaments (80.8%), and depression (57.7%) were seen. Among the significant findings for SQCC as observed using LVSEM, however, a flat shape (81.8%), sparse filaments (72.7%), and non-filament (81.8%) were seen. The overall accuracy of diagnosis using LVSEM was 83.8%: 80.8% for ADC and 90.9% for SQCC. The accuracy of a combination of Papstained slides and LVSEM was 97.3%.
Conclusions: The LVSEM method is useful as an ancillary examination for cytopathology after the classification of Pap-stained slides.
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http://dx.doi.org/10.11480/jmds.640101 | DOI Listing |
Med Mol Morphol
November 2024
Department of Nephrology and Hypertension, Blood Purification Center, Dokkyo Medical University, 880 Kitakobayashi, Mibu, Tochigi, 321-0293, Japan.
Am J Pathol
January 2025
Department of Experimental Pathology, Institute of Medicine, University of Tsukuba, Tsukuba, Japan.
Alport syndrome is a rare kidney disease typically more severe in males due to its X-linked inheritance. However, female patients with heterozygous X-linked Alport syndrome (XLAS) can develop renal failure over time, necessitating accurate pathologic assessment for effective therapy. A key pathologic finding in female patients with XLAS is the mosaic pattern of partial loss of α5 chains of type IV collagen (COL4α5).
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December 2024
Department of Nephrology and Hypertension, Dokkyo Medical University, Tochigi, Japan.
Sci Rep
June 2024
Institute of Combustion Engines and Powertrains, Poznan University of Technology, Pl. Marii Skłodowskiej-Curie 5, 60-965, Poznań, Poland.
Exhaust emissions, which count among the most common causes of premature death worldwide, can cause irreversible changes in cells, leading to their damage or degeneration. In this research, L929 line cells were observed after exposure in the BAT-CELL chamber to exhaust gases emitted from a Euro 6 compression-ignition engine. Real road traffic conditions were simulated, taking into account air resistance while driving at speeds of 50 km/h, 120 km/h and idling engine.
View Article and Find Full Text PDFRev Sci Instrum
May 2024
ICSM, University of Montpellier, CNRS, CEA, ENSCM, Bagnols-sur-Cèze, France.
The FurnaSEM microfurnace was installed in the chamber of a scanning electron microscope to carry out in situ experiments at high temperatures and test its limits. The microfurnace was used in combination with different types of detectors (Everhart-Thornley for the collection of secondary electrons in a high vacuum, gas secondary electron detector for the specific collection of secondary electrons in the presence of gas, and Karmen© detector for the collection of backscattered electrons at high temperature). Experiments carried out on various samples (metal alloys and ceramics) show that the microfurnace operates in both high-vacuum and low-vacuum modes.
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