Exemplos de uso de Hematoxylin-eosin staining em Inglês e suas traduções para o Português
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Observe the endometrial glands at the lower right corner. Hematoxylin-eosin staining.
The slides were subjected to hematoxylin-eosin staining and immunohistochemical study.
Hematoxylin-eosin staining was used to quantify the eosinophils in the peribronchovascular space.
Tissues were paraffin-embedded andhistological evaluation was performed using hematoxylin-eosin staining.
Hematoxylin-eosin staining was used and a Zeiss microscope with a 400x lens.
Among the patients staged as pN0 based on routine hematoxylin-eosin staining, 9 50% were restaged as N1.
The hematoxylin-eosin staining technique demonstrated better preserved cellular structures in the experimental groups compared to the Control Group.
Tissue samples were obtained from all the patients for histopathological examination using hematoxylin-eosin staining.
In the microscopic study,epithelization was qualified after hematoxylin-eosin staining and collagenation after picrosirius staining. .
All specimens were fixed in 10% buffered formalin, androutinely processed for paraffin embedding and hematoxylin-eosin staining.
The pathologic diagnosis of NEAME is primarily based on light microscopy with hematoxylin-eosin staining; the diagnosis is confirmed by immunohistochemical investigation.
The patient charts and medical requests for skin biopsies were the source of the clinical anddemographic data. Histopathology was carried out using routine hematoxylin-eosin staining.
The diagnosis is established by means of histopathological examination using hematoxylin-eosin staining which, when necessary, is complemented by immunohistochemistry of the lesion.
Interwoven network of osteoid trabeculae(black arrow),intermingled with richly vascularized loose connective tissue(green arrow)- hematoxylin-eosin staining, 4× magnification.
The samples were analyzed histologically by hematoxylin-eosin staining techniques, alcian blue and von kossa stains, in order to measure the area of the head versus the tibia epiphysial disc, beyond the thickness of the.
C: Prominent peripheral nerve(arrows)in soft tissues adjacent to the osteoid osteoma nidus- hematoxylin-eosin staining, 10× magnification.
The cases were examined by the Pathology Service using conventional hematoxylin-eosin staining techniques and were later sent to immunohistochemistry to check for expression of antibodies p53 and Ki-67.
Synovial tissue containing dense inflammatory mononuclear infiltrate,with development of lymphoid follicles(arrows)- hematoxylin-eosin staining, 10× magnification.
Cell proliferation was assessed by counting cells through mitosis at hematoxylin-eosin staining and by immunohistochemistry, with the use of the cell proliferation markers PCNA and Ki67.
Figure 3. a: Filiform fragment of fibroadipose tissue showing tubular glands intermingled with spindle cell stroma in one of the extremities hematoxylin-eosin staining, 100× magnification.
Microscopic, data were analyzed using the hematoxylin-eosin staining to verify the inflammatory process; immunohistochemistry, factor VIII, to observe the vascular density, and Masson trichrome to study fibrosis.
B: Squamous and cylindrical glandular epithelium with no atypical finding(asterisk) intermingled with spindle cell stroma with foci of hemorrhage,both with appearance resembling endometrium hematoxylin-eosin staining, 400× magnification.
Hematoxylin-eosin staining showed a chronic, granulomatous perivascular inflammatory process with vasculitis, in addition to thrombosed arteriole with image suggestive of paracoccidioides brasiliensis in its interior Figures 2 and 3.
We postulate that an alternative method, combining tissue microarray analysis and immunohistochemistry, can reduce costs andbe effective in detecting micrometastases in lymph nodes that have previously tested negative for NSCLC by routine hematoxylin-eosin staining.
The descriptive and morphometric histological analyses were performed with hematoxylin-eosin staining, but in the morphometric analysis the estimates of the diameter of the adipocytes Dv, the numerical density of adipocytes Nv and the volume density of adipocytes Vv were carried out.
This suggests that occult micrometastatic tumor cells, which are not detected using the methods currently available clinical staging andconventional histopathological techniques such as hematoxylin-eosin staining, spread to regional lymph nodes or to distant mesenchymal organs prior to the time of surgery.
Objectives: in patients with cervical cancer in stage ib1- iia(figo): 1 to assess the prevalence of pelvic lymph node micrometastasis(mi) through the immunoreactivity of antibody anti pan- cytokeratin ae1/ae3 in lymph node tissue and its correlation with tumor recurrence and overall survival; 2 to describe, in the primary tumor of patients with recurrence tumor and/or lymph node micrometastasis, the immunohistochemical expression(ihc) of the lymphatic endothelial marker d2-40 andtheir correlation with histopathologic findings by conventional hematoxylin-eosin staining.
Slides with hematoxylin-eosin stain were prepared, and were analyzed by a pathologist.
Biopsies went through routine histologic preparation and the slides were hematoxylin-eosin stained.
Figure 3 Vesicular nuclei, eosinophilic cytoplasm andhigh-density fragments could be seen in some cells hematoxylin-eosin stain, magnification 200×.