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Masses in which the echo features were highly characteristic of a benign pathology were categorized as benign.
Fig. 3 Consensus diagnosis by two physicians using std-SPECT/CT according to a three-category scale: M0: no bone metastasis; Me: changes observed on BS that could not be categorized as benign or malignant; and M1: bone metastases.
The observers classified each std-SPECT/CT and UF-SPECT/CT result separately into one of three categories: (1) normal findings or findings considered to represent benign conditions (M0), (2) equivocal findings in which changes were observed on std-SPECT/CT or UF-SPECT/CT but could not be categorized as benign or malignant (Me), or (3) findings of bone metastases (M1).
If so, the nodule can be categorized as benign, and needs no further evaluation.
All IPMN samples categorized as benign displayed low-grade dysplasia by definition.
A disadvantage is that in cases where the protein is not degraded, but still impaired or dysfunctional, the result will be incorrectly categorized as benign.
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When a trained pathologist (JMC) evaluated all stained specimens to confirm their malignancy status and the presence of epithelial tissue, 118 breast tissue samples were re-categorized as benign or malignant, i.e., the core had been taken from a malignant part of the block although the intent had been to get a benign sample or vice versa.
All adverse events were categorized as mild.
As previously described, lesions were categorized as hyperplastic, benign adenoma and adenocarcinoma [ 15].
Cytological diagnoses were categorized as malignant, benign, indeterminate and inadequate [ 1, 14].
For clinical purposes, the majority of intraductal proliferations can be categorized as either (benign) epithelial hyperplasia or carcinoma in situ (usually ductal; i.e. DCIS).
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CEO of Professional Science Editing for Scientists @ prosciediting.com