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1.
Am J Dermatopathol ; 41(11): e139-e143, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31169525

ABSTRACT

Mycosis fungoides (MF) variants with different clinicopathologic and immunohistochemical features have been well-delineated. We report a case of scleromyxedematous changes arising in a patient with long-standing MF who progressed to Sézary syndrome (SS) shortly afterward. Total-skin electron-beam radiation therapy resulted in an excellent response, controlling both the MF/SS and the scleromyxedematous lesions; however, the patient died few months later. Although mucin deposition has been described in association with MF/SS (mainly follicular mucinosis in folliculotropic MF), there are limited reports in the literature on dermal mucinosis and scleromyxedematous changes in MF/SS. The mechanism of this association and its prognostic implications requires further investigation.


Subject(s)
Mycosis Fungoides/pathology , Neoplasms, Multiple Primary/pathology , Sezary Syndrome/pathology , Skin Neoplasms/pathology , Aged , Humans , Male
3.
J Pathol Inform ; 8: 30, 2017.
Article in English | MEDLINE | ID: mdl-28828201

ABSTRACT

CONTEXT: Histopathological characterization of colorectal polyps is critical for determining the risk of colorectal cancer and future rates of surveillance for patients. However, this characterization is a challenging task and suffers from significant inter- and intra-observer variability. AIMS: We built an automatic image analysis method that can accurately classify different types of colorectal polyps on whole-slide images to help pathologists with this characterization and diagnosis. SETTING AND DESIGN: Our method is based on deep-learning techniques, which rely on numerous levels of abstraction for data representation and have shown state-of-the-art results for various image analysis tasks. SUBJECTS AND METHODS: Our method covers five common types of polyps (i.e., hyperplastic, sessile serrated, traditional serrated, tubular, and tubulovillous/villous) that are included in the US Multisociety Task Force guidelines for colorectal cancer risk assessment and surveillance. We developed multiple deep-learning approaches by leveraging a dataset of 2074 crop images, which were annotated by multiple domain expert pathologists as reference standards. STATISTICAL ANALYSIS: We evaluated our method on an independent test set of 239 whole-slide images and measured standard machine-learning evaluation metrics of accuracy, precision, recall, and F1 score and their 95% confidence intervals. RESULTS: Our evaluation shows that our method with residual network architecture achieves the best performance for classification of colorectal polyps on whole-slide images (overall accuracy: 93.0%, 95% confidence interval: 89.0%-95.9%). CONCLUSIONS: Our method can reduce the cognitive burden on pathologists and improve their efficacy in histopathological characterization of colorectal polyps and in subsequent risk assessment and follow-up recommendations.

4.
Exp Mol Pathol ; 103(2): 172-177, 2017 10.
Article in English | MEDLINE | ID: mdl-28822769

ABSTRACT

Advanced stage malignant melanoma often responds poorly to therapy with low survival rates. New therapeutic approaches are based upon a growing understanding of the underlying molecular abnormalities. We demonstrate the feasibility of a next generation sequencing (NGS) assay, which targets hotspots in 50 cancer genes, to assess genotypes that may influence therapeutic selection and response. DNA was extracted from formalin fixed paraffin embedded (FFPE) melanoma specimens to create multiplexed libraries which were sequenced. Of the 121 cases, BRAF mutations were present in 48 cases (40%) and NRAS mutations in 24 cases (20%). We identified other gene variants in 20 BRAF-mutated cases. Additional gene variants were also identified in the 57 BRAF wild-type cases. Four patients harbored different gene mutations at metastatic sites as compared to their primary lesions or metastasis from different sites. Concurrent gene variants may provide additional targets for future therapies and may suggest alternative mechanisms of secondary resistance.


Subject(s)
Biomarkers, Tumor/genetics , DNA Mutational Analysis/methods , GTP Phosphohydrolases/genetics , High-Throughput Nucleotide Sequencing/methods , Melanoma/diagnosis , Membrane Proteins/genetics , Mutation , Proto-Oncogene Proteins B-raf/genetics , Female , Genotype , Humans , Male , Melanoma/genetics , Middle Aged , Neoplasm Metastasis , Paraffin Embedding , Prognosis , Retrospective Studies
7.
J Cutan Pathol ; 43(1): 32-40, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26347360

ABSTRACT

Early cutaneous Lyme disease, erythema migrans, may show different histopathologic patterns. The intent of this case series is to raise awareness of these findings to prevent misdiagnosis and keep this entity in the differential. Erythema migrans develops after a tick bite and subsequent infection with the spirochete, Borrelia burgdorferi. It most commonly manifests as a solitary, annular lesion with a bull's-eye appearance. Classic histopathologic findings include superficial and deep perivascular and interstitial lymphocytic infiltrates mixed with plasma cells and eosinophils. We identified and reviewed eight cases of early erythema migrans. Each patient had confirmed B. burgdorferi IgM seropositivity and IgG seronegativity. Histopathologic evaluation of these biopsies reveals a diversity of patterns. Seven of eight cases show sparse to mild perivascular and interstitial mixed infiltrate of variable amount of lymphocytes, eosinophils, neutrophils and plasma cells, with only one case showing a dense inflammatory infiltrate. Epidermal changes such as spongiosis and interface change are seen in some cases. Additionally, perineural lymphocytic infiltrate is seen in one case, periadnexal infiltrate in four cases and pigment incontinence in one case. Based on variable histopathologic findings, it is important to consider erythema migrans in the differential diagnosis for prompt diagnosis and treatment.


Subject(s)
Borrelia burgdorferi/immunology , Erythema Chronicum Migrans/diagnosis , Tick Bites/microbiology , Adult , Aged , Diagnosis, Differential , Erythema Chronicum Migrans/immunology , Erythema Chronicum Migrans/microbiology , Female , Humans , Immunoglobulin M/metabolism , Male , Middle Aged , Retrospective Studies , Tick Bites/immunology
9.
Endocrinology ; 150(5): 2446-53, 2009 May.
Article in English | MEDLINE | ID: mdl-19116342

ABSTRACT

The primary induced isoflavones in soybean, the glyceollins, have been shown to be potent estrogen antagonists in vitro and in vivo. The discovery of the glyceollins' ability to inhibit cancer cell proliferation has led to the analysis of estrogenic activities of other induced isoflavones. In this study, we investigated a novel isoflavone, glycinol, a precursor to glyceollin that is produced in elicited soy. Sensitive and specific in vitro bioassays were used to determine that glycinol exhibits potent estrogenic activity. Estrogen-based reporter assays were performed, and glycinol displayed a marked estrogenic effect on estrogen receptor (ER) signaling between 1 and 10 microM, which correlated with comparable colony formation of MCF-7 cells at 10 microM. Glycinol also induced the expression of estrogen-responsive genes (progesterone receptor and stromal-cell-derived factor-1). Competitive binding assays revealed a high affinity of glycinol for both ER alpha (IC(50) = 13.8 nM) and ER beta (IC(50) = 9.1 nM). In addition, ligand receptor modeling (docking) studies were performed and glycinol was shown to bind similarly to both ER alpha and ER beta. Taken together, these results suggest for the first time that glycinol is estrogenic and may represent an important component of the health effects of soy-based foods.


Subject(s)
Fermentation/physiology , Flavonols/isolation & purification , Glycine max/chemistry , Glycine max/metabolism , Phytoestrogens/isolation & purification , Binding, Competitive , Cell Proliferation/drug effects , Cells, Cultured , Drug Evaluation, Preclinical , Estrogens/isolation & purification , Estrogens/metabolism , Estrogens/pharmacology , Flavonols/chemistry , Flavonols/metabolism , Flavonols/pharmacology , Gene Expression Regulation/drug effects , Humans , Models, Biological , Models, Molecular , Phytoestrogens/chemistry , Phytoestrogens/metabolism , Phytoestrogens/pharmacology , Pterocarpans/chemistry , Receptors, Estrogen/metabolism , Receptors, Estrogen/physiology , Transcription, Genetic/drug effects
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