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SCI Abstract
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Thyroid Tumors of Uncertain Malignant Potential (UMP)- Clinicopathologic and Molecular Characterization of 324 Cases
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Thyroblastoma Dominated by a Primitive Small Round Cell Component: A Diagnostic Pitfall
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Clinicopathologic and Molecular Features of Poorly Differentiated Thyroid Carcinomas in Adults ≤ 45 Years of Age
The clinical behavior and molecular underpinnings of rare cases of poorly differentiated thyroid carcinoma (PDTC) diagnose...
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Lineage Classification of Pituitary Neuroendocrine Tumors From Whole-Slide Images Using Attention-Guided Graph Representation Learning
Pituitary neuroendocrine tumors (PitNETs) are common sellar neoplasms and represent a major component of routine pituitary...
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Impact of Molecular Testing on Surgical Decision-Making in Indeterminate Thyroid Nodules: A Global Meta-Analysis Across Test Generations
Thyroid nodules with indeterminate cytology represent a clinical challenge owing to uncertain malignancy risk, often leadi...
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Molecular Profiling of Digestive Grade 3 Neuroendocrine Tumors Reveals a Shared Molecular Framework with Lower-Grade Tumors, Marked Heterogeneity, and Therapeutic Opportunities
Well-differentiated neuroendocrine tumors, grade 3 (NETs G3) of the digestive system are high-grade neuroendocrine neoplas...
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Three-Tier Prognostic Stratification of Lung Carcinoids (NET G1-G2-G3) by Multivariable, Data-Driven Integration of Ki-67 and Mitotic Count
Pulmonary neuroendocrine tumors (NETs) include typical and atypical carcinoids, corresponding to low- and intermediate-gra...
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Genomic Catastrophe Defines the Evolutionary Trajectory of Adrenocortical Carcinoma
The mechanisms underlying how adrenocortical carcinoma (ACC) progresses into a metastatic and lethal disease remain poorly...
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Neuroendocrine Tumors of the Gallbladder: A Multicenter Case Series and Systematic Literature Review Indicating Predominantly Non-Aggressive Tumor Behavior and a Common Association with Cholesterol Polyps and Cholesterolosis
Current data on neuroendocrine tumors (NETs) of the gallbladder and cystic duct (GB-NETs) are highly limited, and the avai...
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Distinct ALK Expression Patterns Are Associated with Canonical and Noncanonical Transcript Architectures in Oncocytic Thyroid Neoplasms
Oncocytic thyroid carcinomas are characterized by a unique chromosomal landscape and frequent resistance to radioactive io...
Endocrine Pathology
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An Integrative RNA Spliceosomic Landscape of Pancreatic Neuroendocrine Tumors Identifies Clinically Relevant Molecular Subgroups
Alterations in alternative splicing are emerging as a novel cancer hallmark, offering new insights into tumor biology. How...
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Prevalence and Histologic Features of Multifocal Fibrosing Thyroiditis in the Routine Pathology Practice
Multifocal fibrosing thyroiditis (MFT) is a poorly understood condition characterized by multiple fibrotic scar-like lesio...
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Integrated Pathologic, Genomic, and Transcriptomic Analysis of Renal Neuroendocrine Tumors Reveals Neuroendocrine Transcriptional Programs and Associated Gastrointestinal-Type Epithelium in a Subset of Cases
Renal well-differentiated neuroendocrine tumors (RenNETs) are rare primary renal neoplasms with enigmatic histogenesis. To...
Endocrine Pathology
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Circulating Tumor DNA Analysis in Adrenocortical Carcinoma: A Retrospective Cohort Study
Adrenocortical carcinoma (ACC) is a rare malignancy with high recurrence rates. Circulating tumor DNA (ctDNA) is a minimal...
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Expansion of Germline Variants in Primary Hyperparathyroidism: Fumarate Hydratase Deficiency as a Cause of Parathyroid Adenomas
A substantial fraction (60–85%) of hereditary primary hyperparathyroidism (hPHPT) lacks an identifiable genetic etio...
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A Cauda Equina Neuroendocrine Tumor with Tyrosine Hydroxylase Expression
Asa SL, Ezzat S, Mete O (2018) The Diagnosis and Clinical Significance of Paragangliomas in Unusual Locations. J Clin Med ...
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Tumor Necrosis is Associated with an Increased Metastatic and Cardiovascular Risk in Paragangliomas: A Single-Center Series and Meta-Analysis Comparing Necrosis and Cystic Degeneration in Paragangliomas
Paragangliomas (PGLs) are rare neural crest–derived tumors with highly variable morphology and clinical behavior. Th...
Endocrine Pathology
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Comprehensive Genomic Analysis in Hereditary Adrenal and Extra-Adrenal Paragangliomas
Adrenal and extra-adrenal paragangliomas (PPGLs) are highly heritable non-epithelial neuroendocrine neoplasms. Through a r...
Endocrine Pathology
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Neuroendocrine Neoplasms of the Urinary Bladder: Integrating Molecular Advances into a Refined Classification System
Neuroendocrine neoplasms (NENs) of the urinary bladder are rare but highly aggressive tumors that account for under 1% of ...
Endocrine Pathology
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Real-World-Feasible Immunohistochemistry of ATRX, DAXX, and Menin Identifies a Subgroup of Non-Functioning Pancreatic Neuroendocrine Tumors with low Recurrence Risk to Guide De-Escalating Surveillance
Non-functioning pancreatic neuroendocrine tumors (NF-pNETs) show a variable prognosis. Despite 40–60% of patients re...
Endocrine Pathology
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Digital Immunophenotyping of Lung Atypical Carcinoids and Large Cell Neuroendocrine Carcinomas Identifies Three Subtypes With Specific Tumor-Immune Microenvironment Features
Atypical carcinoids (ACs) and large cell neuroendocrine carcinomas (LCNECs) are defined by the WHO as intermediate- and hi...
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Performance of Immunohistochemistry to Detect Rb/p53 Alterations in High-Grade Neuroendocrine Neoplasms: Staining Patterns and Comparison with Genetic Testing
Rb and p53 status helps distinguishing well from poorly differentiated high-grade neuroendocrine neoplasms (HG-NENs) and m...
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Immunotherapy for Metastatic Pancreatic Neuroendocrine Tumors with High Mutational Burden and Mismatch Repair Alterations Following Treatment with Alkylating Chemotherapy
Alkylating agent-based chemotherapy is one of the main treatment options for patients with metastatic pancreatic neuroendo...
Endocrine Pathology
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Phenotypic Landscape of Pulmonary Neuroendocrine Tumors: Subtyped by OTP/ASCL1 Expression Correlated with Histology, Hormones and Outcome
Recent studies have shown that pulmonary neuroendocrine tumor (NET) subgroups, defined by the transcription factors OTP an...
Endocrine Pathology
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Molecular Subtypes of Pancreatic Neuroendocrine Tumors Mutated in Explain Biological Variability
About 40% of non-functioning (NF) Pancreatic Neuroendocrine Tumors (PanNETs) harbour mutations in MEN1, often co-occurring...
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Follicular Thyroid Carcinoma Relapse Cases - Revisited by X-ray 3D Virtual Histology
The diagnosis and prognosis of follicular thyroid neoplasms are based on the identification of capsular and vascular invas...
Endocrine Pathology
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Correction to: Molecular Subtypes of Pancreatic Neuroendocrine Tumors Mutated in Explain Biological Variability
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, whi...
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The Utility of Cabozantinib in the Therapy of Endocrine Tumours
Endocrine and neuroendocrine malignancies, including epithelial neuroendocrine neoplasms (NENs), phaeochromocytoma/paragan...
Endocrine Pathology
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Multi-center Assessment of DLL3 Expression by Immunohistochemistry in Medullary Thyroid Carcinoma
Medullary thyroid carcinoma (MTC) is a rare neuroendocrine malignancy accounting for 1–2% of thyroid carcinomas. As ...
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Quantitative Assessment of Focus Quality in Whole-Slide Imaging of Thyroid Liquid-Based Cytology Using Laplacian Variance
Reliable focus is essential for digital cytopathology, yet three-dimensional cell clusters in liquid-based cytology (LBC) ...
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