Related Experiment Video
Updated: Jan 7, 2026

Author Spotlight: Genetically Engineered Mouse Models and Pathological Characterization of Neurofibromatosis Type 1 Associated Tumors
Published on: May 17, 2024
The evolving roles of pathologists in paragangliomas and pheochromocytomas
Ozgur Mete1,2,3, C Christofer Juhlin4,5
1Department of Pathology, University Health Network, Toronto General Hospital, 200 Elizabeth Street, 11 Floor, Toronto, ON, M5G 2C4, Canada. ozgur.mete2@uhn.ca.
Abstract:
Intra-adrenal (historically "pheochromocytoma") and extra-adrenal paragangliomas (PPGLs) represent a unique subset of non-epithelial neuroendocrine neoplasms that feature remarkable biological diversity with significant diagnostic complexity. Over the past decade, advances in molecular genetics, biomarker discovery, and integrative tumor classification have transformed our understanding of PPGL pathobiology and redefined the pathologist's role in their diagnosis and clinical management. This review outlines the current multidisciplinary approach to PPGLs, emphasizing practical diagnostic strategies, germline susceptibility testing, and evolving concepts in molecular risk stratification. Pathologists are now central to identifying heritable disease through a thorough morphology assessment and molecular immunohistochemistry, interpreting germline variants of uncertain significance, and integrating genomic and biochemical data into diagnostic reports that inform clinical management. Traditional morphology-based scoring systems such as PASS and GAPP have demonstrated limited prognostic reliability, leading to their replacement by dynamic, multidimensional models that combine histopathological, clinical, biochemical, and molecular features. The 5th edition of the WHO Classification of Endocrine and Neuroendocrine Neoplasms recognizes all PPGLs as malignant non-epithelial (paraneuronal) neuroendocrine neoplasms with variable metastatic potential, underscoring the importance of cell proliferation (Ki67, mitotic count), and accurate biomarker profiling-including SDHB, FH/2SC, CAIX, and molecular cluster-specific markers-to guide the dynamic risk assessment and genetic counseling. By taking into account common daily practice challenges, this review summarizes the evolving pathology practice in PPGLs, highlights the role of biomarkers in the diagnostic workup of these neoplasms, and provides practical pitfalls in the distinction of metastatic disease from germline susceptibility-related multifocal PPGL. It also expands on a modern framework for pathology practice rooted in dynamic risk assessment and integrative endocrine oncology principles.
More Related Videos
08:52Profiling Sensitivity to Targeted Therapies in EGFR-Mutant NSCLC Patient-Derived Organoids
Published on: November 22, 2021
10:13Modeling Astrocytoma Pathogenesis In Vitro and In Vivo Using Cortical Astrocytes or Neural Stem Cells from Conditional, Genetically Engineered Mice
Published on: August 12, 2014
Related Concept Videos
Sympathetic Pathways: Collateral Ganglia and Adrenal Medulla
Collateral Ganglia
Sympathetic preganglionic axons reach the collateral ganglia along the route of splanchnic nerves. These nerves bypass the sympathetic trunk and communicate with sympathetic postganglionic neurons housed in the prevertebral ganglia. These ganglia supply the organs of the abdominopelvic cavity.
The greater splanchnic nerve, formed by the...
Interactions Between Signaling Pathways
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
The Parathyroid Glands
Oxyphil cells, whose functions remain elusive, emerge during late puberty, adding a layer of complexity to the parathyroid gland's intricacies. In contrast, principal parathyroid cells undertake a vital role by...
Tumor Progression
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...