4.4 Article

The Spectrum of Endocrine Pathology

期刊

ENDOCRINE PATHOLOGY
卷 -, 期 -, 页码 -

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HUMANA PRESS INC
DOI: 10.1007/s12022-023-09758-0

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Endocrine pathology; Thyroid; Neuroendocrine cells; Steroidogenic tissues; Morphology; Immunohistochemistry; Molecular genetics

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Endocrine pathology encompasses a wide range of disorders originating from different parts of the body. Understanding this field requires knowledge of the structure and function of the endocrine system, including the signaling pathways involved in hormone synthesis and secretion. Molecular genetics has provided insights into both sporadic and hereditary diseases common in endocrine pathology.
Endocrine pathology comprises a spectrum of disorders originating in various sites throughout the body. Some disorders affect endocrine glands, and others arise from endocrine cells that are dispersed in non-endocrine tissues. Endocrine cells can broadly be classified as neuroendocrine, steroidogenic, or thyroid follicular cells; these three families have distinct embryologic origins, morphologic structure, and biochemical hormone synthetic pathways. Lesions affecting the endocrine system include developmental abnormalities, inflammatory processes that can be infectious or autoimmune, hypofunction with atrophy or hyperfunction caused by hyperplasia secondary to pathology in other sites, and neoplasia of many types. Understanding endocrine pathology requires knowledge of both structure and function, including the biochemical signaling pathways that regulate hormone synthesis and secretion. Molecular genetics has clarified sporadic and hereditary disease that is common in this field.

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