Hypopituitarism classification: Difference between revisions
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Latest revision as of 22:19, 29 July 2020
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Hypopituitarism Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Hypopituitarism classification On the Web |
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American Roentgen Ray Society Images of Hypopituitarism classification |
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Risk calculators and risk factors for Hypopituitarism classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]
Overview
Hypopituitarism can be classified on the basis of location of pathology into primary or secondary hypopituitarism. It can also be classified on the basis of the extent of gland involved into partial or complete glandular involvement.
Classification
Hypopituitarism can be classified on the basis of location of pathology and the extent of glandular involvement:[1]
Classification on the basis of anatomical location:
- Primary hypopituitarism: Represents intrinsic pathology in pituitary and decreased pituitary hormone levels
- Secondary hypopituitarism: Represents pathology in hypothalamus and decreased hypothalamic hormone levels
Classification on the basis of extent of glandular involvement
- Partial hypopituitarism: Means deficiency of one or more than one hormones (can be anterior or posterior pituitary gland lobe)
- Complete/Panhypopituitarism: Means deficiency of all of the pituitary hormones (both anterior and posterior lobes)
References
- ↑ Lamberts, SWJ; de Herder, WW; van der Lely, AJ (1998). "Pituitary insufficiency". The Lancet. 352 (9122): 127–134. doi:10.1016/S0140-6736(98)85043-5. ISSN 0140-6736.