Hypopituitarism classification: Difference between revisions
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=== Classification on the basis of anatomical location: === | === Classification on the basis of anatomical location: === | ||
* Primary hypopituitarism- includes intrinsic pathology in pituitary | * Primary hypopituitarism- includes intrinsic pathology in pituitary and decreased pituitary hormone levels | ||
*Secondary hypopituitarism- includes pathology in hypothalamus | *Secondary hypopituitarism- includes pathology in hypothalamus and decreased hypothalamic hormone levels | ||
=== Classification on the basis of glandular involvement === | === Classification on the basis of glandular involvement === |
Revision as of 15:16, 21 September 2017
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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 and secondary hypopituitarism. It can also be classified on the basis of the portion of gland involvement into partial or complete glandular involvement.
Classification
Hypopituitarism can be classified on the basis of location of pathology and the portion of gland involvement:[1]
Classification on the basis of anatomical location:
- Primary hypopituitarism- includes intrinsic pathology in pituitary and decreased pituitary hormone levels
- Secondary hypopituitarism- includes pathology in hypothalamus and decreased hypothalamic hormone levels
Classification on the basis of glandular involvement
- Partial- includes deficiency of one or more than one hormones (can be anterior or posterior pituitary gland)
- Complete/Panhypopituitarism- includes deficiency of all of the pituitary hormones (both anterior and posterior)
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.