Pituitary apoplexy: Difference between revisions

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List of terms related to Pituitary apoplexy

	Pituitary apoplexy;
ICD-10	E23.6
ICD-9	253.8
DiseasesDB	10049
MedlinePlus	001167
MeSH	D010899

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VisualWikitext

Revision as of 17:14, 19 September 2012

For patient information, click here

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Pituitary gland infarction; pituitary infarct

Overview

Pituitary apoplexy is a form of apoplexy, or infarction, affecting the pituitary gland.^[1]

Headaches are often associated.^[2]

References

↑ "Pituitary Disorders".
↑ Biousse V, Newman NJ, Oyesiku NM (2001). "Precipitating factors in pituitary apoplexy". J. Neurol. Neurosurg. Psychiatr. 71 (4): 542–5. PMID 11561045. Unknown parameter |month= ignored (help)

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Template:WikiDoc Sources

[urlPituitary_Disorders-1] "Pituitary Disorders".

[pmid11561045-2] Biousse V, Newman NJ, Oyesiku NM (2001). "Precipitating factors in pituitary apoplexy". J. Neurol. Neurosurg. Psychiatr. 71 (4): 542–5. PMID 11561045. Unknown parameter |month= ignored (help)

[1]

[2]

@@ Line 1: / Line 1: @@
-'''For patient information, click [[Pituitary apoplexy (patient information)|here]]'''
+__NOTOC__
 {{Infobox_Disease |
    Name           = {{PAGENAME}} |
@@ Line 15: / Line 15: @@
 }}
 {{SI}}
+'''For patient information, click [[Pituitary apoplexy (patient information)|here]]'''
+{{CMG}}
+{{SK}} Pituitary gland infarction; pituitary infarct
 ==Overview==

v t e Endocrine pathology: endocrine diseases (E00-35, 240-259)
Thyroid	Hypothyroidism (Iodine deficiency, Cretinism, Congenital hypothyroidism, Goitre, Myxedema) - Hyperthyroidism (Graves disease, Toxic multinodular goitre, Teratoma with thyroid tissue or Struma ovarii) - Thyroiditis (De Quervain's thyroiditis, Hashimoto's thyroiditis, Riedel's thyroiditis) - Euthyroid sick syndrome
Pancreas	Diabetes mellitus (type 1, type 2, coma, angiopathy, ketoacidosis, nephropathy, neuropathy, retinopathy) - Hypoglycemia - Hyperinsulinism - Zollinger-Ellison syndrome - insulin receptor (Rabson-Mendenhall syndrome)
Parathyroid	Hypoparathyroidism (Pseudohypoparathyroidism) - Hyperparathyroidism (Primary, Secondary, Tertiary)
Pituitary	Hyperpituitarism (Acromegaly, Hyperprolactinaemia, SIADH) - Hypopituitarism (Simmonds' disease / Sheehan's syndrome, Kallmann syndrome, Growth hormone deficiency, Diabetes insipidus) - Adiposogenital dystrophy - Empty sella syndrome - Hypophysitis
Adrenal	Cushing's syndrome (Nelson's syndrome, Pseudo-Cushing's syndrome) - CAH (Lipoid, 3β, 11β, 17α, 21α) - Hyperaldosteronism (Conn syndrome, Bartter syndrome) - Adrenal insufficiency (Addison's disease) - Hypoaldosteronism
Gonads	Ovarian dysfunction (Polycystic ovary syndrome, Premature ovarian failure) - Testicular dysfunction (5-alpha-reductase deficiency) - Testosterone biosynthesis (17-beta-hydroxysteroid dehydrogenase deficiency) - General (Hypogonadism, Delayed puberty, Precocious puberty)
Other	Androgen insensitivity syndrome - Autoimmune polyendocrine syndrome - Carcinoid syndrome - Gigantism - Short stature (Laron syndrome, Psychogenic dwarfism) - Multiple endocrine neoplasia (1, 2) - Progeria - Woodhouse-Sakati syndrome

Pituitary apoplexy
ICD-10	E23.6
ICD-9	253.8
DiseasesDB	10049
MedlinePlus	001167
MeSH	D010899

Pituitary apoplexy: Difference between revisions

Revision as of 17:14, 19 September 2012

Overview

References

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