Hypopituitarism: Difference between revisions

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* Decreased secretion of one or more of 8 hormones normally produced by the pituitary gland at the base of the brain.  
* Decreased secretion of one or more of 8 hormones normally produced by the pituitary gland at the base of the brain.  
*If there is decreased secretion of one specific pituitary hormone, the condition is known as selective hypopituitarism.
*If there is decreased secretion of one specific pituitary hormone, the condition is known as selective hypopituitarism.
*Panhypopituitarism: If there is decreased secretion of most or all hormones
**Panhypopituitarism
**Autoimmune hypophysitis




=== Signs / Symptoms ===


* The most common problem is insufficiency of FSH and/or LH leading to sex abnormalities.
=== Autoimmune hypophysitis ===
* Growth hormone deficiency is more common in people with an underlying tumor than those with other causes.
 
* It can affect Anterior or posterior part of pituitary gland
** Lymphocytic Infundibuloneurohypophysitis (LINH): Posterior pituitary is affected resulting in [[Central diabetes insipidus]].
** Lymphocytic Adenohypophysitis (LAH): Anterior pituitary gland is involved.
** In some cases, pituitary inflammation leads to interruption of dopamine flow from the hypothalamus into pituitary causing [[Prolactin|Hyperprolactinaemia]] Surprisingly HPV and HHV-6 is seen in pituitary adenoma.
 
==== LINH ====
 
* Infundibulo-neuro-hypophysitis is a rare, acquired pituitary hormone deficiency, a type of primary hypophysitis
* It is characterized by an inflammation of the posterior pituitary and the stalk.
* The major clinical manifestation is [[Central diabetes insipidus|diabetes insipidus]] with polyuria and polydipsia.
* It has also Post-Node sign / Symptoms due to pressure effect of Pituitary adenoma including nausea, vomiting, visual disturbances / dizziness
* They may have fatigue, loss of libido, amenorrhea due to 
* Mass effects on adjacent structures (e.g. optic chiasm)
 
==== LAH ====
 
* LAH occurs when the anterior pituitary cells are affected by autoimmune (Lymphocytic) inflammation resulting in
** Adrenal insufficiency (ACTH producing cells are affected)
** Hypothyroidism (TSH producing cells are damaged)
** Hypogonadism (LH and/or FSH producing cells are involved).
* Causation: [[MTB, Mycobacterium tuberculosis|MTB]] ([[Tuberculosis Hypophysitis]])
 
==== [[Prolactin|Hyperprolactinaemia]] ====


* Hyperprolactinemia inhibits the secretion of GnRH / FSH and LH results in hypogonadism.
* Hyperprolactinemia may cause
** Galactorrhea
** [[Infertility remedies|Infertility]]
** Abnormal menstrual period
** [[Hypogonadism]]
** Erectile dysfunction
** Gynecomastia


=== Autoimmune hypophysitis ===
* 17% of [[PCOD, Poly Cystic Ovarian Disease|PCOS]] have Hyperprolactinaemia
*It can lead to deficiencies in one or more pituitary hormones, causing
**Central diabetes insipidus
**Central adrenal insufficiency
**Central hypothyroidism


* Therefore Autoimmune hypophysitis could be considered as secondary Hypogonadism / Hypothyroidism / Adrenal insufficiency


=== Types ===
==== Both anterior and posterior pituitary ====
LAH can thus be classified as:
Lymphocytic infundibular panhypophysitis


# Lymphocytic adenohypophysitis
=== Signs / Symptoms ===
# Posterior pituitary: LINH (Lymphocytic infundibular neurohypophysitis)
# Both LAH and LINH may also lead to symptoms of an intracranial mass such as headache or disturbance of vision


====1- LAH: Lymphocytic adenohypophysitis====
* The most common problem is insufficiency of FSH and/or LH leading to sex abnormalities.
* Growth hormone deficiency is more common in people with an underlying tumor than those with other causes.


* It is characterized by infiltration of the pituitary stalk with lymphocytes, as the name would suggest. Importantly, there is a paucity of plasma cells or granulomas, differentiating it from IgG4-related hypophysitis and granulomatous hypophysitis (e.g. due to neurosarcoidosis) respectively.
* Most common
* It mimics a pituitary adenoma
* It is closely related to other inflammatory conditions in the region, namely orbital pseudotumor and Tolosa-Hunt syndrome.
* It has endocrine hormone deficits (Hypopituitarism)
*TSH producing cell deficit results in secondary Hypothyroidism
*ACTH producing cell  [[Adrenal insufficiency]]
*LH and/or FSH producing cells deficit results in secondary [[Hypogonadism]]
*
*Interruption of dopamine flow from hypothalamus into pituitary, causing high levels of [[Prolactin]]
*Causation: [[MTB, Mycobacterium tuberculosis|MTB]] ([[Tuberculosis Hypophysitis]])






===== Associations =====
Autoimmune conditions such as


=== Related disease ===
* [[Hashimoto thyroiditis|Autoimmune thyroiditis]]: HCV, MMP, EBV, MTB
* [[Hashimoto thyroiditis|Autoimmune thyroiditis]]: HCV, MMP, EBV, MTB
* [[Pernicious anemia]]: EBV, HCV
* [[Pernicious anemia]]: EBV, HCV
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==== 2- LINH : Lymphocytic Infundibuloneurohypophysitis====
=== Hyphophysitis & thyroiditis ===
* Rare
* occurs when the [[posterior pituitary]] is affected resulting in diabetes insipidus.
* Common symptoms include nausea, vomiting, fatigue, loss of libido, amenorrhea, and dizziness.
* Mass effects on adjacent structures (e.g. optic chiasm)
 
==== 3- Both anterior and posterior pituitary ====
Lymphocytic infundibular panhypophysitis
 


====Antibodies====
* 80% of patients with pituitary antibodies also have antibodies to thyroid gland or its hormones.
80% of patients with pituitary antibodies also have antibodies to thyroid gland or its hormones. Likewise, 20% of autoimmune thyroid patients also have pituitary antibodies. It follows that a subset of thyroid patients may have a disease related to autoimmune hypophysitis. Recent research has focused on a defect at the CTLA-4 gene which, coupled with other factors, may result in autoimmunity primarily focusing on certain endocrine glands including the pituitary and thyroid.
* Likewise, 20% of autoimmune thyroid patients also have pituitary antibodies.
* It follows that a subset of thyroid patients may have a disease related to autoimmune hypophysitis

Latest revision as of 00:06, 7 April 2023

Clinic

  • Decreased secretion of one or more of 8 hormones normally produced by the pituitary gland at the base of the brain.
  • If there is decreased secretion of one specific pituitary hormone, the condition is known as selective hypopituitarism.
    • Panhypopituitarism
    • Autoimmune hypophysitis


Autoimmune hypophysitis

  • It can affect Anterior or posterior part of pituitary gland
    • Lymphocytic Infundibuloneurohypophysitis (LINH): Posterior pituitary is affected resulting in Central diabetes insipidus.
    • Lymphocytic Adenohypophysitis (LAH): Anterior pituitary gland is involved.
    • In some cases, pituitary inflammation leads to interruption of dopamine flow from the hypothalamus into pituitary causing Hyperprolactinaemia Surprisingly HPV and HHV-6 is seen in pituitary adenoma.

LINH

  • Infundibulo-neuro-hypophysitis is a rare, acquired pituitary hormone deficiency, a type of primary hypophysitis
  • It is characterized by an inflammation of the posterior pituitary and the stalk.
  • The major clinical manifestation is diabetes insipidus with polyuria and polydipsia.
  • It has also Post-Node sign / Symptoms due to pressure effect of Pituitary adenoma including nausea, vomiting, visual disturbances / dizziness
  • They may have fatigue, loss of libido, amenorrhea due to
  • Mass effects on adjacent structures (e.g. optic chiasm)

LAH

  • LAH occurs when the anterior pituitary cells are affected by autoimmune (Lymphocytic) inflammation resulting in
    • Adrenal insufficiency (ACTH producing cells are affected)
    • Hypothyroidism (TSH producing cells are damaged)
    • Hypogonadism (LH and/or FSH producing cells are involved).
  • Causation: MTB (Tuberculosis Hypophysitis)

Hyperprolactinaemia

  • Hyperprolactinemia inhibits the secretion of GnRH / FSH and LH results in hypogonadism.
  • Hyperprolactinemia may cause
  • 17% of PCOS have Hyperprolactinaemia


Both anterior and posterior pituitary

Lymphocytic infundibular panhypophysitis

Signs / Symptoms

  • The most common problem is insufficiency of FSH and/or LH leading to sex abnormalities.
  • Growth hormone deficiency is more common in people with an underlying tumor than those with other causes.



Related disease


Hyphophysitis & thyroiditis

  • 80% of patients with pituitary antibodies also have antibodies to thyroid gland or its hormones.
  • Likewise, 20% of autoimmune thyroid patients also have pituitary antibodies.
  • It follows that a subset of thyroid patients may have a disease related to autoimmune hypophysitis
  1. CASE REPORT article Front. Endocrinol., 07 October 2020 Sec. Pituitary Endocrinology
  2. Joussen AM, Sommer C, Flechtenmacher C, Voelcker HE. Lymphocytic Hypophysitis Associated With Dacryoadenitis: An Autoimmunologically Mediated Syndrome. Arch Ophthalmol. 1999;117(7):959–962. doi:10.1001/archopht.117.7.959