Endocrine gland disorders Flashcards

1
Q

What is the amino acid that releases the most GH?

A

Arginine

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2
Q

What are the diseases of the pituitary gland?

A

1) Hyperpituitarism

  • Galactorrhea (prolactin)
  • Cushings’s syndrome (ACTH)
  • Hyperthyroidism (TSH)
  • Precocious puberty (GnRH)
  • Hyperpigmentation (MSH)
  • Gigantism
  • Acromegaly
  • Syndrome of inappropriate ADH secretion

2) Hypopituitarism

  • Addison (decreased ACTH)
  • Myxedema (Decreased TSH)
  • Diabetes insipidus (Decreased ADH)
  • Dwarfism (after 4-5y of age)
  • Infantilism (decreased GH and GnRH, dwarf with no sex character)
  • Simmond’s disease (pan-hypopituitarism)
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3
Q

What are the causes of hyperthyroidism?

A
  • In the anterior pituitary

1) Hyperplasia

2) Benign tumor (functioning “secreting hormones)

3) Carcinomas

  • Extra pituitary

1) Like small cell carcinoma

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4
Q

What are the main causes of increased growth hormone?

A

1) Gigantism

  • hyperplasia

2) Acromegaly

  • Tumor in the pituitary gland
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5
Q

What is meant by gigantism?

A
  • It is an increase in GH secretion before the closure of the epiphysis
  • It could be appropriate or disappropriate, when disappropriate the span > then the height, and the lower segments are > then the upper ones
  • They will have hyperglycemia due to the increased GH levels
  • They will have hypogonadism it is usually hyperplastic and in such cases the eosinophilic cells are the ones who are mainly affected
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6
Q

What is acromegaly?

A
  • An increase in GH levels after the closure of the epiphyseal plate, mainly due to pituitary adenoma
  • They will have gynecomastia (due to the prolactin like effect of GH)
  • They will have hyperglycemia (due to increased GH)
  • Sexual dysfunction
  • Visual disturbance (as the adenoma could obscure the optic chiasm)
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7
Q

What are the clinical findings in acromegaly?

A

1) Ape-like face

2) Prominent supra-orbital ridges

3) Proganthism (the jaw forward)

4) Teeth separation

5) Big ear, nose, tongue and lips

6) The hands are spade-like, with elongated fingers

7) The feet are enlarged, and probably they change shoes every month

8) Kyphosis of the vertebrae

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8
Q

What are the common causes of SIADH?

A

1) Small cell lung cancer (سيدة فيها S)

2) Brain Injury (due to the disruption)

3) Drugs (antipsychotic “lithium”)

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9
Q

What is a syndrome of inappropriate ADH secretion?

A
  • Hyponatremia:

1) Dilution of sodium
2) ANP, which increases Na excretion in the urine
3) Decreased sodium reabsorption due to decreased renin

  • Neuronal swelling due to increased osmotic pressure of the plasma, in an attempt to normative blood volume, this will lead to severe neurocognitive effects (confusion, mood swings, hallucinations, seizures, coma)
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10
Q

What are the investigations done for SIADH?

A

1) Urin osmolarity (which is high due to increased Na+ excretion)

2) Urine sodium excretion (also high)

3) Hyponatremia (low serum sodium)

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11
Q

What are the different causes of pan-hypopituitarism?

A
  • AKA Simmonds’ disease

1) Sheehan syndrome (During pregnancy the Ant.pit increases in size but not vascularity, and thus if a hemorrhage occurs during deliver this could damage the whole ant.pituitary)

2) Nonfunctional adenoma (adenoma that does not secrete hormones)

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12
Q

What are the clinical presentations of pan-hypopituitarism?

A

1) Prolactin deficiency (female cannot lactate)

2) Gonadotropin deficiency (secondary hypogonadism, as the cause is not related to gland itself)

3) Secondary hypothyroidism

4) Secondary hypocortisolism

5) No hyperpigmentation (as MSH is decreased with ACTH)

6) Hypoglycemia due to decreased ACTH

7) Skin pallor (due to decreased thyroid hormone = decreased erythropoietin = decreased RBC)

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13
Q

What are the investigations done for hypopituitarism?

A

1) Serum measurement of the hormones

2) Combined insulin tolerance test (we give the hormone and see that it does not increase, in the case of ACTH and GH we give insulin, normally they should increase when we give insulin)

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14
Q

What is diabetes insipidus?

A
  • Deficiency of ADH, with tasteless urine
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15
Q

What are the types of diabetes insipidus?

A

1) Central DI

2) Nephrogenic DI

3) Essential hypernatremia

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16
Q

What is central diabetes insipidus?

A
  • This can be due to Idiopathic, Tumors, or Langerhans cell histiocytoma
  • No ADH
  • Diagnosed by exclusion
17
Q

What is meant by nephrogenic DI?

A

When the renal tubules do not respond to ADH, it could be due to hypokalemia and hypercalcemia (which blunts renal response to ADH)

18
Q

What is essential hypernatremia?

A
  • When the osmoreceptors are defective, they do not feel thirsty, resulting in severe dehydration
19
Q

What are the clinical presentations of diabetes insipidus?

A

1) Polyurea (due to absence of ADH)

2) Polydypsia

3) Dehydration

4) Constipation

20
Q

How to investigate for diabetes insipidus?

A
  • More than 2 times wakes up at night to urinate

1) Water deprivation (in psychotic patients), if DI urine output will remain high

2) Vassopresin test (give ADH if kidney he won’t respond if he responds = central)

3) Hypertonic NaCl test (for essential hypernatremia, a normal person would feel thirsty)

21
Q

What are the different clinical types of pituitary tumors?

A

1) Functional (tumors that secrete hormones into the blood), early presented

2) Non-functional (tumors that do not secrete hormones into the blood), reach big sizes

3) Silent (secrete hormones into nearby tissue, and not blood)

22
Q

What are the pathological types of pituitary gland tumors?

A

1) Anterior lobe

1a) Well-differentiated PitNET (Pituitary neuendocrinetumor “pituitary adenoma”)

1b) Craniopharyngioma

2) Posterior lobe

23
Q

What is the cause of tumors that arise from the somatotrophs and corticotrophs?

A

G-protein mutation

24
Q

Describe the morphology of pituitary adenoma

A

1) Gross

  • Well-circumscribed
  • Oval-round shape
  • Pale/gray in color
  • Small area of hemorrhage
  • Pituitary apoplexy (when severe hemorrhage occurs, enlarging the tumor, destroying the gland)
  • if less than 1 cm it is a microadenoma, if more then it is a macroadenoma (which is usually benign)

2) Microscopic

  • Uniform, arranged in sheets, cords
  • Nuclei have a salt-and-pepper appearance
  • Crooke hyaline change (large eosinophilic cells with a glassy appearance, keratin filaments accumulate, seen in corticotroph cells “due to hypercortisolism”)
25
Q

What are the complications of pituitary adenomas?

A

1) Headache, nausea, vomiting (due to increased intracranial pressure)

  • In large-size non-functioning adenomas:

2) hypopituitarism due to impingement

3) Compression of the optic chiasm

4) Extension into the cavernous sinus

5) Seizure due to the extension into the base of the brain

26
Q

What is craniopharyngeoma?

A
  • It is a grade 1 by WHO (very benign)
  • It develops from the neoplastic transformation of the remnant of the Rathke pouch
  • Diagnosed as a patient comes with headache, dull vision, etc then CT reveals an extra-axial (outside brain tissue) suprasellar mass
  • It has two types, adamntinomatous and papillary
27
Q

Describe the morphology of craniopharyngioma

A

1) Gross

  • In the adamntinomatous type you will find a cystic mass filled with a motor oil-like fluid
  • In the papillary is solid mass

2) Microscopic

  • In the adenomatous
  • Fe keratin + calcification (keratinizing squamous epithelium
  • In papillary
  • Non-keratinized squamous epithelium