Diseases of the endocrine system Flashcards

1
Q

What do the following systems affect:

  • Endocrine
  • Autocrine
  • Paracrine
A
  • E= hormones directly into blood act systemically
  • P= hormones act locally
  • A= affects cell secreting the protein
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2
Q

What are causes of anterior pituitary hypofunction?

A

-Tumours=non secretory adenoma, metastatic carcinoma
-Trauma
-Inflammation= autoimmune, infections, granulomatous
-Infarction
Iatrogenic

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3
Q

Describe primary pituitary tumours

A
  • Majority adenomas & benign
  • Derived from any hormone producing cell
  • Local effects due to pressure on optic chiasma/ adjacent pituitary
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4
Q

What types of anterior pituitary adenomas are there?

A
  • Prolactinoma- menstrual disturbance, galactorrhoea
  • Growth hormone secreting= gigantism in children, acromegaly in adults
  • ACTH secreting-Cushing’s syndrome
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5
Q

Describe acute thyroiditis?

A
  • Acute inflammation of thyroid parenchyma
  • Local or sytemic infection
  • Generalised sepsis
  • Fever, chills, pain, malaise, swelling of anterior neck
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6
Q

What is palpation thyroiditis?

A
  • Microscopic Granulomatous foci centered on thyroid follicles
  • Due to rupture of thyroid follicles
  • Presents as thyroid nodule
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7
Q

What is Riedel thyroiditis?

A
  • Rare fibrosing form of chronic thyroiditis
  • Firm goitre
  • Stridor, hoarseness, dysphagia
  • Benign
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8
Q

Describe Hashimoto’s disease

A

-Autoimmune chronic inflammatory disorder
-Associated with diffuse enlargement of thyroid autoantibodies
-Chronic lymphocytic thyroiditis w/germinal centre formation
-Females most common
-Elevated serum thyroid antibodies
-Many become hypothyroid
-Inc risk of thyroid lymphoma & papillary carcinoma
-

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9
Q

Describe Grave’s disease

A
  • Diffuse hyperplasia
  • May develop permanent hypothyroidism
  • Autoimmune process & diffuse hyperplasia of follicular epithelium
  • Females more common
  • Pretibial myxoedema, hair loss, wide-eyes stare, tachycardia, hyperreflexia, proptosis
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10
Q

Describe a multinodular goitre

A
  • Enlargement of thyroid
  • Most patients euthyroid
  • Tracheal compression or dysphagia may develop
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11
Q

Describe follicular adenoma

A
  • Benign encapsulated tumour
  • Follicular cell differentiation
  • Females most common
  • Painless neck mass
  • Solitary nodule on one lobe
  • Cold nodule on radioactive iodine imaging
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12
Q

What is the most common type of thyroid cancer? Describe it

A
  • Papillary carcinoma
  • Familial, autosomalD non-medullary thyroid carcinoma
  • Activation of RET or NTRK1
  • Chromosomal translocations or inversions, RAS/BRAF mutations,
  • Causes: Cowden’s syndrome, radiation exposure, therapeutic irradiation
  • Granular, cystic, some encapsulated, infiltrative
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13
Q

Describe follicular neoplasms

A
  • Follicular adenoma
  • Minimmaly invasive follicular carcinoma
  • Hurthle cell neoplasms/ oncocytic carcinoma (acidophilic cells in canine thyroid), incidence of cervical lymph node mets
  • Widely invasive follicular carcinoma
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14
Q

Name the types of thyroid carcinoma

A
  • Papillary carcinoma
  • Insular carcinoma
  • Anaplastic carcinoma (rapidly enlarging thyroid mass, inoperable)
  • Medullary carcinoma (differentiation to parafollicular C cells, mutation in RET gene, autosomalD, MEN 2a&2b)
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15
Q

Describe primary thyroid lymphoma

A
  • Associated with lymphocytic thyroiditis
  • Diffuse large B-cell
  • Rapidly enlarging mass, pain, dysphagia, cervical lymphadenopathy
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16
Q

What tumours are likely to metastasise to the thyroid?

A
  • Renal cell carcinoma
  • Melanoma
  • Breast cancer
  • Small cell lung cancer
  • Neuroendocrince carcinoma
17
Q

What are the types of hyperparathyroidism?

A
  • Primary= Excessive section of parathyroid hormone from one of more glands
  • Secondary= Hyperplasia of glands with elevated PTH in response to hypocalcaemia
  • Tertiary= Adenoma associated with longstanding secondary hyperparathyroidism
18
Q

What are causes of secondary hyperparathyroidism?

A
  • Renal insufficiency
  • Vit D deficiency
  • Malabsorption
19
Q

What is the pathogenesis of primary hyperparathyroidism?

A
  • Aging
  • MEN 2a
  • Association with ionizing irradiation
  • Tumorigenesis
  • Arterial hypertension, hypercalcaemia, dec renal function, psych problems, osteoporosis, urolithiasis
  • Mostly single adenoma
20
Q

What is primary chief cell hyperplasia?

A
  • Non neoplastic increase in parathyroid parenchymal tissue
  • Abnormal calcium metabolism
  • Fatigue, lethargy, anorexia, weakness, vomiting
  • Bones, stones, abdo moans
  • Elevated Ca, decrease in organic phosphorous, inc parahormone levels
21
Q

Describe parathyroid adenoma

A
  • Encapsulated benign neoplasms of parathyroid cells
  • symptoms of hypercalcaemia
  • MEN1&2 syndrome, jaw tumour syndrome
  • Single enlarged parathyroid gland remaining glands suppressed & small
22
Q

Describe secondary & tertiary parathyroidism

A
  • non-neoplastic inc in parathyroid parenchymal cell mass within all parathyroid
  • Common with renal failure & dialysis
  • Identical path to primary hyperplasia associated with massive gland enlargement
23
Q

Describe parathyroid carcinoma

A

-Malignant tumour derived from parathyroid parenchymal cells

24
Q

Describe adrenal congenital hypoplasia

A
  • Reduced vol of adrenocorticol tissue leading to adrenal cortical insufficiency
  • High mortality
  • Males, X-linked
  • Hypoadrenalism
  • Managed with mineralocorticoids & glucocorticoids
25
Q

Describe congenital adrenal hyperplasia

A
  • Inherited
  • Deficiency of enzymes required for synthesis of glucocorticoids & mineralocorticoids
  • 21 hydroxylase deficiency most common
  • Deficiencies of corticol & aldosterone secretion
  • Genital ambiguity in F, normal M
  • Advanced bone growth & premature epiphyseal maturation
26
Q

Describe Addison’s disease

A
  • Primary adrenal cortical insufficiency
  • Adrenal destruction
  • Autoimmune form or TB
  • Triad= hyperpigmentation, postural hypotension, hyponatraemia
  • Long term steroid replacement
27
Q

Describe adrenal cortical carcinoma

A
  • Malignant

- Abdominal mass

28
Q

Describe adrenal cortical nodule

A

-Benign non-functional nodules of adrenal cortex

29
Q

Describe an adrenal cortical adenoma

A
  • Benign neoplastic proliferation of adrenal cortical tissue
  • Endocrince hyperfunctioo
  • Aldosterone producing tumours cause Conn’s syndrome
  • Unilateral mass yellow/brown nodules
  • Formed from lipid filled adrenal cortical cells
30
Q

What is Conn’s syndrome

A
  • excess production of aldosterone by the adrenal glands resulting in low renin levels
  • high blood pressure=poor vision or headaches
31
Q

Describe phaeochromocytoma

A
  • Catecholamine secreting tumour from adrenal medulla
  • Sporadic or familial MEN 2a/2b, von reckling, von hippel
  • Elevated urine catecholamines, (nor)adrenaline
  • Anxiety, headaches, palpitations, hypertensions