Clinical Descriptions in Endocrine Flashcards

(73 cards)

1
Q

Most common cause of adrenal insufficiency

A

Addison’s disease

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2
Q

autoimmune destruction of adrenal cortex

A

Addison’s disease

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3
Q

What is Addison’s disease associated with?

A

pernicious anaemia
Type 1 DM
Autoimmune thyroid disease

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4
Q

Lack of CRH/ACTH caused yb pituitary/hypothalmic disease or exogenous steroid use

A

secondary adrenal insufficiency

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5
Q

Disorder of excess cortisol secretion with high mortality, most common in women aged 20-40

A

Cushing’s syndrome

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6
Q

Most common cause of Cushing’s?

A

iatrogenic

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7
Q

Autonomous production of aldosterone independent of its regulators (angiotensin II and potassium)

A

Primary aldosteronism

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8
Q

Commonest secondary cause of hypertension?

A

Primary aldosteronism

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9
Q

What are the subtypes of Primary aldosteronism?

A
Adrenal adenoma (Conn's syndrome)
Bilateral adrenal hyperplasia (most common cause)
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10
Q

Are genetic mutations and unilateral hyperplasia common causes of Primary aldosteronism?

A

no, rare causes

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11
Q

Rare condition associated with enzyme defects in the steroid pathway, commonest is 21a hydroxylase deficiency

A

congenital adrenal hyperplasia

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12
Q

Rare tumours of the adrenal medulla

Curable form of hypertension, but can be potentially fatal

A

Phaeochromocytoma

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13
Q

Phaeochromocytoma is associated with what?

A
Von-hippel-lindau syndrome
Multiple endocrine neoplasia II
Succinate dehydrogenase mutations
Neurofibromatosis
Tuberose Sclerosis
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14
Q

Phaeochromocytoma is associated with what?

A
Von-hippel-lindau syndrome
Multiple endocrine neoplasia II
Succinate dehydrogenase mutations
Neurofibromatosis
Tuberose Sclerosis
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15
Q

activation mutation in tyrosine kinase receptors

A

Multiple endocrine neoplasia II

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16
Q

Mutation in HIF 1-alpha, range of vascular tumours

A

Von-hippel-lindau syndrome

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17
Q

Most common cause of hypothyroidism in the western world

A

Hashimotos Thyroiditis

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18
Q

goitrous hypothyroidism which can be caused by drugs such as amiodarone

A

Iodine deficiency

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19
Q

Is congenital developmental defect hypothyroidism goitrous?

A

no

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20
Q

Typically affects elderly women with long standing but frequently unrecognized/untreated hypothyroidism
high mortality

A

myxoedmea coma

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21
Q

Autoimmune cause of hyperthyroidism

A

Grave’s

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22
Q

Hyperthyroidism in older patients, more insidious onset, glands may feel nodular

A

multinodular goitre

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23
Q

hyperthyroidism most common in females, may be virally triggered, associated with sore throat/fever etc

A

sub-acute thyroiditis/De Quervians

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24
Q

Severe hyperthyroidism causing respiratory and cardiac collapse, hyperthermia, exaggerated reflexes, may be linked with an infection

A

Thyroid Storm

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25
Commonest type of thyroid cancer.
Papillary
26
Type of thyroid cancer ass. with Hashimoto's
Papillary
27
Second most common type of thyroid cancer
Follicular
28
Incidence of this type of thyroid cancer is higher in iodine deficient areas
follicular
29
Thyroid cancer with worse prognosis?
anaplastic
30
primary overactivity of parathyroid eg adenoma
hyperparathyroidism
31
overactivity of parathyroid eg adenoma
primary hyperparathyroidism
32
Physiological response to low calcium
secondary hyperparathyroidism
33
Parathyroid becomes autonomous after many yearse of secondary
tertiary hyperparathyroidism
34
Familial deactivating mutation in the calcium sensing receptor
hypocalciuric hypercalcaemia
35
Causes for this include hypoparathyroidism, vit D deficiency, chronic renal failure, pancreatitis, hyperventilation, osteoblastic bone mets, rhabdomyloysis
Hypocalcaemia
36
Can be a congeital absence (Di George syndrome), destruction, autoimmune, hypomanesaemia or idiopathic
hypoparathyroidism
37
Genetic defect causing PTH resistance
pseudohyperparathyroidism
38
Hypoparathyroidism but with normal calcium
pseudo-pseudohyperparathyroidism
39
Abnormality of bone remodelling resulting in thick but weak bone. Viral cause but with genetic disposition
Paget's disease
40
Fibrous cyst formed, usually presents in teenage years
Thyroglossal cyst
41
Rare, congenital cyst, usually presents in teenage years
dermoid cyst
42
persisting second branchial arch arising in upper part of anterior triangle
Branchial cyst
43
Lymphatic lesion arising in posterior triangle of neck
Cystic hygroma
44
Pain and swelling around mealtimes
salivary gland stone
45
Benign salivary gland neoplasm
Pleomorphic adenoma
46
Excessive release of ADH causing dilutional hyponatraemia, most commonly cause by malignancy or infection
Syndrome of inappropriate ADH secretion
47
Hypo secretion/insensitivity to effects of DADH causing inability to concentrate urine in distal renal tubules
Diabetes insipidus
48
2 types of diabetes insipidus?
Cranial (decreased secretion of ADH) or nephrogenic (decreased ability to concentrate urine cause by resistance to ADH in kidneys)
49
makes up 10% of intra cranial tumours, can be sporadic or associated with MEN1
pituitary adenoma
50
Most common FUNCTIONAL tumour
prolactinoma
51
Second most common functional tumour, GH causes increase insulin like growth factors which stimulate growth of bone cartilage and connective tissue
GH secreting functional pituitary adenomas
52
Usually a micro-adenoma, causes bilateral adrenocortical hyperplasia, symptoms of Cushings
ACTH secreting functional pituitary adenomas
53
usually panhypopituitarism, many causes eg sarcoidosis, infarction (Sheehan's) or tumours
pituitary hypofunction
54
HLA genes represent around 50% of familial risk of what?
T1DM
55
Genetic - Kallman syndrome | or Normosmic IHH
idiopathic hypogonadotrophic hypogonadism
56
condition affecting hypothalmic function and causing amenorrheoa Causes include increased physical exercise, weight loss, anorexia nervosa, stress, chronic alcohol use, chronic illness, haemochromatosis
acquired hypogonadotrophic hypogonadism
57
can be caused by micro or macro prolactinoma or drugs Decreased oestrogen production causes hypothalamic suppresion of GNRH
Hyperprolactinemia
58
Women with only one X chromosome | may have aorta constriction and rudimentary ovaries
Turner syndrome
59
Women with only one X chromosome | may have aorta constriction and rudimentary ovaries
Turner syndrome
60
Menopause before age 40 yrs, usually familial history
Premature ovarian failure
61
Reduced oocyte numbers prematurely
reduced ovarian reserve
62
hyperandrogenism (acne, hirutism) and oligo/amenorrhoea
polycystic ovary syndrome
63
Distally blocked fallopian tube filled with fluid
hydrosalpinx due to PID
64
Presence of endometrial glands outside uterine cavity
Endometriosis
65
What drugs can induce Type 3 DM?
Glucocorticoids, B blockers, diuretics
66
Medical emergency occuring as result of insulin deficiency accompanied by an increase in counter regulatory hormones, leading to severe Hyperglycaemia
DKA
67
Most commonly seen in elderly, happens more to Type 2s than type 1s, can be caused by severe dehydration
Hyperosmolar hyperglycaemic non-ketotic state
68
excess levels of growth hormone stimulate production of growth factor 1, normally caused by excessive secretion of GH from pituitary tumour
acromegaly
69
congenital condition where hymen without opening completely obstructs the vagina
Imperforate hymen
70
When is Imperforate hymen most often diagnosed?
Most often diagnosed in adolescent girls when menstrual blood accumulates in vagina
71
Adhesion/fibrosis of endometrium, typically caused by trauma eg after miscarraige or abortion
Asherman syndrome
72
Ovarian tumours defined by thyroid tissue compromising more than 50% of overall mass
Struma ovarii
73
Caused by ingestion of exogenous thyroxine
Thyrotoxicosis Factita