endocrine pathology Flashcards

1
Q

what are the microscopic and macroscopic histopathological features of:

The anterior pituitary

how they correlate to clinical features

A

made from epithelial cells derived from the developing oral cavity

Have follicles with stroma inbetween

Parafollicular cells are found in between the follicles

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2
Q

pituitary adenomas most commonly affect which cells?

A
  1. Prolactin cell: prolactinoma

next: null cell - make no hormones
then: acth & gh

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3
Q

list the most common cause of hypopituitarism?

A

1.Nonsecretory pituitary adenomas

  1. Ischaemic necrosis
    Most commonly post-partum (Sheehan’s syndrome)
    DIC, sickle cell anaemia, elevated intracranial pressure, shock
  2. Ablation of pituitary by surgery or irradiation
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4
Q

List the clinically important posterior pituitary syndromes

A

Diabetes insipidus
ADH excess eg SIADH

PP hormones:
Vassopressin / antidiuretic hormone (ADH) and oxytocin

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5
Q

List 2 main functions of the thyroid gland?

A

Maintain basal metabolic rate - through t3,4 production

Make calcitonin - Parafollicular cells/C cells. promotes calcium absorption by skeleton

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6
Q

what are non-pathological causes of goitres?

A

non-toxic goitres:

iodine deficiency;

  • environmental eg derbyshire neck
  • diet: cabbages/brassicas
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7
Q

name some common, non-hormonal complications of thyroid goitres?

A

Multinodular goitre can lead to ->

dysphagia and airways obstruction

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8
Q

how does a Multinodular goitre present?

A

non-toxic

can develop hyper functioning nodules -> these release thyroid hormones -> hyperthyroid

causes a hypothyroid state after a while due to negative feedback on TSH

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9
Q

list the presenting triad in the Most common cause of endogenous hyperthyroidism

A

Graves:

  1. Thyrotoxicosis
  2. Infiltrative ophthalmopathy with exophthalmos in up to 40%
  3. Infiltrative dermopathy (pretibibial myxoedema) in a minority of cases
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10
Q

what is the pathogenesis of graves?

A

TSH receptor antibody - most important

Thyroglobulin antibody

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11
Q

a painless goitre is indicative of?

A

Hashimoto’s thyroiditis

papillary carcinoma - just a mass rather than goitre

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12
Q

Lymphoid cells with germinal centres
§ The epithelial cells become large with lots of eosinophilic cytoplasm (Hurthle cells)

the above is seen in which conditions?

A

Hashimoto’s thyroiditis - autoimmune hypothyroidism

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13
Q

Usually solitary
Well circumscribed lesion that compresses the surrounding parenchyma
Well formed capsule
Small proportion cause thyrotoxicosis

is descriptive of?

A

Adenomas of the thyroid

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14
Q

what is the most common origin of carcinomas of the thyroid in order?

A

Papillary (75-85%)
Follicular (10-20%)

Medullary (5%)
Anaplastic (<5%)

PFMA
Please find my answer

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15
Q

how are papillary carcinoma’s diagnosed?

A

Based on nuclear features:

Optically clear nuclei
Intranuclear inclusions - orphan Annie
May be psammoma bodies - (little foci of calcification)

-> May present with cervical lymph node metastasis

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16
Q

what are the characteristics of follicular carcinoma?

A

well demarcated

haematogenours spread -> lungs, bone, liver

17
Q

what is the pathogenensis of Medullary carcinoma?

epidemiology?

A

derived from parafollicular C cells

80% sporadic - adults 5-6th decade

20% familial - MEN - younger patients

18
Q

embryological orgiin of parathyroids?

A

Derive from developing pharyngeal pouches

19
Q

list causes of hyperparathyroid? which are most common?

A

80-90% - solitary adenoma

10-20% hyperplasia of all 4 glands
- Sporadic or component of MEN type 1

<1% carcinoma

20
Q

Neuromuscular irritability - tingling, muscle spasms, tetany
Cardiac arrhythmias
Fits
Cataracts

the above sx are assocaited with which condition? causes?

A

hypoparathyroidism:

Surgical ablation
Congenital absence
Autoimmune

21
Q

most common causes of cushings syndrome?

A

No 1. cause = Exogenous glucocorticoids

Top endogenous cause: Cushings disease (increased ACTH - pituitary adenoma)

others: ectopic acth - usually from lung cancer eg small cell

22
Q

what is seen on histology: cushings syndrome?

A

Exogenous glucocorticoids: Adrenal glands are atrophic

Cushings disease: Nodular adreno-cortical hyperplasia

23
Q

most common causes of Hyperaldosteronism?

A

60 % bilateral adrenal hyperplasia

35 % aldosterone secreting adenoma – Conn’s syndrome

24
Q

Clinical manifestations of which condition are hypertension and hypokalaemia?

A

primary Hyperaldosteronism

25
Q

what is the pathophysiology of CAH Congenital adrenal hyperplasias?

A

Group of autosomal recessive disorders
Hereditary defects in enzymes involved in cortisol biosynthesis

Decreased cortisol results in increased ACTH, adrenal stimulation and increased androgen synthesis
May present in childhood or less commonly in adults

26
Q

list some causes of adrenal insufficiency ?

A
  1. Acute
    Haemorrhage (neonates)
    Sepsis with DIC (Waterhouse-Friderichson syndrome)
    Sudden withdrawal of corticosteroid therapy
  2. Chronic (Addison’s disease)
    Autoimmune (75-90%)
    TB, HIV
    Metastatic tumour (lung and breast particularly)
    Rarely amyloid, fungal infections, haemochromatosis, sarcoidosis
27
Q

what is the difference in presentatoin of adenomas and carcinomas in the adrenals?

A

adenomas:
non-functional. conn’s, cushings

carcinomas:
congenital adrenal hyperplasia, large

28
Q

list some disease of the adrenal medulla?

A

Phaeochromocytoma

Neuroblastoma

29
Q

how are phaeo’s characterised?

A

10% associated with a familial syndrome inc. MEN 2A and 2B, vHL disease and Sturge-Weber syndrome

10% are bilateral
10% are malignant

10% arise outside the adrenal (paragangliomas)