endocrine pathology Flashcards
what are the microscopic and macroscopic histopathological features of:
The anterior pituitary
how they correlate to clinical features
made from epithelial cells derived from the developing oral cavity
Have follicles with stroma inbetween
Parafollicular cells are found in between the follicles
pituitary adenomas most commonly affect which cells?
- Prolactin cell: prolactinoma
next: null cell - make no hormones
then: acth & gh
list the most common cause of hypopituitarism?
1.Nonsecretory pituitary adenomas
- Ischaemic necrosis
Most commonly post-partum (Sheehan’s syndrome)
DIC, sickle cell anaemia, elevated intracranial pressure, shock - Ablation of pituitary by surgery or irradiation
List the clinically important posterior pituitary syndromes
Diabetes insipidus
ADH excess eg SIADH
PP hormones:
Vassopressin / antidiuretic hormone (ADH) and oxytocin
List 2 main functions of the thyroid gland?
Maintain basal metabolic rate - through t3,4 production
Make calcitonin - Parafollicular cells/C cells. promotes calcium absorption by skeleton
what are non-pathological causes of goitres?
non-toxic goitres:
iodine deficiency;
- environmental eg derbyshire neck
- diet: cabbages/brassicas
name some common, non-hormonal complications of thyroid goitres?
Multinodular goitre can lead to ->
dysphagia and airways obstruction
how does a Multinodular goitre present?
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
list the presenting triad in the Most common cause of endogenous hyperthyroidism
Graves:
- Thyrotoxicosis
- Infiltrative ophthalmopathy with exophthalmos in up to 40%
- Infiltrative dermopathy (pretibibial myxoedema) in a minority of cases
what is the pathogenesis of graves?
TSH receptor antibody - most important
Thyroglobulin antibody
a painless goitre is indicative of?
Hashimoto’s thyroiditis
papillary carcinoma - just a mass rather than goitre
Lymphoid cells with germinal centres
§ The epithelial cells become large with lots of eosinophilic cytoplasm (Hurthle cells)
the above is seen in which conditions?
Hashimoto’s thyroiditis - autoimmune hypothyroidism
Usually solitary
Well circumscribed lesion that compresses the surrounding parenchyma
Well formed capsule
Small proportion cause thyrotoxicosis
is descriptive of?
Adenomas of the thyroid
what is the most common origin of carcinomas of the thyroid in order?
Papillary (75-85%)
Follicular (10-20%)
Medullary (5%)
Anaplastic (<5%)
PFMA
Please find my answer
how are papillary carcinoma’s diagnosed?
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
what are the characteristics of follicular carcinoma?
well demarcated
haematogenours spread -> lungs, bone, liver
what is the pathogenensis of Medullary carcinoma?
epidemiology?
derived from parafollicular C cells
80% sporadic - adults 5-6th decade
20% familial - MEN - younger patients
embryological orgiin of parathyroids?
Derive from developing pharyngeal pouches
list causes of hyperparathyroid? which are most common?
80-90% - solitary adenoma
10-20% hyperplasia of all 4 glands
- Sporadic or component of MEN type 1
<1% carcinoma
Neuromuscular irritability - tingling, muscle spasms, tetany
Cardiac arrhythmias
Fits
Cataracts
the above sx are assocaited with which condition? causes?
hypoparathyroidism:
Surgical ablation
Congenital absence
Autoimmune
most common causes of cushings syndrome?
No 1. cause = Exogenous glucocorticoids
Top endogenous cause: Cushings disease (increased ACTH - pituitary adenoma)
others: ectopic acth - usually from lung cancer eg small cell
what is seen on histology: cushings syndrome?
Exogenous glucocorticoids: Adrenal glands are atrophic
Cushings disease: Nodular adreno-cortical hyperplasia
most common causes of Hyperaldosteronism?
60 % bilateral adrenal hyperplasia
35 % aldosterone secreting adenoma – Conn’s syndrome
Clinical manifestations of which condition are hypertension and hypokalaemia?
primary Hyperaldosteronism
what is the pathophysiology of CAH Congenital adrenal hyperplasias?
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
list some causes of adrenal insufficiency ?
- Acute
Haemorrhage (neonates)
Sepsis with DIC (Waterhouse-Friderichson syndrome)
Sudden withdrawal of corticosteroid therapy - Chronic (Addison’s disease)
Autoimmune (75-90%)
TB, HIV
Metastatic tumour (lung and breast particularly)
Rarely amyloid, fungal infections, haemochromatosis, sarcoidosis
what is the difference in presentatoin of adenomas and carcinomas in the adrenals?
adenomas:
non-functional. conn’s, cushings
carcinomas:
congenital adrenal hyperplasia, large
list some disease of the adrenal medulla?
Phaeochromocytoma
Neuroblastoma
how are phaeo’s characterised?
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)