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Follicle and luteal cyst
From unruptured graafian follicles or follicle that ruptured them immediately sealed
Lined by granulosa or luteal cells → shiny cyst
may rupture causing intraperitoneal bleeding and pain
Polycystic ovaries
stein leventhal syndrome
ovaries w multiple cystic follicles
produce excess oestrogen and androgens
increased lh, decreased fsh
sx : hirsutism, puberty characteristics
in t2dm, atherosclerosis etc
Stromal Hyperthecosis
cortical stromal hyperplasia
uniform bilateral enlargement of ovaries
Hypercellular stroma w luteinised stromal cells (like nests w vacuolated cytoplasm)
sx like pcos (imcreased androgens, etc)
Ovarian torsion
usually right, unilateral lower abd pain
ovarian twist itself → decreased blood supply → necrosis
enlarge, infarcted, necrotic cyst
Risk for ovarian cancers
nulliparity (never pregnant)
HRT, esp in oestrogen only
BRCA1, 2
smoking
Ovarian cancer clinical features and spread
poor prognosis : tumours small, if v large alr outside ovary
disease spread to POD and omentum/ln
tx by surgery and chemi but modest imcrease in survival
Ovarian tumour origins (4)
surface epithelial tumours : most frequent, usually malignant
Germ cell tumours
sex chird stromal tumours
metastases
Surface epithelial tumours
From mullerian epithelium that covers surface ofovary
repeated ovulation and scaring → cyst that can undergo metaplasia
Benign (cystic/cysticadenofibroma), malignant cystic/solid and borderline (atypia wo invasion)
epithelial stromal tumours main 4
serous
mucinous
endometrial
clear cell
Serous tumours of epithelial stromal (all types)
most frequent
benign ones are mostly large w smooth glistening capsule w singke layer of tall collumnar epithelium
borderline ones are atypical wo invasion w papillary projection (usually confuned)
malignant ones have nodular irregularities w internal papillary projections, usually w p53 and brca1 tumours (go to LN)
mucinous tumours
mostly benign, lined w mucin secreting epithelial cells
larger than serous tumours but better prognosis
tumour can rupture → mucinous deposits in peritoneum (mucin pseudomyoma peritonei)
kras Mutations
Endometrioid tumours
solid or cystic, composed of tubular hlands
usually malignant w mutatiins in PTEN
Clear cell carcinomas
malignant tumours w broad papillae lined by clear and hobnail cells
bad prognosis
Brenner tumours
encapsulated, usually benign tumours
abundant stroma containung nests
Sex cord stromal tumours (3)
granulosa cell tumours : Sx of excess oestrogen w Call -exner bodies
Sertoli leydig cell tumours :solid tumours resembling testes w tubules, dicer 1
fibroma :Solid grey frbrous cells, sometimes produce meigs syndirme
Teratomas and types
arise in first 2 decades, mostly benign
mature cystic (dermoid) : cyst w epidermal linung + foci ifbone, cartilage, bronchial,etc
immature : solid w areas of necrosis, characterised by immature differentiation of bone, cartilage, muscle nerves, etc
monodermal/ specialised :struma (thyroid), carcinoid or struma, carcinoid
Primitive germ cell tumours (4+ explain)
dysgerminoma : malignant, unilateral large solid mass female counterpart of seminoma, high tx rate
yolk sac tumour : from endoderms, structures, well encapsulated , haemorrhage + necrosis in honeycomb pattern , schiller duval bodies
embryonal : resembles embryonic disc / blastocyst that resemble early presomatic embryo
chriocarcinoma : unilateral, small identical to placental tumour w 2 trophoblast cells
Metastases in ovarian canecr
older women
bilateral, at surface of ovary
from gi, breast, lungs
signet ring mucin secreting cells
Craniopharyngioma
benign tumour of remnant of rathke pouch
anywhere from nasopharynx to diencephalon
sellar mass, tx by rt
Hypopituitarism ant vs post sx
anterior
gh deficiency : dwarfism
acth : hyponatraemia, hypotension
lh/fsh deficiency : infertility, amenorrhea
prolactin deficient : cant lactate
msh deficient : pallor
posterior
adh deficiency : DI
sheehans syndrome
acute infarction w necrosis of ant. pituitary lobe
post partum haemorrhage
mild hypopituitarism (ant pituitary x2 size, partial necrosis)
somatotroph adenomas
gh secreting → acromegaly
acromegally effects :-
mass effect : visual fields
hypopituitarism : disturbs others
metabolic effects : diabetes, htn
ST effects : excessive jaw, internal organs
diagnosed w igf1 (failure to suppress gh on gtt), mri
Prolactinoma
amenorrhea, low lobido, galactorrhea
dx w bloodwork +mri
rx w dopamine agonists (eg cabergoline)
Cushings syndrome
hypercortisolism
acth dependent (if due to pituitary adenima = cushings disease)
acth imdependent : adrenal tumours
sx : truncal obesity, moon face, htn, bruising, hisuitism
nb pseudocushings where clinical cortisol excess wo biochemical data and vv
dx and tx of hyperaldosteronism
check plasma renin (suppressed in primary, elevated in secondary) and aldosterone
salt loading to suppress aldosterone
Androgen excess possibilities
CAH
adrenal tumours : usually malignant
pcos : oligomenorrhea, hirsuitism, ovarian cyst
ovarian hyperthecosis
Addison disease sx
A : apetite loss, weight loss
D : darkened skin
D : dizziness
I : irritability
S . salt craving (hyponatraemia)
O : orthostatic hypotn
N : n&v, abd pain
dx addisons
acth stimulation
insulin tolerance test
ct adrenals
adrenal cortical neoplasm
adenoma : small, functional (cushings or conns)
carcinoma : rare, large , in children unkess mets
Adrenal medulla neoplasm
chromaffin cells
phaechromocytoma
neuroblastic tumours
What and why thyrotoxicosis
elevated free t3/t4
graves (most), multinodular goitre, follicular adenoma
either excess release or extra thyroid source
hyperthyroidism cx
increased bmr → weight loss, heat tolerance
cardiac, ocular, skeletal → tachy, nervous, tremor
thyroid storm
Hypothyroidism
low t3/t4
hashinotos thyroiditis, iodine deficiency, development
sx : fatigue, cold intolerance, weight gain, myxoedma
Hashimotos thyroiditis
autoimmune against tsh receptor
painkess enlargement if thyroid
hurthle cell metaplsia + fibrosis
Granulomatous thyroiditis what, macro and micro
transient, viral likely
gland is adherant to trachea and adjacent strap muscles
neutrophils, aggregation kf macrophage, giant cells
Graves disease
hyperthyroidism due to autoantibodies binding to tsh receptor (eg thyroid stimulating immunoglobulin)
goitre, exopthalmos,pre tibial myxoedema
tx by b blockers ir thyroidectomy (or radioiodine ablation, thinomide)
What is goitre and subtypes
enlarged thyroid gland due to increased tsh
diffuse nontoxic (simple) goitre : endemic ir sporadic
multinodular : from simple goitre, mistaken for tumours
Thyroid storm
extreme hyperthyroidism
common after infection, also after discontinue anti thyroid
sx : elevated T (>40), tachy, arrythmia, vomit
Thyroid neoplasia
solitary palpable thyroid nodule
1% only malignant
in young males, hx radiation tx
if functional most likely benign
follicular adenoma
benign neoplasm
encapsulated
oncocytic (hurthle) cell adenoma another variant
Common thyroid carcinomas (4, common to least)
papillary
follicular
medullary
others
Papillary carcinoma of thyroid
most common due to ionising rafiation
Asx but can also present as mass, hoarseness, dysphagia and met
usually lymphatic invasion but bv also can
genes : braf, rearrangements of chr 10 (eg ret/ptc)
follicular carcinoma of thyroid types
minimally invasive : capsular and vascular invasion, lobectomy usually wo recurrence
widely invasive : extensive, features of malignancy and high chance of met
medullary carcinoma of thyroid
mostly sporadic but some assoc w men2 a/b (ret protooncogene)
solid areas of haemorrhage and necrossi wo infiltration
amyloid stroma from calcitonin
anaplastic carcinoma of thyroid
in elderly, present w local compression
v rapid w v high mortality
braf mutation
spindle cell, giant cell, squamoid variants
Congenital thyroid abnormalities
dyshormonogenesis goitre
thyroid dysgenesis : ectopic, hypoplasia, agenesis