pathology part 2 (wk 4-6)

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46 Terms

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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


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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


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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)


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Ovarian torsion

  • usually right, unilateral lower abd pain

  • ovarian twist itself → decreased blood supply → necrosis

  • enlarge, infarcted, necrotic cyst


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Risk for ovarian cancers

  • nulliparity (never pregnant)

  • HRT, esp in oestrogen only

  • BRCA1, 2

  • smoking


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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


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Ovarian tumour origins (4)

  • surface epithelial tumours : most frequent, usually malignant

  • Germ cell tumours

  • sex chird stromal tumours

  • metastases


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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)


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epithelial stromal tumours main 4

  • serous

  • mucinous

  • endometrial

  • clear cell


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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)


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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


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Endometrioid tumours

  • solid or cystic, composed of tubular hlands

  • usually malignant w mutatiins in PTEN


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Clear cell carcinomas

  • malignant tumours w broad papillae lined by clear and hobnail cells

  • bad prognosis


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Brenner tumours

  • encapsulated, usually benign tumours

  • abundant stroma containung nests


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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


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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


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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


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Metastases in ovarian canecr

  • older women

  • bilateral, at surface of ovary

  • from gi, breast, lungs

  • signet ring mucin secreting cells


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Craniopharyngioma

  • benign tumour of remnant of rathke pouch

  • anywhere from nasopharynx to diencephalon

  • sellar mass, tx by rt


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Hypopituitarism ant vs post sx

  • anterior

  1. gh deficiency : dwarfism

  2. acth : hyponatraemia, hypotension

  3. lh/fsh deficiency : infertility, amenorrhea

  4. prolactin deficient : cant lactate

  5. msh deficient : pallor

  • posterior

  1. adh deficiency : DI


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sheehans syndrome

  • acute infarction w necrosis of ant. pituitary lobe

  • post partum haemorrhage

  • mild hypopituitarism (ant pituitary x2 size, partial necrosis)


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somatotroph adenomas

  • gh secreting → acromegaly

  • acromegally effects :-

  1. mass effect : visual fields

  2. hypopituitarism : disturbs others

  3. metabolic effects : diabetes, htn

  4. ST effects : excessive jaw, internal organs

  • diagnosed w igf1 (failure to suppress gh on gtt), mri


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Prolactinoma

  • amenorrhea, low lobido, galactorrhea

  • dx w bloodwork +mri

  • rx w dopamine agonists (eg cabergoline)


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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


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dx and tx of hyperaldosteronism

  • check plasma renin (suppressed in primary, elevated in secondary) and aldosterone

  • salt loading to suppress aldosterone


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Androgen excess possibilities

  • CAH

  • adrenal tumours : usually malignant

  • pcos : oligomenorrhea, hirsuitism, ovarian cyst

  • ovarian hyperthecosis


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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

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dx addisons

  • acth stimulation

  • insulin tolerance test

  • ct adrenals


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adrenal cortical neoplasm

  • adenoma : small, functional (cushings or conns)

  • carcinoma : rare, large , in children unkess mets


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Adrenal medulla neoplasm

  • chromaffin cells

  • phaechromocytoma

  • neuroblastic tumours


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What and why thyrotoxicosis

  • elevated free t3/t4

  • graves (most), multinodular goitre, follicular adenoma

  • either excess release or extra thyroid source


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hyperthyroidism cx

  • increased bmr → weight loss, heat tolerance

  • cardiac, ocular, skeletal → tachy, nervous, tremor

  • thyroid storm


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Hypothyroidism

  • low t3/t4

  • hashinotos thyroiditis, iodine deficiency, development

  • sx : fatigue, cold intolerance, weight gain, myxoedma


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Hashimotos thyroiditis

  • autoimmune against tsh receptor

  • painkess enlargement if thyroid

  • hurthle cell metaplsia + fibrosis


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Granulomatous thyroiditis what, macro and micro

  • transient, viral likely

  • gland is adherant to trachea and adjacent strap muscles

  • neutrophils, aggregation kf macrophage, giant cells


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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)


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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


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Thyroid storm

  • extreme hyperthyroidism

  • common after infection, also after discontinue anti thyroid

  • sx : elevated T (>40), tachy, arrythmia, vomit


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Thyroid neoplasia

  • solitary palpable thyroid nodule

  • 1% only malignant

  • in young males, hx radiation tx

  • if functional most likely benign


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follicular adenoma

  • benign neoplasm

  • encapsulated

  • oncocytic (hurthle) cell adenoma another variant


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Common thyroid carcinomas (4, common to least)

  • papillary

  • follicular

  • medullary

  • others


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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)


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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


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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


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anaplastic carcinoma of thyroid

  • in elderly, present w local compression

  • v rapid w v high mortality

  • braf mutation

  • spindle cell, giant cell, squamoid variants


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Congenital thyroid abnormalities

  • dyshormonogenesis goitre

  • thyroid dysgenesis : ectopic, hypoplasia, agenesis