Female Reproductive Pathology 2 Flashcards

1
Q

What are the important features of Mullerian malformations?

A
  • associated with abnormalities of the renal and axial skeleton systems
  • have functioning ovaries and age-appropriate external genitalia
  • after onset of puberty, usually present with menstrual disorders
  • late presentations usually with infertility and obstetric complications
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2
Q

What are the important features of vulval cancers?

A
  • majority is squamous cell carcinomas
  • usually develop from pre-cancerous, preinvasive areas called vulval intraepithelial neoplasia
  • 2 subtypes;
  • associated with HPV - younger women
  • associated with chronic vulval skin changes (vulval dystrophy) and lichen sclerosus - older women
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3
Q

Describe some vulval epithelial disorders

A
  • squamous hyperplasia: hyperkeratosis, irregular thickening of ridges, neoplastic potential
  • lichen sclerosus: hyperkeratosis, flattening of ridges, oedema in connective tissue and chronic inflammation, neoplastic potential
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4
Q

Describe the clinical appearance of lichen sclerosus (vulval dystrophy) and its treatment

A
  • sometimes white patches called leukoplakia
  • causes itching (pruritis)
  • picking the skin makes it worse (excoriation)
  • treated with potent topical corticosteroids
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5
Q

What is the main presenting symptom of endometrial cancer?

A

post-menopausal bleeding

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6
Q

Describe some abnormalities of the myometrium

A
  • adenomyosis: endometrial glands and stroma present within the myometrium, causes menorrhagia/dysmenorrhoea
  • smooth muscle tumours: leiomyoma/fibroid (common and associated with menorrhagia and infertility) and leiomyosarcoma
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7
Q

What is endometriosis and its complications?

A
  • endometrial glands and stroma present outside the uterine body

complications:

  • pelvic inflammation
  • infertility
  • pain
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8
Q

What are the possible sites of endometriosis?

A
  • ovary (chocolate cyst)
  • pouch of Douglas
  • peritoneal surfaces, including uterus
  • cervix, vulva, vagina
  • bladder bowel etc.
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9
Q

Where can ovarian cysts originate from?

A

Can be:

  • mesothelial
  • epithelial
  • follicular
  • luteal
  • endometriotic
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10
Q

Describe a possible clinical presentation of polycystic ovary syndrome

A
  • hyperadrogenism
  • hirsutism (growing dark/coarse hair in male pattern)
  • acne
  • alopecia
  • menstrual disturbance
  • infertility
  • obesity
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11
Q

What are the long term complications of polycystic ovary syndrome?

A
  • type 2 diabetes
  • dyslipidaemia
  • hypertension
  • cardiovascular disease
  • endometrial carcinoma
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12
Q

What are some treatment options for PCOS?

A
  • combined contraceptive pill for
  • contraception
  • to prevent development of endometrial hyperplasia and cancer
  • suppress excessive androgen secretion to control acne and hirsutism
  • alternative treatment can be the Mirena intrauterine system (the coil)
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13
Q

How would you describe an ovarian neoplasm?

A
  • solid or cystic
  • benign or malignant
  • classification:
  • epithelial (90%)
  • germ cell
  • sex cord/stromal
  • metastatic
  • miscellaneous
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14
Q

What are different types of epithelial ovarian tumours?

A
  • benign
  • borderline (cytological abnormalities with no stromal invasion)
  • malignant (stromal invasion)
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15
Q

What are the symptoms of ovarian cancer?

A
  • non-specific GI symptoms (bloating/indigestion/)
  • gradually increasing abdominal distension
  • increasing size of tumour causes pressure effects (chronic abdo, pelvic, back pain; increases urinary frequency/urgency; constipation/altered bowel habits; leg swelling/DVT/PE)
  • abnormal vaginal bleeding
  • metastatic symptoms: ascites, pleural effusion, weightloss, fatigue
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16
Q

What is the treatment of ovarian cancer?

A
  • surgical management: exploratory laparotomy for tumour debulking and surgical staging
  • adjuvant chemotherapy
  • response to treatment monitored using CA-125 levels (decreases if treatment is effective and increases on relapse)
17
Q

What is a molar pregnancy?

A
  • abnormal pregnancy resulting from overproduction of the tissue that is supposed to develop into the placenta
  • baby and placenta do not develop normally after conception
  • not compatible with life
  • mother’s have higher than normal hCG levels
18
Q

Describe the different hydatidiform moles

A
  • complete hydatidiform mole: develops when 1 or 2 sperm fertilise an egg that contains no nucleus or DNA, so all genetic material is from father’s sperm cell - no foetal tissue
  • partial hydatidiform mole: develops when 2 sperm fertilise a normal egg, contain some foetal tissue but often just mixed trophoblastic tissue
  • invasive if it has grown into muscular layer of uterus and can develop from both complete or partial moles
19
Q

What is a choriocarcinoma?

A
  • malignant form of gestational trophoblastic disease
  • more likely than other conditions to grow and spread to organs away from uterus
  • half start as molar pregnancies
  • some can arise not related to pregnancy (non-gestational)
20
Q

What is an ectopic pregnancy and its common site?

A
  • implantation of a conceptus outside the endometrial cavity

- commonest site is fallopian tube