FGT Flashcards

1
Q

Describe the urothelium

A
  • Lines the entire conducting passage of the urinary tract, from pelvicalyceal area down the ureter, lining the bladder and urethra
  • Constitutes an impermeable barrier.
  • Stratified (3-7 cells)/multi-layered
  • Umbrella cells (U) at the surface.
  • Lower layers have cells with cuboidal morphology
  • Able to distend.
    • thickness of urothelium depends on how distended bladder is (i.e. thinner if bladder is full)
  • Rests on a basement membrane and lamina propria (LP).
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2
Q

B1 revision

Recall the approach to a lesion of mass

A
  • Non-Neoplastic
    • Congenital
    • Hamartomatous
    • Infection
    • Inflammation
    • Deposits
  • Neoplastic
    • Benign
      • Primary
      • Secondary
    • Malignant
      • Epithelial
      • Mesenchymal
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3
Q

Describe non-neoplastic lesions of the ureter

A

Congenital:
- Duplication/Bifid
- Diverticuli

Infection:
- Secondary to vesicoureteric reflux

Inflammation:
- Ureteritis Cystica

Deposits leading to obstruction:
- Calculi
- Blood clot
- Fibrosis

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4
Q

List non-neoplastic lesions of urinary bladder

A

Congenital
- Exstrophy: skin over lower abdominal wall does not close properly, so bladder is exposed on outer side of abdomen
- Hypoplasia: underdevelopment of tissue
- Diverticuli
#### Infection
- Schistosomiasis esp. in Africa and Asia
#### Inflammation
- eosinophilic
- drugs e.g. cyclophosphamide
- radiation
- idiopathic
#### Deposits
- lithiasis within the lumen
- amyloid within the wall

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5
Q

List non-neoplastic lesions of the urethra

two

A

Congenital
- Accompanies bladder anomalies: Hypospadias
#### Infection
- Gonococcal, Chlamydia, E. coli

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6
Q

List the two types of urothelial neoplasms

A
  • flat
  • papillary
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7
Q

Describe urothelial CIS (a flat urothelial malignancy)

A
  • Presentation: Asymptomatic or symptoms of urinary tract infection not responding to treatment.
  • Cystoscopy: Flat red inflamed-looking mucosa.
  • Histology: Features of malignancy (NC ratio, hyperchromasia, mitotic activity etc): full thickness, urothelium replaced by large pleomorphic atypical cells. No breach in the basement membrane. Haemorrhagic change to urothelium.
  • Macroscopy: haemorrhagic, multifocal flat lesions

Note:
- it may be a diffuse process involving the entire bladder
- important to rule out invasive areas, and any associated papillary lesions

Some risk factors include:
- genetic: HNPCC: inherited genetic mutations in mismatch repair genes– tend to get colon carcinoma but can get different malignancies in other parts of body
- acquired: smoking
Treatment:
- BCG - placed in bladder: causes chronic hypersensitivity inflammatory reaction so entire urothelium becomes inflamed, drops off, dies and falls out

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8
Q

Describe another type of flat malignant neoplasm

A

Urothelial carcinoma
- Invasive carcinoma
- High grade: invasion muscularis propria, low prognosis
- Low grade: invasion into lamina propria
- surface epithelium contains malignant cells that have invaded past BM, which them forms a tumour seen macroscopically by cystoscopy
- Treatment: cystoscopy and replacement with neo-bladder made of ileum

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9
Q

What is the value in differentiating between different levels of invasion?

A
  • Different Treatments
  • Urothelial Carcinoma in situ: Transurethral resection & intravesical BCG
    AND
    Tumor invading through the muscularis propria: Cystectomy
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10
Q

Describe general features of papillary neoplasms

A

Papillary architecture:

It is present in normal tissues e.g. choroid plexus as well as several tumours.
- Architectural Pattern: Finger-like projection - can be seen with cystoscopy: may hypertrophy if bladder chronically obstructed by multiple papillae
- Covering epithelium.
- Microscopy: Core of blood vessels and connective tissue in the center i.e. fibrovascular core.
- Presentation: - Delicate papillae break due to stresses leading to bleeding from the central core of blood vessels.
- This leads to patients present with microscopic or macroscopic hematuria.
- **Hematuria outside of the setting of a UTI is abnormal and must be investigated

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11
Q

Describe benign papillary urothelial neoplasms

A
  • Papilloma
  • Lined by essentially normal urothelium
  • Normal thickness
  • Orderly and organised architecture
  • No mitoses
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12
Q

List the two types of malignant papillary neoplasms

A

Papillary urothelial neoplasm of low
malignant potential/unknown potential
AND
Papillary urothelial carcinoma

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13
Q

Describe papillary urothelial neoplasms of low
malignant potential

A
  • Lined by cytologically troublesome urothelium
  • Increased thickness of urothelium
  • Mild disarray
  • Occasional mitoses
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14
Q

Describe the features of papillary urothelial carcinoma

A
  • Papillary urothelial carcinoma (may be non-invasive or invasive)
    • Lined by cytologically malignant urothelium
    • Very increased thickness of urothelium
    • Complete loss of organisation
    • Several mitoses

Cystoscopic Appearance
- Fronds like a sea anemone, floating in the urine.
#### Macroscopic Appearance
- Finger-like papillary projections.

Cytological Classification (Grade)
- The nuclear appearance gives the grade.

  • Low grade
    • Non-invasive
      • Cells are bland.
  • High grade
    • Invasive
      • Cells are very pleomorphic and large.

Invasion (Stage)
- The depth of invasion gives the stage.
- Muscularis propria invasion is a poor prognosis.
- Low grade
- Non-invasive
- The cells are limited to the urothelium, and there has been no breach of the basement membrane.
- Invasive
- The cells have invaded beyond the basement membrane into the submucosa and muscle.

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15
Q

Describe the fallopian tube

A
  • Muscular (Smooth) tube connecting the ovary with the uterus.
  • Tubular structure with smooth muscle coat
    • Ciliated columnar cells: motilit
    • Non-ciliated columnar cells with apical granules: secrete fluid
    • Intercalated/Peg cells: non-ciliated, may act as stem cells
  • Distal parts have fimbriae (finger-like projections that catch egg in ovulation)
  • Centre of tube has plicae (complicated folds) - large SA to grab egg and move along the tube
  • Movement along the tube due to smooth muscle peristalsis and cilia
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16
Q

List some problems that can occur in the fallopian tube

A
  • infection or inflammation known as salpingitis - acute, chronic, granulomatous, foreign body type
    • obstructive causes: mainly ectopic pregnancy, endometriosis, paratubal cyst
    • benign tumour: adenomatoid
    • malignant neoplasm: primary carcinoma or secondary metastasis from ovary or other abdominal organs
17
Q

Describe salpingitis

A

Aetiology: Infection
- STI (Neisseria gonorrheae, Chlamydia, Mycoplasma).
- Post instrumentation / IUD / post-pregnancy or abortion.
#### Macro
- Adhesion and fusion of fimbria.
- Dilated tube.
- Filled with pus.
- Often asymptomatic or very mild symptoms e.g. low-grade abdominal pain
#### Micro
- Acute (neutrophils) or chronic inflammation (plasma cells).
- Plicae fused.
#### Complications
- Abscess formation.
- Ectopic pregnancy.
- Infertility
- Systemic sepsis and death

18
Q

Describe ectopic pregnancy

A

Aetiology
- Chronic salpingitis: Inflammation fuses the plicae and can, therefore, trap the ovum.
- Congenital abnormalities.
- Functional tubal disturbances.
- Endometriosis.

Macro
- Dilated.
- Hemorrhagic.
- +/- fetus.

Micro
- Chorionic villi.

Treatment
- Salpingectomy - with implications for ferility

Appearance: - Fallopian tubes are distended with ruptured wall exuding hemorrhagic material and fetal tissue.

19
Q

Describe the uterus briefly

A
  • endometrium comprised of glands and stroma
  • myometrium: smooth muscle, lined by endometrium
20
Q

Describe the endometrium

A

Endometrium: tubular glands lined by simple columnar epithelium
- Endometrial stroma: small sesame seed-like specialised fibroblasts closely packed
- Endometriosis: endometrium outside the uterus (can occur anywhere)
- Adenomyosis: endometrium within myometrium
- Look similar microscopically, but are distinct diseases with different prognoses - thickened uterine wall because smooth muscle hypertrophies
- Deposits look like endometrium - have glands with stroma and signs of haemorrhage
- Complications: chronic pain (bleed on cyclical basis causing inflammation and pain), infertility

21
Q

Describe changes to endometrium within menstrual cycle

A

Proliferative Phase to secretory phase over ovulation

22
Q

Describe diseases of endometrium ‘in the wrong location’

A
  • Adenomyosis
    • Endometrium within the myometrium.
  • Endometriosis
    • Endometrium outside the uterus.
    • Complications: Pain, Infertility.

Note that both disease look similar under the microscope, they are distinct diseases, with distinct pathogenesis.

23
Q

Describe endometrial carcinoma

A
  • Endometrial carcinoma
    • Complex glandular and papillary architecture
    • Glands arranged back-to-back without intervening normal stroma
      • Oestrogen-driven disease ∴ cases increasing with obesity (more aromatisation in peripheral fat = ↑ oestrogen levels) and may improve after menopause when oestrogen is driven down
    • Glands and papillae are lined by multiple layers of cells
    • Cells show large nuclei with nucleoli, altered nuclear/cytoplasmic ratio and pleomorphism
    • Malignant glands start to invade myometrium
    • Presentation: PV bleeding intermenstrual, heavy, prolonged or post-menopausal
24
Q

Describe leiomyoma

A
  • Smooth muscle proliferation, homogenous whorled appearance.
  • Complications: Pain, Menorrhagia, Infertility, Compressive symptoms.
  • Leiomyoma: smooth muscle proliferation (fibroids)
    • Microscopy: homogenous, whorled appearance, fascicles of smooth muscle, circumscribed, abundant pink cytoplasm and spindled nuclei
    • Complications: pain (if large/heavy or necrotising), menorrhagia and dysmenorrhoea (uterus so large causing increased endometrial surface area ∴ heavy bleeding), infertility or pregnancy loss as leimyomas interfere with implantation, compressive symptoms
25
Q

List the three parts of the cervix

A
  • endocervix: glandular
    • squamocolumnar junction: transformation zone of squamous to columnar - site where CST taken from
    • ectocervix: squamous
26
Q

Discuss pathology of cervix

A

Cervix - Infection
- Trichomonas.
- Candida.
- HPV.

Cervix - Benign Neoplasm
- Polyps.

Cervix - Malignant Neoplasm
- Squamous cell carcinoma.
- Adenocarcinoma.

27
Q

Describe the vagina and pathology of vagina

A

Vagina
- Fibromuscular canal.
- Mucosal layer – squamous epithelium.
- Lamina propria – elastic fibers.
- Smooth muscle with rugae
- Adventitial layer.

Vagina - Pathology
- Congenital
- Atresia, septate vagina, Gartner duct cysts.
- Infection
- Candida, HPV.
- Benign Neoplasm
- Squamous papilloma.
- Malignant Neoplasm
- Squamous cell carcinoma, Clear cell carcinoma, Embryonal rhabdomyosarcoma.
- Vaginal pathology except for infection is rare.

28
Q

Describe vulva

A
  • normal vulva has stratified non-keratinising squamous epithelium
  • highly vascularised beneath epithelium due to erectile tissue
29
Q

List vulval pathology

A
  • Congenital
    • Ectopic mammary tissue.
  • Inflammation
    • Dermatitis, lichen sclerosus, lichen planus.
  • Infection
    • HPV, candida.
  • Benign Neoplasm
    • Fibroepithelial polyp, nevi, hidradenoma papilliferum.
  • Malignant Neoplasm
    • VIN/Squamous carcinoma, melanoma, Paget’s disease.
30
Q

Describe lichen sclerosis

A
  • Lichen sclerosus
    • Post-menopausal women
    • Pathogenesis: autoimmune, genetic or hormonal
  • Macro: area of leukoplakia (white thickened layer of keratin on mucosal surface -
    hyperkeratosis)
  • Micro: hyperkeratosis, thickening of epidermis, loss of rete pegs, dermal collagen altered
    • Not a pre-malignant condition, but associated with increased risk of SCCNote also:
  • Lichen planus: immune system mistakenly attacking cells of skin/mucous membranes
31
Q

Describe benign neoplasms of the vulva

A

Vulval intraepithelial neoplasia
- Squamous epithelial neoplasia without invasion beyond the basement membrane (pre-invasive).
- Risk factors: HPV, cigarette smoking, lichen sclerosis.
#### Macro
- Leukoplakia.
#### Micro
- Hyperkeratosis, thick epithelium (acanthosis), elongation of rete pegs, nuclear atypia, mitoses.

32
Q

Describe malignant neoplasms of vulva

A

Vulval SCC:
- Age: >60, rare in women younger than 30.
- Risk factors: HPV, cigarette smoking, immunodeficiency.
- Site: Labia majora, also labia minora, clitoris.
- Prognosis: 5-year survival 50-75%.

33
Q

extra

Describe the ovary

A
  • Peripheral darkly staining cortex with follicles
  • Vascular and fibrous central hilar region containing groups of Leydig cells
  • Corpus luteum: very convoluted with steroid secreting cells (large w abundant cytoplasm - appear swollen
    microscopically)
  • Corpus albicans: pale fibrotic structures
  • Primordial follicles: sit within cellular ovarian stroma comprising specialised hormone-responsive
    fibroblast-like cells arranged like shag rug