STDs key points Flashcards

1
Q

what organism is trichomonas vaginalis?

A

protozoa

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2
Q

tx of trichomonas

A

metronidazole

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3
Q

oral effects of trichomonas

A

oral ulcers
rare
if IC

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4
Q

chlamydia organism

A

chlamydia trachomatis

bacteria

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5
Q

chlamydia forms

A

elementary body - metabolically inactive. EC

reticulate body - replicative form. IC

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6
Q

chlamydia tx

A

azithromycin or doxycycline

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7
Q

chlamydia oral effects

A

rare - tonsillopharyngitis
cervical and oropharyngeal lymphogranuloma
rarely vesicles/erosive nodules L lip, ulcers frenum tongue

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8
Q

gonorrhoea organism

A

neisseria gonorrhoeae

bacteria

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9
Q

gonorrhoea oral effects

A

gonococcal tonsillar infection (rare)

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10
Q

gonorrhoea tx

A

IM ceftriaxone

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11
Q

syphilis organism

A

bacteria

treponema pallidum

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12
Q

primary syphilis

A

painless “chancre” ulcer/papule
regional lymphadenopathy
lasts 6-8wks

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13
Q

secondary syphilis

A

typically several weeks after untreated primary. Wide spectrum

  • rash - palms and soles
  • oral: erosions, polymorphic aspect, bullous, erythematous, L lip, tongue, white border surrounding erythematous areas
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14
Q

latent syphilis

A

early (1st year, infectious) and late (usually non-infectious and doesn’t respond well to tx)
absence of clinical manifestations in the setting of serologic detection of syphilis

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15
Q

tx of syphilis

A

IM penicillin x2

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16
Q

congenital syphilis oral effects

A

approx 6yrs
hutchinson teeth
mulberry molars

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17
Q

hutchinson teeth

A

centrally notched, widely spaced, peg shaped U1s

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18
Q

mulberry molars

A

surface has numerous poorly formed cusps surmounting a dome shaped tooth

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19
Q

tertiary syphilis

A
systemic multiorgan disease process
15% untreated pts progress to this
3 main systemic manifestations:
 - neurological
 - CV (aneurysms)
 - gummatous (MC) lesions
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20
Q

what type of virus is HSV?

A

dsDNA

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21
Q

HSV1

A

oral (usually)

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22
Q

HSV2

A

genital

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23
Q

genital herpes lifelong infection

A

viral genome maintained within ganglia for life (latency - episomes
reactivation

24
Q

primary HSV 2 infection outcome

A

usually resolves approx 3 wks

25
HSV2 recurrent infections
can get prodrome (travelling along axons) lesions more likely to be fewer in number, unilateral and generally without systemic symptoms more mild
26
HSV non-primary infection
infection with HSV 1 or 2 in an individual with pre-existing ABs to the other virus manifestations tend to be milder than those of primary infection - presumably due to cross-immunity protection from prior infection with the other HSV type
27
HSV and antivirals
reduce symptoms and likelihood of transmission
28
main risk factor for genital herpes
number of lifetime sex partners
29
what type of virus is HPV?
dsDNA
30
non-oncogenic low risk HPV
6 and 11
31
oncogenic high risk HPV
16 and 18
32
low-risk HPV oral features
``` variety - solitary/multiple verruca vulgaris (common wart) condyloma acuminatum (cauliflower like) squamous papilloma - hairy like (pedunculated) lesions ```
33
squamous cell papilloma
neoformation epithelial origin HPV 6 and 11 slow exophytic growth with wide base or pedicle HPV related - STD screen?
34
squamous cell papilloma histology
``` hyperkeratotic surface papillary (finger-like) projections projections have fibrovascular CT cores SSE covers cores no dysplasia ```
35
condyloma acuminatum
wart HPV 6, 11, 16, 18 tongue and palate acanthotic and sometimes hyperkeratotic epithelium with occasional koilocytosis
36
focal epithelial hyperplasia (Heck's)
asymptomatic benign mucosal disease multiple, painless, soft, sessile papules/plaques/nodules, can coalesce to give larger lesions HPV 13 and 32 associated etc usually need histopathology to confirm exact diagnosis
37
focal epithelial hyperplasia (Heck's) - onset
mostly in specific groups in certain geographical regions - often poverty/low SES usually childhood/adolescence
38
focal epithelial hyperplasia (Heck's) - tx
sometimes resolves spontaneously but tx often indicated - aesthetics/any interference with occlusion no specific tx - SR, laser excision or possibly topical antiviral agents may be of benefit no evidence that it is potentially malignant
39
oncogenic HPV
if infection fails to clear and persists for long time, viral E2 protein fct gets abrogated, leading to overexpression of main viral oncoproteins E6 and E7
40
what type of virus is HIV?
enveloped ssRNA virus
41
revised WHO HIV/AIDS clinical staging system
4 clinical stages for adults | demonstrate at least one clinical condition in that stage's criteria
42
stage 1 acute HIV infection
asymptomatic/persistent generalised lymphadenopathy may remain for several years CD4+ cell count >500 cells/uL
43
stage 2 early/mildly symptomatic HIV
unexplained WL <10% TBW recurrent resp infections dermatological conditions CD4+ cell count 350-499/uL
44
stage 3 late/moderately symptomatic HIV
``` WL >10% TBW, prolonged unexplained diarrhoea pulmonary TB severe systemic bacterial infections MC conditions - ROC, oral hairy leukoplakia, NG/P/S CD4+ cell count 200-349/uL ```
45
stage 4 AIDS
develop AIDS-defining conditions or a CD4 cell count of <200 cells/uL in HIV-infected pts
46
HIV coinfection
TB most prevalent (1 in 4) chronic HBV HCV HPV
47
oral lesions strongly associated with HIV
``` candidiasis: erythematous, pseudomembranous hairy leukoplakia Kaposi sarcoma PDD - LGE - NG/P lymphoma ```
48
LGE
distinct band of erythema of gingival margin
49
HIV oral bacterial infections - TB
painful, superficial lingual ulcer, well-circumscribed with crateriform aspect and slightly elevated and indurated borders
50
HIV oral bacterial infections - syphilis - secondary
mucous patches appeared as white slightly raised plaques on an erythematous base with a serpentine and white/reddish well-defined outline shallow ulcers macular lesions
51
HIV and oral ulcerations
freq increases with HIV progression
52
HIV and SGs
bilateral parotid gland enlargement
53
Kaposi Sarcoma
``` associated with HHV8 infection red/bluish/purplish macular or nodular lesion can ulcerate and bleed small to extensive HP, gingiva and tongue ```
54
NHL
``` clinically - rapidly enlarging necrotic masses - ulcerated/non-ulcerated masses - palate and gingivae most common sites v poor prognosis ```
55
HAART drugs
``` NRTIs NNRTIs INSTIs protease inhibitor entry inhibitor ```
56
HAART recommended initial regimen
2NRTIs plus one from INSTI/NNRTI/PI and a pharmacokinetic (PK) enhancer (also known as a booster) e.g. cobicistat and ritonavir lots of oral HC drug interactions - check
57
orofacial adverse effects of HAART
``` EM ulcers xerostomia taste alteration perioral paraesthesia facial lipodystrophy (hyperpigmentation) (cheilitis) ```