Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
38 Cards in this Set
- Front
- Back
Primary Syphilis = ?
|
Painless chancre
|
|
Secondary Syphilis = ?
|
1. Papules
2. Headache 3. Fevers 4. Arthralgias + Myalgias 5. Generalized Lymphadenopathy 6. Painless mucous membrane lesions |
|
Tertiary Syphilis = ?
|
1. General paresis
2. Aortitis {with aneurysms} 3. Optic atrophy : Argyll - Robertson pupil [ non constrictive to light ; constrict to accommodation ] Highly specific sign of Neurosyphilis 4. Tabes Dorsalis 5. Dementia |
|
Name of reaction that can occur after
antibiotic treatment of secondary syphilis ? |
" Jarisch - Herxheimer reaction"
|
|
What skin lesion initially is an erythematous macule, that evolves into a necrotic, purpuric vesicopustule - asymmetric, and distally placed {hands} ?
|
Disseminated gonococcus.
|
|
5 Features of Disseminated Gonococcus ?
|
1. Systemic septic vasculitis
2. Due to Neisseria gonorrhoea 3. Lesions are : - asymmetric macules - distal - evolve into necrotic purpuric vesicopustules 4. Associated with urethritis + arthralgia |
|
SCORTEN severity score for Toxic Epidermal Necrolysis {TEN} ?
|
S ugar > 14 mmol/L
Cancer / Haematological malignancy Older age > 40 Rate -HR > 120 / min Total HCO3 < 20 Epidermal detachment > 10% BSA Day 1 Nitrogen / Urea > 10 |
|
SCORTEN mortality prediction scoring ?
|
0-1 3% 5%
2 12% 10% 3 33% 30% 4 60% 60% >5 90% 90% |
|
Papule Definition ?
|
|
|
Nodule Definition ?
|
|
|
Purpura Definition ?
|
|
|
Pustule Definition ?
|
|
|
Vesicle definition?
|
|
|
Blister / Bulla Definition ?
|
|
|
Plaque Definition?
|
|
|
Sweet Syndrome ?
[5 features] |
1. "Acute febrile neutrophilic dermatosis"
2. Tender lesions -demarcated plaques to head and upper extremities 3. Unknown cause ? immunological 4. Many Associations: - malignancy {20%} AML / breast Ca - IBD - autoimmune disease - infections [bacterial and viral] 5. females > males 4:1 |
|
Causes of Erythroderma ?
|
1. Eczema 40%
2. Psoriasis 22% 3. Drugs 15% 4. Lymphoma 10% [ Sezary Syndrome] 5. Idiopathic 8% |
|
MOST common causes of vesicular / bullous
skin rash? |
1. Viral [ Herpes simplex ; herpes zoster ]
2. Impetigo 3. Drugs [ sulphonamides / penicillin ] 4. Scabies 5. Insect bites / papular urticaria 6. Bullous eczema / pompholyx |
|
LESS Common Causes of vesicular / bullous skin rash?
|
1. Erythema Multiforme [ Minor / Major ]
[ target lesion + mm involvement] Idiopathic [ 50% ] 2. SJS and TEN |
|
Difference between Bullous pemphigoid {BP} and Pemphigus vulgaris {PV} ?
|
Bullous pemphigoid
= autoantibodies to EPIDERMAL BASEMENT MEMBRANE = autoantibodies to Epidermal karatinocytes = flaccid bullae |
|
Treatment of bullous pemphigoid /
pemphigus vulgaris ? |
1. Steroids
2. Immunosuppressants - Azathioprine - MTX - Cyclophosphamide 3. Burns Unit Mx if widespread |
|
Causes of PALPABLE purpura ?
|
1. Polyarteritis nodosa (PAN)
2. Henoch Schonlein Purpura (HSP) 3. Infective - meningococcaemia - gonococcaemia - staphylococcus - ricketssial {RMSP] - enteroviruses 4. Embolic 5. Allergic [leukocytoclastic] |
|
Classes for Causes of NON-PALPABLE purpura?
|
( Broad categories ) 1. Non-thrombocytopenic2. Thrombocytopenic a. With splenomegaly b. Without splenomegaly |
|
Causes of Non-thrombocytopenic
non-palpable purpura ? |
1. Cutaneous ( Trauma / Sun / steroids / ageing)
2. Systemic Disorders a. Uraemia b. Von-Willebrand's Disease c. Scurvy d. Amyloid |
|
Classification for Causes of
Thrombocytopenic Non-palpable purpura? |
1. With splenomegaly
a. normal marrow b. abnormal marrow 2. Without splenomegaly a. Normal marrow b. abnormal marrow. |
|
Non-palpable purpura: thrombocytopenia WITH SPLENOMEGALY-causes ?
|
1. Normal marrow
a. Liver disease + portal HTN b. Myeloproliferative disorders c. Lymphoproliferative disorders d. Hypersplenism 2. Abnormal marrow a. Leukaemia b. Lymphoma c. Myeloid metaplasia |
|
Non-palpable purpura : thrombocytopenia WITHOUT SPLENOMEGALY-causes ?
|
1. Normal marrow
a. Immune - idiopathic [ITP] / drugs / infections [ HIV] b. Non-immune - vasculitis / sepsis / DIC / HUS / TTP 2. Abnormal marrow - Cytotoxics / aplasia / fibrosis / infiltration / alcohol / THIAZIDES |
|
Associations of Pyoderma gangrenosum?
|
1. IBD inflammatory bowel disease
2. RA rheumatoid arthritis 3. Blood dyscrasias 4. Behcet's Syndrome 5. Malignancy [ myeloma / leukaemia ] |
|
Categories for classifying pruritis?
|
1. With skin disease
2. Without skin disease |
|
Pruritis + skin disease causes? [10]
|
1. Drugs
2. Urticaria 3. Eczema 4. Contact dermatitis 5. Scabies 6. Insect bites 7. parasites [ roundworm] 8. Lichen planus 9. pityriasis rosea 10 . dermatitis herpetiformis |
|
Pruritis WITHOUT skin disease causes ? [6]
|
1. Hepatobiliary
[ jaundice , primary biliary cirrhosis] |
|
What are the 3 main categories causes of
Erythema Multiforme ( EM ) ? |
1. Infection : Herpes Simplex Virus (HSV) / Mycoplasma
2. Drugs: Sulphurs / penicillins 3. Idiopathic : 50% |
|
What is the overlap of Body Surface Area (BSA)
classification for Stevens-Johnson Syndrome and TEN? |
SJS = 10% BSA and 5 % mortality
TEN > 30% BSA and 20-30% mortality Overlap occurs between 10-30% BSA |
|
Which is incorrect regarding Toxic Epidermal Necrolysis (TEN) ?
A. It is more common in Females ( 1.5 : 1 ) B. Is it due to drugs in 90% cases C. It is more common in the young D. It is more common in the immunocompromised (HIV ; Lymphoma ) |
C. Increasing age
|
|
Which is correct regarding SJS ?
A. It is due to drugs in 25% cases. B. It is more common in Females. C. It is strongly associated with Mycoplasma pneumoniae. D. It is more common with increasing age.. |
C.
A = drugs in 50% cases B = Males D. It is more common in younger age groups. |
|
Which is incorrect regarding SJS ?
A. Target lesions are commonly found. B. Skin pain and dusky purpuric skin changes heralds the onset of epidermal destruction. features. |
A. Occassional - makes differentiation from EM difficult.
|
|
Which is incorrect regarding the Management of SJS and TEN ?
A. Immediate cessation of all possible causative drugs is essential - and has been shown to reduce mortality. |
B. TEN = Burns Unit
|
|
Which is incorrect regarding SJS and TEN ?
A. High dose IV immunoglobulin and systemic corticosteroids are proven treatments. B. There is no current accepted therapy for SJS and TEN. C. Corneal rupture and blindness can occur. D. Supportive Care is the mainstay of management. |
A. Controversial
|