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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

Appear 2-10 weeks after primary chancre

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
[ In poorly treated / untreated syphilis]

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
5. Mx with cephalosporin

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 ?
  • Circumscribed
  • firm
  • raised
  • < 0.5 cm diameter
Nodule Definition ?
  • Solid
  • firm
  • elevated
  • palpable
  • > 0.5 cm
Purpura Definition ?
  • Skin / mucous membrane
  • discolouration
  • due to RBC extravasation
Pustule Definition ?
  • Visible accumulation of yellow fluid
  • In form of vesicle / papule
  • containing fluid.
Vesicle definition?
  • Visible accumulation of clear, serous fluid
  • in papule < 5mm
Blister / Bulla Definition ?
  • Visible accumulation of fluid
  • usually large : > 5mm.
Plaque Definition?
  • An area / sheet of elevated skin
  • with distinct edge
  • usually > 1cm
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]
- Mycoplasma / HSV ** / Drugs
[ sulphonamides/penicillins]


Idiopathic [ 50% ]


2. SJS and TEN
[ anticonvulsants / NSAIDS / sulphonamides
penicillins ]
3. Staphylococcal scalded skin syndrome (SSSS)
4. Pemphigus and pemphigoid

Difference between Bullous pemphigoid {BP} and Pemphigus vulgaris {PV} ?
Bullous pemphigoid

= autoantibodies to EPIDERMAL BASEMENT MEMBRANE
= tense bullae
Pemphigus vulgaris


= 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-thrombocytopenic
2. 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]
2. Chronic renal failure {CRF}
3. Haematological [ lymphoma / PRV ]
4. Endocrine [ myxoedema ; thyrotoxicosis]
5. Carcinoma [ lung ; stomach ]
6. Drugs

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.
C. Blistering and epidermal shedding ( desquamation) are Clinical


features.
D. Flu-like symptoms can precede or coincide with the skin blistering.

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. Patients with SJS are best treated in a Burns Unit.
C. Ophthalmology Consultation is essential.
D. Ocular complications can be devastating .

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