Dermatology Flashcards

1
Q

Pompholyx Dermatitis
(dyshidrotic eczema)

A

Triggered by Humidity and High Temperatures

P - Palms and soles (common areas affected)
O - Oozing and blistering lesions
M - Moisture (excessive sweating often triggers it)
P - Pruritus (intense itching is a hallmark symptom)

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2
Q

Porphyria Cutanea Tarda (Uroporphyrinogen Decarboxylase)

Feature
Investigation
Treatment

A

Photosensitive rash with blistering and skin fragility on the face and dorsal aspect of hands
+ Hypertrichosis + Hyperpigmentation

Serum Ferritin
Pink Fluorescence of Urine in Wood Lamp

Chloroquine
Venesection if Ferritin>600

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3
Q

Granuloma Annulare vs Necrobiosis Lipoidica Diabeticorum

A

Hyperpigmented and Centrally Depressed

vs

Well-defined, yellow-brown plaques with atrophic centres and telangiectasia

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4
Q

Seborrheic Dermatitis

Associations
Features
Treatment

A

HIV & Parkinsons

Otitis externa and blepharitis

Scalp -
1. Ketacanazole Shampoo
2. Shampoo with zinc pyrithione or Tar

Body
1. Ketacanazole Topical
2.

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5
Q

Centro Facial Telangiectasia + Pustules / Papules + Flushing –> Think What ?

Treatment ?

A

Acne Rosacea

  1. mild to moderate is topical ivermectin
  2. severe, add oral doxycycline
  3. If Persistent Flushing ONLY –> Topical Brimonidine Gel
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6
Q

Phemigoid Vulgaris vs Bullous Phemigoid

A
  1. no mucosal involvement: bullous pemphigoid
  2. mucosal involvement: pemphigus vulgaris
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7
Q

Phemigus Vulgaris

Pathophysiology and Treatment ?

A

Antibodies against Desmoglein 1&3

Steroids

Acantholysis on biopsy

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8
Q

Phemigus Vulgaris Biopsy Finding

A

Acantholysis on biopsy

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9
Q

Polymorphic Eruptions of Pregnancy (PEP)
vs
Phemigoid Gestationalis

A

Starts with Striae and SPARES UMBILICUS

START WITH UMBILICUS –> Trunk —> Arms

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10
Q

Guttate Psoriasis vs Pityriasis Rosea

Preceding Infections ?
Features ?
Treatment ?

A

Guttate Psoriasis

  1. Preceded by a Sore Throat 3-4 weeks prior
  2. Tear Drop
  3. Self Resolve or UVB
    If Recurrent - Tonsillectomy

Pityriasis Rosea

  1. Preceeded by an URTI
  2. Herald Patch
    Oval Lesions along Lines of Langer - ‘Fir Tree’
  3. Self Limited in 6 weeks time
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11
Q

Systemic Mastocytosis (Neoplastic Proliferation of Mast Cells)

Features
Investigations

A
  1. Urticaria Pigmentosa - produces a wheal on rubbing (Darier’s sign)

Urinary Histamine (Diagnostic)
Serum Tryptase

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12
Q

Acanthosis Agaricans Associations

A

Everything to do with WEIGHT GAIN except Gastric Ca

Grey PATCH

  • Gastric adenocarcinoma (A for acanthos, a for adenocarcinoma. Not squamous cell)
  • PCOS
  • Acromegaly
  • T2DM
  • Cushing’s
  • Hypothyroidism

Prader Willi too —> again Weight Gain

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13
Q

Management of Hirsutism ?

A

Weight Loss
COCP
Facial - Eflornithine

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14
Q

Management of Hypertrichosis ?

A

drugs: minoxidil, ciclosporin, diazoxide

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15
Q

Lichen Planus

  1. Features
  2. Treatment
A
  1. Planus - Polygonal , Pruritic, Purple Papules with White Lines Overlying - Wickenham Striae
  2. Mucosal Involvement - White Lacy in Buccal Mucosa
  3. Longitudinal Nail Ridges and Koebner Phenomenon

Treatment -
Topical Steroids
Benzydamine Oral Mouth Wash

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16
Q

Drugs that can cause Lichen Planus Eruptions ?

A

Gold
Quinine
Thiazides

17
Q

Eczema Herpeticum Features

A

Rapidly Progressing Painful Rash on a BACKGROUND OF EZCEMA
MONOMORPHIC ‘Punched Out Erosions’

LIFE THERATENING —> IV Acyclovir

18
Q

Various HHV and their Skin Pathologies

A

HHV-1—–>HSV-1 (above the belt/cold sores)
HHV-2—-> HSV-2 (below the belt/genital herpes) (HSV 1-2 causes ezcema herpeticum)
HHV-3—–>VZV (chicken pox singles)
HHV-4—–>EBV
HHV-5—–>CMV
HHV-6——> Roseola infantum
HHV-7—–>Pityriasis Rosea
HHV-8—–>Kaposi’s Sarcoma

19
Q

Actinic Keratosis Treatment

A
  1. Avoid Sun Exposure
  2. Topical Fluorouracil for 2-3 weeks
  3. Topical NSAID or Topical Imiquimod
20
Q

Systemic Mastocytosis Diagnostic Criteria

Just remember aggressive !!!

A

Indolent:
No B or C findings

Smouldering = 2 or more B findings (B = burden of disease):

  1. Bone marrow >30% mast cells and/or Tryptase >200 ng/ml and/or KITD816V mutation with a variant allele frequency (VAF) of >10%
  2. Signs of dysplasia or myeloproliferation without frank associated haematological neoplasm, and a normal FBC
  3. Hepatomegaly without liver dysfunction and/or splenomegaly without hypersplenism

Aggressive = 1 or more C findings (C = cytoreduction-requiring i.e. organ dysfunction):

  1. One or more cytopenias (Hb <100, platelets <100, neutrophils <1.0)
  2. Hepatomegaly with liver dysfunction
  3. Osteolytic lesions or fractures
  4. Splenomegaly with hypersplenism
  5. Malabsorption with weight loss due to GI infiltration
21
Q

Ulcerative Colitis with Ragged Edged Ulcer around Stoma Site ?

A

Pyoderma Gangrenosum

22
Q

Erythema Ab Igne
Erythema Marginatum
Erythema Multiforme

A

Over exposure to Heat and Fireplaces

Raised outer area and pale center and also affect the torso (GAS and Rheumatic Fever)

Rad Patches in Hands —> Target Lesions

23
Q
A

No treatment needed if asymptomatic and patient isn’t concerned

Confirmed dermatophyte or Candida infection:

  1. Mild (≤50% nail, ≤2 nails, superficial):
    a. Topical amorolfine 5% lacquer
    b. Duration: 6 months (fingernails), 9–12 months (toenails)
  2. Extensive dermatophyte infection:

a. Oral terbinafine (1st-line)
b. Duration: 6 weeks–3 months (fingernails), 3–6 months (toenails)

Extensive Candida infection:

Oral itraconazole (1st-line), in pulsed weekly courses

24
Q

Squamous Cell Skin Cancer

  1. Risk Factors
  2. Treatment
  3. Poor Prognostic Factors
A
  1. Renal Transplant
  2. Skin Exposure
  3. Long Standing Marjolin Ulcer
  4. Genetic conditions e.g. xeroderma pigmentosum, oculocutaneous albinism

Treatment

If >20mm then Surgical Excision with 6mm margin

If <20mm then Surgical Excision with 4mm margin

Mohs Surgery if Cosmetic Importance

Poor Prognosis if :
1. >20mm
2. >4mm deep
3. Immunosuppressed
4. Poorly Differentiated

25
Treatment for Hyperhidrosis ?
Topical Aluminum Chloride
26
Hereditary Hemorrhagic Telangiectasia Inheritance ? Diagnostic Criteria (4 things only)
Autosomal Dominant Epistaxis + Telangiectasia + Visceral Lesions (GI Telengectasia or AVMs) + Family History 3 Diagnostic 2 Suspected
27
Impetigo Treatment ?
Limited ---> 1. H2O2 2. Topical Fusidic 3. Topical Mupirocin (1st line if MSRA) Extensive 1. Flucloxacillin or Erythromycin Avoid School for 48 hours after Abx or until lesions healed
28
Molluscum Contagium (HIV)
Pinkish or pearly white papules with a central umbilication Alleviate and Encourage not Itch and CONTAGIOUS Self Limiting Ezcema or Inflammation around lesion prior to healing If so - Itch (Hydrocortisone 1%) Infected (Fusidic Acid 2%)
29
Keratosis Piliaris Features
Chicken Skin keratinized hair follicles (rough bumps) over extensors
30
Keloid Scars Most Common Ethnicity Most Common Site Treatment
Africans Sternum Intra-lesional steroids e.g. triamcinolone
31
Bullous Phemigoid Pathophysiology Treatment
Antibodies against hemidesmosome proteins BP180 and BP230 Oral Steroids
32
What Antibody is responsible for Dermatitis Herpertiformis ?
IgA in the Dermis
33
Pyoderma Gangrenosum Causes Mnemonic GRIP My LymphS
GRIP My LymphS (causes of pyoderma gangrenosum) Granulomatosis with polyangitis Rheumatoid arthritis IBD Primary biliary cirrhosis Myleoid leukemia Myeloproliferative disorders Monoclonal gammopathy Lymphoma SLE
34
Bullous Phemigus vs Phemigus Vulgaris
Pemphigus Vulgaris: Rare and life threatening IgG Autoantibodies to Desmoglein (Dsg3) Dsg3 is an adhesion molecule between epidermal cells Antibodies disrupt adhesion causing INTRA-epidermal blistering Affects mucosa and skin Bullous Pemphigoid: More common than Pemphigus Vulgaris Less aggressive and generally not life threatening IgG antibodies to BP180 and/or BP 230, components of hemidesmosomes BP180 anchors hemidesmosomes to lamina densa of basement membrane Blistering is SUB-epidermal Investigation for Both: Skin Punch Biopsy ELISA in specialist setting/centres Management: Pemphigoid Vulgaris: Oral Steroids Bullous Pemphigoid: Topical Steroids In both further treatments --> Immunosuppression / Plasmapheresis