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
Q

Treatment for Hyperhidrosis ?

A

Topical Aluminum Chloride

26
Q

Hereditary Hemorrhagic Telangiectasia

Inheritance ?
Diagnostic Criteria (4 things only)

A

Autosomal Dominant
Epistaxis + Telangiectasia + Visceral Lesions (GI Telengectasia or AVMs) + Family History

3 Diagnostic
2 Suspected

27
Q

Impetigo Treatment ?

A

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
Q

Molluscum Contagium

A

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
Q

Keratosis Piliaris Features

A

Chicken Skin
keratinized hair follicles (rough bumps) over extensors

30
Q

Keloid Scars

Most Common Ethnicity
Most Common Site
Treatment

A

Africans
Sternum
Intra-lesional steroids e.g. triamcinolone

31
Q

Bullous Phemigoid

Pathophysiology
Treatment

A

Antibodies against hemidesmosome proteins BP180 and BP230

Oral Steroids

32
Q

What Antibody is responsible for Dermatitis Herpertiformis ?

A

IgA in the Dermis