Acne Flashcards

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1
Q

Tell me about P acnes

A
  • Gram positive, anaerobic, microaerophilic rod in the sebaceous follicle
  • Produces porphyrins: fluoresces with Woods lamp
  • Density does not correlate with clinical severity
  • Certain ribotypes (4 and 5)are more frequently found in acne patients
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2
Q

Four contributors of acne pathogenesis

A
  1. Follicular hyperkeratosis (microcomedone)
  2. Hormones
  3. Inflammation
  4. P acnes
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3
Q

What causes the black colour in open comedones

A

Melanin and lipid oxidation may be responsible for black colour

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4
Q

Extra-cutaneous features of acne fulminans

A
  • Bones: osteolytic bone lesions: clavicle, sternum, then can also be ankles, humerus, iliosacral joints
  • Systemic: fever, arthralgias, myalgias, hepatosplenomegaly, severe malaise
  • Erythema nodosum
  • SAPHO syndrome can accompany
  • Associated with congenital adrenal hyperplasia and anabolic steroid use (including therapeutic testosterone)
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5
Q

What is PAPA syndrome and its mutation

A
  • Sterile pyogenic arthritis, PG, acne conglobata

- Mutations in PSTPIP1 - proline - serine - threonine - phosphatase interacting protein 1

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6
Q

Morbihan disease

A
  • Distortion of the midline face and cheeks due to soft tissue swelling
  • Woody induration and erythema
  • ?cause: impaired lymphatic drainage and fibrosis in setting of chronic inflammation, some genetic risk
  • Can be seen with rosacea
  • Fluctuations in severity are common
  • Does not resolve spontaneously
  • Rx:
    • Isotretinoin 0.2-1 mg/kg/day for 4-6 months, may need longer
    • Combination with this and ketotifen (H1 antihistamine and mast cell stabiliser) or prednisone may be more beneficial
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7
Q

What weeks for neonatal acne

A

Appear at ~ 2 weeks of age, and resolve by first 3 months

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8
Q

What months for infantile acne

A

2-12 months of age

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9
Q

Hyperandrogenism signs

A
  • Hirsutism
  • Coarsening of voice
  • Muscular habitus
  • Androgenetic alopecia
  • Clitoromegaly with variable posterior labial fusion
  • Increased libido
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10
Q

HAIR-AN syndrome

A

Insulin resistance, acanthosis nigricans and hyperandrogenism: at increased risk of CVS disease and DM

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11
Q

Acne associated with genetic syndromes

A
  • Apert syndrome:
    • Autosomal dominant
    • Disfiguring synostoses of the bones, - hands and feet, vertebral bodies, cranium
    • Increased incidence of severe, early-onset acne that is nodulocystic and more widespread than classic acne - extensors of arms, buttocks and thighs
    • Acne typically resistant to treatment, roaccutane may be beneficial
    • Other cutaneous: seborrhoea, nail anomalies (single nail for second throug fourth digits), diffuse pigmentary dilution of hair and skin
    • Mutation ins FGFR2 - encodes fibroblast growth factor receptor 2 –> effects follicular keratinocyte proliferation, sebaceous lipogenesis, inflammatory cytokine production
  • Borrone dermato-cardio-skeletal syndrome:
    • Autosomal recessive
    • SH3PXD2B mutation
    • Dysmorphic facies, thick skin, acne conglobata, vertebral abnormalitis, mitral valve prolapse
  • PAPA
  • PAPASH
  • PASH
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12
Q

Drug induced acne

A
  • monomorphous eruption of inflammatory papules and pustules
  • Medications - did you MISPLACE your meds Bae?
MEK inhibitors (trametinib)
Iodides, isoniazid
Steroids
Phenytoin, progestins
Lithium
Anabolic steroids - danazol, testosterone
Corticotropin, cyclosporin
EGFR inhibitors

Bromide, B6, B12
Azathioprine

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13
Q

Chloracne

A
  • several weeks after exposure to halogenated aromatic hydrocarbons
  • Can be percutaneous, inhalation of ingestion
  • Found in electrical conductors, insulators, insecticides, fungicides, herbicides, wood preservatives
  • Comedo like lesions and yellowish cysts with minimal inflammation - malar and retroaurciular areas of head and neck, and can be on axillae and scrotum
  • Can persist for several years following exposure
  • Additional: grayish discolouration, hypertrichosis
  • Rx: remove, topical or oral retinoids
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14
Q

Radiation acne

A
  • comedone like papules at sites of previous exposure to therapeutic ionizing radiation
  • appear as acute phase of radiation dermatitis starts to resolve
  • The rays induce epithelial metaplasia within the follicle, creating adherent hyperkeratotic plugs that are resistant to expression
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15
Q

Idiopathic facial aseptic granuloma

A
  • thought to be form of rosacea in children
  • young - 2-4 years of age roughly
  • Dermal lymphohistiocytic infiltrate with foreign body type giant cells
  • > 40% have at least 2 other signs of rosacea: recurrent chalazions, facial flushing, telangiectasias, papulopustules
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16
Q

Hormones

A

Second generation: levonorgesterol

Third generation: anti-androgen - cyprorone acetate, digonest, drosperidone