ALOPECIA Flashcards

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1
Q

complete loss of scalp hair

A

Alopecia totalis

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2
Q

loss of all body hair

A

Alopecia universalis

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3
Q

alopecia associations?

A

Atopic dermatitis, Downs syndrome, Lichen Planus,

SLE, Thyroiditis, Myasthenia Gravis, and Vitiligo

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4
Q

what is this?

Rapid and complete loss of hair in one or several areas (scalp,
bearded area, eyebrows, eyelashes)

Etiology

  • Autoimmune disease targeting follicular cells
  • Hereditary: 25% with +FHx, HLA associations: DR4, DR11, DQ7

Pathology: lymphocytic peribulbar infiltrate around anagen hairs

A

Alopecia Areata

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5
Q

what is this?

  • Early and excessive loss of normal club hairs from normal resting follicles in the scalp
  • Surgery, parturition, fever, drugs, eating disorder protein/nutrient deprivation
  • Hair pull test results in more than 4-6 club hairs.
A

Telogen Effluvium

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6
Q

what is this?

• Loss of anagen hairs usually secondary to chemotherapeutic agents.
• Telogen and catagen hairs are in a resting state and are not
affected.
• Most apparent clinically in 1-2 months after administration
of chemotherapy.
• Resolves in 2-4 weeks after discontinuation of drug but hair
grows back slowly.

A

Anagen Effluvium

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7
Q

what is this?

• Manifests in 20s and 30s with gradual hair loss from the vertex
and frontotemporal regions
• Response of hair follicle to DHT which results in gradual
miniaturization of hair follicles

A

Male-Pattern Baldness

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8
Q

what is this?

• Diffuse hair loss greatest at the crown, sparing the frontal hairline, temporal recession
• Genetic predisposition
• Work up: polycystic ovarian syndrome, free testosterone, ferritin, thyroid function
tests

A

Female Pattern Baldness

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9
Q

what is this?

  • Compulsive practice of plucking hair usually from the scalp, eyebrows, or eyelashes
  • Clinically with patchy alopecia that contain hairs of varying length and the scalp has a rough texture resulting from the short remnants of broken-off hairs.
  • Most common in girls under age 10
  • Worse with stress, associated with OCD
A

Trichotillomania

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10
Q

what is this?

Erythema, atrophy, follicular plugging, mottled hyper- and
hypopigmentation

A

Discoid Lupus Erythematosus

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11
Q

what is this?

  • Perifollicular erythema, ivory white irregular patches
  • Frontal fibrosing alopecia
A

Lichen Planopilaris

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12
Q

what is this?

• Hot comb alopecia, follicular degeneration
syndrome
• Chemical processing, heat, traction, trauma
• May have clinical overlapping features with
folliculitis decalvans

A

Central Centrifugal Cicatricial

Alopecia

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13
Q

what is this?

• Neutrophilic scarring alopecia, pustules are the primary
lesions
• S. aureus induces abnormal suppurative immune
response.
• Recurs after antibiotics are discontinued

A

Folliculitis Decalvans

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14
Q

what is this?

• Part of the follicular occlusion tetrad:
-acne conglobata
-hidradenitis suppurativa
-pilonidal cysts
• Sites of predilection: Vertex and occiput
• TCN, retinoids, intralesional steroids

A

Dissecting Cellulitis

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15
Q

what is this?

• Prolonged tension on the hair
• Tightly braided, ponytail, pulling the hair to straighten
it, habit of twisting the hairs with the fingers.
• Hemorrhage and inflammation lead to scarring and
permanent loss

A

Traction Alopecia

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16
Q

other causes of alopecia?

A

sarcoidosis
pressure alopecia
alopecia neoplastica
syphilis

17
Q

what is this?

• Malformation of hair characterized by twisting of the hair shaft on its own axis leaving the hairs brittle and easily
broken.
• Classic type is AD and presents in childhood and is not
associated with other disorders.

A

Pili Torti

18
Q

what is this?

  • X-linked recessive, “brittle, steel wool” hair
  • Drowsiness, lethargy, convulsive seizures, and severe neurologic deterioration with periodic hypothermia
  • Diffuse cutaneous hypopigmentation, doughy skin, and an exaggerated cupid bow
  • Defective MNK gene (ATP7A) which encodes a copper-transporting ATPase, which is not expressed in the liver (unlike ATP7B, the mutated gene in Wilson’s)
  • Blocks the export of dietary copper from the GI tract which results in a copper deficiency
  • Low serum copper and cerruloplasmin
A

Menkes Kinky Hair Syndrome

19
Q

what is this?

• Pili trianguli et canaliculi: Spun-glass hair
• Triangular hair shaft, central longitudinal groove
• Clinically the defect is noted in the first few years of life as dry, blond, shiny hair that stands straight out from the scalp and cannot be combed.
• Electron microscopy shows longitudinal grooves that
make the hair abnormally rigid.
• AD, AR and sporadic cases reported

A

Uncombable Hair Syndrome

20
Q

what is this?

• AD
• Dry, fragile, sparse scalp hair that appears beaded on trichoscopy
• Mutation in type II hair keratins: KRT81, KRT83,
KRT86 as well as DSG4

A

Monilethrix (beaded hairs)