By Disease Name > Lichen Sclerosus et Atrophicus

Lichen Sclerosus et Atrophicus

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AKA guttate scleroderma

 

clinical:

slightly raised or level with the surface of the skin (later depressed)
typically the surface shows prominent dilated pilosebaceous or sweat duct orifices which often contain yellow or brown, horny plugs
petechiae = clue to diagnosis
ddx:  morphea, atrophic LP
¾ of female patients have one or more organ specific auto-antibody (e.g. thyroid or gastric parietal cells)
LS&A of the penis (aka balanitis xerotica obliterans) - occurs on the glans penis (follicular plugging absent because there are no follicles on the glans)
may degenerate into SCC (especially in the vulva)

 

LS and A of the vulva:

spares the vagina (vulva only)
telangiectasia makes the diagnosis
ddx: intertrigo with atrophy secondary to strong topical glucocorticoids

 

mnemonic (to remember affect age group for these diseases):

vulva LS et A in women:  most common before puberty often will spontaneously improve upon puberty and after menopause
an exact opposite to Fox-Fordyce disease: which begins after puberty and may remain until menopause

 

histology:

thinning of the epidermis but hyperkeratosis
follicular plugging
vacuolar alteration of the basal layer
lymphedema of the papillary dermis; bleeding into skin due to capillary fragility (like the pinch purpura of amyloid)
beneath the edema there is a diffuse, perivascular infiltrate of lymphocytes in the mid dermis