Pigmented lesions Flashcards
elderly mixed black and white man pt [morgan freeman]
multiple
tan/brown macules [gradully enlarges and elevated]
less than 2 cm in size
In the sun a lot [but not sure] and possible mutation of FGFR3
seen on: skin of face, trunk, and extremites
seborrhic keratosis
morgan freeman is black happens 30% of the time so aka
________
clinically descibe the lesion
sharply demarcated:
- fissured
- pitted
- verrucous
but may be smooth
seborrheic keratosis is
ACQUIRED ______ proliferation
basal epidermal cells
benign
3 histofeatures of seborrheic keratosis
1) Hyperkeratosis
2) acanthosis
3) **numerous pseudocytes **
what are pseudocytes
keratin filled invaginations
-surrounding the pseudocytes are basaloid in appearance
tx for seborrheic keratosis
no tx, usually esthetic purposes
lq nitrogen and curettage [just like actinic keratosis]
seborrheic keratosis is not malignant in potential exception for
_____ _____ sign
leser trelat sign
waht is leser trelat sign
sudden apperance numerous seborrheic keratosis and pruritus [pus] associated with
internal malignancy
hyperpigmented **MACULE of the skin **
ephelis [freckles]
1st decade of life
round oval
sharply demarcated
light brown lesion [intensifies with sun]
ephelis
region of increased melanin production
strong genetic predilection
blonde hair blue eyed
red hair green eyed
less than 3 mm in size
ephelis
ephelis NOT like lentigo simplex for 2 reasons
1) not as dark
2) no elongation of rete ridges
ephelis is not like MELANOCYTIC nevus
not elevated
histofeatures of ephelis
1) stratisfied sq epithelium
with abundant melanin
deposition in the basal cell layer
true or false
ephelis is not an increase in melanocyte and in fact can be reduced
2) no tx
true
true, use sunblock
what 2 diseases can be PREVENTED with sunscreen
ephelis
actinic lentigo
olderly white with lesion on skin, dorsum of hand, arm
5 mm - 1 cm
BBM [benign brown macule] from chronic UV light
actinic lentigo = senile lentigo = age spot = liver spot
clinical features:
Well demarcateed
uniformly brown and tan macules
irregular borders
actinic lentigo
actinic lentigo NO CHANGE IN COLOR with intensity of UV light just **unlike which pigmented lesion **
ephelis
waht is the tx for actinic lentigo
no tx unless esthetics:
cyrotherapy
laser
pulsed light therapy
topical
sunblock for prevention
how often does actinic lentigo reoccur
rare
BUT NEW LESIONS CAN ARISE FROM ADJ SKIN ANYTIME
what is actinic lentigo
BBM
benign brown macule
with chronic UV light damage to skin
people with freckles are more likely to develop actinic lentigo
true
what is Addison’s Disease
adrenal cortical insuffeciency
addisons disease
diffuse _____ leads to
geranized brown pigmentation
sun exposed skin
hypermelanosis
B Blk M
multiple circumscribed
dark brown/ black macule
covered with intact mucosa
true or false
oral mucosal lesion typically
1st sign of addisons disease
true
what is the treatment of ORAL lesions from addisons disease
no tx
diagnosis of addisions disease:
1)
2)
hx
elevated plasma levels of ACTH
tx of regular addisons disease
corticosteriod replacement thearpy
what 2 diseases does NOT change with color intensity in sun exposure
which dsiease does change color intensity with sun exposure
does not change color:
1) actinic lentigo
2) lentigo simplex
does change:
ephelis
what is lentigo simplex
BCMH
benign cutanenous melanocytic hyperplasia
usually affects children
unknown cause and not on sun exposed skin
TF
darker than ephelis
true
lentigo simplex is associated with _____ _____syndrome
Peutz Jeghers syndrome
4 histofeatures of lentigo simplex
1) increased # of benign melanocytes
in the **basal cell epidermis **
2) encrustations of rete ridges
3) lots of melanin:
- melanocytes
- basal keratinocytes
4) melanin incontinence
melanin incontinence
melanophages in papilary dermis
waht is the tx for lentigo simplex and
is it malignant
no tx
not malignant
what is Peutz Jeghers syndrome
Autosomal disease
freckle like lesions that affect:
- hands
- perioral skin
- oral mucosa
Jejunum and ileum affected with intestinal polyps [intestinal polyposis] predespostion for GI adenocarcinoma
clinically features of Peutz Jeghers syndrome
1) muliple circumscribed
tan/brown macules
covered by intact mucosa
2) affects:
labial and buccal mucosa, tongue, and palate