5. ROSACEA
• Onset during middle age, with women
being affected somewhat earlier than men.
• Rosacea occurs most frequently in
Caucasians and in those with fair sun-sensitive
skin, i.e. skin phototypes I and II.
• There may be a genetic predisposition to the
disorder, as 10–20% of patients report a
family history of rosacea.
7. SYMPTOMS OF ROSACEA
• ITCHY RASH ON
FACE
• “STINGS”
• “BURNS”
• TOPICAL CREAMS
NOT HELPFUL
• NO NEW MEDS
• NO NEW SOAPS OR
PERFUMES
8. • In 2002, a consensus publication provided a
classification scheme for rosacea into four
major forms with distinct clinical
characteristics.
• Each subtype is graded into mild, moderate and
severe (grades 1–3).
13. Erythematotelangiectatic rosacea.
Persistent erythema of the medial and lateral
cheeks is seen. In this patient, there are no
telangiectasias, indicating mild (grade 1) disease.
16. 2. PAPULOPUSTULAR ROSACEA
• CC//OO: slight tenderness or itch but social distress
caused by the appearance of the eruption far
exceeds the physical symptoms.
• CC//FF: Centrofacial eruption of multiple, small
(<3 mm), dome-shaped, erythematous papules,
some of which are surmounted by a seropustule
can appear singly or in crops.
• Individual lesions last about 2 weeks then
subside into a blotchy erythema, which
gradually fades & others appear.
• Usually no resultant scarring.
21. Moderate to severe
papulopustular rosacea.
There is a typical centrofacial distribution. In
addition, the skin has a scaly, crusty surface and
this is often a sign of more severe disease.
23. 3. PHYMATOUS ROSACEA
• Most commonly rhinophyma
• Occurs primarily in men.
• Reflects hypertrophy of the sebaceous glands &
connective tissue in nasal skin.
• May occur with sever rosacea, but surprisingly,
patients with rhinophyma may only have mild
rosacea.
• Rhinophyma is usually seen in patients with other
features of rosacea but may occur in patients with
acne vulgaris; occasionally it is due to chronic actinic
damage or may arise de novo.
32. 4. OCULAR ROSACEA
• Can occur without accompanying cutaneous
changes or it may be seen in patients with any
of the other subtypes of rosacea.
• CC//OO: nonspecific; itching, tearing, dryness,
gritty sensations, crusting of eyelids & an
inability to wear contact lenses, as well as
frequent styes.
34. OOCCUULLAARR RROOSSAACCEEAA
There may be tiny concretions at the bases of the
cilia (conical dandruff), or mild scaling of the
eyelid margins (scurf).
37. Common, may be first sign of rosacea
variable presentation
38. 4. OCULAR ROSACEA
• May need ophthalmological consultation
especially (grade 3) disease
• Keratitis may lead to blindness
39. VARIANTS OF ROSACEA
1. GRANULOMATOUS
ROSACEA: Persistent red–brown
to skin-colored facial papules with
a characteristic non-caseating
granulomatous histology.
2. ROSACEA CONGLOBATA:
inflammatory facial cysts with
associated scarring.
3. ROSACEA FULMINANS
(pyoderma faciale): characterized
by explosive onset of inflammatory
papules and pustules superimposed
on a back-ground of facial
erythema & fever may occur.
41. WHAT CAUSES ROSACEA?
• The exact cause is unknown.
• May be;
• Demodex mite infestation?
• Solar damage? Heat? Caffiene?
• Lymphatic obstruction? Emotional stress?
59. Histopathology of rosacea
• Telangiectasia of superficial blood vessels;
• Perivascular infiltrates of lymphocytes
(mild to moderate in intensity) and,
sometimes, plasma cells.
• Active pustular lesions show superficial
folliculitis.
• Older lesions show granulomatous
perifolliculitis.
• Demodex mites are noted (20-50% cases)
60. Histopathology of rosacea
• Well-circumscribed collections of epithelioid
histiocytes, usually peri-infundibular.
• Granulomas surrounded usually by
lymphocytes and, sometimes, plasma cells.
• Small collections of neutrophils in some
granulomas.
• Caseous necrosis may be present within some
granulomas.
• Rhinophyma: Sebaceous gland hypertrophy
and scattered follicular plugging.
76. Treatment of rosacea
• On 2013, FDA approved
brimonidine (Mirvaso®)
topical gel, 0.33% for the
(first and only) topical
treatment of persistent
facial erythema of rosacea
in adults 18 years of age or older.
• It is not indicated for the treatment of
inflammatory lesions (papules and pustules) of
rosacea.
• It is selective alpha-2 adrenergic agonist
causing cutaneous vasoconstriction.
86. • Avoid precipitating factors.
• Sometimes, successful treatment of the
inflammatory lesions of papulopustular
rosacea reveals background telangiectasias
(the PERT phenomenon – “post-erythema-revealed
telangiectasias”)
• Topical and systemic therapies used to treat
papulopustular rosacea are often ineffective
in the treatment of erythematotelangiectatic
rosacea and may irritate the skin.
87. EXPECTATIONS
• Tell them to expect improvement in 4-6 weeks
• Tell them to continue regimen until next visit
• May give topicals for maintenance otherwise,
relapse is likely 3 to 6 months after
discontinuation of treatment.
• Inform them there is no cure for rosacea!!!!!!!!
89. LMDF
• Uncommon chronic inflammatory facial
dermatosis. It presents with pale papules
which may be confused with sarcoid or
syringoma clinically.
• Many authors now consider LMDF to be an
extreme variant of granulomatous rosacea.
Others believe it is a distinct entity because
of its characteristic histopathology and
occasional involvement of non-central
facial areas.
90. LMDF
• Age; Young adults in their 20s most often
are affected.
• Etiology; and pathogenesis are unknown.
• Active disease usually involves a 1- to 3-
year course and resolves spontaneously.
• Recurrences are not described.
• LMDF may result in disfiguring scarring.
• Educate patients about the nature of the
disease to help alleviate anxiety and to
establish realistic treatment expectations.
91. C/P of LMDF
• Papules singly or in crops
that are red, brown, or
yellow-brown and appear on
the central face, especially on
and around the eyelids.
• Lesions occasionally may be
generalized and appear on
the extremities or trunk
• May present later as crusts,
pustules ultimately, scars.
92.
93. Histopathology of LMDF
• In LMDF, sections show
round granulomas composed
of epithelioid cells with
central caseating necrosis.
• The granulomas may appear
sarcoidal or tuberculoid
typically arise adjacent to
adnexal structures.
• A chronic inflammatory
infiltrate often present.
• Late lesions show fibrosis
94.
95. Treatment of LMDF
• Surgical:
Scar revision procedures (laser resurfacing,
dermabrasion, chemical peel) may benefit
patients after the disease has run its course.
96. REFERENCES
• Dan Ladd, D.O. Texas/KCOM
Dermatology Residency Program Program
Director Bill V. Way, D.O.
• Bolognia 3rd ed.
• http://dermnetnz.org/acne/rosacea.html
• http://emedicine.medscape.com