美國有一系列醫學教科書稱為「回憶系列(Recall Series)」,包括了內外婦兒急診科的臨床知識,甚至有出病理科與影像科等二線科別的用書。這套教科書都用問答的方式來描述專科的醫學知識,和傳統教科書大相逕庭,看起來很奇怪。
經過回想過的記憶才會長久留存!
神奇的是:當年大五的我自己遮住答案回答完後,還真的把這些複雜的知識都記住了。因此有次教化學家教時,就照這種方式把整個章節「問了」學生一次,結果效果好到懷疑人生(如果當年我知道可以這樣做...)。考量皮膚科沒有出這種教科書,因此煜彬決定自己來纂寫這些章節。
Chapter 29 :: Pityriasis Rubra Pilaris(PRP)
:: Knut Schäkel
鄭煜彬 整理 20191209
EPIDEMIOLOGY
|
|
How much is the male-to-female ratio of PRP?
|
M=F
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CLINICAL FEATURES
|
|
Which 2 features helps to classify PRP?
|
1.
Age of onset (adult or
juvenile)
2.
Course/prognosis (classic or
atypical).
|
What are the six types of PRP?
|
1.
Classic adult (I)
2.
Atypical adult (II)
3.
Classic juvenile (III)
4.
Circumscribed juvenile (IV)
5.
Atypical juvenile, CARD 14
mutation (V)
HIV-associated (VI)
|
What are the first 3 common types of PRP
& the ranking ?
|
1.
Classic adult (>50%)
2.
Circumscribed juvenile (25%)
6.
Classic juvenile (10%)
|
Why PRP is difficult to diagnose in the
beginning?
|
3.
It looks like scaly
dermatitis (well-defined, yellow-orange). (However, it may spread to
erythroderma in 2-3 months)
|
What is the 2 common features of PRP?
|
1.
Salmon-colored scaly plaques
2.
Follicular hyperkeratosis
|
What are the 3 morphological features of
Type I PRP?
|
1.
Erythroderma with nappes
claires
2.
Follicular hyperkeratosis
3.
Waxy diffuse palmoplantar
keratosis
|
What are the 3 morphological features of
Type II PRP?
|
1.
Follicular hyperkeratosis
2.
Sparse scalp hair
4.
Ichthyosiform lesions on legs
|
What are the 3 morphological features of
Type III PRP?
|
1.
Erythroderma with nappes
claires
2.
Follicular hyperkeratosis
3.
Waxy diffuse palmoplantar
keratosis
(as Type I PRP, but earlier onset)
|
What are the morphological features of
Type IV PRP?
|
Well-demarcated scaly, erythematous
plaques at elbow & knee (as psoriasis)
|
What are the 3 morphological features of
Type V PRP?
|
1.
Familial cases
2.
Follicular hyperkeratosis
Scleroderma-like
palms & soles
|
What are the 3 associated features of
Type VI PRP?
|
1.
Acne conglobate
2.
Hidradenitis suppurativa
3.
Lichen spinulosus
3. (as Type I PRP, but HIV+)
|
What is the age of onset of Type I-VI
PRP?
|
I-II: adulthood
III-V: children & adolescents
VI: all ages.
|
What is the distribution of Type I-VI
PRP?
|
IV: localized
Others: generalized, head/neck→caudal
|
What is course of Type I-V PRP?
|
I & III: classic, short, < 3 year,
usually 1-2 years.
II & V: atypical, long, > 20
years.
IV: uncertain, may resolve in teens.
|
ETIOLOGY
|
|
What is the most possible etiology of
sporadic PRP?
|
Infections, such as upper respiratory
tract infections
|
What is the only 2 confirmed etiologies
of PRP up to now?
|
1.
CARD 14(Caspase Recruitment
Domain family member 14), gain of function mutation (in familial cases/type V)
2.
HIV infection(type VI)
|
What is the mechanism of CARD 14 mutation
in PRP type V?
|
CARD 14 mutation→↑CARD 14→activate NF-κB
signaling→activate p65
|
What is the changes of cytokines in PRP
lesions?
|
1.
↑proinflammatory innate
cytokines: TNF, IL-6, 12, 23, & IL-1β
2.
↑ TH1 cytokines
3.
↑ TH17 cytokines(IL-17A/F,
& 22)
|
DIFFERENTIAL DIAGNOSIS
|
|
What is the major differential diagnosis of PRP?
|
Psoriasis
|
What is the clinical difference between
psoriasis & PRP?
|
Psoriasis: extensor, Koebner sign,
plaques with white scales (candle sign), Auspitz sign
PRP: head, salmon-color, islands of
healthy skin, follicular hyperkeratosis, waxy PPK
|
What is the difference between the nail
of psoriasis and PRP?
|
Psoriasis:
salmon patch, oil spot, pitting, subungual hyperkeratosis, onycholysis…
PRP: only hypertrophic nail plate
|
What is the histologic difference between
psoriasis and PRP
|
Psoriasis: hypogranulosis,
elongated rete ridges, vascular dilation, intraepidermal Munro
microabscesses.
PRP: alternating horizontal/vertical
para-/ortho-keratosis, hypergranulosis, thickening rete
ridges, follicular hyperkeratosis
|
TREATMENTS
|
|
What are the effective first-line treatments
of PRP?
|
Topical: emollients,
keratolytic(salicylic acid), vit. D3 analogs(calcipotriol)
Systemic:
retinoids, methotrexate, anti-retroviral tx.
|
What are the effective second-line treatments
of PRP?
|
Topical: corticosteroids,
calcineurin inhibitors, tazarotene
Systemic:
fumaric acid esters, apremilast, TNF inhibitors, anti-IL-12/IL-23p40,
anti-IL-17, azathioprine, cyclosporine
Phototherapy:
PUVA, Re-PUVA, UVA1, NBUVB, BBUVB, Extracorporeal photopheresis
|
Which disease has treatments similar to
PRP?
|
Psoriasis(almost
the same)
|
What is the restriction of the use of
vit. D3 analogs?
|
No more than 30% BSA.
|
What is the dose of oral methotrexate for
PRP?
|
10-25mg/week
|
What is the choice & dose of oral
retinoids ?
|
Acitretin(0.5-0.75mg/kg/day),
isotretinoin(1-2mg/kg/day), alitretinoin.
|
What is the side effects of retinoids for
the prepubertal?
|
Premature closure of epiphyses &
hyperostosis
|
What should you do before the
phototherapy?
|
Phototesting, because phototherapy may
aggravate PRP.
|
Which type of PRP does not response to
ustekinumab?
|
Type IV PRP
|
What is the most effective treatment of
type VI PRP?
|
triple antiretroviral therapy
|
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