玫瑰糠疹雖然不算罕見,大小教科書也都一直會提到,但在臨床實戰上卻沒有那麼容易診斷,甚至需要動用到診斷要件。這種疾病儘管不會有嚴重併發症,卻會造成病人的恐慌,也一直是皮膚科醫師的重要課題。
Chapter 31 :: Pityriasis Rosea
:: Matthew Clark & Johann E. Gudjonsson
鄭煜彬(20200117)
| 
What is the meaning of pityriasis rosea?  | 
Pink (rosea) scales (pityriasis). | 
| 
EPIDEMIOLOGY | |
| 
When is PR found commonly?  | 
In colder months, but not supported by
  all studies.  | 
| 
Why is PR thought as infectious disease?  | 
PR usually has clustering of cases. | 
| 
Which gender has higher prevalence?  | 
Female(F:M=1.39: 1, especially pregnant women) | 
| 
What age group has highest prevalence?  | 
10-35 years(teenagers & young adults) | 
| 
Does PR relapse?  | 
Yes, but rare(only 1.8% to 3.7%). | 
| 
CLINICAL FEATURES | |
| 
HISTORY | |
| 
What is the first lesion of classic PR?  | 
The herald patch: a solitary lesion on
  the trunk or less commonly an extremity. | 
| 
How long is the time between herald patch
  & secondary(2°) eruptions? | 
On average 
l   2 weeks in adults 
l   4 days in children | 
| 
Where is the locations of the 2°
  eruptions of PR?  | 
Trunk & proximal extremities | 
| 
What is the prodromal symptoms before or
  with the 2° eruption? | 
Malaise, nausea, headache,
  gastrointestinal, & upper respiratory symptoms (flu-like), & lymphadenopathy.  | 
| 
What is the most common symptom of PR
  rashes?  | 
Pruritus(severe: mild/moderate: absent=
  1:2:1) | 
| 
What is the variants in pediatric
  patients(< 10 y/o)? | 
Relapsing form: single (multiple is rare)
  episode of relapse within 1 year of the initial episode.  
Persistent form: last for > 12 weeks without
   
Interruption | 
| 
What is the features of relapsing PR? | 
Lack a herald patch, shorter lived, fewer,
  & more localized lesions. | 
| 
What is the features of persistent PR? | 
Has a herald patch, more common oral
  manifestations  | 
| 
How long is the duration of pediatric PR?
   | 
on average 16 days (shorter than that on
  adults) | 
| 
CUTANEOUS FINDINGS | |
| 
What is the features of classic herald patch? | 
One/multiple well-demarcated, thin, oval
  to round, pink/rose/colored/erythematous/ hyperpigmented plaque with a
  slightly depressed center & fine collarette of scale in the periphery. | 
| 
Where is the locations of herald patch? | 
Trunk (50%)>extremities>neck>>
  dorsal feet/face/ scalp/genitalia | 
| 
How big is the size of herald patch?  | 
>3 cm(2-10 cm | 
| 
How much is the incidence of the herald
  patch? | 
80% (12% to 94%) | 
| 
How much is the incidence of the multiple
  herald patch? | 
5% | 
| 
How long is the time between the herald
  patch & 2° eruptions?  | 
2 weeks (a few hours to 3 months), but
  sometimes no 2° eruptions.   | 
| 
What is the features of 2°
  eruption of PR?  | 
Multiple, round-to-oval, 0.5- to 1.5-cm, light
  pink macules, papules, & plaques (smaller herald patch) | 
| 
Where is the locations of 2°
  eruption?  | 
Trunk & proximal extremities>>
  distal extremities >>palms & soles.  | 
| 
What is the specific distribution of 2°
  eruptions of PR?  | 
“Christmas tree” distribution on the
  upper chest & back: long axis of the lesions parallel to lines of
  cleavage (ribs) | 
| 
How about the course of 2°
  eruption?  | 
Appears 2 weeks after herald patch, occurs in crops every few days,
  reaches its maximum 2 weeks later,
  then disappears in 45 days.  | 
| 
How about the relationship between PR &
  sun-exposure?  | 
Some are confined to sun-protected skin; others
  are confined to sun-exposed skin. Most are randomly distributed.  | 
| 
What is the atypical forms of 2°
  eruption? | 
Eczematous, papular, follicular,
  vesicular, urticarial, pustular, & purpuric forms.  | 
| 
What is the configuration of vesicular
  lesions of PR?  | 
They are arranged in a rosette.  | 
| 
What age group has higher incidence of
  vesicular lesions?  | 
Children & young adults | 
| 
How much is the incidence of mucosal
  lesions in PR cases?  | 
16% (uncommon) | 
| 
What is the clinical features of oral
  lesions of PR?  | 
They can be punctate hemorrhagic,
  ulcerative, erythematous macules, plaques, bullous, & annular lesions. Ulcer is most common. | 
| 
What is the atypical variants of PR?
  (hint: 5, distribution) | 
Unilateral(not cross midline), localized(1
  truncal site), & inverse(children’s folds, face, distal limbs),
  blaschkoid, acral variants.  | 
| 
COMPLICATIONS | |
| 
What is the complication of PR in the
  healthy individuals? | 
Anxiety & depression, no long-term
  complications | 
| 
What is the complication of PR in the
  pregnants? | 
PR before 15 weeks: higher miscarriage 
PR after 15 weeks: higher premature delivery
  ± hypotonia, weak motility, & hyporeactivity
   | 
| 
ETIOLOGY & PATHOGENESIS | |
| 
What pathogens may induce pityriasis
  rosea?  | 
HHV-7 and/or HHV-6 | 
| 
What is the relationship between PR &
  HHVs?  | 
PR is the T cell infiltrate (cell-mediated
  immunity) caused by primary infection or reactivation of HHV-7 and/or HHV-6.  | 
| 
What is the changes of cells, cytokines,
  & proteins in PR?  | 
⇧ (1)
  CD4-to-CD8 ratio & Langerhans cells 
(3) IL-17, IFN-γ (4)VEGF, interferon-inducible protein-10 (CXCL10).  | 
| 
DIAGNOSIS | |
| 
What is the clinical diagnostic criteria
  of PR?  | 
3 essential + at least 1 optional, no
  exclusion 
Essential features (圓環屑) 
l   Discrete circular or oval
  lesions 
l   Scaling on most lesions 
l   Peripheral collarette of
  scale with central clearance on ≥ 2
  lesions. 
Optional features (軀近、肋、先) 
l   A truncal & proximal
  limb distribution, < 10% lesions distal to the middle of arms & thighs 
l   Distribution of most lesions
  along the ribs 
l   A herald patch ≥ 2 days before the eruption.  
3 exclusion features 
l   Central, multiple small vesicles
  at ≥ 2 lesions 
l   Most lesions on palmar or
  plantar skin  
l   Clinical or serological evidence of 2° syphilis. | 
| 
LABORATORY TESTING | |
| 
When should you check lab in PR patients?
   | 
To rule out 2° syphilis | 
| 
PATHOLOGY | |
| 
What does PR look like in pathology?  | 
Subacute eczema + extravasated RBC | 
| 
What are the features of PR? | 
Epidermis: focal/multifocal/confluent
  parakeratosis, orthokeratosis, mild acanthosis; a thinned granular layer; &
  spongiosis+ lymphocyte exocytosis 
Dermis: a superficial perivascular
  lymphocytic infiltrate + extravasated RBC  | 
| 
What is the difference of pathology
  between herald patch & 2° eruption? | 
No difference. But herald patch has thicker
  acanthosis & deeper infiltration.  | 
| 
DIFFERENTIAL DIAGNOSIS | |
| 
What diseases can be the differential diagnosis
  of PR?  | 
Papulosquamous disorders:  
l   Nummular eczema (round, no X’mas tree) 
l   Guttate psoriasis(no X’mas tree, no herald patch) 
l   Lichen planus (pruritic, chronic, violet, more distal limbs, no
  collarette of scales) 
l   Pityriasis lichenoides (chronic, relapsing course, no herald patch,
  lesions in various stages, limbs) 
l   Tinea corporis(KOH) 
l   Parapsoriasis(no X’mas tree, no herald patch, chronic course) 
l   Seborrheic dermatitis(face & scalp),  
l   Secondary syphilis (oral/palmoplantar lesions, persistent LAP,
  serology+, split papules, moth-eaten alopecia, condyloma lata ). | 
| 
What are the possible culprits of
  drug-induced PR?   | 
Barbiturates,
  captopril, clonidine, gold, metronidazole, d-penicillamine, isotretinoin,
  levamisole, NSAID, omeprazole, terbinafine, imatinib, & adalimumab.  | 
| 
Why does adalimumab induce PR-like
  eruption?  | 
Adalimumab dampens T-helper 1 cell
  response and predispose to viral infection or reactivation.  | 
| 
What is the difference between PR &
  drug-induced PR? | 
Drug-induced PR has more hyperpigmentation
  & lichenoid morphology. 
More interface dermatitis, dyskeratotic
  keratinocytes, & eosinophils in pathology.  | 
| 
CLINICAL COURSE AND PROGNOSIS | |
| 
How long is the duration of PR?  | 
Average: 45 days (range: 2 weeks to 5
  months) | 
| 
What is the definition of persistent PR?  | 
Eruptions last > 3 months (12 weeks) | 
| 
What is the cutaneous sequela of PR?  | 
Post-inflammatory hyper/hypopigmentation | 
| 
MANAGEMENT | |
| 
What should you do to most cases of PR?  | 
No treatment is necessary because it is self-limited
   | 
| 
How to treat PR?  | 
l   Topical: steroids & antihistamines (just improve pruritus) 
l   Oral: acyclovir (800 mg 5 time) >> macrolide (erythromycin
  & azithromycin)  
l   UVB | 
| 
How to prevent PR?  | 
No way. | 
 

