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CHAPTER
Papulosquamous
Disorders
102 New SARP Series Skin
This group includes disorders presenting with papules/plaques having scales (term “papulo” means papules and
“squamous” means scaling.)
Pityriasis also means scaling, so all disorders prefixed with term “pityriasis” are also included here.
All disorders starting with term pityriasis (like P. alba, P. versicolor, P. rosea, P. rubra pilaris etc.) have scaly lesions
ic
“ReD Li’PS”
ReD Lips
PSORIASIS
Definition (Fig. 1)
It is a chronic, multifactorial, inflammatory and proliferative condition with multiple genetic (PSORS 1-8 genes) and
environmental (trauma, infection drugs) factors having a critical role (Fig. 1).
Etiology
TABLE 1: Genetic and environmental factors of psoriasis
Pathogenesis
Basically disease of “T-cells”
zz Epidermal → CD8 + T-cells
Th 17 cells
zz Dermal → CD4+ T-cells subsets → → Stimulate IL 23 → respectively produce IL17 and IL22
Th 22 cells
which mediate dermal inflammation and epidermal hyperplasia.
Biochemical Changes n e mo n
M
ic
Levels of
Calmodulin↑, cGMP↑ (But cAMP↓)
Arachidonic acid↑
Proteinases and polyamines↑ CAP↑ increases
A B
Types
Psoriasis Vulgaris (Figs 4 to 9)
Psoriasis vulgaris (chronic plaque psoriasis) (Fig. 3) → Most common type.
Points to Remember
“Vulgaris” means “commonest”Q
Clinical features
Well demarcated, erythematous, indurated plaque with silvery white (mica like)
scalingQ over scalp, extensors (elbows, knees, knuckles and lower back)Q, palm,
sole (also flexures). Fig. 3: Psoriasis vulgaris with
erythematous plaque having silvery
Points to Remember white scaling over extensor (Back)
Fig. 4: Periumbilical lesion of inverse psoriasis Fig. 5: Psoriasis vulgaris with Fig. 6: Psoriasis vulgaris with
extensive involvement extensor and scalp involvement
Fig. 7: Scalp psoriasis Fig. 8: Rupoid psoriasis with Fig. 9: Palmoplantar psoriasis
heaped up scales
Memory Aid
Limpet is a conical shell fish, very adherent to rocks
Treatment
Self-resolving in weeks to months.
Topical corticosteroids and phototherapy also useful (Role of antistreptococcal
antibiotics is controversial).
ic
Nail POLISH
A B C
Treatment
MethotrexateQ (DOC), cyclosporine (for rapid control), acitretin.
Fig. 17: Pustular psoriasis Figs 18A and B: Acropustulosis Fig. 20: Nail involvement with
onycholysis and pitting
108 New SARP Series Skin
Precipitating factors
Withdrawal of steroidsQ or application of irritant topical therapy.
Treatment
AcitretinQ (DOC), methotrexate, cyclosporine.
In impetigo herpetiformisQ: systemic steroidsQ >cyclosporineQ
Both, erythrodermic and pustular psoriasis develops after the application of irritant topical therapy or
withdrawal of systemic steroids. So, systemic steroids are avoided in psoriasis, except for Impetigo herpetiformisQ
where both acitretin, methotrexate can not be used (as they are teratogenic). So systemic steroidsQ >cyclosporineQ
is used. (Systemic Steroid are pregnancy category ‘B’ while cyclosporine is pregnancy category ‘C’ drug).
Psoriatic Arthritis
Seronegative arthritis, seen in <40% all psoriasis patients.
Associated with HLA B27.
Diagnostic criteria used for psoriatic arthritis is CASPAR- [Classification criteria for (P = Psoriatic, AR = ARthritis)]
Wright and moll criteria is used for classifying psoriatic arthritis.
Treatment
Methotrexate (DOC)Q, NSAID’s, Sulfasalazine, Leflunomide, Biological (TNF-alpha inhibitors).
n e mo n
M
ic
O.P. DAS: O = Oligoarthritis, P = Polyarthritis, D = Distal interphalangeal arthritis, A = Arthritis mutilans, S = Spondylitis
and sacroiliitis
MC 2nd MC
Papulosquamous Disorders 5 Chapter 109
Clinical Sign
On scratching the lesions of psoriasis
Grattage test → Accentuation of scales
Candle Grease sign → Coming off scales attached together like onion-peels
Auspitz’s signQ → Pin point bleeding spots (Fig. 22)
� On removing the scales, a glistening white adherent membrane known as Berkley’s membraneQ
appears, which when removed produce pin point bleeding spots.
� Psoriatic plaque is often surrounded by hypopigmented margin due to prostaglandin E2 (PGE2)Q known as Wornoff
ringQ.
Investigations
On Histology (Fig. 23)
Epidermal changes
ParakeratosisQ—retention of nuclei in stratum corneum
Acanthosis—thickening of stratum spinosum
Absence of stratum granulosumQ
Munro’s micro abscessQ—collection of neutrophils in stratum corneum
Spongioform pustules of KOGOJQ—collection of neutrophils in stratum spinosum (also stratum granulosum)
Elongated rete ridges—broad at the base, giving “camel foot” appearance.
Suprapapillary thinningQ—thinning of epidermis above dermal papilla.
Dermal change n e mo n
M
ic
Dermal papillae enlarged
Lymphocytic infiltration
Dilated and tortuous dermal vesselsQ
P = Parakeratosis
S = Suprapapillary thinning
O = Loops(dermal capillary)
Scoring System in Psoriasis
R = Regular acanthosis
PASI → for psoriasis (Psoriasis area severity index) I = Infiltration of CD 4 T cells in dermis
NAPSI → for nail psoriasis (Nail Psoriasis Severity A = Abscess (munro’s microabscess)
Index) S = Spongioform pustules of kogoj and
CASPAR → Diagnostic criteria for psoriatic arthritis I = Infiltration of CD8 T cells in epidermis
Due to high risk of metabolic syndrome is psoriasis S = Stratum granulosum absent
many cardiovascular diseases (eg. Myocardial
infarction, pulmonary emboli, CVA) are associated.
Treatment
Topical [preferred in localized disease i.e. <10% body surface area (BSA) involvement]
Wait for
8-methoxypsoralen 2 hours Exposure to UVA (chamber)Q
(0.6–0.8 mg/kg) (Initial exposure depending on
alternate day MPD-minimal phototoxic dose)
MPD is determined by exposing the patient to increasing dose of UVA, 2 hrs after ingestion of psoralens
and finding minimum dose of UVA which produces erythema at 72 hrs
Papulosquamous Disorders 5 Chapter 111
Variant of PUVA
PUVA sol → Sunlight (SOLar) instead of UVA chamber
Topical PUVA → topical psoralen wait for½ hour UVA exposure
Bath PUVA → Soak in psoralen water wait for½ hour UVA exposure
Biologicals
Not used as 1st line therapy
Preferred in moderate to severe disease with following:
zz Not responding to conventional therapy
zz Drug intolerance/toxicity
zz Erythrodermic/pustular/psoriatic arthritis
M
ic
‘3H’
Hypertension
Hypertriglyceridemia
Hypertrichosis
Etiology
Autoimmune.Q It is a cell-mediated immune response of unknown antigen.
Clinical Features
It is an autoimmune inflammatory disease involving skin, mucosa, nail and
hair. Lesions are pruriticQ and have flexural predispositionQ.
5 Ps →Plane (flat), purple (violaceous), polygonal, pruritic, papules
Surface of lesions have white streaks called wickham’s striaeQ, (Fig. 28) becomes
prominent if thin layer of oil is applied over the lesions Fig. 24: Hypertrophic Lichen
Sites → FlexorsQ (wrists), ankles, chin and lower back. planus
Papulosquamous Disorders 5 Chapter 113
Fig. 25: Ulcerative lichen planus Fig. 26: Lichen planus of the buccal mucosa reticular form
Associations
Mucosa (50% patients with cutaneous lichen planus (LP) have mucosal involvement): Asymptomatic or may be
associated with burning and pain (on consuming spicy food).
Dental amalgamQ (dental filling having mercury ) may be causative.
Oral mucosa may present with →
zz Reticulate (lacy) patternQ (commonest type), The buccal mucosa, tongue, and gingiva are the common sites
which tend to be bilateral and symmetrical.
zz Erosive/ulcerative type- rare but have premalignant potential (may give rise to Squamous cell carcinomaQ)
Genital mucosa presents with → annular lesions
The following were identified as Risk of malignant Comments
potentially malignant disorders by the conversions in 10 years
WHO’s working group on oral cancer
• Erythroplakia Very high risk (70–85%) A fiery red patch or bright red velvety
plaques that cannot be characterized
clinically or pathologically as any other
definable disease.
Contd…
114 New SARP Series Skin
• Leukoplakia High risk (10–30%)- non A keratotic white patch or plaque that
homogenous cannot be scraped off and cannot be
Low risk (1–5%) – characterized clinically or pathologically
homogenous as any other disease. Most common pre
malignant lesion in the oral cavityQ.
• Oral submucous fibrosis (SMF) High risk (10–30%) Particularly associated with areca nutQ
chewing, the main component of betel quid
• Oral lichen planus (Fig. 29) Low risk (below 1%) Erosive/ulcerative type
A B C
Fig. 29: Oral lichen planus Figs 30A to C: Lichen planus nail (Arrow indicates wing shaped
projection pterygium)
Abbreviations: NP, Nail plate, PNF, Proximal nail fold
ic
“PALE”
P = Psoriasis
A = Alopecia areata
L = Lichen planus
E = Eczema
SCALP → Follicular eruptions on scalp with cicatricial or scarring alopeciaQ (Lichen plano pilaris)Q (Fig. 32)
Palm and sole → Yellowish, Keratotic grouped papules or plaques may be seen in case of palm and sole involvement.
Other Findings
Koebner’s phenomenonQ
Association with HCV, HBV (Hepatitis C and B virus infection) and primary biliary cirrhosisQ
Lesions heal with hyperpigmentationQ (disease is self-limitingQ within 1–2 years)
Lichenoid eruptions
Lichen planus like eczematous eruptions with prominent scaling and absent Wickham’s striae develop over sun-
exposed area commonly triggered by drugsQ like:
ACE inhibitors, Antimalarials
β-blockers
Penicillamines
116 New SARP Series Skin
Lichenoid drug eruptions can look same as lichen planus, but can be differentiated with help of following
features:
� Extensive rash distributed symmetrically over the trunk and limbs
� Photodistribution.
� Rash may be scaly resembling eczema or psoriasis
� Wickham striae are usually absent
� Nail and mucosa involvement is uncommon
� More likely to resolve leaving marked pigmentation
� On histology: Parakeratosis with eosinophils
n e mo n
M
ic
“ABP”
ECG
Papulosquamous Disorders 5 Chapter 117
ic
Treatment
Localized → Topical steroids
Widespread → PUVA
Steroids (oral mini pulse)
Azathioprine
Acitretin
Hypertropic LP → Steroids + salicylic acid (applied under occlusion for better penetration)
Mucosal LP → Steroids + Dapsone
n e mo n
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ic
A B
Clinical Features
Age: 10-35 years; FemalesQ >Males
Initial appearance of 1st lesion known as HeraldQ/mother
patch (Figs 35A and B). Annular lesion with salmon
pink color, cigarette paper like scales at the periphery
(collarette of scale)Q.
Scales are attached at edges and free toward the center.
When lesion is stretched along long axis, scales fold across
the lines of stretch, called “Hanging Curtain” signQ.
Initial lesions are followed by appearance of multiple similar
appearing smaller, less scaly, less erythematous lesions
along the lines of the ribs giving fir-tree/Christmas tree
appearanceQ (Fig. 37).
Lesions of pityriasis rosea may mimic lesions of secondary
syphilisQ. They can be differentiated by past history of
Fig. 37: Fir-tree/Christmas tree appearance
chancre, positive VDRL and involvement of palms and soles
in secondary syphilis.
Most Common site—TrunkQ (Fig. 36).
Self-limitingQ disease usually in 6–10 weeks.
Fig. 38: Pityriasis rosea Flowchart 1: Clinical course followed by pityriasis rosea
Papulosquamous Disorders 5 Chapter 119
Treatment
Asymptomatic → Reassurance
Symptomatic
Itchy → Antihistamine
Calamine
Topical steroid
Severe/Erythematous/Scaly → Coal tar
Topical steroids
Recalcitrant → Phototherapy
PUVA/PUVASOL
NBUVB
Age of Onset
Juvenile variant = 5–10 years
Adult variant = 40–60 years
Clinical Features
Scaly (pityriasis), orange to red (Rubra), follicular (pilaris) papules,
coalesce to form large plaques, with islands of normal skinQ in
between. Sometimes >90% body surface involved (ErythrodermaQ)
(Figs 41A and B).
Most common site: Trunk (lesions evolve in cephalocaudal direction)
(Fig. 39). Fig. 39: Distribution of pityriasis rubra pilaris
Other Sites
Digits →follicular lesions (Nutmeg grater)
Palm and sole → Keratoderma (thicking) of palm and sole (Keratodermic sandals) Fig. 42.
Nails → Yellowish discoloration with thickened nail plate
Griffith’s classification → 6 types
1. Classic adult type
2. Atypical adult type
3. Classic Juvenile type
4. Atypical juvenile type
5. Circumscribed juvenile type
6. HIV associated
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New SARP Series Skin
A B
Figs 41A and B: Pityriasis rubra pilaris with islands of Fig. 42: Keratodermic sandals
normal skin
Treatment
Topical → Corticosteroids
Salicylic acid
Systemic → Acitretin
Methotrexate
Papulosquamous Disorders 5 Chapter 121
PARAPSORIASIS
Parapsoriasis describes a group of cutaneous diseases that can be characterized by scaly papules and/or plaques dispersed
on the trunk or proximal extremities that have a resemblance to psoriasis. Because of the variation in clinical presentation
and a lack of a specific diagnostic finding on histopathology, an uniformly accepted definition of parapsoriasis is lacking.
Brocq described 3 major entities that fit the description:
Pityriasis lichenoides (Acuta and chronica)
Small plaque parapsoriasis
Large plaque parapsoriasis (Parapsoriasis en plaque)
zz Pityriasis lichenoides (Acuta and chronica)
Pityriasis lichenoides variants is scaly dermatoses with necrotic papules that are clinically and histologically
different from parapsoriasis. These diseases generally are benign and undergo spontaneous resolution.
zz Difference between small plaque parapsoriasis and large plaque parapsoriasis
M
ic
features asymmetrical, erythematous, scaly plaques
Mnemonic to remember
erythematous + with presence of
features of Poikiloderma = ATP
scaly plaques • Induration and
• Poikiloderma (atrophy, A = Atrophy
pigmentation, telangiectasia) T = Telangiectasia
• Treatment Not aggressive Aggressively treated P = Pigmentation
Conjunctivitis
ic
Urethritis
Balanitis Circinata → Lesions over glans penis with ring like border (circinate)
Iridocyclitis and infections →
zz Sexually acquired (STI) → Chlamydia trachomatisQ CUBIKA
zz Enteric acquired (infection) → Shigella, Salmonella
Keratoderma blenorrhagica → Crusted, exudated plaques over palm and sole
Arthritis → Acute, Asymmetrical, Arthritis of lower Limb with sacroilitis.
122 New SARP Series Skin
n e mo n
M
ic Another mnemonic
CU KABIR on 27th
C = Conjunctivitis
U = Urethritis
K = Keratoderma blennorrhagicum
A = Arthritis
B = Balanitis circinata
I = Iridocyclitis
R = Rupioid psoriasis
27 = HLA B27
ic
“ID-SCALP”
Idiopathic → MC (30%)
DRUG (Anti-epileptics, carbamazepine), Ca2+Ch-blockers, Antibiotics (penicillin)
Seborrheic dermatitis, Sezary syndrome
Contact dermatitis
Atopic dermatitis, airborne contact dermatitis
Lymphoma and Leukemia
Psoriasis, pityriasis rubra pilaris and pemphigus foliaceus
LICHEN NITIDUS
Multiple discrete, tiny, pinheadQ sized skin colored papules common in children over forearms, dorsumQ of hand,
penis, chest, abdomen and buttock (Fig. 44).
Koebner phenomenon present
Histology: “Claw and ball” appearance
Elongated rete ridges with focal dense lymphohistiocytic infiltrate in upper dermis
Elongated rete ridges resembles ‘claw’ and lymphohistiocytic infiltrate appears like a ‘ball’.
Papulosquamous Disorders 5 Chapter 123
A B C
Treatments
Topical • Corticosteroids
• Calcineurin inhibitors
Phototherapy
Systemic • Corticosteroides
• Cyclosporin
• Acitretin
124 New SARP Series Skin
ONE LINERS
Pityriasis amiantacea→Seen in psoriasis, atopic dermatitis, seborrheic dermatitis, Tinea capitis
↓ ↓
scaling asbestos like
It may be complicated by secondary staphylococcal infection.
n e mo n
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ic
PAST
P = psoriasis
A = atopic dermatitis
S = seborrheic dermatitis, staphylococcal infection
T = Tinea capitis
Due to thickness of stratum corneum, lesions of psoriasis have less obvious erythema on palm and sole.
Seborrheic dermatitis → Lesions do not spill onto forehead and nape of neck from scalp.
Yellow greasy scales on seborrheic areas, severe in HIVQ: seborrheic dermatitis.
Greasy scales over scalp of infant: cradle capQ (seborrheic dermatitis)
Pityriasis capitis is commonly known as dandruff (no inflammation), inflammation is present in seborrheic
dermatitis.
Psoriasis → Lesions may spill onto forehead and nape of neck.
Dactytitis→ Digits become sausage shaped due to inflammation of tendons, joint and soft tissue
Enthesitis→ Inflammation of entheses
Dactytitis and enthesitis is typical manifestations of psoriatic arthritis
Post sexual (chlamydia) and post enteric (shigella, salmonella) are infective causes of Reiter’s disease/reactive arthritis.
PS-clinical features
ORI-nail changes
ASIS- Histological findings
Dental filling (amalgam)/MercuryQ → can cause oral lichen planus.
Ulcerative/erosive oral L.P. → rare but premalignant.
Civette bodiesQ are seen in lichen planus.
Griffith’s classification is used for pityriasis rubra pilaris
Wornoff ring seen in psoriasis is due to prostaglandinsQ
Following clinical history/clues in the questions are suggestive of:
zz Scaly (pityriasis), orange to red (Rubra), follicular (pilaris) papules, coalesce to form large plaques: pityriasis
rubra pilaris
Papulosquamous Disorders 5 Chapter 125
zz Keratotic sandalsQ (thickening of palm and sole), with islands of normal skinQ in between: pityriasis rubra
pilaris
zz Classic triad of arthritis, urethritis and conjunctivitis. Reactive arthritis/reiter’s disease.
zz “Lake of pus “ or “sheet of pus”Q in MCQ indicates: Impetigo herpetiformis/pustular psoriasis/von
zumbusch disease.
Diagnostic Box
Understanding biological therapies used in psoriasis
Basic interplay between T-cells, antigen presenting cell (APC) and cytokines is well established in psoriasis
126 New SARP Series Skin
Recent Advances
Psoriasis Genes: PSORS 1-8 genes (PSORiasis susceptibility)
PSORS 1→ Located in MHC (chromosome 6p21.3)
Most replicated psoriasis susceptibility locus
PSORS 2 → 2nd most replicated psoriasis susceptibility locus
PSORS 5 → Linked to psoriasis in Swedish families
PSORS 8 → Susceptibility gene for Crohn’s disease and also implicated in psoriatic arthritis.
Multiple HLA alleles associated with psoriasis
HLA CW6 →psoriatic arthritis and early onset psoriasis
HLA B27
B38 Also associated with psoriatic arthritis
B39
HLA B27 → Strongly associated with the axial variant of psoriatic arthritis.
Recent Biologicals
Ixekizumab (phase III completed) anti IL-17A
Brodalumab (phase II completed) bind to IL-17 receptor A
Tofacitinib Janus kinase (JAK) Inhibitors → prevent cytokine receptor signaling → receptors
Baricitinib for IL 2, 6, 22, 23, IFN-y, TNF-α
Golimumab
TNF α inhibitor
Certolizumab pegol
Briakinumab
Tildrakizumab IL-23
Guselkumab
Voclosporin Calcineurin inhibitor (similar to cyclosporine)
Papulosquamous Disorders 5 Chapter 127
1. Which of the following is/are not a subtype of 8. Regarding Lichen Planus all are true, except:
lichen planus: (PGI May 2018) a. Hypopigmentation in most residual disease
a. Ulcerative lichen planus b. Lymphocytic infiltration in supradermal layer
b. Lichen nitidus c. Itchy polygonal purple papules
c. Hypertrophic lichen planus d. Skin, hair and oral mucosae are normal
d. Lichen scrofulosorum 9. Sawtooth rete ridges are seen in:
e. Lichen planus pigmentosus a. Erythroderma b. Psoriasis
2. Nail changes in psoriasis is/are: (PGI May 2018) c. Darier’s disease d. Lichen planus
a. Onycholysis 10. A young lady presents with lacy lesions in oral
b. Oil drop discolouration cavity and genitals, and her proximal nail fold
c. Subungual hyperkeratosis has extended onto the nail bed. What is the likely
d. Nail pitting diagnosis:
e. Pterygium formation a. Psoriasis b. Geographic tongue
3. A lady with bilateral buccal reticulate white c. Lichen planus d. Candidiasis
streaks. Pain increases on intake of spicy food and 11. Vitamin D analogue calcitriol is useful in the
patient gives no H/O tobacco but show amalgam treatment of:
on 3rd molar. Diagnosis? (AIIMS Nov 2015) a. Lichen planus b. Psoriasis
c. Pemphigus d. Leprosy
12. Complication of chronic Lichen planus:
a. Dermatofibroma
b. Malignant melanoma
c. Basal cell carcinoma
d. Squamous cell carcinoma
13. Nappes claires is seen in:
a. Pityriasis versicolor b. P. alba
c. P. rubra pilaris d. P. rosea
a. Leukoplakia b. Lichen planus 14. A 35-year-lady presents with bilateral buccal
c. Aphthous stomatitis d. Candidiasis reticulate white streaks as shown in, pain and
burning sensation on eating spicy food. There
4. Pityriasis rosea true:
is no history of tobacco chewing but shows
a. Self-limiting
amalgamated 3rd molar tooth is present. What is
b. Chronic relapsing
most likely cause?
c. Life threatening infection (autoimmune disease)
d. Caused by dermatophytes
5. Least common site involvement in psoriasis is:
a. Scalp involvement b. Nail involvement
c. CNS involvement d. Arthritis
6. A patient with psoriasis was started on systemic
steroids. After stopping treatment, the patient
developed generalized pustules all over the body.
The cause is most likely to be:
a. Drug induced reaction b. Pustular psoriasis
c. Bacterial infections d. Septicemia
7. The only indication of giving corticosteroids in
pustular psoriasis is:
a. Psoriatic erythroderma with pregnancy
b. Psoriasis in a patient with alchoholic cirrhosis
c. Moderate arthritis a. Candida b. Aphthous stomatitis
d. Extensive lesions c. Lichen planus d. Leukoplakia
128 New SARP Series Skin
15. A 7 months pregnant lady with diabetes comes 21. This type of psoriasis is commonly seen in children
with lesions all over the body, mainly trunk as and may follow a streptococcal sore throat:
in the picture below. Which of these drugs is the (PGMEE 2014)
appropriate treatment? a. Pustular b. Stable plaque
c. Arthropathic d. Guttate
22. Goekarman regimen used in for treatment of
psoriasis is: (PGMEE 2015)
a. Coal tar plus anthralin
b. UVB plus coal tar
c. UVB plus anthralin
d. UVB plus methotrexate
23. Among various types of psoriatic arthritis, which
variety is most common: (PGMEE 2015)
a. Classic b. Spondylitis
a. Cyclosporine b. Azathioprine c. Rheumatoid d. Oligoarticular
c. Methotrexate d. Retinoids 24. The treatment of choice for erythrodermic
16. In which of the following, Koebner phenomenon is psoriasis is: (PGMEE 2014)
NOT seen: (PGMEE 2015) a. Topical corticosteroids
a. Erythema multiforme b. Corticosteroids
b. Lichen sclerosis c. Coaltar topically
c. Lichen simplex chronicus d. Methotrexate
d. Lichen planus 25. A primigravida female presented with
17. A Hanging Curtain Sign is seen in: erythematous skin changes and lesions with
a. Hordeolum externum b. Psoriasis multiple pus lakes. Which of the following should
c. Lichen Planus d. Pityriasis Rosea be the most appropriate: (PGMEE 2010)
18. First topical retinoid approved by us FDA for a. Psorolen + PUVA b. PUVA
psoriasis: (PGMEE 2016-17) c. Atretin d. Corticosteroids
a. Isotretinoin b. Tazaroten 26. Psoriasis is exacerbated by: (PGMEE 2015)
c. Acitretin d. Calcipotrine a. Antimalarials b. Lithium
19. Tiny bleeding spots after removal of deep scales in c. β-blockers d. All of the above
Plaque Psoriasis is Known as: (PGMEE 2015-16) 27. The most common association with coarse pitting
a. Koebner’s Sign b. Burkley’s Sign of nails and onycholysis is: (PGMEE 2014)
c. Candle Wax Sign d. Auspitz Sign a. Cicatricial alopecia
20. 45-year-old male presents with scaly lesions over b. Well defined scaly plaques
back. Most likely diagnosis is: (PGMEE 2016-17) c. Polygonal papule
d. Violaceous papules
28. A young female presented with lacy linear lesions
on tongue since a month with elongation of nail
fold beyond the nail bed. What is the diagnosis:
a. Lichen planus (PGMEE 2010)
b. Psoriasis
c. Candidiasis
d. Geographic tongue
29. Characteristic bodies in Lichen planus:
a. Civatte bodies (PGMEE 2016-17)
b. HP bodies
c. Warthin Fiekendly Bodies
d. Negri bodies
30. Not a histological feature of lichen planus is:
a. Lichen planus a. Neutrophils in stratum (PGMEE 2014)
b. Pustular psoriasis b. Hyperkeratosis
c. Erythrodermic psoriasis c. Pigment incontinence
d. Psoriasis vulgaris d. Acanthosis
Papulosquamous Disorders 5 Chapter 129
31. The most characteristic finding in lichen planus
is: (PGMEE 2013)
a. Violaceous lesions
b. Civatte bodies
c. Thinning of nail plate
d. Basal cell degeneration
32. Cicatrising alopecia with perifollicular blue-gray
patches is most commonly associated with:
a. Pitting of nails (PGMEE 2011)
b. Discoid plaques in the face
c. Arthrtis
d. Whitish lesions in the buccal mucosa
33. A young boy presented to OPD with multiple shiny
a Lichen nitidus b. Lichen planus
pinhead size white papules over dorsum of head,
c. Scabies d. Phrynoderma
forearm and penis. What would be the diagnosis?
40. A 7 month pregnant lady comes with the following
a. Lichen planus (PGMEE 2014)
lesions all over the body. Picture shows multiple
b. Lichen nitidus
small pustules over skin. Which of these drugs is
c. Scabies
an appropriate treatment?
d. MC
34. Case with curtain like sign and Christmas tree
Pattern along the ribs: (PGMEE 2016-17)
a. Pityriasis rosea
b. Pityriasis versicular
c. Pityriasis lichenoides chronica
d. Pityriasis rubra pilaris
35. Multiple erythematous annular lesions with
peripheral collarette of scales arranged
predominantly on trunk are seen in:
a. Pityriasis vesicular (PGMEE 2012)
b. Pityriasis rubra pilaris a. Cyclosporine b. Azathioprime
c. Pityriasis rosea c. Methotrexate d. Retinoids
d. Pityriasis lichennoides chronica 41. Black follicular prominences seen over scalp,
36. Annular herald patch is seen in: (PGMEE 2013) leading to scarring alopecia along with nail
a. Psoriasis b. Nocardiasis dystrophy leading to anonychia. Diagnosis:
c. P.alba d. P. rosea
37. Keratodermic sandal is a feature of: (PGMEE 2013)
a. Psoriasis
b. Lichen planus
c. Pityriasis rubra pilaris
d. Pityriasis rosacea
38. All of the following are primary cutaneous
disorder except: (PGMEE 2012)
a. Icthiosis
b. Reiter’s disease
c. Lichen planus
d. Psoriasis a. Scalp psoriasis with nail changes
39. A child came with similar lesions over dorsum of b. Black dot tinea capitis with onychomycosis
hand, shaft of penis and forearm. Picture shows c. Lichen planus
Pinhead discrete but grouped papules. Diagnosis. d. Alopecia areata
130 New SARP Series Skin
1. Ans. a. Ulcerative lichen planus, d. Lichen Variants of P.R: Papular, vesicular, pustular,
scrofulosorum hemorrhagic, purpuric, inverse, EMF like, giant,
urticarial without herald patch.
The clinical presentation of lichen planus has several
forms: actinic (in sun-exposed areas), annular, Treatment
atrophic, erosive/ulcerative, follicular, hypertrophic, •• Essentially symptomatic [antihistamine, calamine
linear, pigmented, and vesicular/bullous. lotion]
Lichen scrofulosorum is a type of tuberculid which
occurs due to mycobacterial hypersensitivity. 5. Ans. c. CNS involvement
Lichen nitidus is a rare skin condition that usually [Ref: 8th edition chapter 20]
appears as tiny, skin-colored, glistening bumps on
the surface of your skin. Lichen nitidus results from Scalp is a common site of involvement in psoriasis.
abnormal inflammatory activity in skin cells, but the Corona psoriatica is a band of psoriasis, projecting
cause of inflammation is unknown. beyond hairline on forehead.
Nail changes in psoriasis are pitting, onycholysis,
2. Ans. a. Onycholysis, b. Oil drop discolouration, subungual hyperkeratosis, splinter hemorrhages,
c. Subungual hyperkeratosis, d. Nail pitting uneven surface.
Pterygium (Proximal nail fold extends onto and fuses 6. Ans. b. Pustular psoriasis
with nail bed) formation is seen in lichen planus.
•• Dorsal pterygium is seen in lichen planusQ [Ref: IADVL 4th edition page no: 1030]
•• Ventral pterygium is seen in:- Pustular Psoriasis
Scleroderma with Raynaud’s phenomenon
•• Acute widespread lakes of pus
Causalgia of median nerve
•• Precipitated by steroid withdrawal.
Trauma
•• Von Zumbusch reaction is a very severe
3. Ans. b. Lichen planus generalized pustular psoriasis
•• Pustular psoriasis is also aggravated by local
White reticulate pattern is commonly seen associated infections, hypocalcemia, topical application of
with lichen planus. History of amalgam filling in anthralin
teeth is also suggestive of lichen planus. •• Pustular psoriasis in pregnancy is called impetigo
herpetiformis
4. Ans. a. Self-limiting
7. Ans. a. Psoriatic erythroderma with pregnancy
Pityriasis Rosea
It is an acute, self-limiting disease, probably 8. Ans: a. Hypopigmentation in most residual disease
infective in origin, affecting mainly children and
young adults, characterized by a distinctive skin Post-residual Hyperpigmentation is seen most
eruption and minimal constitutional symptoms. commonly in residual disease
Etiology
9. Ans. d. Lichen planus
Most common: Human herpes virus HHV 7 and HHV 6
Drugs: Arsenic, bismuth, lithium, metronidazole, HPE of Lichen Planus
barbiturates, captopril, ketotifen. •• Hyperkeratosis
Vaccination: Hep B / BCG •• Hypergranulosis
Mother/herald patch–Solitary annular plaque •• Acanthosis
which heralds the disease [site trunk, arm]. •• Basal cell degeneration producing Civatte bodies
Followed by multiple oval shaped symmetrically •• Max-Joseph Space
arranged collarette scaly plaques along the lines of •• Band like infiltration of Lymphocytes at dermo-
cleavage [Christmas tree pattern] involving bathing epidermal junction.
trunk area. •• Saw toothing of Rete – Ridges
Papulosquamous Disorders 5 Chapter 131
10. Ans. c. Lichen planus from 1 to about 4 weeks before healing. Aphthae
typically are multiple round or ovoid ulcers with a
[Ref: 8th edition chapter 41.1] circumscribed margin, erythematous halo and a
Lichen Planus yellow or grey floor.
•• It is an idiopathic, chronic, inflammatory disease Option (D) Leukoplakia
that affects the skin, mucous membranes and The World Health Organization defines leukoplakia
appendages as a white patch or plaque on the mucosa that cannot
•• 5’p’s of LP – pruritus, plane (flat) topped, be rubbed off and that is not recognized as a specific
polygonal, purple (violaceous), papules and disease entity, which implies a diagnosis of exclusion
plaques. (e.g. of LP, candidiasis). The term is also used
•• Sites: Flexer aspect of wrist, forearm extensor irrespective of the presence or absence of epithelial
surface of lower legs, lumbosacral area. dysplasia, although there is a small malignant
•• Lesions heal with hyperpigmentation potential to some keratoses.
•• Oral cavity: White streaks in lacy pattern in
posterior buccal mucosa seen. 15. Ans. a. Cyclosporine
•• Nails: Pterygium: Thinning, splitting, ridging. [Ref: Bolognia 3rd Ed page 2242, IADVL 2nd Ed page
•• Kobner’s phenomenon is positive 1054, Roxburgh’s 18th ed page 148-150, Fizpatrick 7th
•• Wickham striae: Dedicate white lines seen over ed page 959-960]
lesions better viewed with oil application.
The clinical picture is consistent with Pustular
11. Ans. b. Psoriasis Psoriasis of Pregnancy AKA Impetigo Herpitiformis.
Systemic steroids followed by impetigo
herpetiformis Cyclosporine is the drug of choice
12. Ans. d. Squamous cell carcinoma
in impetigo herpetiformis. As retinoids, PUVA
and Methotrexate are contraindicated in pregnancy,
13. Ans. c. P. rubra pilaris cyclosporine and/or steroid is used. Localized
disease is treated by topical steroid while generalized
The islands of sparing in PRP is known as Nappes
disease is treated by systemic steroid. Systemic
claire’s
steroid should be avoided in routine care of Psoriasis,
14. Ans. (c) Lichen planus because the disease requires progressively higher
dose and withdrawal of steroid is associated with
[Ref: Rook dermatology 8th ed page 41.1] relapse into more severe forms.
Clues in the Question are
•• Bilateral reticulate white streaks is very characterstic 16. Ans. c. Lichen simplex chronicus
of wickham’sstriae seen in lichen planus. [Ref: IADVL Textbook of Dermatology 4th edition vol
•• Dental amalgams are known to predispose to 1 pg 131]
lichen planus symptoms of burning on intake of
spicy food can occur in all the mentioned options, Lichen simplex chronicus also known as
so let’s rule out the options. neurodermatitis occurs due to excessive scratching
at particular site and is not associated koebner’s
Option (A) Oral Candida phenomenon
The characteristic sign of this condition is a sharply
defined patch of creamy, crumbly, curd-like white 17. Ans. d. Pityriasis Rosea
pseudomembrane, which, when removed, leaves
[Ref: Andrew’s Diseases of the Skin: Clinical
an underlying erythematous base. This membrane
Dermatology 12th/e pg. 199; Multiple References]
consists of desquamated epithelial cells, fibrin,
leukocytes and fungal mycelium that attaches it to Hanging certain sign, collarette of scales, cigarette
the inflamed epithelium. Present in preterm babies, paper scales all are seen pityriasis rosea
immunocompromised conditions such as AIDS.
18. Ans. b. Tazaroten
Option (B) Recurrent Aphthous Stomatitis (RAS)
[Ref: IADVL Textbook of Dermatology 4th edition vol
It is characterized by recurring episodes of ulcers,
1 pg 1051]
typically from childhood or adolescence, each lasting
132 New SARP Series Skin
22. Ans. b. UVB plus coal tar [Ref: IADVL Textbook of Dermatology 4th edition vol
1 pg 1098]
[Ref: IADVL Textbook of Dermatology 4th edition vol
Elongation of nail fold is known as pterygium
1 pg 1051]
These are two phototherapy regimen used in psoriasis 29. Ans. a. Civatte bodies
•• Ingram regimen: Dithranol followed by light
[Ref: IADVL Textbook of Dermatology 4th edition vol
exposure
1 pg 1101]
•• Goeckerman regimen: Coal tar followed by light
exposure Civatte or colloid bodies are apoptotic (degenerating)
basal keratinocytes
23. Ans. d. Oligoarticular
30. Ans. a. Neutrophils in stratum
[Ref: IADVL Textbook of Dermatology 4th edition vol
1 pg 1037] [Ref: IADVL Textbook of Dermatology 4th edition vol
1 pg 1101]
Asymmetrical oligoarticular type of psoriatic
arthritis is most common Neutrophilic collection in epidermis are seen in psoria-
•• Most common joint involved in psoriatic arthritis sis known as munro’s Microabscess and Kogoj pustules
is DIP (Distal interphalangeal joint)
Following findings are also associated with psoriatic 31. Ans. d. Basal cell degeneration
arthropathy [Ref: Rook’s Textbook of Dermatology 9th edition
•• Sausage digit inflammation of entire digit pg37.14]
•• Pencil in cup deformity (on plain radiograph)
Most characteristic histological finding is basal cell
•• Opera glass deformity (telescoping fingers)
degeneration.
24. Ans. d. Methotrexate Most characteristic nail finding is pterygium
[Ref: IADVL Textbook of Dermatology 4th edition vol 32. Ans. d. Whitish lesions in the buccal mucosa
1 pg 1057] [Ref: IADVL Textbook of Dermatology 4th edition vol
•• DOC for erythrodermic psoriasis: Methotrexate 1 pg 1099]
•• DOC for pustular psoriasis: Acitretin It’s a case of lichen planus
Papulosquamous Disorders 5 Chapter 133
33. Ans. b. Lichen nitidus Lichen nitidus
Disorder Distribution
Lichen Trunk, dorsum of hand, shaft of penis and
nitidus forearm (flexors of upper extremities).
Lichen Extremities (flexors of wrists, ankles and
planus shin) and lower back.
Variants: Phrynoderma
Annular –face and glans
Actinic – face
Linear –extrimities
Follicular – scalp
Hypertrophic- shin
Pigmentosus – photoexposed and flexures
Scabies Web spaces, wrists, ulnar aspect of forearm,
groin. Face, palm and sole spared in adults
and involved in infants.
Phryno- Elbows, knees
derma
134 New SARP Series Skin