Dermatology Flashcards

1
Q

Name some skin disorders a/w Diabetes

A
  • Necrobiosis lipoidica
  • Infection: Candida, Staphylococcal
  • Granuloma annulare
  • Neuropathic ulcer
  • Vitiligo
  • Lipoatrophy
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2
Q

What is Necrobiosis lipoidica ??

A
  • typically seen on SHINS
  • Shiny, PAINLESS, area of yellow/red/brown skin
  • a/w TELANGIECTASIA
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3
Q

What is Granuloma annulare ??

A
  • Papular lesions
  • slightly Hyperpigmented + centrally depressed
    Site: Dorsal Hands & feet, Extensors of Arms & legs
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4
Q

Causes of Acanthosis Nigricans ??

A

Symmetrical, brown, velvety plaque on Neck, Axilla, Groin
- GI Cancer
- Obesity
- PCOS
- Acromegaly, Cushing’s disease
- Hypothyroid
- T2DM
- Prader-Willi
- Nicotinic acid
- COCPs
- Familial

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5
Q

What is the pathophysiology of Acanthosis N ??

A

Insulin resistance==> HYPERINSULINAEMIA==> interaction with IGF receptor-I ==> KERATINOCYTES & Dermal FIBROBLASTS proliferation

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6
Q

Name the skin conditions a/w Pregnancy

A
  • Atopic eruption of pregnancy (MC)
  • Polymorphic eruptions
  • Pemphigoid gestationis
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7
Q

Features of Atopic eruptions of Pregnancy ??

A
  • MC skin disorder seen
  • Eczematous + Itchy + Red rash
  • No specific treatment
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8
Q

Features of Polymorphic eruptions of Pregnancy ??

A
  • Pruritic condition a/w LAST Trimester
  • 1st appears in Abd. STRIAE
  • Rx.(based on severity)- Emollients, mild potency topical steroids, Oral steroids
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9
Q

Features of Pemphigoid gestationis ??

A
  • Pruritic blistering lesions
  • starts at Peri-Umbilical region ==> later spreading to trunk, back, buttocks & arms
  • 2nd or 3rd trimester
  • RARELY seen in 1st pregnancy
  • Rx.- Oral Corticosteroids
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10
Q

What are the skin disorders a/w TB ??

A
  • LUPUS VULGARIS (50% cases)
  • Erythema nodosum
  • Scarring alopecia
  • Scrofuloderma
  • Verrucosa cutis
  • Gumma
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11
Q

What is Lupus Vulgaris ??

A

MC form of Cutaneous TB seen in Indian subcontinent
- Site: Face, common around Nose & Mouth
- Initial- Erythematous flat plaque
- Later- Elevated & ulcerates

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12
Q

What is Scrofuloderma ??

A

Breakdown of skin overlying a TB focus

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13
Q

What skin condition is a/w the following
- Oesophageal Ca
- Gastric Ca
- Pancreatic Ca
- GI & Lung Ca

A
  • Tylosis
  • Acanthosis nigricans
  • Migratory thrombophlebitis
  • Acquired hypertrichosis lanuginosa
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14
Q

What skin condition is a/w the following
- Lymphoma
- Myeloproliferative disorder
- Glucogonoma

A
  • Acquired ichthyosis, Erythroderma
  • Pyoderma gangrenosum (Bullous & Non-bullous form)
  • Necrolytic Migratory erythema
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15
Q

What skin condition is a/w the following
- Lung Ca
- Ovarian & Lung ca
- GI & Lung Ca

A
  • Erythema gyratum repens
  • DERMATOMYOSITIS
  • Acquired hypertrichosis lanuginosa
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16
Q

Which skin conditions are a/w Haematological malignancy eg.- Myelodysplasia- tender, purple plaques ??

A

Sweet’s syndrome (Acute febrile Neutrophillic dermatosis)
- sudden onset well defined tender plaques or nodules
- Fever
- Arthralgia
- Ocular inflammation
- Systemic symptoms
Lesions reveal Neutrophilic Infiltrates

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17
Q

RF for SCC of skin ??

A
  • Excessive Sunight
  • Psoralen UVA therapy
  • Immune suppression (Post-Renal transplant, HIV)
  • Smoking
  • Actinic keratosis, Bowen’s disease
  • MARJOLIN’s ulcer (long standing leg ulcer)
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18
Q

Which genetic condition is a/w SCC of skin ??

A

Xeroderma pigmentosum
Oculocutaneous albinism

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19
Q

Rx. of SCC of skin ??

A

Surgical excision
- Tumour < 20mm, excise with 4mm margin
- Tumour > 20mm, excise with 6mm margin
Mohs Micrographic Sx.
- used in High risk pts.
- Cosmetically important sites

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20
Q

Prognosis of SCC of skin ??

A

Good prognosis
- Well differentiated, < 20mm diameter, < 2mm deep, Not a/w any disease
Poor prognosis
- Poorly diferentiated, > 20mm diameter, > 4mm deep, Immunosuppression for any reason

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21
Q

Which is the MC type of skin cancer in the western world ??

A

BCC aka Rodent ulcers
- Slow growing with local invasion
- Metastases is extremely rare

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22
Q

Features of BCC ??

A

MC type is NODULAR type
- Site- Head & Neck
- Sun exposed areas
- Initial: Pearly lesion
- Later: Ulcerate leaving a central ‘Crater’
ROUTINE Referral made

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23
Q

Rx. of BCC of skin ??

A
  • Surgical removal
  • Curettage
  • Cryotherapy
  • Topical cream: IMIQUIMOD, FLUROURACIL
  • Radiotherapy
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24
Q

What are the types of Malignant Melanoma ??

A
  • Superficial spreading (70% cases)
  • Nodular (2nd MC, MOST AGGRESSIVE)
  • Lentigo Maligna (Less common)
  • Acral Lentiginous (Rare)
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25
Q

Describe Superficial spreading Malignant melanoma

A
  • Young people
  • Site: Arm, Leg, back & chest
  • Appearance: Growing mole + Dx. criteria
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26
Q

Describe Nodular Melanoma

A
  • Most aggressive form
  • Middle aged people
  • Sun exposed areas
  • Appearance: Red/ Black lump (or) lump which bleeds/ oozes
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27
Q

Describe Lentigo maligna

A

Is a type of Melanoma in situ
- Older people
- Chronic sun exposed areas
- Progresses slowly, at some stage stage becomes invasive causing Lentigo maligna melanoma
- Appearance: Growing mole + Dx. criteria

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28
Q

Describe Acral lentiginous

A
  • African Americans or Asians
  • Nails, Palm or Soles
  • Appearance: Subungual pigmentation (HUTCHINGSON’s Sign) (or) on Palms or Feet
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29
Q

Name some rare forms of Malignant Melanoma

A
  • Desmoplastic M
  • Amelanotic M
  • Melanoma arising from other parts of body eg. Ocular M
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30
Q

What are the Dx. Criteria of Malignant Melanoma ??

A

Major Criteria
- Change in Size
- Change in Shape
- Change in Colour
Minor Criteria
- Diameter >= 7mm
- Inflammation
- Oozing or Bleeding
- Altered Sensation

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31
Q

Rx. of Malignant Melanoma ??

A
  • Suspicious lesion: Excision Biopsy
  • Lesion should be removed en mass
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32
Q

How is the Margins of excision related to Breslow thickness ??

A

Lesions 0-1mm thick = 1cm
Lesions 1-2mm thick = 1-2cm (depending on the site & pathological features
Lesions 2-4mm thick = 2-3cm (depending on site & pathological features)
Lesions > 4mm thick = 3 cm

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33
Q

What is the single most imp. factor that determines the prognosis in Malignant Melanoma ??

A

Breslow DEPTH (invasion depth of tumour)
< 0.75mm = 95-100% (5 year survival)
0.76- 1.5mm = 80-96%
1.51- 4mm = 60- 75%
> 4mm = 50%

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34
Q

What is Mycosis Fungoides ??

A

aka Alibert-Bazin synd. or Granuloma Fungoides
- Rare form of Blood Cancer (T-Cell Lymphoma) causing Skin lesions
- Itchy, flat, scaly, pink or red patch
- Plaque that can be red, scaly & itchy

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35
Q

What is Sezary syndrome ??

A

type of T-Cell Cutaneous Lymphoma
- Pruritis
- Erythroderma of Palms, Soles & Face
- Lymphadenopathy
- Hepato-splenomegaly
- Atypical T-cells

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36
Q

What is Systemic Mastocytosis ??

A

Neoplastic proliferation of Mast cells
- Urticaria pigmentosa- produces a wheal on rubbing (Darier’s sign)
- Flushing
- Abdominal pain
- Monocytosis on Blood film

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37
Q

How do we Dx. Systemic Mastocytosis ??

A

Raised S. Tryptase levels
Monocytosis
Urinary histamine

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38
Q

What is Keratoacanthoma ??

A

BENIGN epithelial tumour
MC with advancing age & rare among young people

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39
Q

Features of Keratoacanthoma ??

A

Looks like volcano or crater
- Initial: smooth dome-shaped papule
- Rapidly growing to become Crater centrally filled keratin
Spontaneous regression within 3 months is common
- they should be urgently excised (to exclude SCC)

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40
Q

What is Actinic Keratosis ??

A

Solar keratoses is a common PRE-MALIGNANT lesion
- Chr. Sun exposure
- Sun exposed areas (eg. Temple region)
- Small, crusty or scaly lesions
- Pink/Red/Brown/same colour as skin
- Multiple lesions may be present

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41
Q

Rx. of Solar or Actinic Keratosis ??

A
  • Flurouracil cream [(2-3 wks course), use Hydrocortisone cream if skin becomes red & inflamed]
  • Mild AKs: Topical Diclofenac
  • Topical Imiquimod
  • Cryotherapy
  • Curettage & Cautery
  • Sun avoidance, Sun-screen
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42
Q

What causes Impetigo ??

A

Bacterial skin infection (very contageous)
Staph. aureus or Strept. pyogenes
- ‘Golden crusted skin around mouth’

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43
Q

Rx. of Impetigo ??

A

Pts. who are NOT systemically unwell or at high risk of complication
- H2O2 (1% )cream
Topical Abx. cream
- Fusidic acid
- Mupirocin (IF resistant to Fusidic acid) & also in MRSA
Extensive disease
- Oral FLUCLOXACILLIN
- Oral Erythromycin (if penicillin allergic)

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44
Q

What is the School exclusion criteria for Impetigo ??

A

Until lesions are Crusted & healed (or)
48hrs after starting Abx. Rx.

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45
Q

Molluscum contagiosum causitive organism ??

A

MC virus (POX-VIRIDAE family)
- Direct transmission: Personal contact
- Indirect transmission: via FOMITES (contaminated surfaces)

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46
Q

RF for Molluscum C ??

A
  • Childern
  • Kids with ATOPIC Dermatitis
  • Max. incidence: Preschool [1-4 yrs]
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47
Q

What are the presentations of Molluscum C infection ??

A

Pinkish/ Pearly white papule with central umbilication; upto 5mm in diameter
Site
- Children: Trunk & Flexures; but anogenital lesions may occur
- Adults: Sexual contact- genitalia, pubis, thighs & lower abdomen; rarely Oral mucosa & on Eyelids

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48
Q

Rx. of Molluscum C ??

A

Self limiting (spontaneous resolution in 18 months)
But things like the following can be done
- After bath: Squeezing (with fingernails) or Piercing (Orange stick)
- Cryotherapy (older kids & adults)
If a/w Eczema/ Inflammation
- Mild topical Steroids (HC 1%)
If infected (eg.-oedema, crusting)
- Topical Fusidic acid 2%

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49
Q

When is referral considered in Molluscum C cases ??

A
  • HIV (+) with extensive lesions = HIV specialist
  • Eye-lid margins/ Ocular lesions = Ophthalmologist
  • Adults + Ano-genital lesions = GUM clinic (for STI screening)
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50
Q

What is Erythema ab igne ??

A

Skin disorder caused by over exposure to INFRARED Radiations
- Reticulated, Erythematous patches with Hyperpigmentation & Telengiectasia
- “Elderly women who sits next to the open fire”
- Risk of SCC development

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51
Q

What is Erythrasma ??

A

CORYNEBACTERIUM Minutissimum overgrowth
- Asymptomatic, flat, slightly scaly, pink/brown rash at GROIN or AXILLAE

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52
Q

Dx. & Rx. of Erythrasma

A
  • Wood’s light examination reveals Coral-Red fluorescence
  • Mild: Topical Miconazole or Antibacterials
  • Extensive: Oral ERYTHROMYCIN
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53
Q

What is Tinea infection & its types ??

A

Dermatophyte fungal infections
3 main types
- T corporis: Trunk, Leg, Arm
- T capitis: Scalp
- T pedis: Feet (Athlete’s foot)
- T cruris

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54
Q

Hallmark features of T capitis (Scalp Ringworm) ??

A
  • MCC: Trichophyton tonsurans in UK % USA
  • Also caused by Microsporum canis (cats & dogs)
    Dx- Fluorescence under Wood’s Lamp
  • M canis: GREEN
  • T tonsurans: do not fluoresce
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55
Q

Ix. & Rx. of T capitis ??

A
  • Scalp scrapings
  • Oral Antifungals
    — T tonsurans: TERBINAFINE
    — M canis: GRISEOFULVIN
    Topical KETOCONAZOLE shampoo for 2 wks. to reduce transmission
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56
Q

Hallmark of T corporis

A

Trichophyton rubrum & T verrucosum (eg. from contact with Cattles)
- Well defined annular, erythematous lesions with pustules & papules
Rx.- Oral FLUCONAZOLE

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57
Q

Hallmark of T pedis ??

A

Athlete’s foot
- Itchy, peeling skin b/w toes
- common in Adolescence

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58
Q

What is Pityriasis Versicolor ??

A

aka Tinea versicolor, is a Superficial Fungal infection
- MALASSEZIA Furfur

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59
Q

Features of Pityriasis versicolor ??

A
  • MC site: TRUNK
  • Hypopigmented, pink/brown (hence Versicolor); more noticeable under Sun-tan
  • Scales is common, Mild Pruritis
    RF: Immunosuppression, Malnutrition, Cushing’s
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60
Q

Rx. of Pityriasis Versicolor ??

A
  • Topical Anti-fungals
  • Ketoconazole shampoo

If Rx. failure
- Send scrapings to confirm Dx.
- Oral ITRACONAZOLE

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61
Q

What is Pityriasis Rosea ??

A

Acute, self-limiting rash (after 6-12 wks) seen in Young adults
- HERPES HOMINIS Virus 7 (HHV-7) may play a role.

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62
Q

Features of Pityriasis Rosea ??

A
  • No prodrome; but minority of pts. give a H/o recent viral infection
  • HERALD Patch (on Trunk)
  • followed by Erythematous, oval, scaly patches
    The longitudinal diameters of the oval lesions run parallel to Line of langer ==> ‘Fir tree’ appearance
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63
Q

What is Onycholysis & mention a few causes ??

A

Separation of nail plate from nail bed
- Idiopathic
- Trauma (eg. over manicuring)
- Infection (usually FUNGAL)
- Psoriasis, Dermatitis
- PVD (eg.- Raynaud’s)
- Hyper/Hypo-thyroidism

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64
Q

What is Onychomycosis & mention the causes ??

A

Fungal infection of nails
- Dermatophytes: T rubrum (90% cases)
- Yeasts: Candida
- Non-Dermatophyte moulds

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65
Q

Mention some hallmarks of Onychomycosis

A

RF: DM & Increasing age
C/F- Thick, Rough, Opaque nails & Unsightly nails
Ix.- Nail clippings, Scrapings from nails

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66
Q

Rx. of Onychomycosis ??

A

Asymptomatic + Pt. not bothered by looks : NO need of Rx.
Dermatophyte infection:
- 1st line: Oral TERBINAFINE
- 2nd line: Oral Itraconazole
- Finger nail : 6wks to 3 months Rx
- Toenail : 3 to 6 months
Candida infection:
- Mild: Topical Antifungals (AMOROLFINE)
- Severe: Oral ITRACONAZOLE (12wks)
- Finger nail : 6 months Rx.
- Toe nails : 9 to 12 months Rx.

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67
Q

Is scabies an infection or a reaction ??

A

Delayed Type 4 HS reaction to mites/ eggs which occur 30 days after initial manifestation

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68
Q

Features of Scabies

A

Sarcoptes scabiei
- Mites burrow into skin & lay eggs in Stratum CORNEUM
- Widespread pruritis
- Linear burrow on sides of finger, webspaces & wrist flexors
Infants: Face & Scalp can be affected

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69
Q

Rx. of Scabies ??

A

1st line: Permethrin 5%
2nd line: Malathion 0.5%
Allow the cream to dry & leave on the skin for : Permethrin- 8 to 12 hrs & Malathion- 24 hrs before washing off
REPEAT Rx. after 7 days
- Pruritis persists for upto 4-6 wks post eradication
- Blanket therapy

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70
Q

What is Crusted Scabies ??

A
  • aka Norwegian scabies
  • Common in Immunosuppressed specially in HIV pts.
  • Rx.- IVERMECTIN + Isolation
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71
Q

HLA a/w Psoriasis ??

A

Chr. skin disorder a/w increased risk of Arthritis & CVS disease

B13, B17 & Cw6
Strong concordance (70%) in identical twins

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72
Q

What is the Pathogenesis of Psoriasis ??

A

Immunological & Environmental
- Abnormal T-cell activity==+==> KERATINOCYTE proliferation (mediated by Th-cells producing IL-17, designated Th-17)
Worsened by - Skin trauma & Stress
Triggered by - Strept. infection
Improved by - Sunlight
- Munro microabscess (Collection of neutrophils) found on skin biopsy

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73
Q

In Psoriasis, how much time does it take for Keratinocytes to transform to Anucleate Corneocytes ??

A

3 days
[Normally it takes 28 to 30 days]
- Epidermal cells fail to secrete adequate amount of LIPIDS => Scaling (due to loss of S Corneum integrity)

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74
Q

Name the subtypes of Psoriasis

A

Plaque psoriasis (MC subtype)
Flexural P (skin is smooth in this type)
Guttate P
Pustular P (common on PALMS & SOLES)

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75
Q

Describe Plaque Psoriasis

A

MC subtype of P
- Typical well-demarcated red, scaly patches
- Extensor surface, Sacrum, Scalp

76
Q

Describe Guttate Psoriasis

A

Transient psoriatic rash commonly triggered by STREPTOCOCCAL infection (Sore throat 2-4 wks prior).
- Multiple, red, TEAR-drop lesions on the body
- MC in Children & Adolescents

77
Q

What are the exacerbating factors for Psoriasis ??

A

Trauma
Alcohol
Drugs
- ACEi & Beta-blockers
- Lithium
- Antimalarials (CQ & HCQ)
- NSAIDs
- Infliximab
- Systemic Steroid withdrawal

78
Q

Rx. of Chr. Plaque Psoriasis

A
  • 1st line (tried for 4 wks) : Potent CS (od) + Vit.D analogue (od) [applied at separate times- one in morning & one at evening]
  • 2nd line (tried if no improvements after 8 wks) : Vit. D analogue (bd)
  • 3rd line (if no improvement after 8 to 12 wks) : Potent CS (bd) for 4 wks (OR) Coal tar preparations (od or bd)
    Short acting DITHRANOL can also be used
79
Q

Rx. for Scalp psoriasis ??

A

Potent Topical CS (od) for 4 wks.
If no improvement after 4 wks, then either use
- Different formulation of the potent CS (eg. shampoo or mousse) &/or
- Topical agent to remove adherent scalp (eg. salicylates/emmolients/oils) before applying potent CS

80
Q

Rx. for Face, Flexure & Genital Psoriasis ??

A

Mild to Moderate potency CS applied (od) or (bd) for <= 2 wks

81
Q

Which phototherapy is used in Psoriasis ??

A

ToC- Narrow band UV-B light for <= 3 wks
Photochemotherapy can also be used- PUVA (psoralen + UV-A)

82
Q

What is the S/E of Phototherapy used in Psoriasis ??

A

Skin aging
SCC (not Melanoma)

83
Q

Drug of choice for Psoriasis with Joint disease ??

84
Q

Why should topical steroids not used for long time in Psoriasis ??

A
  • Steroid skin atrophy (very common in Scalp, Face & Flexures)
  • Stria
  • Rebound symptoms
85
Q

Give some eg. of Vit D analogues

A
  • Calcipotriol (Dovonex)
  • Calcitriol & Tacalcitol
    NOTE: They reduce scales & thickness of plaque but NOT Erythema.
86
Q

Which elective procedure is done in pts. with Recurrent Guttate Psoriasis ??

A

TONSILLECTOMY

87
Q

What is Erythema nodosum ??

A

Inflammation of Subcutaneous fat (Panniculitis)
- Tender + Erythematous + Raised red/ violet Nodular
- Site: SHINS (also Forearms, thighs)
Resolves within 6 wks.
Heals without Scarring
NSAIDs can reduce the symptoms

88
Q

Which infections cause Erythema nodosum??

A

BTS
- Brucellosis, TB, Streptococci
[Also seen in Sarcoidosis, IBD, Behcet’s]
-Pregnancy
- COCPs (use Non-Oestrogen based Contraceptions)

89
Q

What is Erythema Multiforme ??

A

HS reaction triggered by Infection
- Divided into Minor & Major forms
- Major form is a/w Mucosal involvement

90
Q

Features of Erythema Multiforme ??

A
  • Target lesions
  • Initially: Hands/ Feets before spreading to Torso
  • ULs&raquo_space;> LLs
  • Pruritis is mild

MCC is HSV infection

91
Q

What is Orf ??

A

Skin disease of sheep & goats
PARAPOX Virus
Can cause Erythema Multiforme

92
Q

What is Erythroderma ??

A

Term used when > 95% of skin is involved in a RASH of ANY kind
Sometimes called ‘Red man Synd.’
Causes
- Idiopathic
- Psoriasis, Eczema
- Drugs: Gold
- Lymphomas, Leukaemias

93
Q

Rx for Erythroderma Psoriasis ??

A

1st line: Ciclosporin
Infliximab (if 1st line is CI or ineffective)

94
Q

What is Lichen Planus ??

A

Skin disorder of unknown etiology, most probably is Immune mediated
- Itchy, papular rash
- Site: Palm & Soles, Genitalia & Arm flexors
- Wickham’s striae: Polygonal rash + ‘white lines’ pattern on surface
- Koebner phenomenon can be seen

95
Q

Features of Lichen Planus ??

A
  • Wickham’s Striae: Polygonal rash + ‘White lines’ pattern on surface
  • Koebner’s phenomenon (new skin lesion appearing on site of trauma)
  • Oral involvement (50% cases):White-lace pattern on buccal mucosa
  • Nails: Thinning, Longitudinal ridges
96
Q

Causes & Rx. of Lichen Planus ??

A

Lichenoid drug eruptions- causes:
- Gold, Quinine, Thiazides
Rx.
- Potent Topical Steroids
- Benzydamine mouth wash/spray
- Severe: Oral steroids or Immunosuppression

97
Q

What is Pemphigus vulgaris ??

A

Autoimmune disease caused by antibodies directed against
- Desmoglein-3 (Cadherin-type epithelial cell adhesion molecule)
MC in Ashkenazi Jewish pepole

98
Q

Features of Pemphigus Vulgaris ??

A

Mucosal ulceration (MC); Oral involvement in 50-70% pts.
Skin blistering
- Flaccid, easily ruptured vesicles & bullae
- PAINFUL but NOT Itchy
Nikolsky’s sign: Spread of bullae following application of horizontal, tangential pressure to the skin
ACANTHOLYSIS on biopsy

99
Q

Rx. for Pemphigus Vulgaris ??

A

1st line: STEROIDS
2nd line: Immunosuppressants

100
Q

What is Bullous Pemphigoid ??

A

Autoimmune condition causing Sub-epithelial blistering of skin secondary to development of antibody against
- Hemi-Desmosomal proteins BP180 & BP230
MC in Elderly

101
Q

Features of Bullous Pemphigoid ??

A
  • ITCHY, tense blisters typically at Flexures
  • Blisters heal without Scarring
  • NO Mucosal involvement (Mouth spared) BUT in reality, 10 to 50% have mucosal involvement
  • Exam purpose: mucosa not involved
102
Q

Ix. & Rx. of Bullous Pemphigoid ??

A

Dermatologist referral for biopsy & Dx. confirmation
- Skin biopsy: Immunofluorescence shows IgG & C3 at Dermo-epidermal junc.
Rx.
- Oral Corticosteroids (mainstay)
- Topical CS, Immunosuppressants & Abx. are also used

103
Q

Differentiate b/w
- Pemphigus Vulgaris
- Bullous Pemphigoid

A

BOTH are autoimmune diseases
- Antibodies (IgG) against Desmoglein 3; Mucosa inolved; PAINFUL but NOT Itchy; Ashkenazi Jewish
- Antibodies against Hemi-desmosamal proteins BP180, BP230; Mucosa NOT involved; ITCHY; Elderly

104
Q

What is Pemphigus & Pemphigoid ??

A
  • a/w Penicillamine & Captopril; tends to present as ulcers with fragile small blisters that quickly breakdown. Mouth & Genitals can be affected
  • Large flaccid blisters; DPP4 inhibitors is a/w Pemphigoid
105
Q

What is Stevens-Johnson Synd. ??

A

Severe systemic reaction affecting skin & mucosa ie. almost always due to DRUG Reaction
- Common in CHINESE/ Thai descents due to the presence of HLA-B1502
- Increased risk in European, a/w HLA-A3101

106
Q

Features of SJS ??

A
  • Maculopapular; typical ‘Target lesions’
  • May develop into vesicle/bullae
  • Mucosa involved
  • Fever, Artharlgia
107
Q

Drugs causing SJS ??

A

‘NO SLAP’
- NSAIDs. - OCPs
- Sulfonamides
- Lamotrigine, Carbamazepine, Phenytoin
- Allopurinol. - Penicillins
- INDAPAMIDE (it has Sulfonamide moiety)
Rx.
- Admit & Supportive care

108
Q

What is Toxic Epidermal Necrolysis ??

A

Life threatening skin disorder MC seen secondary to DRUG Reaction
- Skin develops a SCALDED appearance over an extensive area
- TEN is the extreme end of a spectrum of skin disorder which includes E multiforme & SJS

109
Q

Causes & Features of TEN ??

A

Causes
- NSAIDs. - Sulfonamides
- Carbamazepine, Phenytoin
- Allopurinols. - Penicillins
C/F
- Pyrexia, Tachycardia
- Nikolsky’s sign (+)ve

110
Q

Rx. of TEN ??

A
  • STOP ppt. factors
  • 1st line: IVIGs
  • Immunosuppressive agents (Ciclosporin, Cyclophosphamide)
  • Plasmapheresis
    Supportive care
    -ICU
  • Correct volume loss & electrolyte derangement
111
Q

Rx. of Hyperhidrosis ??

A
  • 1st line: Topical AlCl prep. (main s/e is skin irritation)
  • Iontophoresis (particularly useful in Palmer, Plantar & Axillary symptoms)
  • Botox for axillary symptoms
  • Endoscopic Transthoracic Sympathectomy (risk of compensatory sweating)
112
Q

What is Pompholyx ??

A

Dyshidrotic Eczema
Type of eczema that affects
- Hands: Cheiropompholyx
- Feet: Pedopompholyx
Ppt. by HUMIDITY (Sweating) & High Temp.

113
Q

Hallmarks of Pompholyx ??

A

‘Pt. has been on summer holidays in hot area where he was sweating a lot’
- Small blisters on Palms & Soles
- Pruritic; often intensely Itchy & Burning
- Once blisters burst, skin may become dry & crack

114
Q

Rx. of Pompholyx or Dyshidrotic Eczema ??

A

Cool compresses
Emollients
Topical Steroids

115
Q

What is Seborrhoeic Dermatitis ??

A

Chr. dermatitis due to proliferation of normal skin commensal MALASSEZIA Furfur (formerly-Pityrosporum Ovale)

116
Q

Features of Seborrhoeic Dermatitis ??

A

Eczematous lesions on sebum rich areas
- Scalp (may cause dandruff)
- Periorbital, Auricular & NL folds
- O Externa & Blepharitis may occur
a/w HIV & Parkinson’s disease

117
Q

Rx of Seborrhoeic Dermatitis ??

A

Scalp disease
- 1st line: Zn Pyrithione (Head & Shoulders) & Tar (Neutrogena T/Gel)
- 2nd line: Ketoconazole
- Selenium sulphide & Topical CS
Face & Body disease
- Topical Antifungals: Ketoconazole
- Topical Steroids: for Short period
- RECURRENCE is common

118
Q

What is Nickel dermatitis ??

A

Type 4 HS reaction
- Caused by jewelry (eg.- Watches)
Dx.- SKIN PATCH test

119
Q

What are the 2 main types of Contact Dermatitis ??

A

Irritant CD (Common)
- Non allergic
- Due to Weak acids & alkalis (eg. detergents)
- Common in Hands
- ERYTHEMA is typical
Allergic CD
- Type 4 HS reaction
- Uncommon- seen on head after hair dye
- Acute weeping eczema, predominantly affects Hairline MARGINS rather than Scalp itself

120
Q

What kind of dermatitis is seen with Cement exposure ??

A

BOTH types
- Its Alkaline nature: Irritant CD
- Dichromates in cement: Allergic CD

121
Q

What is Eczema Herpeticum ??

A

Severe primary infection of skin by Herpes Simplex V 1 or 2
- MC in Children with atopic eczema
- Rapid progressing Painful Rash
- Monomorphic, punched out erosions (circular, depressed, ulcerated lesions)
- 1 to 3 mm in diameter

122
Q

Rx. of Eczema Herpaticum ??

A

Life threatening in Children
- Admit + IV Aciclovir

123
Q

What is Dermatitis Herpetiformis ??

A

Autoimmune Blistering skin disorder a/w Coeliac disease
- Caused by IgA Deposition in Dermis (dermal papillae).
Itchy vesicular skin lesions on extensor surfaces (elbows, knees, buttocks)

124
Q

Ix. & Rx. of Dermatitis Herpetiformis ??

A

Skin biopsy:
- Direct Immunofluorescence shows “Granular pattern IgA deposition in Upper DERMIS”
Rx.
- Gluten free diet
- DAPSONE

125
Q

What is Acne Rosacea ??

A

Rosacea is a chronic skin condition of unknown aetiology
- Site: Nose, Cheeks & Forehead
- 1st sign: Flushing => later persistent Erythema with papules & pustules
- Rhinophyma
- Blepharitis
- Sunlight can exacerbate symptoms
- Telangiectasia are common

126
Q

Rx. of Acne Rosacea ??

A
  • Mild (limited no. of papules, pustules, NO plaques) : Topical Metronidazole & Azelaic acid
  • Flushing predominant + limited Telangiectasia: Topical Brimonidine gel
  • More severe: Systemic Abx. Oxytetracycline
  • Prominent Telangiectasia: Laser
  • High factor Sun-screen
  • Rhinophyma: Dermatology referral
127
Q

What is Acne Vulgaris ??

A

Common skin disorder- Adolescence
- Site: face, Neck, Upper trunk
Follicular epidermal hyper-proliferation=> Keratin plug formed => obstructs Pilosebaceous follicle ==> causes Comedones, Inflam. & Pustules
PROPIONOBACTERIUM Acne colonization

128
Q

Rx. of Acne Vulgaris ??

A
  • Single topical therapy (Retinoids, Benzoyl peroxide)
  • TOPICAL combination therapy (Abx., Benzoyl peroxide, Retinoids)
  • Oral Abx. (Single oral Abx. for 3 m)
  • COCPs are an alternative to Oral Abx. in women
  • Oral Isotretinoin (Specialist supervision) [Topical & oral forms are CI in Pregnancy]
129
Q

What are the Oral Abx. used in Acne Vulgaris ??

A

TTCs: Lymecycline, OxyTTC, Doxy.
- Avoided in: Pregnant/ Breastfeeding < 12yrs old
ERYTHROMYCIN is used in Pregnancy
Topical Retinoids/ Benzoyl peroxide is always co-prescribed with Oral Abx.
[Topical + Oral] Abx. - NOT used
Gram (-) Folliculitis can occur with long term Abx. use => High dose Oral TRIMETHOPRIM

130
Q

How is COCPs used as a Rx. in Acne Vulgaris ??

A

used in combination with Topical agents
- 2nd line: CO-CYPRINDIOL (Dianette) is used as it has Anti-androgen property (But increased risk of VTE compared to other COCPs) & is only given for 3 months.

131
Q

What is Pellagra ??

A

Skin condition due to Nicotinic acid (Niacin, Vit B3) deficiency
Causes
- Isoniazid {Tryptophan ==(-)==> Niacin}
- Alcoholics

132
Q

Features of Pellagra ??

A

4 D’s
- Dermatitis: Brown scaly rash on SUN-exposed sites- Casal’s necklace if around neck
- Diarrhoea
- Dementia, Depression
- Death (if not treated)

133
Q

What is Porphyria Cutanea Tarda (PCT) ??

A

It is the most common HEPATIC Porphyria
- Inherited defect in Uroporphyrinogen decarboxylase (or)
- Hepatic damage eg.- Alcohol, HCV, Oestrogen

134
Q

Features of Porphyria Cutanea Tarda ??

A
  • PHOTOSENSITIVE Rash with Blistering
  • Skin fragility on Face & Dorsal Hands (MC feature)
  • Hypertrichosis
  • Hyperpigmentation
135
Q

Ix. for Porphyria Cutanea Tarda ??

A

Urine: elevated Uroporphyrinogen
Wood’s Lamp: Pink fluorescence of urine
Guide therapy: S. Iron Ferritin levels

136
Q

Rx. of Porphyria Cutanea Tarda ??

A
  • Chloroquine
  • Venesection (preferred if iron ferritin >= 600 ng/ml)
137
Q

How does Zinc deficiency manifest ??

A

Acrodermatitis Enteropathica
- A R inherited defect of intestinal Zn absorption

138
Q

Features of Acrodermatitis Enteropathica ??

A

Acrodermatitis: Red, crusted lesions
- Acral distribution
- Peri-orificial
- Peri-anal
Short stature, Hypogonadism
Alopecia
Hepatosplenomegaly
GEOPHAGIA (Clay/Soil ingestion)
Cognitive impairment

139
Q

What is Pyogenic granuloma ??

A

aka Eruptive Haemangioma
- BENIGN skin condition
- Its a misnomer (they are neither true granuloma nor pyogenic)
- MC in Women & Young adults

140
Q

Features of Eruptive Haemangioma aka Pyogenic granuloma ??

A

Linked to Trauma & Pregnancy
- Site: Head/Neck, Upper trunk & Hands
- Oral mucosa lesions (common in Pregnancy)
Initially- Small red/brown spot
Rapidly progresses in days to weeks forming Raised, red/brown lesion, spherical in shape
Can bleed profusely/ ulcerate

141
Q

Rx. of Eruptive Haemangioma aka Pyogenic Granulona ??

A
  • Lesions a/w pregnancy: often Resolve Spontaneously
  • Other lesions usually persists
  • Excision, Curettage & Cauterisation, Cryotherapy
142
Q

Difference b/w Hirsutism & Hypertrichosis ??

A

Hirsutism: Androgen DEPENDENT hair growth
Hypertrichosis: Androgen INDEPENDENT hair growth

143
Q

Drug causes of
- Hirsutism ??
- Hypertrichosis ??

A
  • Androgen therapy, Phenytoin, Corticosteroids
  • Minoxidil, Ciclosporin, Diazoxide
144
Q

Choice of COCPs for Hirsutism ??

A

Co-cyprindiol (Dianette): not used on long term basis due to risk of VTE
Ethinylestradiol
Drospirenone (Yasmin)

145
Q

Rx. of Facial Hirsutism ??

A

Topical Eflornithine (CI in pregnancy & Breast-feeding)

146
Q

How to assess Hirsutism ??

A

Ferrimen-Gallwey Scoring System
- 9 body areas are assigned a score of 0-4; score > 15 = Moderate or Severe
[Note: MCC is PCOS]

147
Q

Causes of Hypertrichosis ??

A

Congenital Hypertrichosis lanuginosa
Porphyria Cutanea Tarda
ANOREXIA NERVOSA
Congenital Hypertrichosis terminalis
Drugs: Minoxidil, Ciclosporin, Diazoxide

148
Q

What is Livedo Reticularis ??

A

Caused by obstruction of capillaries resulting in swollen venules
- Purplish, Non-blanching, reticulated rash
- MCC is Idiopathic

149
Q

Causes pf Livedo Reticularis ??

A
  • Idiopathic (MCC)
  • PAN
  • SLE
  • Cryoglobulinaemia
  • APLA synd.
  • Ehlers-Danlos Synd.
  • Homocystinuria
150
Q

What is a Keloid & how is it treated ??

A

Tumour like lesion of scar, which arises from Connective tissue of a scar which extends beyond the original wound dimension
Rx.
- Early keloid: Intra-lesional Steroid injection eg.- Triamcinolone
- Excision

151
Q

Hallmark features of Keloid scar ??

A
  • More common in Dark skinned
  • MC in Young adults, less common in elderly
  • Sites: Sternum, Shoulder, Neck, Face, Trunk, Extensors of limbs

They are LESS likely to occur if incision is made along relaxed skin tension lines
- Langer lines: used to determine optimal incision lines (but produces WORSE cosmetic results than when following skin tension lines

152
Q

What is vitiligo ??

A

Autoimmune condition which results in loss of Melanocytes ==> Skin depigmentation
- Typically seen in 20 to 30 yrs old

153
Q

Features of vitiligo ??

A
  • Well demarcated, depigmented
    skin patches
  • PERIPHERIES (most affected)
  • Koebner’s phenomenon (+)ve - Trauma may ppt. new lesions
154
Q

What conditions are a/w Vitiligo & how is it treated ??

A

Type 1 DM, Addison’s disease
Autoimmune thyroid disease
Pernicious anaemia
Alopecia areata
Rx.
- Topical Steroids (can reverse if used early)
- Topical Tacrolimus & Phototherapy
- Sun-block for affected areas

155
Q

What is the difference b/w Scarring & Non-scarring Alopecia ??

A

Scarring: LOSS of hair follicle
Non-scarring: Hair follicle preserved

156
Q

What are the causes for Scarring alopecia ??

A
  • Trauma & Burns
  • Radiotherapy
  • LICHEN PLANUS
  • DISCOID Lupus (ANA negative)
  • Tinea capitis (if KERION develops in untreated cases)
157
Q

What is Telogen Effluvium ??

A

Hairloss following stressful period (eg. Surgery)

158
Q

What is Alopecia Areata ??

A

Autoimmune condition( increase INF-gamma ==> T-cell infiltration => Follicular epithelium damage) causes - Localised, well demarcated patches of hair loss
- Edge of hair loss: small, broken ‘exclamation mark’ hairs

159
Q

Rx. of Alopecia Areata ??

A

Eventually, the hair will grow back in majority pts.
- Topical/Intralesional Corticosteroids
- Topical Minoxidil
- Phototherapy
- Dithranol
- Contact immunotherapy

160
Q

In which skin lesions can Koebner’s phenomenon can be seen ??

A

Lichen Planus
Lichen Sclerosis
Molluscum Contagiosum
Psoriasis
Vitiligo
Warts

161
Q

Name the skin lesions seen on Shin

A

PEN
Pretibial myxoedema (Grave’s)
- Symmetric, Erythematous;
- Shiny, Orange peel skin
Pyoderma gangrenosum
Erythema nodosum
Necrobiosis Lipoidica Diabeticorum
- Shiny, painless yellow/red skin areas in diabetics
- a/w Telangiectasia

162
Q

What is Yellow nail synd. ??

A

Slowing of nail growth leads to the characteristic thickened & discoloured nails
a/w
- Congenital Lymphoedema
- Pleural effusion
- Bronchiectasis
- Chronic sinus infection

163
Q

What is 1 finger tip unit / Finger tip rule ??

A

0.5 g - sufficient to treat a skin area about 2x that of the flat of an adult hand

164
Q

What are the types of Vasculitides??

A

Large vessel
- Temporal arteritis
- Takayasu
Medium vessel
- Polyarteritis nodosa
- Kawasaki disease
Small vessel
- ANCA associated
- Immune complex associated

165
Q

What are the types of Small Vessel Vasculitides ??

A

ANCA associated
- Wegener’s granulomatosis (GPA)
- Churg-Strauss synd. (E-GPA)
- Microscopic Polyangitis
Immune Complex associated
- Henoch-Schonlein purpura
- Goodpasture’s synd.
- Cryoglobulinaemic vasculitis
- Hypocomplementemic Urticarial (anti-C1q vasculitis)

166
Q

Hallmark features of Venous ulceration ??

A

Typically seen above Medial malleoli
- ABPI is important in Non-healing ulcers (it assesses the arterial flow)
- > 1.4 : Calcified/hardened vessel
- 1.0 to 1.4 : Normal
- 0.9 to 1.0 : Acceptable
- 0.8 to 0.9 : Some arterial disease
- 0.5 to 0.8 : Moderate arterial disease
- < 0.5 : Severe arterial disease

167
Q

Rx. of Venous ulceration ??

A

Compression bandaging (4 layers) most effective
Oral Pentoxifylline (peripheral vasodilator, improves healing)
- Flavinoids
- Hydrocolloid dressings, topical GF, Ultrasound therapy & Intermittent Pneumatic compression

168
Q

What is Osler-Rendu-Weber synd. ??

A

Hereditary Haemorrhagic Telangiectasia
- Autosomal DOMINANT
- 20% occurs spontaneously
Multiple telangiectasia over skin & mucous memb.

169
Q

Diagnostic criteria of Osler-Rendu-Weber synd. ??

A

4 main criteria
- Epistaxis
- Telangiectasis
- Visceral lesion (GI telangiectasia, Pulm. AV malformation, Hepatic AVM, Cerebral AVM, Spinal AVM)
- Family Hx. (1st degree relative)
2/4 : Possible HHT
>= 3/4 : Definite HHT

170
Q

What is Lichen Sclerosus ??

A

aka L S et atrophicus
- Inflammatory condition that usually affects the genitalia & is more common in Elderly females
- Leads to atrophy of the epidermis with white plaques forming

171
Q

Features & Rx. of Lichen Sclerosus ??

A

White patches that may scar
ITCH is prominent
Pain during Intercourse or Urination
Rx.-
- Topical Steroids & Emollients

172
Q

Dx. of Lichen Sclerosus ??

A

Clinical basis + Biopsy (if atypical features are present)
- Skin Biopsy NOT necessary if Dx. can be made clinically & typical presentation
- Atypical presentation or Diagnostic uncertainity or Suspicion of Neoplasia (Hyperkeratosis, erosion, erythema or new warty or papular lesion)=> HISTOLOGY & Biopsy
Do BIOPSY if :
- Rx. failure
- Extragenital or overlap with Morphea
- Pigmented areas (to exclude abnormal melanocyte proliferation)
- Second line therapy has to be used

173
Q

Which cancer is commonly seen in pts. with Lichen Sclerosus ??

A

Vulval Cancer

174
Q

What is Pyoderma gangrenosum ??

A

Rare, non-infectious, Inflammatory disorder which causes painful ulcerations
- It is classified as Neutrophilic dermatosis: a skin condition characterised by dense infiltration of neutrophils in the affected tissue & is often seen on biopsy

175
Q

Causes of Pyoderma gangrenosum ??

A
  • IDIOPATHIC (50% cases)
  • IBD (10 to 15% cases)
  • RA & SLE
  • Myeloproliferative disorder, Lymphoma, Myeloid leukaemias, Monoclonal gammopathy
  • Granulomatosis with P
  • Primary Biliary Cirrhosis
176
Q

Features of Pyoderma gangrenosum ??

A

Site: Lower limbs (typical)
Soften at the site of a minor injury as this is known as Pathergy (Exageratted skin reaction to minor trauma => Papules, Pustules)
Initial c/f:- Sudden onset + Small Pustule, Red bump or Blood-blister
Later:
- Skin breaks => Ulcer (PAINFUL)
- Edge of ulcer: Purple, voilaceous & UNDERMINED
- Ulcer may become deep & necrotic
- Fever & Myalgia

177
Q

Dx. & Rx. of Pyoderma Gangrenosum ??

A

Characteristic appearance, a/w other diseases; presence of Pathergy & Histology
Rx.
- 1st line: Oral Steroids
- Immunosuppressive Rx.- Ciclosporin & Infliximab in severe cases
- ANY Sx. should be postponed until the disease is controlled

178
Q

What is Dermatitis Artefacta ??

A

Psycho-dermatological condition characterised by self-inflicted skin lesions. Pts. typically deny that these are self induced
- MC in Adolescents & Females
- a/w Personality disorders, Dissociative & Eating disorders
- 33% of pts. with Bulimia & Anorexia

179
Q

Features of Dermatitis Artefacta ??

A
  • Linear/ Geometric lesions; well demarcated from normal skin
  • Lesion appearance depends on mechanism of injury
  • Lesions appear suddenly eg- Overnight
  • Appear whole, complete & do not evolve over time
  • Multiple lesions at various stages of healing
  • Common sites: Face (specially cheeks), Dorsum of hand
  • Despite the severity of skin lesions, pt. is nonchalant, ‘la belle difference’ aka Mona lisa smile
  • H/o recent life events or triggers- marital dispute or bereavement
180
Q

Dx. of Dermatitis artefacta ??

A

Based on history & after exclusion of other skin conditions
Psychiatric assessment- to rule out Munchausen synd., Malingering

181
Q

Rx. og Dermatitis Artefacta ??

A
  • Good rapport
  • Co-managed by Dermatologist, Psychologist & Psychiatrists
  • SSRIs & CBT may be helpful
182
Q

What is Anagen Effluvium ??

A

Occurs when all hairs enter the ANAGEN phase of growth at the same time. This leads to Rapid hair loss; Seen in
- Cancer CT
- Radiotherapy
- Pemphigus vulgaris

183
Q

Virus causing Kaposi Sarcoma ??

A

Human Herpes Virus 8
- Multiple Red-brown Nodular lesions affecting arms, legs & torso
Rx. of skin lesions
- IFN alpha
- Liposomal Anthracyclines
- Paclitaxel

184
Q

What disease is caused by HHV 6 ??

A

Exanthem subitum aka Roseola infantum or Sixth disease
[Less commonly caused by HHV-7]

185
Q

Disease caused by the virus in HIV
- CMV
- EBV

A
  • Infectious Mononucleosis like synd., CMV retinitis
  • Reactivation of Lymphoma
186
Q

Resistant Eczema Rx. ??

A

Ciclosporin, Azathioprine & Mycophenolate mofetil