Pediatric Dermatosis: Nevi
1. Verrucous Epidermal Nevi (VEN)

- Along Blaschko's lines
- Verrucous plaque
- Asymptomatic
- Present soon after or after birth
- Treatment: lasers
2. Inflammatory Linear Verrucous Epidermal Nevi (ILVEN)

- Aka: Eczematous Epidermal Nevi
- Linear and inflammatory
- More red, eczematous
- Resistant to usual treatment
- Needs topical steroid
3. Becker's Nevus

- Aka:
- Becker's Melanosis
- Pigmented Hairy Epidermal Nevi
- Presents in adolescence
- Starts as hyperpigmented lesion

- Develops hypertrichosis on lesion
- Role of androgen suspected
- Not congenital melanocytic nevi
4. Infantile Hemangioma

- Three stages:
- Growth:
- Usually at 3 months
- Maturation:
- Usually by 3-9 months
- Resolution:
- Starts at 9 months
- Leaves telangiectasias
- Capillary proliferations
- Appear as:
- Vascular lesions with telangiectasias
- Erythematous plaques
- Anywhere on body
- On nose:
- Pinocchio or Siren nose appearance

- Spontaneous resolution
- Treatment required if:
- Over vital organs
- Undergo ulcerations
- Bleeding
- Drugs for treatment:
- Systemic steroids
- propranolol
5. Capillary Malformations
Salmon Patch
- Aka: Erythema Nuchae, Stork Bite
- Autosomal dominant inheritance
- Very common condition
- Reddish patch
- On neck or face
- Usually resolves by 1 year
- Area of erythema and telangiectasia
- On nape of neck or face

Port-wine Stain


- Aka: Nevus Flammeus
- Capillary malformation
- Strict midline demarcation
- Stable course (keeps growing)
- Does not resolute
- Strictly unilateral
- Commonly on face
- Very vascular reddish patch
Treatment:
- Lasers (pulse dye laser)
Associated with Sturge-Weber Syndrome:

- Neurocutaneous are AD except
- Sturge Weber → Sporadic → GNAQ mutation
ㅤ | Seen in |
GNAS | • Mccune Albright • Cardiac Myxoma |
GNAS 1 | • Pseudohypoparathyroid/ Albright Hereditary Osteodystrophy |
GNAQ | • Sturge Weber (Sporadic) |
- Port-wine stain in trigeminal distribution
- Leptomeningeal Angiomatosis (ipsilateral)
- cavernous angioma (vascular malformation).
- Convulsions (Focal)
- behavioural problems,
- Mental retardation
- Choroidal Hemangiomas
- Ocular complications
- ipsilateral glaucoma,
- blindness,
- congestion
- Buphthalmos
- Unilateral weakness
- d/t tumor compressing corticospinal pathway.
CT scan:
- S-shaped intracranial calcifications
- S for Sturge-Weber, S for S shaped


- Tram track appearance or rail road calcification
- NOTE: Also seen in
- membranoproliferative glomerulonephritis,
- bronchiectasis.
- Mnemonic: Web of storage (Sturg Weber) of Portwine factories () → connected by rail tram tracks (Tram track apearance)
Urticaria Pigmentosa


- Urticarial wheals with pigmentation
- Form of cutaneous mastocytosis (increased mast cells)
- CD 117/CKIT
- Usually in children < 2 years
- No systemic involvement
- Typical urticarial itchy wheals on trunk
- Heal with pigmentation
- Itching due to increased mast cell
Darier's sign:
- Not a feature of Darier's disease
- Stroking skin with blunt object causes linear urticarial wheals
- Due to histamine release from mast cells
Biopsy caution:
- Anesthesia can degranulate mast cells
Urticaria and Angioedema
Urticaria
- Erythematous, edematous, itchy papules and plaques
- Evanescent
- disappears in hours, no marks
- High IgE causing mast cell histamine release
Acute Urticaria: < 6 weeks
- Causes (mnemonic: 5 Is):
- Infections
- Injections (or drugs)
- Inhalation
- Ingestion (food items)
- Idiopathic
Chronic Urticaria: > 6 weeks
- Mostly physical in nature
- Includes Urticarial Vasculitis
Physical Urticaria

1

- Most common chronic type
- Physical force causes urticaria
Dermographism (most common)
- Skin writing, linear itchy wheals on stroking

Other forms:
- Cold Urticaria (cold)
- Heat Urticaria (heat)
- Solar Urticaria (sun)
- Aquagenic Urticaria (water)
- Cholinergic Urticaria (increase in core body temperature)
- Delayed Pressure Urticaria (pressure)
- Appears later, painful, lasts > 24 hours
Treatment of Urticaria

- First line: Second-generation H1 antihistamines (standard dose)
- If no response: Increase dose to four-fold
- If still no response:
- Add omalizumab,
- cyclosporin,
- montelukast, or
- first-generation antihistamines
4. Omalizumab
- Monoclonal antibody against IgE
- Used for
- Urticaria
- prophylaxis of severe persistent Bronchial asthma
- Not effective in atopic dermatitis
- Given subcutaneously
- Kochinu asthma (asthma) vannapo maran Om Kreem (Om) kuttichathaennu prnj ammumma
Urticarial Vasculitis

- Differences from typical urticaria:
- Lesions more persistent (> 24 hours)
- Heal with pigmentation
- More tender than itchy
- Form of chronic urticaria, actually vasculitis
- Biopsy: Leukocytoclastic vasculitis
- Associated with connective tissue disorders and malignancies
Angioedema

- Swelling of skin or mucosa
- Deeper, less defined, more painful, less erythematous
- Hypodermis and submucosa involvement
- Takes longer to resolve
- Can be:
- Mast cell mediated:
- With urticaria, treated like urticaria
- Bradykinin mediated: Just angioedema
Hereditary Angioedema (HAE)

- Also: Quincke's Disease
- Autosomal dominant
- Bradykinin mediated
- NOT HISTAMINE MEDIATED
- Defect: C1 esterase inhibitor deficiency
- Leads to uncontrolled complement cascade
- C1 inhibitor normally controls C1 pathway.
- Deficiency → uncontrolled complement → episodic swelling (edema).
- Types based on C1 inhibitor:
- Type 1: Low C1 inhibitor protein concentration
- Type 2: Loss of C1 inhibitor function (quantity normal)
- Type 3: Normal C1 inhibitor → Factor 12?? (unknown defects)
- Presentation:
- Recurrent laryngeal edemas
- Colicky abdominal pain
- Recurrent angioedema
- Positive family history
- Evaluation:
- Screening: Low C4 level
- Specific: C1 inhibitor levels
- Treatment:
- Acute: Airway management
- IV C1-esterase inhibitor concentrate (C1-INH)
- Fresh frozen plasma (contains C1 inhibitor)
- DOC: Danazol
- Icatibant, Ecallantide
- Lanadelumab
- Ee kaatile Ee kallan Anade adyil
- Prophylaxis: Tranexamic acid, anabolic steroids
- Anabolic steroid Danazol may help.
Vector-Borne Diseases
Leishmaniasis
- Protozoal disease
- Vector: Sandfly
- Three types:
- Cutaneous,
- Mucocutaneous,
- Visceral (Kalazar)
Old World Cutaneous Leishmaniasis

- Endemic to India (NE, Rajasthan)
- Also: Delhi Boil, Baghdad Boil
- Caused by (mnemonic: MAIT):
- L. Major
- L. Tropica
- L. Aethiopica
- L. Infantum
- Seen in exposed areas
- Typical lesion: Annular lesion with crusting
- Papule -> ulcerates -> crusts

New World Cutaneous Leishmaniasis

- Seen in Mexico
- Caused by L. Mexicana
- Chronic ear cartilage ulcer: Chiclero's Ulcer
Mucocutaneous Leishmaniasis

- Destruction of nasal and oral mucosa
- Grossly deformed condition: Espundia
Post-Kalazar Dermal Leishmaniasis (PKDL)



- Consequence of visceral leishmaniasis
- Develops 1-2 years after treatment.
- Presents as hypopigmented nodules.
- History of kalazar (fever, splenomegaly, hepatomegaly) in childhood
- Develops years later
- Caused by: L. Infantum, L. Chagasi, L. Donovani
- Endemic to NE India
- Lesions:
- Raindrop-like hypopigmented lesions on trunk
- Succulent erythematous papules and nodules around muzzle area of face
- Not leprosy (no loss of sensation)
Smear:
- Leishman in Donovan bodies
- LD bodies, amastigote form in macrophages

Treatment:
- DOC: Oral Miltefosine
- Antimonials,
- Amphotericin B,
Erythema Chronicum Migrans (ECM)
- Cutaneous feature of Lyme Disease
- Caused by spirochete Borrelia burgdorferi
- Vector: Ixodes ticks
Presentation:

- Erythema
- Central bite usually present
- Expanding erythema from bite
- Clears centrally within a week
- Advances up to 50 cm diameter
Classical sign:
- Bite in center, expanding ring
Common Tests
Test | Method | Applications |
Diascopy | Press glass slide against skin | 1. Differentiate purpura (non-blanchable) and erythema (blanchable) |
ㅤ | ㅤ | 2. Differentiate Nevus Depigmentosus and Nevus Anemicus |
ㅤ | ㅤ | 3. See apple jelly nodules in granulomatous disorder |



Woods Lamb Examination

Mnemonic:
- NO (9% Nickel oxide) Bullshit (Barium silicate) in Woods
- 365 days (365nm) in wood
- Woman with green cap (tinea capitis green), yellow beaded pedant (yellow versicolor) around neck and red bikini (red → erythrasma) inside a forest full of wood (Woods lamp)
- Low output mercury arc lamp
- Covered with Wood’s filter (barium silicate + 9% nickel oxide)
- Emits UV light (320–450 nm, peak 365 nm)
- Clinical Uses:
Condition | Wood’s Lamp Finding |
Vitiligo | Lesions accentuate |
Tinea capitis | Greenish fluorescence |
Pityriasis versicolor | Yellow fluorescence |
Erythrasma | Coral red fluorescence |
Congenital erythropoietic porphyria | Reddish fluorescence |
Melasma | Differentiates epidermal vs dermal types |





Skin Biopsy Types
- Incision biopsy:
- Small part of lesion excised
- Shave biopsy:
- Superficial;
- seborrheic or actinic keratosis
- Punch biopsy:
- Most common
- Uses circular punch of various sizes
- Area is sutured after removal
- Excision biopsy:
- For suspected malignancy
- Entire lesion is removed

