Skin Tumours😍

Broad Classification

  • Skin tumours:
    • Benign
    • Malignant

Benign Skin Tumours

Skin Tags:

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  • Description:
    • Loose fibrous tissue
    • dead skin
  • Identification: Common, identifiable by appearance

Syringomas:

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  • Mnemonic: Syrincoma () → comma cells → comma () yil kidakkunna aalde kannil synringe (periorbital are) vach valich → watery fluid () vann
  • Description: Benign tumour of the acrosyringium
    • eccrine sweat glands
  • Appearance:
    • Grouped, shiny
    • asymptomatic
  • Location: Periorbital area
  • Contents: Watery fluid
  • Borders: Angular
  • Histopathology:
    • Tadpole or comma cells

Dermatofibroma (Benign Fibrous Histiocytoma):

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  • Description: Solitary lesion
    • Hyperpigmented to skin colour
    • Round or oval shape
    • Papule, nodule, or plaque
  • Key Sign: Dimple sign
    • Dimpling in center when stretched
  • Location: Lower legs
  • Histopathology:
    • Storiform, cartwheel, or whorled pattern
      • Elongated spindle cells with elongated nuclei
      • Radiating from central point

Malignant Skin Tumours (Skin Cancers)

  • Types: Melanoma, non-melanoma
    • Non-melanoma:
      • BCC: No precursors
      • SCC: Has precursors

Non-Melanoma Skin Cancers

Precursors of SCC (Pre-lesions):

Actinic Keratosis (AK):

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  • Description: Small papules
    • Rough, scaly surface
    • Adherent yellowish crust
    • Pinpoint bleeding when crust removed
  • Premalignant
  • Location:
    • Photoexposed parts of elderly or white populations
    • Lips, forearms
  • Mnemonic: Actors Bleed when exposed

Bowen's Disease (Intraepidermal or In situ SCC):

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  • UV light exposed
  • Description: Malignant, stays in situ
    • Plaque with adherent crust
    • No pinpoint bleeding
  • Location:
    • Lower legs of elderly females
  • Mnemonic: Bowen → Bowing → Ladies, Legs

Squamous Cell Carcinoma (SCC):

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  • Origin: Epidermal keratinocytes or appendages
  • Commonality: Second most common skin tumour
  • Immunocompromised:
    • Commonest in these states (e.g., HIV, renal transplant)
  • Spread: Low rate of spread
    • Local, regional, distant

Presentation:

  • Varied
    • Papule, nodule, or ulcer with crusting
    • Photoexposed areas
    • Difficult to diagnose clinically

Histopathology:

  • Keratin pearls
    • notion image

Keratoacanthoma (KA):

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  • Mnemonic:
    • Akkante () Breast → well defined rounded mounted
    • Akkante () Lip (epidermal lipping) suck cheyth (SCC)
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  • Classical Feature:
    • Well-defined, round with central crater
    • Large papule/nodule
    • central keratinic crust/plug
    • Filled with necrotic keratinic material
  • Reclassification: Well-differentiated SCC with good prognosis
  • Location: Face (common), hands
  • Phases: Growth, maturation, resolution (resolves on its own)
  • Histopathology: Epidermal lipping
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Molluscum
Molluscum
  • Differentiation: Not to be confused with Henderson-Patterson bodies
    • molluscum contagiosum

Basal Cell Carcinoma (BCC) / Basalioma / Rodent Ulcer:

SCC → below line joining angle of mouth to earlobe
SCC → below line joining angle of mouth to earlobe
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Nodules
Nodules
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  • AKA Rodent ulcer / Basalioma
    • Vismayam → Vismodegib
Rodent ulcer
Hedgehog pathway inhibitor
Artificial (Artefact) Palaruvi (Peripheral True Palisading)
      Vismayam Vismodegib
      Rodent ulcer
      Hedgehog pathway inhibitor
      Artificial (Artefact) Palaruvi (Peripheral True Palisading)
  • Commonality:
    • Most common human cancer
  • Growth & Metastasis:
    • Very slow-growing
    • Very locally invasive
    • Rarely metastasizes (good prognosis)
  • A/w Gorlin syndrome
  • Origin: Basal layer of epidermis or follicular structures
  • Features:
    • Locally invasive (does not metastasize)
    • lymph nodes negative.
  • M/c subtype is Nodular

Clinical:

  • Most common site:
    • Face (medial canthus)
    • above line joining angle of mouth to earlobe
      • above a
        above a
  • Pearly nodule with 
    • rolled out edges, indurated margins.
  • Ulcer with
    • overhanging thready margins
  • Telangiectasias (fine blood vessels)
  • Bleeds on touch

Microscopic Features:

  • Peripheral True palisading.
  • Retraction artifact.
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Treatment for BCC:

  • Mohs micrographic surgery
  • Small, low-risk, or superficial:
    • Imiquimod,
    • 5-Fluorouracil,
    • Photodynamic Therapy (PDT),
    • intralesional alpha 2B therapy
  • Large or recurrent:
    • Wide local excision
  • Targeted:
    • Vismodegib (hedgehog pathway inhibitor)

Photodynamic Therapy (PDT)

  • Principle: Photosensitizer + light + oxygen → ROS → cell death.
  • Uses: Cancers, precancerous lesions, dermatology.
  • Advantages: Selective destruction, spares normal tissue.

Color changes:

  • Lesion remain unchanged or turn red dark brown/blackcrust falls off.

Malignant Melanoma

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Subungual melanoma
Subungual melanoma
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  • Origin: Melanocytes
  • Metastasis: Very common

Predisposing Factors:

  • UV radiation
  • white population,
  • Certain precursor lesions
  • Familial atypical mole melanoma syndrome.
  • Genetic: CDKN2A gene
  • Mnemonic:
    • Melanoma → ABCDE
    • CD Keettu enne → CDKN2A

Types:

Nodular melanoma
Nodular melanoma
Lentigo maligna
Lentigo maligna
Type
Description
Superficial spreading
• m/c in pre-existing mole
• Seen in
sun exposed areas
• e.g :
Subungual melanoma (Hutchinson sign)
Lentigo maligna
• In situ melanoma in elderly
Best prognosis
Insitu melanoma
Acral melanoma
• m/c in dark skinned patients
Nodular melanoma
Most aggressive, rapid vertical phase of growth
Worst prognosis
Amelanotic melanoma : Variant of nodular type

Hutchinson's

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  • HHerpes Zoster Ophthalmicus
  • UsubUngual Melanoma (superficial spreading melanoma)
    • Hutchinson sign
      • notion image
  • TTriad congenital syphillis
    • Peg shaped teeth
    • Interstitial Keratitis (IK + SNHL)
    • SNHL
  • CH Chauffeur's Fracture/Backfire Fracture
    • Intra articular #
  • Son looking olderHutchison Gilford
    • LMN A gene defect (laminopathy).
    • Progeria (onset: Child)
  • PUPIL Hutchinson Pupil
    • Herniation of uncus (medial temporal lobe) → compresses ipsilateral CN III → same side pupillary dilatation.
    • Kernohan’s notch phenomenon:
      • False localizing sign
        • Ipsilateral pupil dilatation
        • Ipsilateral UMN palsy

Precursor Lesions:

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  • Large congenital melanocytic nevi (CMN):
    • Trunk, especially >20 cm with satellite lesions
    • High chance of conversion
  • Junctional nevi: Highest risk of transformation
    • notion image
  • Atypical or dysplastic nevi

Investigations:

  • Biopsy (Confirmatory):
  • IHC markers
    • S-100, Melan-A, HMB-45.

ABCDE Changes (for pre-existing mole -> malignant transformation):

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  • Asymmetry: Mole asymmetrical
  • Borders: Irregular
  • Color: Different colours
  • Diameter: Larger than pencil eraser
    • >6 mm.
  • Evolution: Sudden changes in size, shape, colour

Staging:

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  • Clarke & Breslow:
    • Depends on depth of invasion.
  • TNM staging.
 

Management: 

  • Wide local excision.
  • Margins measured before excision, based on Breslow depth
  • Sentinel lymph node biopsy

Prognostic Factor: 

  • Lymph node status >>> Breslow thickness
  • mitotic rate, ulceration

  • Special Stains:
    • Masson fontana
    • Enzyme stain: 
      • Dopa oxidase.
    • Immunohistochemistry: 
      • HMB45
      • S100
  • Mnemonic: Her Brain was full of Black Malam (Brain has melanin in substantia nigra) → She was dumb (Mandana masson fontana)→ But Dope (Dopa oxidase) looking and good hump (HMB45) and base (Stratum basale)

Mycosis Fungoides (MF)

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  • Paul (Pautriers) tried sex (sesary) with
    • mike (mycosis) → 45 yr old and
    • dani (denileukin) → 4 yr old
    • → Into brain (cerebriform nucleus)
  • Description:
    • Cutaneous T-cell lymphoma (CTCL) variant
    • T-cell tumour in skin
  • Cell Proliferation:
    • CD4 positive &
    • CD45 RO positive helper T-cells
  • Course: Very indolent
  • Metastasis: Very commonly seen
  • Skin biopsy: 
    • Pautrier's microabscesses (cancer cell clusters).
      • Mnemonic: PM → MP (Pautrier's for Mycosis, Munro's for Psoriasis).
        Mnemonic: PM → MP (Pautrier's for Mycosis, Munro's for Psoriasis).
  • Blood spread → Sézary Syndrome.
    • Sézary cells with cerebriform nuclei (brain-like).
  • DNA analysis
    • Clonal arrangement of T cell receptor genes (TCR gene)Standard now
    • Mycoides → Fungal → Flower like
    • Fungoides → T cell cancer ⇒ Clonal arrangement of TCR

Clinical Presentation:

  • Location:
    • Trunk (central girdle),
    • upper lower limb
    • Central body
  • Stages:
    • Patches,
    • plaques,
    • tumour/nodular,
    • erythroderma

Sezary Syndrome:

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Triad

  1. Erythroderma
  1. Peripheral lymphadenopathy
  1. Sezary cells (>20% lymphocyte count OR >1000 cells/mm³)
      • Atypical lymphocytes
      • Grooved or cerebriform nucleus
      • Seen in tissue & blood
      • Mnemonic: Sezary cell → Sezary seed → middle groove (+)
  • Cerebriform appearance
    • Inverted papilloma → Thala (Cerebriform) thirinjavan

Histopathology:

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  • Epidermotropism:
    • Many T-lymphocytes in epidermis
  • Pautrier's microabscesses:
    • Collections of T-cells forming microabscesses in epidermis
    • Poultry → easily infected with fungus → fungoides
      • notion image

Treatment:

  • Total Skin Electron Beam Therapy (treatment of choice)

Newer Drug:

  • Denileukin Diftitox (IL2 fusion toxin)
  • Mnemonic: Di → Di → 2