Skin😍

Skin

Types of Ulcers (Based on Edge)

  • Sloping
    • Venous ulcer, healing ulcer.
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  • Punched out:
    • Arterial ulcer, neuropathic ulcer, bed sores, syphilis.
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  • Undermined:
    • TB ulcer.
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  • Rolled out:
    • Basal cell carcinoma (Rodent ulcer),
    • Marjolin's ulcer.
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  • Cauliflower:
    • Squamous cell carcinoma.
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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)

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
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  • 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
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  • 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)

 

Marjolin's Ulcer

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  • Low-grade squamous cell carcinoma arising from:
    • chronic venous ulcers (e.g., venous ulcer)
    • Post-burn scar
    • Chronic osteomyelitis
    • Post-radiation ulcer
  • Slow growing
    • Due to being relatively avascular
  • Painless
    • Due to absence of nerves in scar tissue
  • No secondary deposits
    • Due to no lymphatics in scar tissue
  • Radioresistant
    • Due to avascularity

Management:

  • Wedge biopsy
  • Wide Local Excision (WLE).

Erythrasma

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  • Contributing factors:
    • Warm and humid environments
    • Poor hygiene
  • Appearance: Red or brown patches
  • Organism features:
    • Corynebacterium minutissimum
    • Gram-positive bacterium
    • Colonizes the skin
  • Common sites:
    • Groin
    • Armpits
    • Between toes

Soft Tissue Sarcoma (STS)

Site of Soft Tissue Sarcoma in Order

  • Lower limb (Commonest site) > Upper limb > Trunk > Retroperitoneum > Head and neck.

Most Common Types:

  • Overall STS:
    • Liposarcoma.
  • M/c Retroperitoneal tumor
    • Liposarcoma
  • STS in children:
    • Rhabdomyosarcoma.
  • STS in males:
    • Malignant fibrous histiocytoma.

Clinical Features: 

  • Lump/mass (most common).

Spread: 

  • Hematogenous > Lymphatic (Rare).
    • Limbs to Lungs.
    • Retroperitoneum to Liver.
  • Exceptions (STS spreading to LN)
    • Mnemonic: MARCES:
      • Malignant fibrous histiocytoma
      • Angiosarcoma
      • Rhabdomyosarcoma
      • Clear cell
      • Epithelioid
      • Synovial
    • Management for these:
      • Lymph node (LN) clearance.

Investigations:

  • Tru-cut/Core biopsy (Confirmatory).
  • Staging: PET-CT.

Management: 

  • Wide local excision + Radiotherapy + Chemotherapy.

Prognostic Factor: 

  • Grade of tumor (most important)

Desmoid Tumour

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  • Type: STS of anterior abdominal wall.
  • Location: Seen at scar sites.
  • Features: Increased chances of recurrence.
  • Association: Gardner Syndrome.
  • Management: Wide local excision.

Gardner Syndrome

  • Skin: Sebaceous cysts.
  • Fibrous tissue: Fibromas.
  • Bone: Osteomas.
  • Dental: Supernumerary teeth
  • GI: Intestinal polyposis.
  • Desmoid tumor
  • Mnemonic: Gardener (gardening through body layers)

Fibrosarcoma

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  • Microscopic Pattern: Herringbone pattern
  • Hypoglycemia - Paraneoplastic syndrome
  • Mnemonic: Fibrosarcoma → Tiger nte skin (pattern similar app.) um bonum (Herringbone) vachitulla fiber

Leiomyosarcoma (Smooth Muscle Cancer)

  • Mnemonic:
    • Leo (Leomyosarcoma) → Vijay (Vimentin) with Cigar (Cigar shaped nuclei) → smooth (smooth muscle) actor (Actin positive)
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  • Malignant smooth muscle tumor.
  • Microscopic: Nuclei appear like cigars.
  • M/c Smooth muscle sarcoma of Stomach
  • IHC Stains: 
    • Vimentin positive (all sarcomas) and 
    • Smooth muscle actin positive.
  • Exhibits cigar-shaped nuclei.
    • Cigar-shaped nuclei seen in
      • anything to do with smooth muscle
        • Normal smooth muscle
        • Leiomyoma
        • Leiomyosarcoma
  • Diagnostic criterion for Leiomyosarcoma
    • Mitosis (≥ 10 mitosis per 10 HPF).

Rhabdomyosarcoma (Skeletal Muscle Cancer)

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  • Embryonal Rhabdomyosarcoma:
    • Known as Sarcoma Botryoides.
    • "Botryoides" means grape-like 
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  • Microscopic:
    • Cambium layer (cells accumulated in one area).
    • Cells are very long → strap cells or tennis racket cells.
  • Special Stain: 
    • PTAH (Phosphotungstic Acid Haematoxylin).
      • "PTAH" sounds like "pai" (strength for skeletal muscle).
  • IHC Stains: 
    • Vimentin positive 
    • Desmin positive
    • MyoD positive.
  • Mnemonic: Rhabdomyosarcoma → → Sar (Vimal (Vimentin)) →
    • Tennis (Tennis racket cells) kambiyil (Cambium layer) strap chyth → Ptah (PTAH → Phosphotungistic acid hematoxylin) nnu adich
    • Myran (myoD) Desp (desmin) ayi

Tennis Racket Appearance

 
Condition
Context / Type
Rhabdomyosarcoma
Skeletal muscle tumor
Langerhans cell histiocytosis
Seen on electron microscopy
Giardia lamblia
Parasite (microbiology)
Clostridium tertium
Bacteria (not tetani)
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Angiosarcoma

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  • Most Common Organ:
    • Most commonly in the liver.
  • Most common cause for malignant cancer of heart in adults
  • Causes: VAT chemicals:
    • V: Vinyl chloride (plastics, polyvinyl chloride).
    • A: Arsenic (pesticides).
    • T: Thorotrast (thorium-based contrast dye, old radiology use).
      • Thorotrast,
        • Thorotrast linked to
          • HCC,
          • cholangiocarcinoma &
          • renal cell carcinoma.
          • Angiosarcoma (VAT → Plastic)
  • Histology:
    • Anastomosing vascular channels.
    • Highly pleomorphic cells.
  • IHC markers:
    • von Willebrand factor.
    • Factor VIII.
    • VEGF.
    • CD31 (PCAM)
  • Mnemonic: Plastic (Plastic industry) ittu Vaattan (VAT) poyapo Liveril blood cancer vannnu

Stewart-Treves Syndrome/Lymphangiosarcoma

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  • Development:
    • Angiosarcoma
    • Long Standing (8-10 years) Lymphedema
  • Features:
    • Bluish/reddish skin nodules.
  • Increased Incidence: 
    • LN removed above axillary vein
    • RT given to axilla after clearance