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MALIGNANT TUMORS OF SKIN
DR MUKHILESH R M.S.,
Salient Features Of Skin Malignancies
 Most commonly epidermal origin

 Basal cell carcinoma
 Squamous cell carcinoma
 Malignant melanoma
 Skin adnexal tumors are rare.
 Chemical carcinogens play a major role.
Basal Cell Carcinoma
 Most common skin tumor, originates from basal layer of epidermis
 Slowly growing , locally invasive – RODENT ULCER.
 26 histological variants.
 Most common are
 Nodular

 Superficial speading
 Infiltrative
 Pigmented & Morpheaform
Predisposing factors
UV rays

Arsenics,
coal , tar

BCC
White
skin,
genetics

Middle
aged,
men
Pathogenesis
 No apparent precursor lesion
 Locally infiltrative.
 Rarely metastasise.
 Never lympatic spread
 Ovoid cells in nests with outer pallisading layer.
Contd…
 Nodulocystic
 Waxy , cream coloured with rolled, pearly borders
surrounding central ulcer.
 Morpheaform
 Type IV collagenase and spread rapidly
 Flat, plaque like lesion
 Basosquamous variant
 Highly aggressive

 Metastasize similar to SCC and aggressive treatment required.
Prognosis
 High risk BCC

 >2cm
 Specific location – nose , ear, eyes
 Ill-defined margins

 Recurrent tumors
 immunosuppression
Management of BCC
 Surgical VS Non Surgical

 Non surgical
 Curettage
 Electrodessication
 Laser vapourisation
 Destroy any potential tissue sample for pathological confirmation and
margin analysis
Surgical Management
 Complete tumor removal , with pathological confirmation and margin analysis.

 Large tumors invading adjacent structure with aggressive histology – WIDE LOCAL EXCISION
 0.5-1cm margin
 Reconstructive procedures
MOHS Micrographic Surgery
 Excision of skin cancer under microscopic control.

 Minimise recurrent rates with maximum conservation.
 Indicated in
 Poorly demarcated,
 Recurrent / incompletely excised
 Near vital structures

 Can also be used for SCC, lentigo maligna,DFS
Contd…

Under local
anesthesia
Saucerising excision
of primary tumor

Sample and defect
are marked and
oriented
Stained with H&E.

Examination of
slide for residual
tumor

Excise more tissue
from mapped area.
Contd…
Other Modalaties
 Radiotherapy

 Topical treatments
 5-fluorouracil
 Imiquimod
 Cryotherapy
Cutaneous Squamous Cell Carcinoma
 Malignant tumor of keratinising epithelium of epidermis

 2nd most common tumor
 Cumulative sun exposure and damage
 Associated with pre-existing scars, osetomyelitis, burn.
 Marjolin’s ulcer
Pathogenesis
Sun exposure

Scars and
sinuses

Chemical
carcinogens

SCC

Tobacco use

HPV 5 & HPV
16
Pathology
 Smooth nodular to verrucous , papillamatous and ulcerating lesions.

 Everted edges and surrounded by inflamed, indurated skin.
 Distant metastasis.
 Secondary lymph nodes involvement.
Differential Diagnosis Of SCC
 Actinic keratosis

 BCC
 Keratoacanthoma
 Pyoderma gangrenosum
 Warts
Microscopic Appearance
 Irregular masses of squamous epithelium proliferate and invade dermis.

 KERATIN PEARLS
 Perineural / vascular invasion
 Positive for cytokeratin 1 and 10
 Border’s histological grading
 Ratio of pleomorphic and anaplastic to normal cells
Prognosis
 Invasion
 Depth – deeper lesion , worse the prognosis
 Surface size - >2 cm
 Histological grade
 Site
 Lips and ears – increase recurrent rate
 Immunosuppression
 Perineural and vascular involvement

 Aetiology
TNM Classification
Size
• T1 - <2cm
• T2 - 2-5 cm
• T3 - >5cm
• T4 - muscle or
bone
involvement

Nodes
• N0 - no
regional
nodes
• N1 - regional
nodes

Metastasis
• M0 - no
metastasis
• M1- distant
metastasis

Grade
• G1- low grade
• G2moderately
differentiated
• G3- high
grade
Management
 Surgical excision – accurate histology

 Margins to be assessed
 4mm clearance for <2cm
 1 cm clearance for >2cm
 Radiotherapy resistant – Veruccus carcinoma
Malignant Melanoma
 Cancer of melanocytes

 Wherever melanocytes exist
 Bowel mucosa
 Retina
 Leptomeninges
Macroscopic Features In Nevi
Suggesting Malignant Melanoma
Contd…
 Tingling

 Itching
 Serosanguinous discharge
 Blood supply
 Melanomas >1mm have blood supply – doppler positive pigmented
lesion
Types Of Malignant Melanoma
 Superficial spreading

 Nodular melanoma
 Lentigo maligna melanoma
 Acral lentiginous melanoma
 Amelanotic melanoma
 Desmoplastic melanoma
Superficial Spreading Melanoma
 Commonest type – 70%

 Arise from pre – existing nevus
 Rapid growth of darker pigmented are in a junctional nevus.
 Predominantly radial growth phase.
 Nodularity can occur – vertical growth phase.
Nodular Melanoma
 More aggressive

 Increased vertical growth than radial phase
 Middle age men.
 Usually trunk.
 Sharply demarcated, blue-black papules 1-2cm.
 Lack horizontal growth phase.
Lentigo Maligna Melanoma
 Hutchinson’s melanotic freckle

 Slow growing, variegated, brown macule
 Intense sun exposure.
 Women > men
 Less metastaic potential
 Better prognosis
Acral Lentiginous Melanoma
 Soles of feet and palms of hand
 Rare in white skinned people
 Flat, irregular macule.
 Can mimic a fungal infection
 Biopsy of the nail matrix rather than just the pigment.

 Hutchinson’s sign nail-fold pigmentation then widens progressively to
produce a triangular pigmented macule with nail dystrophy.
Miscellaneous
 Amelanotic melanoma
 Not pigmented
 Poor prognosis

 Desmoplastic melanoma
 Head and neck
 Perineural invasion

 High recurrent rate
Histology
 Malignant changes of melanocytes in basal epidermis
 Horizontal growth phase – cells spread along the dermo-epidermal
junction
 Vertical growth phase – dermis may be invaded and increased metastatic
potential.
 Satellite nodules
 Lesions situated with in 2-5cm of the primary
 Intransit lesions
 Situated >5cm , proximal to lymphnode basin
Management
 History and clinical examination

 Excision biopsy with 2mm margin of skin and subdermal fat.
 Incisional biopsy – large lesion / facial lesions where excision results in
scarring.
 Staging of melanoma
 Clarkes’ staging

 Breslows’ classification
Staging Of Melanoma
Management Of Malignant Melanoma
Pigmented
lesion
Biopsy

Diagnosis of melanoma
<1mm depth
Excision - 1cm
margin

2-4mm
depth
Excision -2cm
margin

>4mm depth
Excision – 3cm
margin
Management of lymphnodes
 Based on breslow thickness.

 <1mm least beneficial with prophylactic dissection.
 >4mm increased chance of both lymphatic and distant metastasis.
 Intermediate thickness
 Elective prophylactic lymph node dissection
 Sentinel lymphnode biopsy
Sentinel Lymphnode Biopsy
Sentinel Lymphnode Biopsy
Other Modalities
 Chemotherapy

 Melphalan
 Vemurafenib
 Isolated limb perfusion therapy

 Immunotherapy
 IFN / TNF ALPHA
 Radiotherapy
Malignant tumors of skin

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HỌC TỐT TIẾNG ANH 11 THEO CHƯƠNG TRÌNH GLOBAL SUCCESS ĐÁP ÁN CHI TIẾT - CẢ NĂ...HỌC TỐT TIẾNG ANH 11 THEO CHƯƠNG TRÌNH GLOBAL SUCCESS ĐÁP ÁN CHI TIẾT - CẢ NĂ...
HỌC TỐT TIẾNG ANH 11 THEO CHƯƠNG TRÌNH GLOBAL SUCCESS ĐÁP ÁN CHI TIẾT - CẢ NĂ...
 

Malignant tumors of skin

  • 1. MALIGNANT TUMORS OF SKIN DR MUKHILESH R M.S.,
  • 2. Salient Features Of Skin Malignancies  Most commonly epidermal origin  Basal cell carcinoma  Squamous cell carcinoma  Malignant melanoma  Skin adnexal tumors are rare.  Chemical carcinogens play a major role.
  • 3. Basal Cell Carcinoma  Most common skin tumor, originates from basal layer of epidermis  Slowly growing , locally invasive – RODENT ULCER.  26 histological variants.  Most common are  Nodular  Superficial speading  Infiltrative  Pigmented & Morpheaform
  • 4. Predisposing factors UV rays Arsenics, coal , tar BCC White skin, genetics Middle aged, men
  • 5. Pathogenesis  No apparent precursor lesion  Locally infiltrative.  Rarely metastasise.  Never lympatic spread  Ovoid cells in nests with outer pallisading layer.
  • 6. Contd…  Nodulocystic  Waxy , cream coloured with rolled, pearly borders surrounding central ulcer.  Morpheaform  Type IV collagenase and spread rapidly  Flat, plaque like lesion  Basosquamous variant  Highly aggressive  Metastasize similar to SCC and aggressive treatment required.
  • 7. Prognosis  High risk BCC  >2cm  Specific location – nose , ear, eyes  Ill-defined margins  Recurrent tumors  immunosuppression
  • 8. Management of BCC  Surgical VS Non Surgical  Non surgical  Curettage  Electrodessication  Laser vapourisation  Destroy any potential tissue sample for pathological confirmation and margin analysis
  • 9. Surgical Management  Complete tumor removal , with pathological confirmation and margin analysis.  Large tumors invading adjacent structure with aggressive histology – WIDE LOCAL EXCISION  0.5-1cm margin  Reconstructive procedures
  • 10. MOHS Micrographic Surgery  Excision of skin cancer under microscopic control.  Minimise recurrent rates with maximum conservation.  Indicated in  Poorly demarcated,  Recurrent / incompletely excised  Near vital structures  Can also be used for SCC, lentigo maligna,DFS
  • 11. Contd… Under local anesthesia Saucerising excision of primary tumor Sample and defect are marked and oriented Stained with H&E. Examination of slide for residual tumor Excise more tissue from mapped area.
  • 13. Other Modalaties  Radiotherapy  Topical treatments  5-fluorouracil  Imiquimod  Cryotherapy
  • 14. Cutaneous Squamous Cell Carcinoma  Malignant tumor of keratinising epithelium of epidermis  2nd most common tumor  Cumulative sun exposure and damage  Associated with pre-existing scars, osetomyelitis, burn.  Marjolin’s ulcer
  • 16. Pathology  Smooth nodular to verrucous , papillamatous and ulcerating lesions.  Everted edges and surrounded by inflamed, indurated skin.  Distant metastasis.  Secondary lymph nodes involvement.
  • 17. Differential Diagnosis Of SCC  Actinic keratosis  BCC  Keratoacanthoma  Pyoderma gangrenosum  Warts
  • 18. Microscopic Appearance  Irregular masses of squamous epithelium proliferate and invade dermis.  KERATIN PEARLS  Perineural / vascular invasion  Positive for cytokeratin 1 and 10  Border’s histological grading  Ratio of pleomorphic and anaplastic to normal cells
  • 19. Prognosis  Invasion  Depth – deeper lesion , worse the prognosis  Surface size - >2 cm  Histological grade  Site  Lips and ears – increase recurrent rate  Immunosuppression  Perineural and vascular involvement  Aetiology
  • 20. TNM Classification Size • T1 - <2cm • T2 - 2-5 cm • T3 - >5cm • T4 - muscle or bone involvement Nodes • N0 - no regional nodes • N1 - regional nodes Metastasis • M0 - no metastasis • M1- distant metastasis Grade • G1- low grade • G2moderately differentiated • G3- high grade
  • 21. Management  Surgical excision – accurate histology  Margins to be assessed  4mm clearance for <2cm  1 cm clearance for >2cm  Radiotherapy resistant – Veruccus carcinoma
  • 22. Malignant Melanoma  Cancer of melanocytes  Wherever melanocytes exist  Bowel mucosa  Retina  Leptomeninges
  • 23.
  • 24. Macroscopic Features In Nevi Suggesting Malignant Melanoma
  • 25. Contd…  Tingling  Itching  Serosanguinous discharge  Blood supply  Melanomas >1mm have blood supply – doppler positive pigmented lesion
  • 26. Types Of Malignant Melanoma  Superficial spreading  Nodular melanoma  Lentigo maligna melanoma  Acral lentiginous melanoma  Amelanotic melanoma  Desmoplastic melanoma
  • 27. Superficial Spreading Melanoma  Commonest type – 70%  Arise from pre – existing nevus  Rapid growth of darker pigmented are in a junctional nevus.  Predominantly radial growth phase.  Nodularity can occur – vertical growth phase.
  • 28. Nodular Melanoma  More aggressive  Increased vertical growth than radial phase  Middle age men.  Usually trunk.  Sharply demarcated, blue-black papules 1-2cm.  Lack horizontal growth phase.
  • 29. Lentigo Maligna Melanoma  Hutchinson’s melanotic freckle  Slow growing, variegated, brown macule  Intense sun exposure.  Women > men  Less metastaic potential  Better prognosis
  • 30. Acral Lentiginous Melanoma  Soles of feet and palms of hand  Rare in white skinned people  Flat, irregular macule.  Can mimic a fungal infection  Biopsy of the nail matrix rather than just the pigment.  Hutchinson’s sign nail-fold pigmentation then widens progressively to produce a triangular pigmented macule with nail dystrophy.
  • 31. Miscellaneous  Amelanotic melanoma  Not pigmented  Poor prognosis  Desmoplastic melanoma  Head and neck  Perineural invasion  High recurrent rate
  • 32. Histology  Malignant changes of melanocytes in basal epidermis  Horizontal growth phase – cells spread along the dermo-epidermal junction  Vertical growth phase – dermis may be invaded and increased metastatic potential.
  • 33.  Satellite nodules  Lesions situated with in 2-5cm of the primary  Intransit lesions  Situated >5cm , proximal to lymphnode basin
  • 34. Management  History and clinical examination  Excision biopsy with 2mm margin of skin and subdermal fat.  Incisional biopsy – large lesion / facial lesions where excision results in scarring.  Staging of melanoma  Clarkes’ staging  Breslows’ classification
  • 36.
  • 37. Management Of Malignant Melanoma Pigmented lesion Biopsy Diagnosis of melanoma <1mm depth Excision - 1cm margin 2-4mm depth Excision -2cm margin >4mm depth Excision – 3cm margin
  • 38. Management of lymphnodes  Based on breslow thickness.  <1mm least beneficial with prophylactic dissection.  >4mm increased chance of both lymphatic and distant metastasis.  Intermediate thickness  Elective prophylactic lymph node dissection  Sentinel lymphnode biopsy
  • 41. Other Modalities  Chemotherapy  Melphalan  Vemurafenib  Isolated limb perfusion therapy  Immunotherapy  IFN / TNF ALPHA  Radiotherapy