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‫الرحيم‬ ‫الرحمن‬ ‫ال‬ ‫بسم‬
By: Dr. Aliaa
Alshorbagy
 Introduction
 Aetiology
 Types
 Invasion and Metastasis
 Risk Factors
 Diagnosis and Staging
 Treatment and Prevention
Structure of the
skin
 Melanocytes:
In stratum basale
Pale “halo” of cytoplasm
Neural crest
Produce melanin and pass it
on to nearby keratinocytes
Melanin covers nuclei of
nearby keratinocytes
Skin colour depends on
melanocytes activity, rather
than the number present
 A tumour arising from
melanocytes of the
basal layer of the
epidermis
 Less commonly –
uveal tract (eye) and
meningeal
membranes
 MM is the only common life –
threatening problem in
dermatology.
 Primary cutaneous melanoma may
develop in precursor melanocytic
nevi (common acquired, congenital
and atypical types ), although more
than 50 % of cases are believed to
arise without apreexisting
pigmented lesion .
 The cause is unknown.
 Excessive exposure to sunlight
 Genetic predisposition
EpidemiologyEpidemiology
 Melanoma accounts for only 4 % of all
skin cancers , however ,it causes the
greatest number of cancer-related
deaths .the incidence of MM is
increasing more rapidly that of any other
cancer, making it the 5th
most common
invasive cancer in men and women .
1-Excessive sun exposure.
2-Race : MM is more common in
white races .
3-Previous cutaneous MM.
4- Family history of MM.
5- Increase numbers of
acquired nevi.
6- Presence of potential
precursors of MM e.g
dyeplastic nevi and CMN.
 Occur anywhere on the skin
Females (commonest is lower leg)
Males ( back).
 Early melanoma is pain free. The
only symptom if present is mild
irritation or itch.
GLASGOW SYSTEM
Major:
 Change in size
 Irregular pigment
 Irregular outline
Minor:
 Diameter >6mm
 Inflammation
 Oozing/bleeding
 Itch/altered sensation
AMERICAN ‘ABCDE’
SYSTEM
 Asymmetry
 Border
 Colour
 Diameter
 Examination
Evolving; a
mole or skin
lesion that
looks
different
from the rest
or is
changing in
size, shape,
or color
Evolving; a
mole or skin
lesion that
looks
different
from the rest
or is
changing in
size, shape,
or color
 Superficial spreading Malignant
melanoma
 Nodular melanoma
 Lentingo maligna melanoma
 Acral melanoma
 The most common type
of MM in the white-
skinned population –
70% of cases
 Commonest sites –
lower leg in females
and back in males
 In early stages may be
small, then growth
becomes irregular
 Commoner in males
 Trunk is a common site
 Rapidly growing
 Usually thick with a
poor prognosis
 Black/brown nodule
 Ulceration and
bleeding are common
 In white-skinned
population this accounts
for 10% of MMs, but is
the commonest MM in
nonwhite-skinned
nations
 Found on palms and
soles
 Usually comprises a flat
lentiginous area with an
invasive nodular
component
 Rare
 Often diagnosed late –
confusion with benign
subungal naevus,
paronychial infections,
trauma
 Hutchinson’s sign –
spillage of pigment onto
the surrounding nailfold
 Occurs as a late
development in a
lentigo maligna
 Mainly on the face in
elderly patients
 May be many years
before an invasive
nodule develops
Superficial spreading
melanomas: Benign
melanocytic naevi
Superficial spreading
melanomas: Benign
melanocytic naevi
Nodular melanomas
Vascular tumor
Histiocytoma
Nodular melanomas
Vascular tumor
Histiocytoma
Latingo maligna
melanoma
Seborrhic
keratoses
Latingo maligna
melanoma
Seborrhic
keratoses
Stages Of MelanomaStages Of Melanoma
Level I: Lesions involving only the epidermis (in
situ melanoma); not an invasive lesion.
Level II: Invasion of the papillary dermis but does
not reach the papillary-reticular dermal interface.
Level III: Invasion fills and expands the papillary
dermis but does not penetrate the reticular dermis.
Level IV: Invasion into the reticular dermis but
not into the subcutaneous tissue.
Level V: Invasion through the reticular dermis into
the subcutaneous tissue.
Clark Classification (Level of Invasion)
 The Breslow thickness is
the single most
important prognostic
variable (distance in mm
of the furthest tumour
cell from the basal layer
of the epidermis)
Breslow
depth
5 year
survival
In situ 95-100%
<1mm 95-100%
1-2mm 80-96%
2.1-4mm 60-75%
>4mm 50%
Scalp lesions worse prognosis, then
palms and soles, then trunk, then
extremities
Younger women appear to do better than
either men at any stage or women over
50
Ulceration of the tumour surface is a high
risk factor
Surgical resection of
tumour
Lymph node dissection
Chemotherapy
Radiotherapy
Immunotherapy
 Keep out of the strong midday sun
(between 10 am and 3 pm)
 Remember clothing is an effective
sunscreen (particularly fine
woven cotton clothing)
 Use hats in the sun, particularly
broad brimmed hats
 Use a sunscreen to protect from
UVR.
 Sunscreens should be liberally applied and
reapplied every two hours if exposure to the
sun continues.
 Protect children and infants from strong sunlight
at all times. Use a sunscreen with a high sun
protection factor number (>15) .
 Avoid using sunbeds and sunlamps.
Malignantmelanoma 091229021816-phpapp01

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Malignantmelanoma 091229021816-phpapp01

  • 3.  Introduction  Aetiology  Types  Invasion and Metastasis  Risk Factors  Diagnosis and Staging  Treatment and Prevention
  • 5.  Melanocytes: In stratum basale Pale “halo” of cytoplasm Neural crest Produce melanin and pass it on to nearby keratinocytes Melanin covers nuclei of nearby keratinocytes Skin colour depends on melanocytes activity, rather than the number present
  • 6.  A tumour arising from melanocytes of the basal layer of the epidermis  Less commonly – uveal tract (eye) and meningeal membranes
  • 7.  MM is the only common life – threatening problem in dermatology.  Primary cutaneous melanoma may develop in precursor melanocytic nevi (common acquired, congenital and atypical types ), although more than 50 % of cases are believed to arise without apreexisting pigmented lesion .
  • 8.  The cause is unknown.  Excessive exposure to sunlight  Genetic predisposition
  • 9. EpidemiologyEpidemiology  Melanoma accounts for only 4 % of all skin cancers , however ,it causes the greatest number of cancer-related deaths .the incidence of MM is increasing more rapidly that of any other cancer, making it the 5th most common invasive cancer in men and women .
  • 10. 1-Excessive sun exposure. 2-Race : MM is more common in white races . 3-Previous cutaneous MM. 4- Family history of MM. 5- Increase numbers of acquired nevi. 6- Presence of potential precursors of MM e.g dyeplastic nevi and CMN.
  • 11.  Occur anywhere on the skin Females (commonest is lower leg) Males ( back).  Early melanoma is pain free. The only symptom if present is mild irritation or itch.
  • 12. GLASGOW SYSTEM Major:  Change in size  Irregular pigment  Irregular outline Minor:  Diameter >6mm  Inflammation  Oozing/bleeding  Itch/altered sensation AMERICAN ‘ABCDE’ SYSTEM  Asymmetry  Border  Colour  Diameter  Examination
  • 13. Evolving; a mole or skin lesion that looks different from the rest or is changing in size, shape, or color Evolving; a mole or skin lesion that looks different from the rest or is changing in size, shape, or color
  • 14.  Superficial spreading Malignant melanoma  Nodular melanoma  Lentingo maligna melanoma  Acral melanoma
  • 15.  The most common type of MM in the white- skinned population – 70% of cases  Commonest sites – lower leg in females and back in males  In early stages may be small, then growth becomes irregular
  • 16.  Commoner in males  Trunk is a common site  Rapidly growing  Usually thick with a poor prognosis  Black/brown nodule  Ulceration and bleeding are common
  • 17.  In white-skinned population this accounts for 10% of MMs, but is the commonest MM in nonwhite-skinned nations  Found on palms and soles  Usually comprises a flat lentiginous area with an invasive nodular component
  • 18.  Rare  Often diagnosed late – confusion with benign subungal naevus, paronychial infections, trauma  Hutchinson’s sign – spillage of pigment onto the surrounding nailfold
  • 19.  Occurs as a late development in a lentigo maligna  Mainly on the face in elderly patients  May be many years before an invasive nodule develops
  • 20. Superficial spreading melanomas: Benign melanocytic naevi Superficial spreading melanomas: Benign melanocytic naevi Nodular melanomas Vascular tumor Histiocytoma Nodular melanomas Vascular tumor Histiocytoma Latingo maligna melanoma Seborrhic keratoses Latingo maligna melanoma Seborrhic keratoses
  • 22. Level I: Lesions involving only the epidermis (in situ melanoma); not an invasive lesion. Level II: Invasion of the papillary dermis but does not reach the papillary-reticular dermal interface. Level III: Invasion fills and expands the papillary dermis but does not penetrate the reticular dermis. Level IV: Invasion into the reticular dermis but not into the subcutaneous tissue. Level V: Invasion through the reticular dermis into the subcutaneous tissue. Clark Classification (Level of Invasion)
  • 23.  The Breslow thickness is the single most important prognostic variable (distance in mm of the furthest tumour cell from the basal layer of the epidermis) Breslow depth 5 year survival In situ 95-100% <1mm 95-100% 1-2mm 80-96% 2.1-4mm 60-75% >4mm 50%
  • 24. Scalp lesions worse prognosis, then palms and soles, then trunk, then extremities Younger women appear to do better than either men at any stage or women over 50 Ulceration of the tumour surface is a high risk factor
  • 25. Surgical resection of tumour Lymph node dissection Chemotherapy Radiotherapy Immunotherapy
  • 26.  Keep out of the strong midday sun (between 10 am and 3 pm)  Remember clothing is an effective sunscreen (particularly fine woven cotton clothing)  Use hats in the sun, particularly broad brimmed hats  Use a sunscreen to protect from UVR.
  • 27.  Sunscreens should be liberally applied and reapplied every two hours if exposure to the sun continues.  Protect children and infants from strong sunlight at all times. Use a sunscreen with a high sun protection factor number (>15) .  Avoid using sunbeds and sunlamps.

Notes de l'éditeur

  1. Important to differentiate the navi from early malanoma 5% familial – genes arnd chrmosome 9p21 appears to be involved.
  2. 1 major and 1 or more minor should be considered for exicion and diagnostic biopsy.