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Dr. Utham Murali. M.S ;
M.B.A.
 Weight - 16% TBW
 Surf. Area - 2 sq.m
 Thickness - 0.5 - 4mm
 Layers - Epidermis
- Dermis
- Subcutaneous Layer
 5% of the total skin
 Thickness - 0.05 -1mm
 Different layers [K/S/S/E]
Stratum corneum
Stratum lucidum
Stratum granulosum
Stratum spinosum
Stratum basale
 Cells –
Keratinocytes
Melanocytes
 Dermis - 95% of the skin.
 Dermis is 15-40 times thicker
 Thickness - 0.6 - 3mm
 2 layers papillary
reticular
 Contains - Skin appendages
 Basement membrane
 Barrier to the environment:
trauma, radiation, pathogens
 Temperature and H2o
homeostasis
 Excretion (e.g. urea, sodium
chloride, potassium, water)
 Endocrine and metabolic
functions
 Sensory organ - pain, pressure
and movement.
Types
Congenital
Infective / Inflammatory
Cystic / Neoplastic
Vascular
Others
Classification
NEUROFIBROMATOSIS
 It is tumour arising from connective tissue of the
nerve sheath. It can be single or multiple.
 Neurofibromatosis (NF) 1 or von Recklinghausen’s
disease is the more common variant, affecting
approximately 1:4000 births.
 Skin manifestations can appear in early life, with the
development of > 5 smooth-surfaced café-au-lait
spots, armpit or groin freckling & Lisch nodules.
OTHERS
 Dermoid Cyst
 Gorlin’s syndrome
 Xeroderma pigmentosum
 Gardner’s syndrome
 Ferguson-Smith syndrome
 Chronic Inflammatory disease of
apocrine sweat glands.
 Common in Axillae and groin.
 Common in females 4 : 1.
 Strongly associated with obesity and
smoking.
 Multiple discharging sinuses, with
nodules in the skin which is tender.
 Antibiotics.
 Excision of the involved area widely
followed by skin grafting or flaps.
HIDRADENITIS SUPPURATIVA
 It is characterized by cutaneous ulceration
with purple undermined edges.
 It occurs secondary to heightened,
immunological reactivity, usually from
another disease process.
 Cultures from ulcers often grow Gram-
negative streptococci.
 These skin lesions generally respond to
steroids. Surgery is rarely indicated.
PYODERMA GANGRENOSUM
 It is highly infectious superficial skin
infection caused by staphylococci /
streptococci organisms.
 Usually seen in children.
 Formation of multiple blisters that
rupture and coalesce, to cover as
“honey coloured crust”.
 Treatment is oral antibiotics and
topical antiseptics.
IMPETIGO
 This is a sharply demarcated
streptococcal infection of the
superficial lymphatic vessel.
 Area affected is erythematous &
oedematous.
 Febrile and have a leucocytosis.
 Common in young / old.
 Erysipelas & Cellulitis overlap.
 Treatment is Penicillin.
ERYSIPELAS
 It is a bacterial (Streptococcus
pyogenes) infection of the skin and
subcutaneous tissue.
 Previous skin trauma or ulceration.
 Expanding area of erythematous,
oedematous tissue that is painful
and associated with a fever & warm
skin.
 Elevation / Antibiotics / Dressing.
CELLULITIS
 Surgical emergency.
 Polymicrobial synergistic infection.
 80% have a history of previous
trauma or infection.
 Rapid progression to septic shock.
 Urgent resuscitation, antibiotics and
surgical debridement.
 Mortality 30–50%.
NECROTISING FASCITIS
 It is a localized collection of pus in a
cavity lined by granulation tissue,
covered by pyogenic membrane.
 Both gram + / - bacteria.
 Visible (pointing) pus, tenderness,
fluctuation – features of abscess.
 Sites – anywhere in the body.
 Investigations, relevant to specific
types.
 Complications – Antibioma.
 Treatment - Hilton’s method of draining
an abscess.
OTHERS
 Boil
 Carbuncle
 Pott’s puffy tumour
 It is a retention cyst. It is due to
blockage of the duct of sebaceous
gland, causing a cystic swelling.
 Common in face, scalp, scrotum.
 Fixed to the skin and usually have a
central punctum and are often
indentable with pressure.
 Treatment depends on the clinical
state of the cyst.
SEBACEOUS CYST
 It is a cystic swelling occurring in relation to
tendon sheath or synovial sheath or joint
capsule.
 Site – Dorsum of wrist.
 Cystic degenertion – tendon sheath.
 Well localised / Restricted mobility.
 Asymptomatic – left alone.
 Excision – Firm crepe bandage.
 High recurrence rate – 30%.
GANGLION
OTHERS
 Lymph Cyst
 Milia
 Bursa
 Parasitic cyst
 Haematoma
 Benign overgrowth of basal layer of
epidermis.
 Common – elderly / Sites – face, trunk
& tongue.
 Raised, soft, well demarcated brown
lesion. The surface may be smooth,
velvety, or verrucous.
 Most have a “stuck-on” appearance
and waxy texture. The surface tends to
crumble when picked.
 Bleeding / ulceration / infection /
malignancy.
 Excision / Curettage / Cryosurgery.
 These are patches of overgrown skin with
hyperkeratosis.
 More common in children / adolescents /
young adults.
 It may be familial but often stimulated by
virus. [ HPV ]
 Sites – finger tips / face / axilla / sole of the
feet.
 They are dry / painful and disfiguring.
 Repeated rubbing may cause infection. It
can spread to other finger & other parts.
 It can persist for long time or disappear
spontaneously.
 The most common benign tumour.
 Universal / Ubiquitous tumour.
 Occur anywhere – except Brain.
 Sites & Types.
 It can be diffuse / localized.
 Mobile / Slips / Semi-fluctuant / Non-
tranilluminant.
 Single / Multiple.
 Complications.
 Excision.
 Moles (melanocytic naevi) as they are due to
a proliferation of melanocytes.
 Moles may be flat or protruding. They vary in
colour from pink to dark brown or black.
 The number of moles a person has depends
on genetic factors and on sun exposure.
 Melanocytic naevi may be present at birth
(congenital) but more usually begin to grow
during childhood although new ones can
appear at any age.
 Junctional naevus
 Compound naevus
 Intradermal naevus
 Spitz naevus
 Spindle cell naevus
 Halo naevus
 Dysplastic naevus
 Naevus spilus
 Naevus of Ota & Ito
 Blue naevus
- Tumours arising – acc. Skin structures - sweat glands / hair follicle
- Less common
- Protrudes as well – localized swelling in skin
Syringo
ma
- Raised /
pedicled
lesions
Hidraden
oma
- Blue
cystic
nodules
Tricholemmoma
- Hamartoma from hair
follicle
- Can turn into BCC –
10%
Trichoepithelioma
- Usually seen –
nasolabial fold
- Presents as small cut.
nodule
 Rhinophyma is an end-stage sequela of
acne rosacea.
 It is hypertrophy and hyperplasia of the
sebaceous glands and tends to affect
elderly men (male to female ratio 12:1).
 Nose is bluish red in colour with dilated
capillaries.
 Up to 3% of cases may have an occult
BCC.
 Treatment by dermabrasion or laser
resurfacing produces good results.
 Actinic Keratosis / Solar Keratosis
 Bowen’s disease of skin
 Cutaneous horn / Chronic scars
 Dysplastic Naevus
 Erythroplasia of Queyrat / Extramammary
disease of Paget
 Giant Naevus [GCPN]
 Keratoaconthoma
Malignant
Lesions
Basal Cell Carcinoma
Squamous Cell Carcinoma
Malignant Melanoma
 It is a slow-growing, locally
invasive malignant tumour
arising from basal epidermis
and hair follicles.
 Pre-disposing factors.
 It occurs in the middle-aged
or elderly.
 90% of lesions found on the
face above a line from the
lobe of the ear to the corner
of the mouth.
BCC
UV rays
Middle
aged,
men
White
skin,
genetics
Arsenics,
coal , tar
 Localised (nodular, nodulocystic,
cystic, pigmented and naevoid)
 Generalised can be superficial
(multifocal or superficial spreading) or
infiltrative (morphoeic, ice pick and
cicatrising).
 Nodular and nodulocystic - 90% of
BCCs.
 There are ‘high-risk’ and ‘low-risk’
BCCs. High-risk BCCs are (> 2 cm).
 Ovoid cells in nests with outer
‘palisading’ layer.
 Rarely metastasise.
 Never lympatic spread.
 Radiosensitive
 Wide excision (2 cm clearance) with
skin grafting or flap is the procedure of
choice.
 Laser surgery.
 Topical – 5 Fu.
 Cryosurgery.
 MOHS (Microscopically Oriented
Histographic 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
 It arises from squamous
layer of the kin.
 2nd most common tumor
 Usually - elderly – men.
 SCC is also associated
with chronic inflammation
& immunosuppression.
 SCC may vary from
smooth nodular to
verrucous, papillomatous &
ulcerating lesions.
 Marjolin’s ulcer
SCC
Sun
exposure
Chemical
carcinogens
HPV 5 &
HPV 16
Tobacco
use
Scars and
sinuses
 Keratin pearl – onion
skin
 Perineural / vascular
invasion
 Broder’s histological
grading
 Regional lymph nodes
are commonly involved
but blood spread does
not occur.
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
• G2-
moderately
differentiated
• G3- high
grade
 Surgical excision –
< 2cm - 4mm clearance
> 2cm - 1cm clearance
 Radiotherapy
 Chemotherapy –
Methotrexate / Vincristine /
Bleomycin
 Amputation
 Field therapy
 Melanoma is a tumour
arising from the epidermal
melanocytes.
 Can arise in skin, mucosa,
retina & the meninges.
 Risk factors – “PIGMENT”
 MM accounts for 3 % all
malignancy worldwide.
 Most likely naevi to form
MM are the junctional &
compound types.
Clark’s Breslow’s AJCC
• T T
N.S
• Thin < 1 mm < 10%
• I.M 1-4 mm 20-5%
• Thick > 4 mm 60%
 Tingling
 Itching
 Serosanguinous discharge
 Doppler + lesions >1mm
 Satellite lesions
Superficial spreading
65-70% / Most common
Nodular Melanoma
15-30% / Most aggressive
Lentigo maligna
5-15% / Less common
Acral lentiginous
5% / Least common
Amelanotic melanoma
Worst type
Desmoplastic melanoma
Peri-neural invasion
Tumour markers Investigations
Local spread
(Satellite nodules)
Lymphatic spread
(Transit nodules)
Distant spread -
Blood
MELAN-A
S 100
LDH
HMB 45
(Hydroxy Methyl bromide)
No incision biopsy
Excision biopsy
Punch biopsy
FNAC of LN
U/S - abd
Chest X-ray
SLNB
Spread
Margin & Depth
In-situ = 0.5cm
< 1mm = 1cm
1-2mm = 1-2cm
( 1.5cm )
> 2mm = 2-3cm
Hardley’s ( WLE )
# Lymphatic mapping &
SLNB
# Palpable mobile L.N –
If FNAC + → Regional
Block dissection is done
# Fixed L.N – only CT
because it is inoperable.
# Elective lymph node
dissection ( ELND )
 Isolated limb perfusion
therapy
 Laser ablation
 Chemotherapy –
* DTIC [Dacarbazine]
* Melphalan
* CVD
 Immunotherapy / Biotherapy
 Radiotherapy
 It is a benign endothelial tumour seen
commonly in children. (Girls)
 They may go unnoticed at birth or be evident
as a faint ‘herald’ patch.
 It grows rapidly in first year & slowly 70%
involution in 7 yrs.
 Common in head & neck region ( 60% ).
 Large haemangiomas may be associated
with visceral anomalies.
 Ulceration / bleeding / airway block and visual
disturbances - complications.
 Majority of haemangioma require no specific
treatment.
Strawberry naevus Port-wine stainSalmon patch
 Campbell de Morgan
spots
 Spider naevi
 Pyogenic granuloma
 Glomus tumour
 Angiosarcoma
 Kaposi’s sarcoma
 Occurs anywhere in the body.
 Not genetically predisposed.
 It is limited to the scar tissue
only. It will not extend to normal
skin.
 It is pale brown in colour, not
painful, nontender.
 Often self limiting also.
 It responds very well for
steroid injection.
 Recurrence is uncommon.
 Genetically predisposed. Often familial.
 Common site – sternum.
 It continues to grow even after 6 months
– years.
 It extends into adjacent normal skin.
 It is brownish black/pinkish black (due to
vascularity) in colour, painful, tender and
sometimes hyperaesthetic.
 Recurrence – very high – 50%.
 Treatment – various methods.
Ulcer Type
Traumatic Non-specific
Neuropathic Non-specific
Gravitational Non-specific
Pressure sores / Ischaemic Non-specific
Secondary Infective Non-specific
Iatrogenic Non-specific
Dermatitis artefacta Non-specific
Aphthous Non-specific
Peptic Non-specific
Primary Infective Specific
GIT / Skin Malignant
 Sinus – It is a blind track lined by
granulation tissue leading from an
epithelial surface into the surrounding
tissues.
Means – “Hollow” or “a bay” [ Latin ]
 Fistula – It is an abnormal
communication between the lumen of
one viscus to another or the body
surface or between the vessels.
Means – “flute” or “a pipe or tube”
Congenital Acquired
T-O-F Post-surgical
Branchial Fistula-in-ano
E C F
A V F
Congenital Acquired
Pre-auricular Post-surgical
Umbilical Pilonidal
Urachal Suture
Coccygeal Specific – TB / Crohn’s
Sacral Actino. / Ostemyelitis
 Functional anatomy of skin
 Types of Skin & Soft-tissue lesions
 Description of each lesions
 Investigation methods & Treatment
 Other specific lesions
THANK YOU

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Skin & soft tissue lesions

  • 1. Dr. Utham Murali. M.S ; M.B.A.
  • 2.
  • 3.
  • 4.  Weight - 16% TBW  Surf. Area - 2 sq.m  Thickness - 0.5 - 4mm  Layers - Epidermis - Dermis - Subcutaneous Layer
  • 5.  5% of the total skin  Thickness - 0.05 -1mm  Different layers [K/S/S/E] Stratum corneum Stratum lucidum Stratum granulosum Stratum spinosum Stratum basale  Cells – Keratinocytes Melanocytes
  • 6.  Dermis - 95% of the skin.  Dermis is 15-40 times thicker  Thickness - 0.6 - 3mm  2 layers papillary reticular  Contains - Skin appendages  Basement membrane
  • 7.  Barrier to the environment: trauma, radiation, pathogens  Temperature and H2o homeostasis  Excretion (e.g. urea, sodium chloride, potassium, water)  Endocrine and metabolic functions  Sensory organ - pain, pressure and movement.
  • 8. Types Congenital Infective / Inflammatory Cystic / Neoplastic Vascular Others Classification
  • 9.
  • 10. NEUROFIBROMATOSIS  It is tumour arising from connective tissue of the nerve sheath. It can be single or multiple.  Neurofibromatosis (NF) 1 or von Recklinghausen’s disease is the more common variant, affecting approximately 1:4000 births.  Skin manifestations can appear in early life, with the development of > 5 smooth-surfaced café-au-lait spots, armpit or groin freckling & Lisch nodules.
  • 11. OTHERS  Dermoid Cyst  Gorlin’s syndrome  Xeroderma pigmentosum  Gardner’s syndrome  Ferguson-Smith syndrome
  • 12.
  • 13.  Chronic Inflammatory disease of apocrine sweat glands.  Common in Axillae and groin.  Common in females 4 : 1.  Strongly associated with obesity and smoking.  Multiple discharging sinuses, with nodules in the skin which is tender.  Antibiotics.  Excision of the involved area widely followed by skin grafting or flaps. HIDRADENITIS SUPPURATIVA
  • 14.  It is characterized by cutaneous ulceration with purple undermined edges.  It occurs secondary to heightened, immunological reactivity, usually from another disease process.  Cultures from ulcers often grow Gram- negative streptococci.  These skin lesions generally respond to steroids. Surgery is rarely indicated. PYODERMA GANGRENOSUM
  • 15.
  • 16.  It is highly infectious superficial skin infection caused by staphylococci / streptococci organisms.  Usually seen in children.  Formation of multiple blisters that rupture and coalesce, to cover as “honey coloured crust”.  Treatment is oral antibiotics and topical antiseptics. IMPETIGO
  • 17.  This is a sharply demarcated streptococcal infection of the superficial lymphatic vessel.  Area affected is erythematous & oedematous.  Febrile and have a leucocytosis.  Common in young / old.  Erysipelas & Cellulitis overlap.  Treatment is Penicillin. ERYSIPELAS
  • 18.  It is a bacterial (Streptococcus pyogenes) infection of the skin and subcutaneous tissue.  Previous skin trauma or ulceration.  Expanding area of erythematous, oedematous tissue that is painful and associated with a fever & warm skin.  Elevation / Antibiotics / Dressing. CELLULITIS
  • 19.  Surgical emergency.  Polymicrobial synergistic infection.  80% have a history of previous trauma or infection.  Rapid progression to septic shock.  Urgent resuscitation, antibiotics and surgical debridement.  Mortality 30–50%. NECROTISING FASCITIS
  • 20.  It is a localized collection of pus in a cavity lined by granulation tissue, covered by pyogenic membrane.  Both gram + / - bacteria.  Visible (pointing) pus, tenderness, fluctuation – features of abscess.  Sites – anywhere in the body.  Investigations, relevant to specific types.  Complications – Antibioma.  Treatment - Hilton’s method of draining an abscess.
  • 21. OTHERS  Boil  Carbuncle  Pott’s puffy tumour
  • 22.
  • 23.  It is a retention cyst. It is due to blockage of the duct of sebaceous gland, causing a cystic swelling.  Common in face, scalp, scrotum.  Fixed to the skin and usually have a central punctum and are often indentable with pressure.  Treatment depends on the clinical state of the cyst. SEBACEOUS CYST
  • 24.  It is a cystic swelling occurring in relation to tendon sheath or synovial sheath or joint capsule.  Site – Dorsum of wrist.  Cystic degenertion – tendon sheath.  Well localised / Restricted mobility.  Asymptomatic – left alone.  Excision – Firm crepe bandage.  High recurrence rate – 30%. GANGLION
  • 25. OTHERS  Lymph Cyst  Milia  Bursa  Parasitic cyst  Haematoma
  • 26.
  • 27.  Benign overgrowth of basal layer of epidermis.  Common – elderly / Sites – face, trunk & tongue.  Raised, soft, well demarcated brown lesion. The surface may be smooth, velvety, or verrucous.  Most have a “stuck-on” appearance and waxy texture. The surface tends to crumble when picked.  Bleeding / ulceration / infection / malignancy.  Excision / Curettage / Cryosurgery.
  • 28.  These are patches of overgrown skin with hyperkeratosis.  More common in children / adolescents / young adults.  It may be familial but often stimulated by virus. [ HPV ]  Sites – finger tips / face / axilla / sole of the feet.  They are dry / painful and disfiguring.  Repeated rubbing may cause infection. It can spread to other finger & other parts.  It can persist for long time or disappear spontaneously.
  • 29.  The most common benign tumour.  Universal / Ubiquitous tumour.  Occur anywhere – except Brain.  Sites & Types.  It can be diffuse / localized.  Mobile / Slips / Semi-fluctuant / Non- tranilluminant.  Single / Multiple.  Complications.  Excision.
  • 30.  Moles (melanocytic naevi) as they are due to a proliferation of melanocytes.  Moles may be flat or protruding. They vary in colour from pink to dark brown or black.  The number of moles a person has depends on genetic factors and on sun exposure.  Melanocytic naevi may be present at birth (congenital) but more usually begin to grow during childhood although new ones can appear at any age.
  • 31.  Junctional naevus  Compound naevus  Intradermal naevus  Spitz naevus  Spindle cell naevus  Halo naevus  Dysplastic naevus  Naevus spilus  Naevus of Ota & Ito  Blue naevus
  • 32. - Tumours arising – acc. Skin structures - sweat glands / hair follicle - Less common - Protrudes as well – localized swelling in skin Syringo ma - Raised / pedicled lesions Hidraden oma - Blue cystic nodules Tricholemmoma - Hamartoma from hair follicle - Can turn into BCC – 10% Trichoepithelioma - Usually seen – nasolabial fold - Presents as small cut. nodule
  • 33.  Rhinophyma is an end-stage sequela of acne rosacea.  It is hypertrophy and hyperplasia of the sebaceous glands and tends to affect elderly men (male to female ratio 12:1).  Nose is bluish red in colour with dilated capillaries.  Up to 3% of cases may have an occult BCC.  Treatment by dermabrasion or laser resurfacing produces good results.
  • 34.  Actinic Keratosis / Solar Keratosis  Bowen’s disease of skin  Cutaneous horn / Chronic scars  Dysplastic Naevus  Erythroplasia of Queyrat / Extramammary disease of Paget  Giant Naevus [GCPN]  Keratoaconthoma
  • 35. Malignant Lesions Basal Cell Carcinoma Squamous Cell Carcinoma Malignant Melanoma
  • 36.  It is a slow-growing, locally invasive malignant tumour arising from basal epidermis and hair follicles.  Pre-disposing factors.  It occurs in the middle-aged or elderly.  90% of lesions found on the face above a line from the lobe of the ear to the corner of the mouth. BCC UV rays Middle aged, men White skin, genetics Arsenics, coal , tar
  • 37.  Localised (nodular, nodulocystic, cystic, pigmented and naevoid)  Generalised can be superficial (multifocal or superficial spreading) or infiltrative (morphoeic, ice pick and cicatrising).  Nodular and nodulocystic - 90% of BCCs.  There are ‘high-risk’ and ‘low-risk’ BCCs. High-risk BCCs are (> 2 cm).  Ovoid cells in nests with outer ‘palisading’ layer.  Rarely metastasise.  Never lympatic spread.
  • 38.  Radiosensitive  Wide excision (2 cm clearance) with skin grafting or flap is the procedure of choice.  Laser surgery.  Topical – 5 Fu.  Cryosurgery.  MOHS (Microscopically Oriented Histographic Surgery)
  • 39.  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
  • 40.  It arises from squamous layer of the kin.  2nd most common tumor  Usually - elderly – men.  SCC is also associated with chronic inflammation & immunosuppression.  SCC may vary from smooth nodular to verrucous, papillomatous & ulcerating lesions.  Marjolin’s ulcer SCC Sun exposure Chemical carcinogens HPV 5 & HPV 16 Tobacco use Scars and sinuses
  • 41.  Keratin pearl – onion skin  Perineural / vascular invasion  Broder’s histological grading  Regional lymph nodes are commonly involved but blood spread does not occur.
  • 42. 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 • G2- moderately differentiated • G3- high grade
  • 43.  Surgical excision – < 2cm - 4mm clearance > 2cm - 1cm clearance  Radiotherapy  Chemotherapy – Methotrexate / Vincristine / Bleomycin  Amputation  Field therapy
  • 44.  Melanoma is a tumour arising from the epidermal melanocytes.  Can arise in skin, mucosa, retina & the meninges.  Risk factors – “PIGMENT”  MM accounts for 3 % all malignancy worldwide.  Most likely naevi to form MM are the junctional & compound types.
  • 45. Clark’s Breslow’s AJCC • T T N.S • Thin < 1 mm < 10% • I.M 1-4 mm 20-5% • Thick > 4 mm 60%
  • 46.  Tingling  Itching  Serosanguinous discharge  Doppler + lesions >1mm  Satellite lesions
  • 47. Superficial spreading 65-70% / Most common Nodular Melanoma 15-30% / Most aggressive Lentigo maligna 5-15% / Less common Acral lentiginous 5% / Least common Amelanotic melanoma Worst type Desmoplastic melanoma Peri-neural invasion
  • 48. Tumour markers Investigations Local spread (Satellite nodules) Lymphatic spread (Transit nodules) Distant spread - Blood MELAN-A S 100 LDH HMB 45 (Hydroxy Methyl bromide) No incision biopsy Excision biopsy Punch biopsy FNAC of LN U/S - abd Chest X-ray SLNB Spread
  • 49.
  • 50. Margin & Depth In-situ = 0.5cm < 1mm = 1cm 1-2mm = 1-2cm ( 1.5cm ) > 2mm = 2-3cm Hardley’s ( WLE )
  • 51. # Lymphatic mapping & SLNB # Palpable mobile L.N – If FNAC + → Regional Block dissection is done # Fixed L.N – only CT because it is inoperable. # Elective lymph node dissection ( ELND )
  • 52.  Isolated limb perfusion therapy  Laser ablation  Chemotherapy – * DTIC [Dacarbazine] * Melphalan * CVD  Immunotherapy / Biotherapy  Radiotherapy
  • 53.
  • 54.  It is a benign endothelial tumour seen commonly in children. (Girls)  They may go unnoticed at birth or be evident as a faint ‘herald’ patch.  It grows rapidly in first year & slowly 70% involution in 7 yrs.  Common in head & neck region ( 60% ).  Large haemangiomas may be associated with visceral anomalies.  Ulceration / bleeding / airway block and visual disturbances - complications.  Majority of haemangioma require no specific treatment.
  • 55. Strawberry naevus Port-wine stainSalmon patch
  • 56.  Campbell de Morgan spots  Spider naevi  Pyogenic granuloma  Glomus tumour  Angiosarcoma  Kaposi’s sarcoma
  • 57.
  • 58.  Occurs anywhere in the body.  Not genetically predisposed.  It is limited to the scar tissue only. It will not extend to normal skin.  It is pale brown in colour, not painful, nontender.  Often self limiting also.  It responds very well for steroid injection.  Recurrence is uncommon.
  • 59.  Genetically predisposed. Often familial.  Common site – sternum.  It continues to grow even after 6 months – years.  It extends into adjacent normal skin.  It is brownish black/pinkish black (due to vascularity) in colour, painful, tender and sometimes hyperaesthetic.  Recurrence – very high – 50%.  Treatment – various methods.
  • 60. Ulcer Type Traumatic Non-specific Neuropathic Non-specific Gravitational Non-specific Pressure sores / Ischaemic Non-specific Secondary Infective Non-specific Iatrogenic Non-specific Dermatitis artefacta Non-specific Aphthous Non-specific Peptic Non-specific Primary Infective Specific GIT / Skin Malignant
  • 61.  Sinus – It is a blind track lined by granulation tissue leading from an epithelial surface into the surrounding tissues. Means – “Hollow” or “a bay” [ Latin ]  Fistula – It is an abnormal communication between the lumen of one viscus to another or the body surface or between the vessels. Means – “flute” or “a pipe or tube”
  • 62. Congenital Acquired T-O-F Post-surgical Branchial Fistula-in-ano E C F A V F Congenital Acquired Pre-auricular Post-surgical Umbilical Pilonidal Urachal Suture Coccygeal Specific – TB / Crohn’s Sacral Actino. / Ostemyelitis
  • 63.  Functional anatomy of skin  Types of Skin & Soft-tissue lesions  Description of each lesions  Investigation methods & Treatment  Other specific lesions
  • 64.