squamous cell carcinoma, basal cell carcinoma, sebaceous gland carcinoma
DESCRIPTION
Clinical presentation of SCC, BCC and SGC.TRANSCRIPT
Squamous cell carcinoma, basal cell carcinoma &
sebaceous gland carcinoma
Epidemiology, classification & histologyNoor Aniah Azmi
MBBCh (Cairo University, Egypt)
Objectives of this presentation
① To understand the difference between SCC, BCC and SGC
a. Better diagnosis
b. Better management
② To understand which is the local and metastasizing tumour
③ Be able to identify the histological slidesa. OSCE exam for part I
Normal Layers of the Skin
Normal Histology of the Eyelid
Basal Cell CarcinomaSquamous Cell Carcinoma
Sebaceous Gland Carcinoma
Basal Cell CarcinomaMost common eyelid tumor
90% of all
eyelid tumour
Arises fromStratum basale Outer root sheath of the hair follicle
Only in hair-bearing tissue
Commonly at lower eyelid
Slowly-growing tumour, locally invasive
Non-metastasizing
Can recur if incompletely treated – more difficult to treat
Common sites
(1) Inferior 50-60%
(2) Medial 25-30%- Most dangerous- Spread via lacrimal
system and spread
(4) Lateral 5%
(3) Superior 15%
Risk FactorsProlonged exposure to sunlight
Fair-skinned
Blue-eyed, red-haired
English, Irish or Scottish ancestry
Male, > 50 years old
History of cigarette-smoking
Prior basal cell carcinomas
Family history of skin cancer
Young patients or positive family history – look for possible system
associations
Basal Cell Nevus syndrome (Gorlin’s syndrome)- Multiple nevoid- Skeletal anomaly
Xeroderma pigmentosa- Excessive sensitivity to sun- Defect in repair mechanism
for UV-induced DNA damaged-cells
Clinical Types
1. Nodular BCC
2. Noduloulcerative BCC (Rodent Ulcer)
3. Sclerosing BCC (morphoeic)
1. Nodular BCC• Slowly-growing
• 1-2 years to reach 0.5 mm diameter
• Shiny and firm
• Pearly nodule
• With dilated surface vessels
2. Rodent Ulcer• Central ulceration
• Pearly raised rolled edges
• Dilated vessels over its margins
• Telangectasis
3. Sclerosing BCC
• Less common and difficult to diagnose – beneath the epidermis
• Indurated plaque
• Loss of lashes
Mistaken diagnosis: Chronic blepharitis
Histological Featuresepithelial proliferation arising from the basal layer of the epidermis
Normal dermis Desmoplastic stroma – pale-pink stroma supporting neoplastic cells
Histological Features
Peripheral palisades
Mitotic figures
Histological Features
Higher magnification
Atypical cells- High nuclear-
cytoplasmic ratio- Hyperchromatic nuclei- Pleomorphic
Histological Features
Sclerosing BCC
Thin cords radiate
peripherally
Basal Cell CarcinomaSquamous Cell Carcinoma
Sebaceous Gland Carcinoma
Squamous Cell Carcinoma
40 times less than BCC
Arises from the squamous layer
May ariseDe novoFrom pre-existing actinic keratosisFrom carcinoma in-situ
SPREAD
Regional LN 20% of cases
Lymphatics and perineural invasion
Common sites
(1) Lower eyelid 49%
(2) Medial canthus 36%
(3) Upper eyelid 23%
Risk FactorsElderly
Fair skin
History of chronic sun exposure
ImmunocompromisedAIDSRenal transplant
Clinical Types
1. Nodular SCC
2. Ulcerating SCC
3. Cutaneous horn
1. Nodular SCC• Hyperkeratotic nodule
• Crusting erosions and fissures
2. Ulcerating SCC
• Red base
• Sharply defined
• Indurated and everted borders
Ulcerating SCC vs Rodent Ulcer
Ulcerating SCC- Everted borders- Pearly margin- No telangectasia
Rodent Ulcer- Pearly margins with rolled
edges- Telangectasia present
3. Cutaneous Horn
• With underlying invasive SCC
Histological FeaturesUlcerated region overlying
Infilrates the dermis deeply
Histological Features
Keratin pearls
Mitotic figures
Pseudosarcomatous change
Basal Cell CarcinomaSquamous Cell Carcinoma
Sebaceous Gland Carcinoma
Sebaceous Gland Carcinoma
Highly-malignant
Arises fromMeibomian glandsGlands of ZeisSebaceous gland of the caruncle, eyebrow or face
Commonly at upper eyelid
Multifocal origin, spread superficially
EpidemiologyFemales, > 50 years old
Most common eyelid tumour after BCC
1.5-5% of all eyelid tumour
Adverse Prognostic FactorUpperlid involvement
Tumour size > 10mm
Duration of symptoms > 6 months
Mortality rate 22%
SpreadVia lymph node
Perineural to intracranial via orbit
Clinical Types
1. Nodular SGC
2. Spreading SGC
3. Pagetoid SGC
1. Nodular SGC• Discrete hard nodule
• Yellowish discolouration – lipid
• Commonly at upper tarsal plate
Mistaken diagnosis: chalazion
How to differentiate between nodular SGC and chalazion?
Nodular SGC Chalazion
Nodule at tarsal plateMaybe tender if inflammed
2. Spreading SGC
• Diffuse thickening of lid margin
• Infiltrates into dermis
• Loss of lashes
• Multifocal non-contiguous origin
Mistaken diagnosis: chronic blepharitis
How to differentiate between SGC and chronic blepharitis?
Spreading SGC Chronic Blepharitis
3. Pagetoid Spread
• Extension of tumour within epithelium
• Including palpebral, forniceal and bulbar conjunctiva
Mistaken diagnosis: inflammatory condition
Normal Histology
Histological FeaturesLarge tumour nodules in the dermis,Irregular lobular mass of cells resembling adenoma but more aggressive
Central necrosis
Histological Features
Hyperchromatic atypical nuclei Scanty cytoplasm
Histological FeaturesPagetoid Spread
Spread through epidermis
Dermis layer
Histological FeaturesOil red-O fat stain
Cytoplasm of abnormal cells
Please remember…Any chronic unilateral blepharitis should raise
the possibility of sebaceous gland carcinoma.
Any case of recurrent chalazion, think of malignancy!
In summary
SCC BCC SGC
Epidemiology 5-10% of eyelid malignancy
90% of eyelid tumour
1.5 – 5% of eyelid tumour
Origin Epidermis, extending beyond stratum basale
Stratum basale of epidermis
Meibomian gland, sebaceous gland
Common sites Lower eyelid Lower eyelid Upper eyelid
Behaviour Very aggressive Not very aggressive
Highly-malignant
Spread Lymphatic transmission, perineural spread
Locally invasive, does not spread
Via lymph node
Clinical types Nodular, ulcerating, cutaneous
Nodular, noduloulcerative,sclerosing
Nodular, spreading, pagetoid
Pathognomonic histological feature
Keratin pearls Palisading peripheral cells
Foamy cytoplasm
Let’s try to identify the slides
Choose one answerSquamous cell carcinoma in situ is defined as a pathologic anatomic limitation by which one of the following:
a) Superficial epithelium
b) Stromal keratocytes
c) Basal epithelium
d) Basement membrane
Choose one answerAppropriate management of multiple or recurrent chalazia includes:
a) Needle biopsy
b) Local antibiotics
c) Full-thickness biopsy
d) Shave biopsy
Referencehttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2992157/
Jack J Kanski, Clinical Ophthalmology 6th Edition
Jack J Kanski, Clinical Ophthalmology Systemic Approach 7th Edition
Myron Yanoff, Ocular Pathology 6th Edition
AAO, Ophthalmic Pathology and Intraocular Tumours
AAO, Orbit, Eyelid and Lacrimal System