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Squamous cell carcinoma, 
basal cell carcinoma & 
sebaceous gland carcinoma 
Epidemiology, classification & histology 
Noor 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 slides 
a. OSCE exam for part I
Normal Layers of the Skin
Normal Histology of the Eyelid
Basal Cell Carcinoma 
Squamous Cell 
Carcinoma 
Sebaceous Gland 
Carcinoma
Basal Cell Carcinoma 
Most common eyelid tumor
 90% of all 
eyelid tumour 
 Arises from 
 Stratum 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 Factors 
 Prolonged 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 Features 
epithelial 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 Carcinoma 
Squamous Cell 
Carcinoma 
Sebaceous Gland 
Carcinoma
Squamous Cell Carcinoma
 40 times less than BCC 
 Arises from the squamous layer 
 May arise 
 De novo 
 From pre-existing actinic keratosis 
 From 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 Factors 
 Elderly 
 Fair skin 
 History of chronic sun exposure 
 Immunocompromised 
 AIDS 
 Renal 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 Features 
Ulcerated region 
overlying 
Infilrates the 
dermis deeply
Histological Features 
Keratin 
pearls 
Mitotic 
figures 
Pseudosarcomatous change
Basal Cell Carcinoma 
Squamous Cell 
Carcinoma 
Sebaceous Gland 
Carcinoma
Sebaceous Gland Carcinoma
 Highly-malignant 
 Arises from 
 Meibomian glands 
 Glands of Zeis 
 Sebaceous gland of the caruncle, eyebrow or face 
 Commonly at upper eyelid 
 Multifocal origin, spread superficially
Epidemiology 
 Females, > 50 years old 
 Most common eyelid tumour after BCC 
 1.5-5% of all eyelid tumour 
Adverse Prognostic Factor 
 Upperlid involvement 
 Tumour size > 10mm 
 Duration of symptoms > 6 months 
 Mortality rate 22%
Spread 
 Via 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 plate 
Maybe 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 Features 
Large 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 Features 
Pagetoid Spread 
Spread through epidermis 
Dermis layer
Histological Features 
Oil 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 answer 
Squamous 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 answer 
Appropriate management of multiple or recurrent chalazia 
includes: 
a) Needle biopsy 
b) Local antibiotics 
c) Full-thickness biopsy 
d) Shave biopsy
Reference 
 http://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

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Squamous cell carcinoma, Basal cell carcinoma, Sebaceous gland carcinoma

  • 1. Squamous cell carcinoma, basal cell carcinoma & sebaceous gland carcinoma Epidemiology, classification & histology Noor Aniah Azmi MBBCh (Cairo University, Egypt)
  • 2. 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 slides a. OSCE exam for part I
  • 3. Normal Layers of the Skin
  • 4. Normal Histology of the Eyelid
  • 5. Basal Cell Carcinoma Squamous Cell Carcinoma Sebaceous Gland Carcinoma
  • 6. Basal Cell Carcinoma Most common eyelid tumor
  • 7.  90% of all eyelid tumour  Arises from  Stratum basale  Outer root sheath of the hair follicle  Only in hair-bearing tissue  Commonly at lower eyelid
  • 8.  Slowly-growing tumour, locally invasive  Non-metastasizing  Can recur if incompletely treated – more difficult to treat
  • 9.
  • 10. Common sites (1) Inferior 50-60% (2) Medial 25-30% - Most dangerous - Spread via lacrimal system and spread (4) Lateral 5% (3) Superior 15%
  • 11. Risk Factors  Prolonged 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
  • 12. 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
  • 13. Clinical Types 1. Nodular BCC 2. Noduloulcerative BCC (Rodent Ulcer) 3. Sclerosing BCC (morphoeic)
  • 14. 1. Nodular BCC • Slowly-growing • 1-2 years to reach 0.5 mm diameter • Shiny and firm • Pearly nodule • With dilated surface vessels
  • 15. 2. Rodent Ulcer • Central ulceration • Pearly raised rolled edges • Dilated vessels over its margins • Telangectasis
  • 16. 3. Sclerosing BCC • Less common and difficult to diagnose – beneath the epidermis • Indurated plaque • Loss of lashes  Mistaken diagnosis: Chronic blepharitis
  • 17. Histological Features epithelial proliferation arising from the basal layer of the epidermis Normal dermis Desmoplastic stroma – pale-pink stroma supporting neoplastic cells
  • 18. Histological Features Peripheral palisades Mitotic figures
  • 19. Histological Features Higher magnification Atypical cells - High nuclear-cytoplasmic ratio - Hyperchromatic nuclei - Pleomorphic
  • 20. Histological Features Sclerosing BCC Thin cords radiate peripherally
  • 21. Basal Cell Carcinoma Squamous Cell Carcinoma Sebaceous Gland Carcinoma
  • 23.  40 times less than BCC  Arises from the squamous layer  May arise  De novo  From pre-existing actinic keratosis  From carcinoma in-situ SPREAD  Regional LN 20% of cases  Lymphatics and perineural invasion
  • 24.
  • 25. Common sites (1) Lower eyelid 49% (2) Medial canthus 36% (3) Upper eyelid 23%
  • 26. Risk Factors  Elderly  Fair skin  History of chronic sun exposure  Immunocompromised  AIDS  Renal transplant
  • 27. Clinical Types 1. Nodular SCC 2. Ulcerating SCC 3. Cutaneous horn
  • 28. 1. Nodular SCC • Hyperkeratotic nodule • Crusting erosions and fissures
  • 29. 2. Ulcerating SCC • Red base • Sharply defined • Indurated and everted borders
  • 30. Ulcerating SCC vs Rodent Ulcer Ulcerating SCC - Everted borders - Pearly margin - No telangectasia Rodent Ulcer - Pearly margins with rolled edges - Telangectasia present
  • 31. 3. Cutaneous Horn • With underlying invasive SCC
  • 32. Histological Features Ulcerated region overlying Infilrates the dermis deeply
  • 33. Histological Features Keratin pearls Mitotic figures Pseudosarcomatous change
  • 34. Basal Cell Carcinoma Squamous Cell Carcinoma Sebaceous Gland Carcinoma
  • 36.
  • 37.  Highly-malignant  Arises from  Meibomian glands  Glands of Zeis  Sebaceous gland of the caruncle, eyebrow or face  Commonly at upper eyelid  Multifocal origin, spread superficially
  • 38. Epidemiology  Females, > 50 years old  Most common eyelid tumour after BCC  1.5-5% of all eyelid tumour Adverse Prognostic Factor  Upperlid involvement  Tumour size > 10mm  Duration of symptoms > 6 months  Mortality rate 22%
  • 39. Spread  Via lymph node  Perineural to intracranial via orbit
  • 40. Clinical Types 1. Nodular SGC 2. Spreading SGC 3. Pagetoid SGC
  • 41. 1. Nodular SGC • Discrete hard nodule • Yellowish discolouration – lipid • Commonly at upper tarsal plate  Mistaken diagnosis: chalazion
  • 42. How to differentiate between nodular SGC and chalazion? Nodular SGC Chalazion Nodule at tarsal plate Maybe tender if inflammed
  • 43. 2. Spreading SGC • Diffuse thickening of lid margin • Infiltrates into dermis • Loss of lashes • Multifocal non-contiguous origin  Mistaken diagnosis: chronic blepharitis
  • 44. How to differentiate between SGC and chronic blepharitis? Spreading SGC Chronic Blepharitis
  • 45. 3. Pagetoid Spread • Extension of tumour within epithelium • Including palpebral, forniceal and bulbar conjunctiva  Mistaken diagnosis: inflammatory condition
  • 47. Histological Features Large tumour nodules in the dermis, Irregular lobular mass of cells resembling adenoma but more aggressive Central necrosis
  • 48. Histological Features Hyperchromatic atypical nuclei Scanty cytoplasm
  • 49. Histological Features Pagetoid Spread Spread through epidermis Dermis layer
  • 50. Histological Features Oil red-O fat stain Cytoplasm of abnormal cells
  • 51. Please remember…  Any chronic unilateral blepharitis should raise the possibility of sebaceous gland carcinoma.  Any case of recurrent chalazion, think of malignancy!
  • 53. 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
  • 54. Let’s try to identify the slides
  • 55.
  • 56.
  • 57. Choose one answer Squamous 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
  • 58. Choose one answer Appropriate management of multiple or recurrent chalazia includes: a) Needle biopsy b) Local antibiotics c) Full-thickness biopsy d) Shave biopsy
  • 59. Reference  http://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

Notes de l'éditeur

  1. The proliferated cells appear blue and are present in nests of different sizes. Note the sharp demarcation of the pale-pink area of stroma supporting the neoplastic cells from the underlying (normal) dark-pink dermis (d, relatively normal dermis). This stromal change, called desmoplasia (ds, desmoplastic stroma), is characteristic of neoplastic lesions. Compare with the benign lesions in Figs 6.24 to 6.27, where the dermis does not show such a change.
  2. The nests are composed of atypical basal cells and show peripheral palisading (pp). Mitotic figures are present. Again, note the pseudosarcomatous change (desmoplasia) (ds, desmoplastic stroma) of the surrounding supporting stroma, which is light-pink and contains proliferating fibroblasts.
  3. Higher magnification illustrates characteristic features of basal cell carcinoma, including atypical cells and separation artifact between nests of cells and desmoplastic surrounding connective tissue.
  4. he most frequent sites of periocular involvement are the lower eyelid (49%), medial canthus (36%), and the upper eyelid (23%).
  5. Histologic section of the excisional biopsy shows epithelial cells with an overall pink color that infiltrate the dermis deeply. The overlying region is ulcerated.
  6. C, Increased magnification shows the invasive squamous neoplastic cells making keratin (pearls) in an abnormal location (dyskeratosis). Numerous mitotic figures are present. Note the pseudosarcomatous (dysplastic) change in the surrounding stroma.
  7. Oil red-O fat stain shows marked positivity in the cytoplasm of abnormal cells. Any recurrent or suspect chalazion should be sampled for biopsy.
  8. SCC
  9. SCC
  10. Answer: D
  11. Answer: C