15.6 KHURANA OF EYELIDS Flashcards

1
Q

These include; simple papilloma, naevus, angioma, haemangioma, neurofibroma and sebaceous adenoma.

  • Benign tumours
  • Pre-cancerous conditions
  • Malignant tumours
A

Benign tumours

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2
Q

These are solar keratosis, carcinoma in situ and xeroderma pigmentosa.

  • Benign tumours
  • Pre-cancerous conditions
  • Malignant tumours
A

Pre-cancerous conditions

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3
Q

Commonly observed tumours include squamous cell carcinoma, basal cell carcinoma, malignant melanoma and sebaceous gland adenocarcinoma.

  • Benign tumours
  • Pre-cancerous conditions
  • Malignant tumours
A

Malignant tumours

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4
Q

are the most common benign tumours arising from the surface epithelium.

  • Papillomas
  • Xanthelasma
A

Papillomas

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5
Q

These are creamy-yellow plaque-like lesions which frequently involve the skin of upper and lower lids near the inner canthus

  • Papillomas
  • Xanthelasma
A

Xanthelasma

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6
Q

represents lipid deposits in histiocytes in the dermis of the lid.

  • Papillomas
  • Xanthelasma
A

Xanthelasma

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7
Q

common type of birthmark that are usually red or purple.

  • Haemangioma
  • Neurofibroma
A

Haemangioma

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8
Q

These may be superficial and bright red in colour (strawberry naevus) or deep bluish or violet in colour.

  • Capillary haemangioma
  • Naevus flammeus (port wine stain)
  • Cavernous haemangiomas
A

Capillary haemangioma

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9
Q

It may occur pari passu or more commonly as a part of Sturge-Weber syndrome.

  • Capillary haemangioma
  • Naevus flammeus (port wine stain)
  • Cavernous haemangiomas
A

Naevus flammeus (port wine stain)

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10
Q

It consists of dilated vascular channels and does not grow or regress like the capillary haemangioma.

  • Capillary haemangioma
  • Naevus flammeus (port wine stain)
  • Cavernous haemangiomas
A

Naevus flammeus (port wine stain)

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11
Q

developmental venous anomaly and usually occur after first decade of life.

  • Capillary haemangioma
  • Naevus flammeus (port wine stain)
  • Cavernous haemangiomas
A

Cavernous haemangiomas

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12
Q

It consists of large endothelium-lined vascular channels and usually does not show any regression.

  • Capillary haemangioma
  • Naevus flammeus (port wine stain)
  • Cavernous haemangiomas
A

Cavernous haemangiomas

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13
Q

Lids and orbits are commonly affected in neurofibromatosis (von Recklinghausen’s disease).

  • Haemangioma
  • Neurofibroma
A

Neurofibroma

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14
Q

The tumour is usually of plexiform type

  • Haemangioma
  • Neurofibroma
A

Neurofibroma

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15
Q

occur as nonpigmented protrusions with a keratin filled central crater.

  • Keratoacanthomas
  • Naevi
A

Keratoacanthomas

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16
Q

common cutaneous lesions that arise from the arrested epidermal melanocytes .

  • Keratoacanthomas
  • Naevi
A

Naevi

17
Q

located at the epidermis/dermis

  • Junctional naevi
  • Dermal naevi
  • Compound naevi
A

Junctional naevi

18
Q

are flat, brown in appearance

  • Junctional naevi
  • Dermal naevi
  • Compound naevi
A

Junctional naevi

“brown appearance, flat”

19
Q

located within the dermis, are elevated lesions which may not be visibly pigmented.

  • Junctional naevi
  • Dermal naevi
  • Compound naevi
A

Dermal naevi

“no visible pigment, elevated”

20
Q

share features of junctional and dermal naevi

  • Junctional naevi
  • Dermal naevi
  • Compound naevi
A

Compound naevi

21
Q

though a common lesion of sun exposed skin is relatively uncommon on the eyelids.

  • Actinic keratosis
  • Xeroderma pigmentosa
A

Actinic keratosis

22
Q

Characteristic features of this autosomal recessive
(AR) disease are:
• Progressive cutaneous pigmentation resulting from
damage on exposure to natural sunlight.
• Bird-like facies is typical of this condition.
• Predisposition to develop lid tumours

  • Actinic keratosis
  • Xeroderma pigmentosa
A

Xeroderma pigmentosa

23
Q

Predisposing factors include increasing age, white skin, sun exposure, xeroderma pigmentosa and basal
cell naevus syndrome.

  • Basal cell carcinoma
  • Squamous cell carcinoma
A

Basal cell carcinoma

24
Q

It forms the second commonest malignant tumour
of the lid. It is commonly arises from the lid margin (mucocutaneous junction) in elderly patients
de novo or from pre-existing lesion such as actinic
keratosis, Bowen’s disease and radiation dermatosis.

  • Basal cell carcinoma
  • Squamous cell carcinoma
A

Squamous cell carcinoma

25
Q

Risk factors include sun exposure, radiation, fair skin, injury or other irritative insults.

  • Basal cell carcinoma
  • Squamous cell carcinoma
A

Squamous cell carcinoma

“sun exposure”

26
Q

There is a male predilection.

  • Basal cell carcinoma
  • Squamous cell carcinoma
A

Squamous cell carcinoma

27
Q

It is a rare tumour arising from the meibomian glands
(western literature)

  • Sebaceous gland carcinoma
  • Malignant melanoma (Melanocarcinoma)
A

Sebaceous gland carcinoma

28
Q

Clinical features. It usually presents initially as a nodule (which may be mistaken for a chalazion), more frequently on the upper eyelid. Which then grows to form a big growth

  • Sebaceous gland carcinoma
  • Malignant melanoma (Melanocarcinoma)
A

Sebaceous gland carcinoma

29
Q

is a rare tumour of the lid (less than 1% of all eyelid lesions).

  • Sebaceous gland carcinoma
  • Malignant melanoma (Melanocarcinoma)
A

Malignant melanoma (Melanocarcinoma)

30
Q

It may arise from a pre-existing naevus, but usually arises de novo from the melanocytes present in the skin.

  • Sebaceous gland carcinoma
  • Malignant melanoma (Melanocarcinoma)
A

Malignant melanoma (Melanocarcinoma)