Plastics/orbit lesions Flashcards

1
Q

benign/malignant lymphoid conjunctival lesion

A

Type of lymphoma - characterized by cell surface markers and flow cytometry. Specimen has to be fresh/ unpreserved for these tests.

90% are non-Hodgkins B-cell lymphoma.

Primary intraocular lymphoma is also B-cell derived.

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2
Q

Bowen’s disease

A

squamous cell caricnoma in situ (SCCIS)

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3
Q

actinic keratoses (AK)

A
Premalignant (22% becomes SCC)
Thick, scaly, crusty lesion
Usu. elderly white men
Linked to sun exposure
Parakeratosis
Tx: excision, cryotherapy, topical 5-FU
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4
Q

Lentigo (solar, maligna, simplex)

A

Solar lentigo occurs in older patients that are sun exposed. (Resemble freckles but are larger in size and occur in old age.)

Lentigo simplex resembles freckles but are larger and are not related to sun exposure nor age.

Lentigo maligna lesions appear similar to solar lentigo except that they have irregular pigmentation. 30-50% of these lesions progress to melanoma.

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5
Q

freckle vs nevus

A

Freckle 2/2 melanocytes producing TOO MUCH pigment (and not from an over-abundance of melanosomes).

Nevus is derived from UNDIFFERENTIATED MELANOCYTES found at the epidermal/dermal border.
-Nests of dermal melanocytes (Derived from neural crest cells). Increased in pigment & size with puberty

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6
Q

BCC

A

MC eyelid malignancy

More common on?
Lower lid  (50-60%) > medial canthus (25-30%) > upper lid  (15%) > lateral canthus  (5%)

Pathology?
Basal cell nests
Peripheral palisades

1) MC = nodular - firm, raised, pearly nodule sometimes with telangiectasia.
Histologically, nodular BCC has “peripheral palisading” of basal cells. When the center ulcerates it has the classic “rodent ulcer” type of appearance.
2) Morpheaform = Much more aggressive
Firm, flat with indistinct borders
Slender tendrils. pagetoid spread
3) Other BCC types: ulcerative, pigmented and sclerosing

Treatment?
Excision w/ Mohs’ surgery
Rarely metastasize
Medial canthal basal cell carcinomas are particularly prone to infiltrate deeper tissues.

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7
Q

what to worry about after a face lift

A

In a patient having had a face-lift procedure, the surgeon is most worried about post-operative hematoma, which can–if untreated–lead to necrosis of the flap. This is an emergency and the hematoma should be drained immediately.

The typical time course of a hematoma is within the first twelve hours after surgery, and they are more common in men.

Untreated hematomas can lead to skin necrosis of the flap.

Nerve injuries are uncommon after facelift, occuring about 1-2% of the time.

Infections occur less than 1% of the time, and most patients are routinely covered with oral antibiotics perioperatively.

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8
Q

trichofolliculoma

A

A trichofolliculoma presents as a solitary and sometimes umbilicated lesion.

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9
Q

Trichoepithelioma

A

Firm flesh-colored nodule w/ telangiectasia, resembles BCC
Usu. on forehead, eyelids, usu. In females
Basaloid cells surrounding keratin center

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10
Q

Pilomatrixoma appearance/path. Systemic assoc?

A

Solitary firm deep nodule
reddish-purple subcutaneous mass attached to the overlying skin.

Affects young adults

Pathology?
Islands of epithelial cells surrounded by basophilic cells with shadow cells
Purple blends into pink

Association?
Myotonic dystrophy
Gardner’s syndrome

Treatment? Excision

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11
Q

trichilemmoma. Systemic assoc?

A

Small crusty, ulcerated, resembles verruca
Usu. on face
Glycogen-rich clear cells of outer hair sheath

Cowden’s disease?
multiple facial tricholemmomas
marker for breast or thyroid CA

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12
Q

MC site for orbital lymphoma to occur?

A

50% of orbital lymphoproliferative lesions are located in the LACRIMAL FOSSA (the one in the frontal bone and not the one housing the lacrimal sac).
90% of orbital lymphomas are non-Hodgkin B-cell lymphoma, 40%-60% of which are of the MALT variety. Fresh biopsies not in fixative should be sent to pathology.

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13
Q

MC epitheloid lacrimal gland

A

Lacrimal fossa lesions are generally of three types: inflammations (pseudotumor), lymphoproliferative lesions (lymphoma), and tumors of the lacrimal gland itself. One characteristic finding with lacrimal gland tumors is that they can impinge on the globe and cause inferior displacement of the globe. Lymphoproliferative lesions generally mold around the bone. Pleomorphic adenoma is the most common epithelial lacrimal gland tumor. The thing to remember about this lesion is that it should be removed in total. Violation of the pseudocapsule and leaving remnants behind is thought to increase recurrence. It should not be biopsied. Adenoid cystic is the most common malignant lacrimal gland tumor. These tumors are associated with a lot of pain and have a Swiss-cheese pattern on pathology.

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14
Q

Rhabdo location

A

Rhabdomyosarcomas = derived from undifferentiated pluripotential MESENCHYMAL cells and not from muscle. -typically occur in patients 8-10 years old.

MC type is embryonal (80% of cases) SUPERONASAL quadrant.
-good survival rate (94%)

Alveolar = awful (10-year survival rate of 10%)
-lower orbit location

Rx: XRT & chemotherapy (mainstays for all types)
Surgical removal of the lesion is not indicated unless the lesion is small and encapsulated.

Mnemonic for the types of rhabdo: Everyone gets Embryonal (most common, 80%); Alveolar is Awful (most lethal, survival <10%); Pleomorphic Please (best survival rate, 97%, so if someone gets rhabdo please let it be this type)

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15
Q

hemifacial spasm

A

MCC: The facial nerve may be compressed as it exits the brainstem by an ectactic vertebral artery or anterior inferior cerebellar artery (AICA).

In a patient presenting with hemifacial spasm, it is recommended to obtain an MRI/MRA of the head and neck to evaluate for mass lesions that may be compressing the 7th nerve.
DDx: stroke to this region, multiple sclerosis, or trauma

Rx: neuromodulatory injections such as botulinum toxin or neurosurgery (the Jannetta procedure) in which a sponge is placed in between the nerve and ectatic vessel to distract it away from compressing the nerve. This procedure has a high success rate in hemifacial spasm caused by vascular compression.

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16
Q

Seborrheic keratosis

A

Benign basaloid neoplasm
Smooth, greasy, stuck-on
Acanthosis, hyperkeratosis, horn or pseudohorn cysts
MC start to appear in middle age

Leser-Trelat sign?
Sudden appearance of multiple SK associated with internal malignancy (GI adenocarcinoma).

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17
Q

Nevus (early in life to late in life)

A

Nevi start out at the junctional level between the epidermis and dermis. Then, they extend into the epidermis and dermis where they are referred to as compound. Loss of the epidermal portion comes next, leaving just the dermal portion. They are then referred to as dermal.

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18
Q

Dacryocystitis in adults

A

Dacryocystitis in adults is almost always secondary to obstruction of the nasolacrimal duct. Probing and irrigation will not relieve strictures in adults. (Only indicated in children where there is a suspicion of a non patent valve of Hasner).

Topical antibiotics are not indicated because they do not penetrate into the skin.

Most adults with a history of dacryocystitis secondary to total NLDO will need a dacryocystorhinostomy (DCR).

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19
Q

Sebaceoucs carcinoma etiology of papillary conj

A

Pagetoid spread (PS) is responsible for its appearance as a papillary palpebral conjunctivitis. PS occurs intraepidermally, whereby cells proliferate singly or in nests at all levels of the epidermis. This finding is most commonly seen in association with neoplasms (most of which are malignant).

When sebaceous gland carcinoma involves the conjunctival epithelium and spreads (pagetoid spread), it can spread very rapidly. Excision of the lesion is indicated with sentinel lymph node biopsy
XRT - NOT effective.

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20
Q

Lacrimal gland fistula

A
  • occurs when a ductule from the lacrimal gland goes to the external skin
  • generally an overlying extra few eyelashes near the fistula. It is treated by excising the ductules.
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21
Q

dacryocystocele

A

=lacrimal sac distension 2/2 a nasolacrimal sac distension and is filled with amniotic fluid or mucus
-If infection is present, IV antibiotics in children or oral antibiotics in adults may be indicated to clear the infection.

Conservative treatment is indicated first which includes lacrimal sac massage. Because of the high rate of infection, topical antibiotics should be considered. Lacrimal system probing is indicated if this fails to clear the obstruction in 1-2 weeks.

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22
Q

NLDO in adult with bloody tears

A

Epiphora = defined as an overflow of tears. +/-mucus discharge and mattering of the eyelids. Dry eye may be a concomitant complaint although often dry eye and tearing suggests a reactive hypersecretion.

Presence of bloody tears = possibility of a malignancy in the lacrimal drainage apparatus.
MC malignancy of the lacrimal sac = squamous cell carcinoma (risks: smoking)
DDx (specific for lacrimal sac): Lymphoma, inverted papilloma (a benign lesion that may progress to SCC), and other malignancies

If you plan to perform a DCR and the patient complains of bloody tears, it is important to get a biopsy of the lacrimal sac at the time of surgery in order to diagnose an occult malignancy.

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23
Q

ON meningioma

A

Most arise from arachnoid villi

Si/Sx: typically present as painless loss of vision with an APD and sometimes with proptosis.
Optic nerve disc optociliary shunt vessels should raise suspicion.
Bilateral cases are associated with neurofibromatosis.

Rx: similar to optic nerve gliomas =observation unless intracranial or chiasmal extension is noted. In these cases, resection of the entire nerve may be indicated as well as possible radiation.

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24
Q

MCC of optociliary shunt vessels

A

A: ON meningioma

Optociliary shunt vessels (aka retinochoroidal collaterals) are a dilation of the naturally-occurring veins that drain from the peripapillary retinal circulation into the choroidal circulation.

  • Similar to hemorrhoids or esophageal varices,
  • optociliary shunt vessels evolve 2/2 chronically-poor drainage of the central retinal vein.

DDx:

  • sphenoid wing meningioma (30% of patients)
  • optic nerve sheath meningioma
  • low-grade optic nerve glioma
  • chronic papilledema
  • chronic glaucoma
  • old central retinal vein occlusion
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25
Q

Rx for PAM

A

Excision with cryotherapy is the current treatment for primary acquired melanosis (PAM).

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26
Q

rx for uveal melanoma

A

brachytherapy

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27
Q

tear meniscus/tear breakup times

A

Jones I involves placing fluorescein onto the ocular surface and then placing a swab in the nose at 2 and 5 minutes to see if the lacrimal drainage system is intact.

Normal tear meniscus R/O hypersecretion

Tear breakup times < 10 seconds are suggestive of dry eye. > 15 seconds are normal.

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28
Q

verruca

A
Verruca Vulgaris
Wart caused by HPV
Hard, rough-surfaced lesion
Children/adolescents, esp. immunosuppressed
Acanthosis, hyperkeratosis
Treatment: cryotherapy

DDx: trichilemmoma

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29
Q

Cutaneous horns 2/2?

A

Cutaneous horns are a result of hyperkeratosis.

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30
Q

Tolosa-Hunt Syndrome

A

Idiopathic sterile inflammation of the cavernous sinus; along spectrum with orbital pseudotumor

Signs:
Severe unilateral headaches and painful ophthalmoplegia

Cavernous sinus syndrome:
(Multiple cranial neuropathies including CN 5 (facial pain and numbness), Horner syndrome)

Treatment:
Steroids

31
Q

Cavernous sinus syndrome Ddx:

A
Aneurysm
Meningioma
Schwannoma
Pituitary adenoma
Metastasis
Sarcoidosis
Cavernous sinus thrombosis
C-C fistula (dilated episcleral vessels, pulsated exophthalmos, ocular bruit)
32
Q

Superotemporal location (pediatric orbit)

A

On skin = Dermoid CYST

On eye:
eosinophilic granuloma
Epibulbar Osseous Choristoma
Dermolipoma

33
Q

Superonasal

A

Mucocele
Encephalocele
Embryonal rhabdomyosarcoma

capillary hemangioma
lymphangioma

34
Q

INFERONASAL

A

Inferonasal to the medial canthus
Dacryocystocele
Lacrimal fistula

Inferonasal orbit = Alveolar rhabdomyosarcoma

Dermoid on eye

35
Q

Periorbital inflammation DDx peds

A
Periorbital cellulitis
Ruptured dermoid cyst
Rhabdomyosarcoma
Orbital pseudotumor
Leukemia
Histiocytosis X (Eosinophilic granuloma)
Infantile cortical hyperostosis
36
Q

Periorbital ecchymosis DDx

A

Lymphangioma
Neuroblastoma
Leukemia in orbit
Trauma

37
Q

DDx of adult with recurrent periorbital ecchymosis?

A

Orbital varix

Amyloidosis

38
Q

Capillary hemangioma:

A
Usu. appears at 1-2 wks, rapid growth over 1st year
Most involute after 1 year, 75% absent by 4 years
Rarely bleeds
Association with PHACE:
Posterior fossa abnormalities
Hemangiomas
Arterial cerebrovascular anomalies
Cardiac defects
Eye anomalies

Kassabach-Merritt Syndrome
Thrombocytopenia from platelet sequestration
Treatment: Steroid injection, PO propanolol

39
Q

Lymphangioma

A

Usu. appears in 1st decade; often persists
Increases w/ respiratory infections
Bleeding common (“chocolate cyst”)
?Origin – no lymphatics in orbit
Check for intracranial involvement
Tx = observation if possible (difficult to remove due to poor margins)

40
Q

Varix

A

Increases with valsalva or head down position (“positional proptosis”)
30% have phleboliths

41
Q

Rhabdomyosarcoma

A

Most common primary malignancy of orbit in kids
Usu. presents with unilateral proptosis at age 7-8
Often develops quickly (1-2 wks) and painless
Arises from pluripotent mesenchymal cells, not extraocular muscles

Location?
Superonasal most common

Pathology types?
Embryonal =Most common, Good survival
Alveola = Worst prognosis, Honeycomb appearance
Pleomorphic = Least common, Best prognosis
Botryoid = Grapelike, Secondary tumor from paranasal sinuses or conj

Treatment?
Chemo / radiation, NOT local excision
Exenteration if large

42
Q

Second most common metastases to orbit?

A

Ewing’s sarcoma (usu. 2nd or 3rd decade)

43
Q

Most common orbital metastases in kids

A

Neuroblastoma
Unilateral or bilateral proptosis with ecchymosis (raccoon eyes)

Originates from?
Adrenal gland, or sympathetic chain

Opsoclonus?
Not related to orbital involvement
Associated with a good prognosis

Test?
Urine for catacholamines
Path shows rosettes

Prognosis poor but better if?
Diagnosed before age 1
Opsoclonus
Rarely but can self regress

44
Q

Histiocytosis X

A

a.k.a. Langerhans cell histiocytosis
Accumulation of proliferating histiocytes in tissues
Children (ages 5-10)

Symptoms: proptosis, pain, periorbital swelling

3 types?
1) Eosinophilic granuloma =Localized and benign bone lesion
2) Hand-Schuller-Christian = Disseminated and aggressive, Lytic skull lesions & proptosis
Associated with diabetes insipidus
3) Letterer-Siwe disease
Most aggressive and fatal, Multisystemic soft tissue lesions
Rarely involves eye

Treatment:
Excision and radiation

Prognosis:
Ranges from benign to chronic dissemination and death

CT?
Sharply demarcated osteolytic lesion

Path?
Birbeck granules (racket-shaped)
+S100, +Vimentin

45
Q

Fibrous histiocytoma

A

Most common mesenchymal tumor of orbit
Benign mass of fibroblasts & histiocytes

Path? Storiform (cartwheel) pattern

46
Q

Hemangiopericytoma

A

Rare orbital tumor from capillary pericytes
Usually middle-age women
A-scan: med-low reflectivity

CT: encapsulated tumor, well-circumscribed
Benign, but may undergo malignant transformation
More symptomatic than cavernous hemangioma

Path: capillary channels in staghorn pattern
Treatment: Surgery

47
Q

Cavernous Hemangioma

A

Most common benign intraorbital tumor
Increased growth in pregnancy
Tx? usu. observation, surgery if needed

48
Q

Hyperostosis Ddx?

A

Fibrous histiocytoma, metastatic prostate CA, sphenoid wing meningioma

49
Q

Pleomorphic adenoma

A

Most common benign lacrimal gland tumor
a.k.a. Benign mixed tumor

Symptoms:
Painless proptosis
Downward displace of globe

Pathology?
Pseudocapsule
Mix of epithelial (E) + stromal (S) tissue

Treatment?
Complete excision of tumor & pseudocapsule
If remnants left behind, malignant tumor may recur (therefore do not biopsy

50
Q

Adenocystic carcinoma

A

Most common malignant lacrimal tumor

Symptoms:
Pain from perineural invasion and bone destruction
Rapid growth

Pathology?
No capsule
Swiss cheese pattern

Treatment?
Aggressive, may need to remove adjacent bone by exenteration
Poor prognosis

51
Q

How to biopsy lacrimal mass?

A

Orbital part only (ductules travel through palpebral lobe)

52
Q

Lymphoma

A

Painless mass molding the globe
No bony destruction
non-Hodgkin’s B-cell lymphoma (90%) > MALT (40%)

Most common location?
Lacrimal fossa

Risk of systemic lymphoma?
Eyelid (2/3) > Orbit (1/3) > Conjunctiva

53
Q

Burkitt’s lymphoma

A
In kids, consider Burkitt’s lymphoma
B-cell non-Hodgkin lymphoma
Endemic in Africa
Often affects maxilla
Path: “Starry sky” appearance
54
Q

Encephalocele

A

Neural tube defect resulting in sac-like protrusion into orbit
Increases with valsalva
Give protective eye wear!

55
Q

Pulsatile Proptosis Ddx?

A

C-C Fistula
NF 1 (absent sphenoid wing)
Encephalocele
AVM

56
Q

Mucocele

A

Cystic lesion when sinus ostium obstructed from chronic sinusitis
Mucus expands, causing bony erosions

57
Q

Silent sinus syndrome

A

Chronic maxillary sinus disease eroding orbital floor causing enophthalmos

58
Q

Aspergillosis

A

Septate, acute-angle branching hyphae
Spread from sinus
Usu. immunocompromised (e.g. leukemia, lymphoma, liver transplant)
Stains poorly w/ H&E

Treatment?
amphotericin B, debridement

Septate
fuSarium – natamycin
aSpergillus – ampho, nata

59
Q

Mucormycosis

A

Non-septate, large-angle branching hyphae
Spread from sinus
Usually DM patient
Vascular thrombosis
Black eschar on nasal endoscopy or roof of palate
Stains well w/ H&E

Treatment?
ampho B, debridement (controversial), hyperbaric O2 (inc ampho delivery)

nOn-Septate
mucOr – amphotericin
rhizOpus – azole

60
Q

Hyperkeratosis

A

thickening of keratin layer

61
Q

Parakeratosis

A

incomplete keratinization with nuclei in keratin layer

62
Q

Acanthosis

A

thickening of squamous layer

63
Q

Squamous Papilloma

A

Benign basaloid neoplasm
Flesh-like, sessile or pedunculated lesion
Finger-like projections with fibrovascular core, hyperkeratosis, acanthosis
Similar to SK on path

64
Q

Keratoacanthoma

A
Dome-shaped low-grade squamous carcinoma
Central keratin-filled crater and elevated rolled edges
Rapid onset in elderly
Resembles SCC
Treatment: excision, steroid injection
65
Q

Molluscum contagiosum

A

Viral skin infection
Pearly, dome-shaped w/ umbilicated center
Large cells with granular eosinophilic cytoplasm, small peripheral nucleus
Treatment: excision

66
Q

Xanthelasma

A

Pathology: Lipid laden histiocytes (macrophages) with foamy cytoplasm and intracellular lipid
Located in dermis
30% associated with hypercholesterolemia

Associated systemic disease?
Erdheim-Chester disease
Xanthelasma + proptosis
Histiocytosis in adults
Affects bones, lungs, heart
Usually death in few years
67
Q

Chalazion

A

Pathology: Zonal granuloma around lipid core
Multinucleated giant cells with extracellular lipid
Inflammatory meibomian glands or glands of Zeis (not Moll)

68
Q

Name a malignant lesion with extracellular lipid?

A

Sebaceous cell carcinoma

69
Q

Sebaceous cell carcinoma

A

Mimics chronic blepharitis or recurrent chalazion
More common in upper lid where there are more meibomian glands

Pathology?
Foamy cytoplasm
Pagetoid spread (intraepidermal spread of clusters of tumor cells)
“skip lesions”

Special stain?
Oil red O stains lipid in cytoplasm (must be fresh/frozen, as paraffin embedding destroys lipids)
Highly malignant

70
Q

Muir-Torre Syndrome?

A

Multiple sebaceous neoplasms
Keratoacanthosis
Visceral tumors (colon CA most common)
Inheritance: AD

71
Q

Syringoma

A

Common sweat gland eccrine tumor
Small yellow-white papules, resembles milia
Benign proliferation of eccrine structures

72
Q

Hydrocystoma

A

Apocrine gland tumor (sometimes eccrine)
Transparent cysts filled with protein
Cystic cavity with eosinophilic protein content

73
Q

Types of nevus:

A

Intradermal (dermal only) = Most common & most benign

Junctional (epidermal / dermal) = Most malignant potential

Compound (intradermal / junctional)

74
Q

Melanoma types

A

Types:
1) Lentigo maligna (flat macule) = Usually in elderly
Usually sun-exposed areas. Most common; less aggressive

2) Superficial spreading -Usually in young, Unrelated to sun-exposure

3) Nodular = Usually in 50s; male:female = 2:1
Aggressive due to vertical extension