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
Rx for PAM
Excision with cryotherapy is the current treatment for primary acquired melanosis (PAM).
26
rx for uveal melanoma
brachytherapy
27
tear meniscus/tear breakup times
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.
28
verruca
``` Verruca Vulgaris Wart caused by HPV Hard, rough-surfaced lesion Children/adolescents, esp. immunosuppressed Acanthosis, hyperkeratosis Treatment: cryotherapy ``` DDx: trichilemmoma
29
Cutaneous horns 2/2?
Cutaneous horns are a result of hyperkeratosis.
30
Tolosa-Hunt Syndrome
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
Cavernous sinus syndrome Ddx:
``` Aneurysm Meningioma Schwannoma Pituitary adenoma Metastasis Sarcoidosis Cavernous sinus thrombosis C-C fistula (dilated episcleral vessels, pulsated exophthalmos, ocular bruit) ```
32
Superotemporal location (pediatric orbit)
On skin = Dermoid CYST On eye: eosinophilic granuloma Epibulbar Osseous Choristoma Dermolipoma
33
Superonasal
Mucocele Encephalocele Embryonal rhabdomyosarcoma capillary hemangioma lymphangioma
34
INFERONASAL
Inferonasal to the medial canthus Dacryocystocele Lacrimal fistula Inferonasal orbit = Alveolar rhabdomyosarcoma Dermoid on eye
35
Periorbital inflammation DDx peds
``` Periorbital cellulitis Ruptured dermoid cyst Rhabdomyosarcoma Orbital pseudotumor Leukemia Histiocytosis X (Eosinophilic granuloma) Infantile cortical hyperostosis ```
36
Periorbital ecchymosis DDx
Lymphangioma Neuroblastoma Leukemia in orbit Trauma
37
DDx of adult with recurrent periorbital ecchymosis?
Orbital varix | Amyloidosis
38
Capillary hemangioma:
``` 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
Lymphangioma
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
Varix
Increases with valsalva or head down position (“positional proptosis”) 30% have phleboliths
41
Rhabdomyosarcoma
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
Second most common metastases to orbit?
Ewing’s sarcoma (usu. 2nd or 3rd decade)
43
Most common orbital metastases in kids
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
Histiocytosis X
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
Fibrous histiocytoma
Most common mesenchymal tumor of orbit Benign mass of fibroblasts & histiocytes Path? Storiform (cartwheel) pattern
46
Hemangiopericytoma
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
Cavernous Hemangioma
Most common benign intraorbital tumor Increased growth in pregnancy Tx? usu. observation, surgery if needed
48
Hyperostosis Ddx?
Fibrous histiocytoma, metastatic prostate CA, sphenoid wing meningioma
49
Pleomorphic adenoma
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
Adenocystic carcinoma
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
How to biopsy lacrimal mass?
Orbital part only (ductules travel through palpebral lobe)
52
Lymphoma
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
Burkitt’s lymphoma
``` In kids, consider Burkitt’s lymphoma B-cell non-Hodgkin lymphoma Endemic in Africa Often affects maxilla Path: “Starry sky” appearance ```
54
Encephalocele
Neural tube defect resulting in sac-like protrusion into orbit Increases with valsalva Give protective eye wear!
55
Pulsatile Proptosis Ddx?
C-C Fistula NF 1 (absent sphenoid wing) Encephalocele AVM
56
Mucocele
Cystic lesion when sinus ostium obstructed from chronic sinusitis Mucus expands, causing bony erosions
57
Silent sinus syndrome
Chronic maxillary sinus disease eroding orbital floor causing enophthalmos
58
Aspergillosis
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
Mucormycosis
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
Hyperkeratosis
thickening of keratin layer
61
Parakeratosis
incomplete keratinization with nuclei in keratin layer
62
Acanthosis
thickening of squamous layer
63
Squamous Papilloma
Benign basaloid neoplasm Flesh-like, sessile or pedunculated lesion Finger-like projections with fibrovascular core, hyperkeratosis, acanthosis Similar to SK on path
64
Keratoacanthoma
``` 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
Molluscum contagiosum
Viral skin infection Pearly, dome-shaped w/ umbilicated center Large cells with granular eosinophilic cytoplasm, small peripheral nucleus Treatment: excision
66
Xanthelasma
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
Chalazion
Pathology: Zonal granuloma around lipid core Multinucleated giant cells with extracellular lipid Inflammatory meibomian glands or glands of Zeis (not Moll)
68
Name a malignant lesion with extracellular lipid?
Sebaceous cell carcinoma
69
Sebaceous cell carcinoma
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
Muir-Torre Syndrome?
Multiple sebaceous neoplasms Keratoacanthosis Visceral tumors (colon CA most common) Inheritance: AD
71
Syringoma
Common sweat gland eccrine tumor Small yellow-white papules, resembles milia Benign proliferation of eccrine structures
72
Hydrocystoma
Apocrine gland tumor (sometimes eccrine) Transparent cysts filled with protein Cystic cavity with eosinophilic protein content
73
Types of nevus:
Intradermal (dermal only) = Most common & most benign Junctional (epidermal / dermal) = Most malignant potential Compound (intradermal / junctional)
74
Melanoma types
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