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TABLE 35.1. Summary of Chemotherapeutic Agents Used in Orbital Disease. (continued)

Class

Type of agent

Other names

Orbital disease

Clinical toxicity

 

Taxoids

Docetaxel

Squamous cell carcinoma of head and neck

Myelosuppression, asthenia, nausea, vomiting,

 

 

 

 

hepatotoxicity, parasthesias, allergic reaction

 

 

Paclitaxel

Squamous cell carcinoma of head and neck

Myelosuppression, asthenia, nausea, vomiting,

 

 

 

 

hepatotoxicity, parasthesias, allergic reaction

 

Biological response

Interferon alfa

Basal cell carcinoma

Flulike symptoms

 

modifiers

 

Squamous cell carcinoma

 

 

 

 

Malignant melanoma

 

 

 

Interleukin 2

Malignant melanoma

Flulike symptoms, cardiotoxicity, gastrointestinal

 

 

 

 

disorders, dyspnea, metabolic disorders, rash,

 

 

 

 

leukopenia

 

 

GM-CSF

Malignant melanoma

Flulike symptoms, gastrointestinal disorders,

 

 

 

 

metabolic disorders, rash

Miscellaneous

Platinum

Cisplatin

Adenoid cystic carcinoma

Peripheral neuropathy, renal toxicity, ototoxicity,

agents

coordination

 

Sarcomas/Osteosarcoma

nausea, vomiting

 

complexes

 

Basal cell carcinoma

 

 

 

 

Squamous cell carcinoma of head and neck

 

 

 

Carboplatin

Adenoid cystic carcinoma

Myelosuppression

 

 

 

Sarcomas/Osteosarcoma

 

 

 

 

Basal cell carcinoma

 

 

 

 

Squamous cell carcinoma of head and neck

 

 

Substituted Urea

Urea

Conjunctiva and corneal dysplasia and neoplasia

Hematopoietic depression

 

Immunosuppressive

Cyclosporine

Thyroid eye disease

Nephrotoxicity, hypertension, hepatotoxicity,

 

agents

 

Pseudotumor

neurotoxicity, nausea, vomiting, diarrhea

 

 

Azathioprine

Thyroid eye disease

Gastrointestinal disorder, leukopenia,

 

 

 

 

thrombocytopenia

 

Immune modulation

Dinitrochlorobenzene

Conjunctival and corneal dysplasia

Myelosuppression

 

 

(DNCB)

and neoplasia

 

 

Corticosteroids

Prednisone,

Thyroid eye disease

Fluid and electrolyte abnormalities, hypertension,

 

 

prednisolone

Pseudotumor

hyperglycemia, osteoporosis, myopathy,

 

 

 

Lymphoma

behavioral disturbances, cataracts, growth arrest,

 

 

 

Rosai–Dorfman

striae, ecchymoses, hirsutism

 

Monoclonal

Infliximab

Pseudotumor

Septicemia, latent tuberculosis reactivation, optic

 

antibodies

 

 

neuritis, dymelinating disease

 

 

Rituximab

Lymphoma

Interstitial pneumonitis, Stevens–Johnson disease,

 

 

 

 

tumor lysis syndrome

 

 

Cetuximab

Squamous cell carcinoma of head and neck

Fever, asthenia, transaminase elevation nausea, skin

 

 

 

 

toxicity

 

 

 

 

 

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fluorouracil, and tegafur. The predominant side effects of these drugs include myelosuppression, nausea, vomiting, and mucositis.

Vincristine is a Vinca alkaloid and has associated neurological side effects, such as paresthesias, neuritic pain, muscle weakness, ptosis, and diplopia. Etoposide is an epipodophyllotoxin. Its most common side effects are myelosuppression, alopecia, and gastrointestinal disturbances. Secondary acute myelogenous leukemia has been reported following chemotherapy with etoposide. Dactinomycin, doxorubicin, bleomycin, and mitomycin C are antibiotics. In toxicity profile, they are similar to the alkylating agents already discussed. Doxorubicin may cause a cardiomyopathy. Ventricular ejection may be monitored during treatment to detect early cardiotoxicity. A reversible alopecia also occurs with doxorubicin. Bleomycin has been reported to cause pulmonary toxicity. Mitomycin C induces a severe myelosuppression and thus has limited utility for systemic administration. Topical mitomycin C is well tolerated when delivered onto an intact conjunctival and corneal epithelium. Reported side effects have been transient and resolved upon discontinuation of the drug. These include conjunctival injection, chemosis, epiphora, and punctate keratitis.90–92,109,110 This is in contrast to earlier studies in which topical mitomycin C was applied to bare sclera, with a resultant scleral necrosis.16,117 The taxoids docetaxel and paclitaxel are derivatives of the yew tree. Their principal toxicity is myelosuppression and a severe allergic reaction. The first dose of should be administered under close observation. Interferon-alfa, interleukin 2, and granulocyte colony-stimulating factor cause flulike symptoms that may be accompanied by a rash or metabolic abnormalities.

The platinum-coordinated complexes include cisplatin and carboplatin. Their most significant side effect is myelosuppression. Cisplatin, unlike carboplatin, is more likely to be associated with nephrotoxicity and ototocixity. Cyclosporine and azathioprine are immunosuppressive agents. Cyclosporine can cause nephrotocixity, neurotoxicity, and hepatoxicity, while azathioprine’s most significant side effects are leukopenia and gastrointestinal distress.

Numerous side effects have been associated with prolonged use of corticosteroids. Most notably these include avascular necrosis of the hip, cataracts, cushingoid features, diabetes, glaucoma, hypertension, increased appetite, mood disturbances, osteoporosis, and gastric ulcers. Corticosteroid use should be limited to a few months. Agents that protect against osteoporosis and gastric irritation should be considered.

The monoclonal antibodies represent a new approach to chemotherapy, targeting specific cell surface markers in an attempt to maximize therapeutics and minimize toxicity. Infliximab, an inhibitor of tumor necrosis factor- , has been associated with severe

septicemia and reactivation of latent tuberculosis.32,33,118,119 Rare cases of optic neuritis and exacerbation of demyelinating diseases have been reported in patients receiving infliximab.120,121 Rituximab, an anti-CD20 monoclonal antibody, has been associated with hypersensitivity reactions resulting in interstitial pneumonitis and Stevens–Johnson syndrome.122,123 Rapid cell death following administration may result in tumor lysis syndrome and acute renal failure.124 Phase I to III trials with cetuximab, an antiepidermal growth factor receptor antibody, have reported fever, asthenia, transaminase elevation, nausea, and skin toxicities as the most adverse reactions.87–89

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Index

A

differential diagnosis of, 235

incidence of, age-related increase

Adenocarcinoma, 216, 217, 269–270

exenteration of

in, 17–18

Adenoma, pituitary, 275–276

potential complications of, 237

infections mimicking, 323–325

ALT. See Alternative lengthening of

prognosis and follow-up of, 237

presentation of, 323

telomeres

histopathology of, 236

rhino-orbital mucormycosis as,

Alternative lengthening of telomeres

investigation of, 235–236

324

(ALT), mechanisms effecting,

management of, 236

sino-orbital mucormycosis as,

19

orbital invasion by, 234–235, 236

323–324

Alveolar soft part sarcoma, 188, 195

orbital malignancy, secondary and,

invasion and, metastasis, 34, 39

clinical features of, 195

425

ionizing radiation and, 22–24

management and prognosis of, 195

BCC. See Basal cell carcinoma

mutations in, 11–12

morphologic features of, 195

Bone-forming lesions, 174–177

DNA and, 11–12

radiologic features of, 195

osteoblastoma, 174

somatic, 11

Amputation neuroma, 188t, 196–197

osteogenic sarcoma, 174–176

phenotypes of, 3

clinical features of, 197

clinical manifestations of, 175

progression of, metastatic event in

management and prognosis of, 197

incidence of, 175–176

temporal, 34

morphologic features of, 197

parosteal, 176–177

skin, immunosuppression and,

radiologic features of, 197

radiologic studies of, 175

28–29

Angiography

osteoma, 174, 175

telomerase activity in, 19

fistula classification with, 92

Breast carcinoma, 280, 283–284

treatment of, viruses and, 21–22

orbital tumor imaging with, 91–92

 

viruses and, 20–22

Angiolymphoid hyperplasia,

C

Cancer research

159–160

Cancer

DNA and, 3

clinical features of, 159

age-associated, 17–18

immunology and, 17

management and prognosis of, 160

MSI and, 18

Carcinomas, 82, 198. See also

morphologic features of, 159–160

antigens in

Adenocarcinoma

radiologic features of, 159

tumor-associated, 14

acinic cell, 217

Angiosarcoma, 142t, 154–155

tumor-specific, 14

adenoid cystic, 212–216, 424

clinical features of, 155

cells of, oncogene activation in, 7

clinical features of, 212–213, 214,

management and prognosis of, 155

chemicals and, 22–24

215

morphologic features of, 155

chemokines and, 16–17

management and prognosis of,

radiologic features of, 155

chromosomal alterations and, 3

214–216

Antigen presenting cells (APC)

development of

pathology of, 213–214

anticancer response and, 15–16

molecular models of, 3–12

radiologic features of, 213, 214,

antigen processing with, 16

two-hit hypothesis of, 6

215

APC. See Antigen presenting cells

DNA mutations and, 7

breast, 280, 283–284

(APC)

etiology of, 24

mucoepidermoid, 216

Arteriovenous fistulas and

genes in, 3

squamous, 225–226

malformations, 142, 156–159

expression and downregulation

Cartilage-forming lesions, 177–178

clinical features of, 156–157, 158

of, 36

chondroma as, 177

management and prognosis of, 157,

genetic disease and, 24

chondrosarcoma as, 177, 178

158–159

genomic instability in, 23

mesenchymal chondrosarcoma as,

morphologic features of, 157

immune response in, 14–17

177

radiologic features of, 157

cell-mediated, 15, 16

multiple enchondromatoses as,

 

humoral, 14–15, 16

177–178, 179

B

immune surveillance mechanisms

Maffucci syndrome, 178, 179

Basal cell carcinoma (BCC), 233–237

in, 14–24

Ollier disease, 178

clinical features of, 233–234

immunosuppression and, 27–29

Chemokines, 16–17

4 3 3

4 3 4

I N D E X

 

 

 

Chemotherapy

mismatched repair genes of, 7–8

fibrous histiocytoma as, 164–166

GD, 422–423

MSI and, 8

dermatofibrosarcoma

lymphoproliferative disease,

mutations of

protuberans, 165–166

422–423

cancer and, 7, 11–12

giant cell fibroblastoma, 166, 167

orbital inflammation and, 422–424

new perspectives on, 7–8

histiocytoses and, 166–172

orbital lymphoma, 137

replication of, 18

Langerhans cell, 166–168

orbital tumor, 422–429

telomere length and, 18–19

non-Langerhans cell, 166–172

pediatric, 410–418

RNA synthesis from, cancer

xanthogranuloma, 166, 167, 168,

side effects of, 426–429

research and, 3

169–170

SMN, 44

sequencing of, tissue diagnosis

imaging of

Cholesteatoma, 339–342, 341

with, 124–126, 127, 128

CT, 164–165

Chondrosarcoma, 177, 178

strand breaks in, 22

MRI, 164–165

mesenchymal, 177

 

pseudosarcoma, 163

Computed tomography (CT)

E

xanthogranuloma, 166, 171

advantages and disadvantages of, 88

EBRT. See External beam

bilateral, 172

artifacts of, 85, 88

radiotherapy

cutaneous, 170–172

bone window imaging with, 86

EBV. See Epstein-Barr Virus

Erdheim-Chester disease, 168,

computer image guidance with,

Ecchymosis, 58

169–170

391–392

Enchondromatoses, multiple,

juvenile, 168, 170

image interpretation with, 84

177–178, 179

necrobiotic, 170

imaging with, fibrohistiocytic

Endothelial hyperplasia, intravascular

orbital, 168

tumor, 164–165

papillary, 142, 155–156

treatments for, 171–172

indications for, 87

clinical features of, 155

Fibro-osseous lesions, 178–180

optic nerve lesions detected by,

management and prognosis of, 156

fibrous dysplasia as, 178–179, 180,

87–89

morphologic features of, 155–156

181

orbital tumor imaging with, 84–85,

radiologic features of, 155

diagnosis of, 179

86, 102, 105, 166

Eosinophilia, 159–160

imaging method of, 179

parameters of, 85

clinical features of, 159

ossifying fibroma as, 180, 181

risk of, 85

management and prognosis of, 160

 

Computer image guidance

morphologic features of, 159–160

G

biopsy and, 397

radiologic features of, 159

GD. See Graves disease

craniotomy, extended and, 393,

Epithelial tumors

Giant cell-rich lesions, 180–182

395–396

adenocarcinoma as, 269–270

giant cell reparative granuloma as,

CT, 391–392

esthesioneuroblastoma as, 270

180–181

MRI, 391–392

lacrimal gland, 204, 205

giant cell tumor, 182, 183

noninvasive approaches to, 397

orbital tumors originating from

osteitis fibrosa cystica as, 181–182

orbital tumors and, 392–393

sinonasal tract and, 266–270

hyperparathyroidism and, 181

image fusion for, 392–395

SCC, 266–269

Granular cell tumor, 188t, 194–195

radiosurgery and, 396

Epstein-Barr Virus (EBV), 30–31

clinical features of, 194

skull-based strategies and, 391–397

Erdheim-Chester disease, 168, 169–170

management and prognosis of, 195

techniques and set-up for, 392, 393

Esthesioneuroblastoma, 270, 416–417

morphologic features of, 194–195

Conjunctival tumors, 245–255, 246

Ewing tumors, 414

radiologic features of, 194

melanoma as, 249–255

Exophthalmos, 54

Granulocytic sarcoma, 413

SCC as, 245–249

External beam radiotherapy (EBRT)

Granulomatosis, Wegner’s, 66,

Craniopharyngioma, 275

Rb, 42

345–347

Crohn’s disease, 345

SMN, 44–45

Graves disease (GD), 328–333

CT. See Computed tomography

Extraocular palsy, 330

chemotherapy and, 422–423

Cystic lesions, 182–184

Eyelid tumors, 233–243

clinical features of

bone cyst as

BCC, 233–237

orbital, 329–331

aneurysmal, 182–184

melanoma as, 241–243

systemic, 328–329

simple, 182

radiation treatment for, 399,

differential diagnosis of, 332–333

 

403–404

echography of, differentiation with,

D

SCC, 237–239

331–332

Dacryocystectomy, 227, 228

SGC as, 239–241

extraocular palsy, restrictive in,

Dacryops, 205–206, 208

 

330

Dermolipoma, 296–297, 298

F

histopathology, orbital of, 329

DNA

Fibroblastic tumors, 163–164, 165

inflammatory stage of, 329

damaged, 23

Fibrohistiocytic tumors, 163–172. See

management and prognosis of, 333

gene expression of, histone

also Fibroblastic tumors

nerve dysfunction, optic in, 330

acetylation and, 12

fibromatoses, 163–166

orbital content volume stage of, 329

genome instability and, 8

aggressive, 163

orbital inflammation and, 328

methylation of, 9–12

reactive, 163

pathogenesis of, 328

radiation treatment of, 399 radiologic features of, 331–332 sign(s) of, 329–330

proptosis, bilateral as, 330 tests of, orbital change, 331 unilateral, lymphoma and, 332

H

Hemangioma, 219, 417 capillary, 142, 144–148

clinical features of, 145 management and prognosis of,

146–148

morphologic features of, 144, 146 radiologic features of, 145, 146

cavernous, 141–144, 142 clinical features of, 141–142 management and prognosis of,

144

morphologic features of, 143–144 ophthalmoscopic findings in, 143 radiologic features of, 143

Hemangiopericytoma, 142, 152–154 clinical features of, 152–153 management and prognosis of, 154 morphologic features of, 153–154 radiologic features of, 153

Hematic cyst, 339–342 Histiocytoses, 166–172

Langerhans cell, 166–168 non-Langerhans cell, 166–172 xanthogranuloma, 166, 167, 168,

169–170

Histone acetylation, 9–11 acetylase and

deacetylase, 10–11 histone, 10–11

gene expression and, 12 TSG and, 10

Hypothalamus dysfunction, 405

I

Idiopathic orbital inflammation (IOI), 312–321

myositis, orbital as, 318–321 biopsy of, 320–321 diagnosis of, 318 treatment of, 320

Immune system. See also Immunosuppression

antigen discrimination of, self/nonself, 15

cancer and response of, 14–17 APCs and, 15–16

major histocompatibility complex and, 15

orbital tumors and response of, 24 Immunosuppression

cancer and, 27–29 skin, 28–29

infection and, 29–30 invasive aspergillosis, 29

I N D E X

mucormycosis, 29–30 orbital tumors and, 29

viruses and, 27–28 orbital tumors and, 28t

IOI. See Idiopathic orbital inflammation

K

Kimura disease, 159–160 clinical features of, 159

management and prognosis of, 160 morphologic features of, 159–160 radiologic features of, 159

L

Lacrimal drainage system tumors, 221–229. See also Lacrimal gland tumors

biopsy and, 223 dacryocystectomy, 227, 228 investigation of, 222–226 lacrimal sac fossa region,

differential diagnosis of masses in, 221

lacrimal sac tumor presentation in, 221–222

suspected, 221–222 unsuspected, 221

management of, 226–227 papillomas of, 223–225 pathology of, 223

SCC as, 237–239, 245–247 squamous carcinomas as, 225–226 suspected sac tumor of, 221–222,

226–227 management of, 226

unsuspected sac tumor of, 221, 226 management of, 226

Lacrimal gland tumors, 204–219 acinic cell carcinoma as, 217 adenocarcinoma as, 216, 217

management and prognosis of, 216

adenoid cystic carcinoma as, 212–216

clinical features of, 212–213, 214, 215

management and prognosis of, 214–216

pathology of, 213–214 radiologic features of, 213, 214,

215

dacryops as, 205–206, 208 epithelial, 204, 205t hemangioma as, 219 malignant mixed tumors as,

211–212

clinical features of, 211, 212 management and prognosis of,

211–212 pathology of, 211

radiologic features of, 211

4 3 5

malignant rhabdoid tumor as, 219 mucoepidermoid carcinoma as, 216 management and prognosis of,

216 nonepithelial, 204 oncocytoma as, 219 orbital, 81–82

carcinoma as, 82 dacryoadenitis as, 82 lymphoid tumors of, 81 pleomorphic adenoma as, 81

pleomorphic adenoma as, 206–211 clinical features of, 206, 208, 209 management and prognosis of,

208, 209, 211 pathology of, 209–211

radiologic features of, 207–209 radiation treatment of, 401

SCC as, 219

solitary fibrous tumor as, 218, 219 spindle cell myoepithelioma as,

219

staging of, 355–356 Warthin tumor as, 219

Leiomyoma, 142, 159 clinical features of, 159

management and prognosis of, 159 morphologic features of, 159 radiologic features of, 159

Loss of heterozygosity (LOH), tumor cells and, 5, 6

Lymphangioma, 99, 100, 142, 148–152

clinical features of, 148–149 hemorrhage, spontaneous of, 146,

148

location of, 148, 149, 150 management and prognosis of,

150–151

morphologic features of, 150 proptosis of, 148

radiologic features of, 150 Lymphoma, 31

unilateral, 332 Lymphoproliferative disease, 77–78,

422–423

M

Maffucci syndrome, 178, 179 Magnetic resonance imaging (MRI),

89

advantages and disadvantages of, 88 artifacts of, 90, 91

computer image guidance with, 391–392

image interpretation with, 84 imaging with, fibrohistiocytic

tumor, 164–165 indications for, 87 nanoparticle, 110–111

optic nerve lesions detected by, 87–89

4 3 6

I N D E X

 

 

 

Magnetic resonance imaging

Metastatic tumors, 279–287

clinical features of, 190–191

(continued)

clinical findings of, 279–281

management and prognosis of, 192

orbital tumor imaging with, 84,

diagnostic procedures for, 281–282

morphologic features of, 191, 192

86–91, 102, 105, 166

orbital imaging as, 281–282

radiologic features of, 191, 192

signal types in, 89

tissue diagnosis as, 282

Neurofibromatosis, 198–201

parameters of, 89

epidemiology of, 279

ophthalmic manifestations of type

risk of, 90–91

incidence of, 279

1, 198–201

techniques for, 106–108

management and prognosis of,

ophthalmic manifestations of type

diffusion-weighted magnetic

282–283

2, 201

resonance images as, 106

orbital, origins of, 283–287

diagnosis of, 199

magnetic resonance dynamic

breast carcinoma as, 280,

NHL. See Non-Hodgkin’s lymphoma

color mapping, 107–108, 109,

283–284

(NHL)

110

paraneoplastc orbital syndrome

Non-Hodgkin’s lymphoma (NHL), 27,

magnetic resonance

as, 286–287

28, 135b, 137–139

spectroscopy, 106–107

sites, miscellaneous primary as,

 

tissue characterization by, 89

283–286

O

Malignant peripheral nerve sheath

sites, unknown primary as, 281,

Ocular tumors, 257–264

tumor, 188, 192–193

286

melanoma as, choroidal, 260–264

clinical features of, 192–193

pediatric, 311–312

retinoblastoma as, 257–260

management and prognosis of, 193

Microsatellite instability (MSI), 8

Ollier disease, 178

morphologic features of, 193

cancer, age-associated and, 18

Oncocytoma, 219

radiologic features of, 193

DNA mismatched repair genes

Oncogenes, 4

Melanoma, 241–243

and, 8

activation of

choroidal, 260–264

orbital tumors and, 8–9

cancer cell, 7

clinical features of, 241–242

Mohs microsurgical technique,

TSGs and, 5

conjunctival, 249–255

120–121

tumor development and, 4

clinical features of, 249–250

MRI. See Magnetic resonance

Oncogenesis

histopathology variations of,

imaging

aging and, 17–20

250–255

MSI. See Microsatellite instability

current concepts of, 1–46

differential diagnosis of, 242

(MSI)

viruses and, 20–22

histopathology of, 242–243

Mucocele

Ophthalmoscopy, 64

investigation of, 242

orbital, 342–343

Optic nerve glioma, 307–310, 416

management of, 243

presentation of, 342–343

diagnosis of, 308–309

orbital invasion by, 242

primary, 342

imaging of, 309–310

prognosis and follow-up of, 243

secondary, 342

incidence of, 307–308

Melanotic neuroectodermal tumor,

orbital inflammation and, 342–343

prognosis of, 308

197

orbital tumors and, 79

treatment of, 310

clinical features of, 197

pediatric, 301

Orbit. See also Orbital lymphoma;

management and prognosis of, 197

Mucormycosis

Orbital tumors; Paraneoplastc

morphologic features of, 197

rhino-orbital, 324

orbital syndrome

radiologic features of, 197

sino-orbital, 323–324

biopsy of, 113–128

Meningioma, 69

Myoepithelioma, spindle cell, 219

core, 114–115, 116

ectopic, 274–275

 

excisional, 113, 114, 119

optic nerve sheath, 69–70

N

fine-needle aspiration, 115–118

radiation treatment of, 399–400

Neoplasia. See also Tumors

incisional, 113

sphenoid ridge, 272–274

inflammation and infection of the

intraoperative, 118–121

Metastasis

orbit v., 317–326

sentinel node, 121–122

cancer progression and, 34

inflammation mimicked by,

techniques for, 114

cascade of, carcinogenic steps

321–323

tissue diagnosis for, 122–128

during, 35

biopsy of, 322–323

bony, 102

disease of

diagnosis of, 322

clinical evaluation of, 51–59

orbital tumor, 39

rhabdomyosarcoma as, 322,

history and, 51

orbit and, 38–39

324–325

ocular examination and, 51–53

dissemination and, 34

inflammation mimicking, 317–321

dissemination in, 37, 38

distant, 36

allergic fungal disease of the

ecchymosis in, 58

gene expression, 37

nose and paranasal sinuses as,

enucleation of, 376–377

invasion and, 34, 39

325, 326

implants and, 377

orbital, 36–39, 426

imaging of, 317–318, 319

indication of, 376

local orbital environment and,

IOI as, 317–321

surgical techniques for, 376–377

36–38

Neuroblastoma, 197–198, 311–312,

examination of, 53–59

origins of, 283–287

413–414

exophthalmos and, 54

orbital tumor, 34–39, 78, 79

Neurofibroma, 188, 189–192

globe displacement and, 56, 57

 

I N D E X

4 3 7

 

 

levator function and, 53–54

specific, 343–347

investigation of, 134–136, 137

neuro-ophthalmologic, 61–70

tissue destruction and, 342

management of, 136–139

proptosis and, 54–55

tumor development and, 335–347

modality therapy for, 137

exenteration of, 378–384

Wegner’s granulomatosis as,

morphological features of, 133–134

bone resection and, 379

345–347

primary versus secondary, 135t

eyelid removal and, 380, 381

intracranial disease extension into,

radioimmunotherapy for, 137–139

granulation process of, 380–381

66–70

rituximab in, 138–139

healing process after, 381–382,

adult malignant glioma as, 69

Zevalin in, 138–139

383

meningiomas as, 69

radiotherapy for, 136–137

implants and, 381, 382, 383

optic nerve sheath meningiomas

staging workup for, 135, 136

objective of, 378–379

as, 69–70

studies of, 134

orbitocraniofascial approach to,

optic pathway glioma as, 66–69

Orbital myeloid sarcoma, 312

383

malignancy of

Orbital tumors. See also Bone-

procedure approaches to, 380

adenoid cystic carcinoma as, 424

forming lesions; Cartilage-

reconstruction after, 383–384

BCC as, 425

forming lesions; Conjunctival

subtotal, 378

carcinomas as, 424

tumors; Cystic lesions; Eyelid

total, 378, 379–380

melanoma, malignant as, 426

tumors; Fibrohistiocytic

exploration of, surgical, 375

osteosarcoma as, 425

tumors; Fibro-osseous lesions;

extraocular muscle thickening in

primary, 424

Giant cell-rich lesions; Graves

assessment of, 79–80

sarcomas as, 424–425

disease; Lacrimal drainage

metastatic tumors and, 79–80

SCC as, 425–426

system tumors; Lacrimal gland

orbital inflammatory disease and,

secondary, 425–426

tumors; Metastatic tumors;

79

metastasis in, 38, 426

Ocular tumors; Orbital

slow-draining carotid cavernous

local orbital environment and,

lymphoma; Pediatric orbital

fistula and, 80

36–38

tumors; Periocular tumors;

thyroid eye disease and, 79, 80

radiation treatment of, 400

Periorbital tumors; Peripheral

globe displacement in, 56, 57

mucocele in, 342–343

nerve tumors; Pseudotumors;

cavernous hemangioma, 142

presentation of, 342–343

Vascular orbital tumors

Graves disease in, 79, 80

primary, 342

anatomic site

hemorrhage of, 339–340

secondary, 342

autopsy classification of, 353,

hyperemia in, 57–58

nerve assessment of, 80–81

354

imaging of, 65–66, 67

normal, 74

clinical classification of, 353–354

basics of, 84–92

optic disk atrophy and, 54

pathologic classification of, 353,

CT, 84–85, 86

optic nerve lesions in, 80–81

354

developments in, 105–110, 107

optic neuritis in, 80

retreatment classification of, 353,

MRI, 84

proptosis in, 54–55

354

new concepts in, 104–111

asymmetrical, 56

anterior-inferior, 57

purposes of, 104

diagnosis of, 56

anteriorly located, palpation of, 58

infections of, 335–338

examination of, 56

assessment of, 73–79

cancer mimicked by, 323–325

exophthalmometers and

biopsy of, 113–128, 364

fungal, 335–336, 338

measurement of, 55–56

incisional, 369

parasitic, 336–338, 339

pseudotumor cerebri in, 80

bone changes induced by, 95–96

tuberculosis as, 335

sarcoidosis in, 66, 343–347

hyperostosis and, 96

inflammation of

diagnosis of, 344

bony orbit and, 102

amyloid deposits as, 346, 347

treatment of, 343, 344–345

calcification detection in, 96

bone destruction and, 341–342

systemic disorders and affect on,

cancer etiology and, 24

chemotherapy and, 422–424

66

changing nature and behavior of,

cholesteatoma as, 339–342

giant cell arteritis as, 66

27–31

Crohn’s disease as, 345

Polyarteritis nodosa as, 66

chemosis in, 51, 52

GD as, 328–333

sarcoidosis as, 66

chemotherapy for, 422–429

hematic cyst as, 339–342

Wegner’s granulomatosis as, 66

side effects of, 426–429

idiopathic, 423

tumorlike conditions in, 315–347

chorioretinal folds in, 51–52

mucocele, 342–343

xanthelasmas in, 58

computer image guidance and,

neoplasia mimicked by, 317–321

Orbital lymphoma, 133–139. See also

392–393

neoplasia mimicking of, 321–323

Orbital tumors

conjunctiva congestion and, 52

neoplasia v. infection and,

chemotherapy for, 137

craniotomy, extended approaches

317–326

classification of, 134, 135–136

and, 393, 395–396

nonspecific, 338–343

clinical features of, 133, 134

cystic features of, imaging

pseudotumor, orbital as, 338–339

diagnosis of, 135, 137

technique detection of, 100

sarcoidosis as, 343–345

non-Hodgkin’s, 135b

debulking procedure of, 369

signs of, 322

management of, 137–139

diagnosis of, 49–128

Sjögren’s syndrome as, 340, 345

immunotherapy for, 137–139

imaging in differential, 94–102