The Orbits: Orbital Masses
Diagnosis | Findings | Comments |
Retinoblastoma Fig. 4.122, p. 374 Fig. 4.123, p. 374 | Radiograph/CT: usually calcified mass in child < 3 y. | (see Table 4.30 ) |
Hemangioma | CT/MRI: usually intra-/extraconal but may spread to involve globe. Best imaged with MRI to assess extent. | (see Table 4.35 ) |
Melanoma | MRI: T1 hypointense mass related to choroids, which enhances with contrast. CT: enhancing mass. | Older children/teenagers. Best imaged with MRI. |
Diagnosis | Findings | Comments |
Optic nerve glioma | MRI: Best to evaluate extent. Mass isointense/slightly hyperintense to normal white matter on T1 and T2 and shows prominent CE. Causes fusiform enlargement of nerve, which is buckled and kinked. | One-third in the setting of NF1 and characteristically bilateral. |
Hemangioma | CT/MRI: usually extraconal but some lesions intraconal. | (see Table 4.35 ) |
Inflammatory pseudotumor | CT/MRI: unilateral or bilateral uveoscleral thickening with enhancement, an enhancing retro-ocular mass, or enlargement of extraocular muscles, tendons, and lacrimal gland. | Idiopathic disorder with inflammatory, lymphoid infiltration of intraorbital tissues. |
Lymphoma and metastases | CT/MRI: Lymphoma: diffuse infiltration of entire intraconal region. Shows slight to moderate enhancement. | Lymphoma best imaged with MRI. |
Metastases: neuroblastoma/rhabdomyosarcoma, usually also with extraconal and orbital wall involvement. | ||
Hematoma | CT: Hyperdense if acute. CT best for evaluating fractures. | If traumatic, assess for foreign body. |
Rhabdomyosarcoma | CT/MRI: May be primary or secondary. Usually intraconal or involving muscle but may extend extraconal and intracranial. MRI best for extent: T1 iso-/hypoin-tense relative to muscle and T2 hyperintense. Degree of enhancement varies. Enhanced scans in coronal plane best for evaluating intracranial extension. | Usually embryonal subtype. |
Diagnosis | Findings | Comments |
Dermoid/epidermoid Fig. 4.129, p. 378 | CT/MRI: well-demarcated, anterior extraconal mass with fatty, fluid, or mixed contents. Majority superolateral related to frontozygomatic suture. CT shows osseous remodelling ± fine calcification in cyst wall. | MRI if features are not diagnostic or suspect deep extension into sinuses, masticator space, or intracranially. |
Teratoma Fig. 4.130, p. 378 | MRI: best for assessing extent. CT: best for showing calcification. Usually complex with cystic and solid elements, composed fat/fluid/calcium and soft tissue. Often marked expansion of the orbit and displacement of the globe. | Benign but cause severe progressive proptosis in infancy. Transspatial. |
Capillary hemangioma | MRI is imaging modality of choice to show extent especially if suspected intracranial extension. Use enhanced T1 and T2, axial, and coronal planes. T1 iso- or hypointense, showing diffuse intense enhancement postcontrast. T2 heterogeneous/hyperintense with frequent flow voids. MRA unhelpful as vascular component is at capillary level. CT: slightly hyperdense homogeneous mass with intense enhancement. | Usually present before 6 mo. Only imaged if symptomatic or fail to involute. |
Lymphatic, venous, and venolymphatic malformations | MRI best to show extent; use fat-saturated axial and coronal sequences. See multilocular, transspatial, variably enhancing mass. Fluid-fluid levels with signal corresponding to age of blood products. Pure lymphatic malformation is nonenhancing. Venolymphatic variable. | Present in childhood with progressive, slow-growing mass. Usually extraconal but often transspatial. Include brain imaging for associated intracranial abnormalities especially in venolymphatic malformations. |
Malignancy (lacrimal gland/lymphoma/leukemia) Fig. 4.131, p. 378 | Primary lacrimal gland malignancy rare and associated with bony destruction. Lymphoma/leukemia: well-defined high-density mass involving lacrimal gland or isolated soft-tissue mass. | May present with exophthalmos (see Table 4.36 ). |
Orbital cellulitis/subperiosteal abscess Fig. 4.132, p. 378 | CECT: thickening and edema of orbital soft tissues representing cellulitis and/or phlegmon. Low-density, rim-enhancing area represents subperiosteal abscess. Usually extraconal but can extend intraconally. Procure axial and coronal images. | Need brain imaging (CT or MRI) to evaluate intracranial complications of sinusitis. MRI more sensitive. |
Diagnosis | Findings | Comments |
Metastases/lymphoma/leukemia | Radiograph/CT: show defect or destruction often not confined to orbits. CT/MRI shows adjacent soft-tissue mass and exophthalmos. | Most common causes are neuroblastoma, hematological malignancy, rhabdomyosarcoma, and Ewing sarcoma. |
Extension from lacrimal gland/tumor | Radiograph/CT/MRI: Localized wall expansion adjacent to tumor. Lesions have a sclerotic rim. | |
Spread of adjacent infection | CT: usually subperiosteal abscess but if longstanding may cause destruction of orbital wall. | Wall involvement usually due to aggressive pathogen particularly aggressive fungal sinus infections such as mucormycosis and aspergillosis (see Table 4.35 ). |
Adjacent tumor | CT: ethmoid or maxillary antral tumors invade by direct extension. | |
Mucocoele | Radiograph/CT: Bony expansion of adjacent sinus, which protrudes into orbit. Sinus may be sclerotic if chronically infected. Contains nonenhancing soft tissue. | Present with unilateral proptosis. Most common is frontal sinus with palpable mass in superome-dial orbit. |
LCH | Radiograph/CT: Single or multiple lytic lesions with beveled edges and adjacent soft-tissue mass. Often have exophthalmos. MRI needed if sphenoid bone involved and present with diabetes insipidus. | Need skeletal survey to look for other bone lesions. |