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Definition: Lacrimal gland dermoids (LGDs) represent congenital, non-neoplastic choristomas, containing cytologically normal tissue not normally found at that location.
Synonym: anterior orbital dermoid (AOD).
Classic clue: Young child presents with smooth scalloping of orbital wall by adjacent unilateral lacrimal-gland mass having hyperdense wall, decreased attenuation center, increased T1 signal intensity, and no postcontrast enhancement.
LGDs are typically unilateral well-defined cyst-like masses containing fluid or fat.
LGDs may contain calcifications.
LGDs are habitually filled with hypodense material (see Figure 41-1 ).
LGDs are typically nonenhancing postcontrast, but may exhibit enhancement if infected.
Central cavity may contain keratin and other cystic debris.
LGDs commonly cause scalloping or sclerosis of adjacent bone.
LGDs may cause proptosis with medial displacement of globe (see Figure 41-1 ).
LGDs may show “dirty fat” when infected (see Figure 41-2 ).
LGDs are well circumscribed initially retaining lacrimal gland shape.
T1 increase secondary to fatty components is nearly pathognomonic for dermoid in this location.
T2 hyperintense to extraocular muscles (EOMs).
T1 + Gd exhibits no enhancement (unless infected).
Internal debris can cause heterogeneous intracystic signal.
Dedicated orbital imaging thin-section, fat saturation, Gd-enhanced, axial, and coronal sequences are essential for the best evaluation.
Frequently found in the first year of life.
Present as a palpable painless nodule near the lacrimal gland.
May become infected (see Figure 41-2 ).
Surgery is the accepted standard treatment.
Excision is recommended to prevent impromptu rupture or cutaneous fistula formation.
Leakage of cyst contents can cause significant inflammation and postoperative recurrence.
Lesions excised with the capsule intact rarely recur.
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