Multiple Lucent Skull Lesions
Miral D. Jhaveri, MD
DIFFERENTIAL DIAGNOSIS
Common
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Skull Normal Variants
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Venous Lakes
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Emissary Veins, Transcranial
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Arachnoid Granulations
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Prominent Convolutional Markings
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Parietal Foramina
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Treatment-Related
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Burr Holes
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Surgical Defects, Calvarial
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Metastases, Skull
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Osteoporosis
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Myeloma
Less Common
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Langerhans Cell Histiocytosis
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Hyperparathyroidism
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Lymphoma, Metastatic, Intracranial
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Hemangioma
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Leukemia
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Osteomyelitis, Skull
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Osteoradionecrosis
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Chiari 2 (Lacunar Skull)
Rare but Important
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Neurosarcoid
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Neurofibromatosis Type 1 (Lambdoid Defects)
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Syphilis, Acquired
ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
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As with solitary lucent skull lesion, margins helpful
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Sharply demarcated: Treatment-related, myeloma
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Permeative: Metastasis, osteomyelitis
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Beveled: Histiocytosis
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Inner table involvement: Convolutional markings, arachnoid granulations
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Helpful Clues for Common Diagnoses
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Skull Normal Variants
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Venous Lakes
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Diploic venous can usually be traced to area of lucency
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Slightly ragged configuration, poorly defined margin
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Emissary Veins, Transcranial
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Extremely variable positions
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Common in frontal and parietal bones
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Very thin walls
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Communicate with meningeal veins and dural sinuses
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Arachnoid Granulations
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Punched out defects inner table subjacent to dural venous sinuses
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CSF density/intensity
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Prominent Convolutional Markings
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Related to pulsation of brain
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Inner table, frequent in children
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Become prominent in craniosynostosis, chronic raised intracranial pressure
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Parietal Foramina
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Two symmetric openings on each side of sagittal suture in the upper edge of parietal bones
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Usually very small, permit passage of emissary veins
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Treatment-Related
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Burr holes, shunt-related, surgical defects
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Sharply marginated
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Metastases, Skull
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Permeative skull destruction ± scalp/dural soft tissue
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Often known primary malignancy
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Commonly lung, breast, renal, thyroid
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Osteoporosis
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Older age group
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Spotty demineralization appearing as lucent lesions
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Myeloma
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Multiple, well-circumscribed, lytic, punched out, round lesions
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Skeletal survey helpful
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Helpful Clues for Less Common Diagnoses
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Langerhans Cell Histiocytosis
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Sharply marginated lytic defect with bevelled margins
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Associated soft tissue mass
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Large lesions: Geographic destruction
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Brain: Thick enhancing infundibulum, absent posterior pituitary bright spot
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2-5 years: Multifocal disease
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Hyperparathyroidism
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Hemangioma
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Sharply marginated expansile lesion
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Diploic space, honeycomb, or sunburst appearance pattern
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1/3 have thin sclerotic rim
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Multiple uncommon
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Leukemia
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Osteopenia with multiple lytic lesions
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Sutural diastasis: Produced by ↑ intracranial pressure
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Tubular and flat bones more commonly involved
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Skeletal survey may be helpful
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Osteomyelitis, Skull
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Permeative destruction ± scalp/epidural soft tissue
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Usually occurs as a complication of trauma or sinusitis
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Brain abscess is most common complication
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Osteoradionecrosis
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Mixed region of lysis and sclerosis
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Radiates outward from epicenter of radiation portal
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Chiari 2 (Lacunar Skull)
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Caused by inherited mesenchymal defect, not hydrocephalus/increased intracranial pressure
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Not same as prominent convolutional markings (normal variant)
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Present at birth, largely resolves by 6 months
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Minor changes may persist into adulthood
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Involves both inner, outer tables
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Squamous portions of temporal/occipital bones, parietal bones
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Helpful Clues for Rare Diagnoses
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Neurosarcoid
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Uncommon
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Well-circumscribed lytic lesion
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Involves inner, outer tables of calvarium
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Sharp, non-sclerotic margins
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Neurofibromatosis Type 1 (Lambdoid Defects)
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Lambdoid suture defect
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Associated sphenoid wing dysplasia
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Plexiform neurofibromas of scalp, orbit common
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