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