Neuroradiology #37

Clinical Data

40-year-old female presents with acute severe headache at the emergency department.
The neurologist wants to rule out an intracranial haemorrhage and orders a CT brain.

Showing images CT without contrast

More images: MRI

What do you see?

What do you see?

CT shows
* low attenuating suprasellar lesion (fat density) with rim calcification.
* multiple scattered smaller similar subarachnoid lesions supra and infratentorial.
* enlarged supratentorial ventricles.

MRI shows
* the suprasellar lesion shows T1 heterogenous and T2-hyperintense signal,
* multiple scattered T1-hyperintense foci subarachnoid and intraventricular in the left frontal horn (arrows).
* no enhancement.
* no diffusion restriction (not shown).

What is the most likely diagnosis?

What is the most likely diagnosis?

Ruptured suprasellar dermoid cyst.

Ruptured intracranial dermoid cyst

Intracranial dermoid cysts are often incidental findings and most do not cause symptoms. Both dermoid and epidermoid cysts are ectodermal in origin and lined by stratified squamous epithelium. In addition, dermoid cysts contain epidermal appendages such as sebaceous glands which secrete sebum, an oily substance.

Symptoms occur due to mass effect or rupture. In case of rupture, dermoid material (sebum droplets) can leak into the subarachnoid space which can lead to chemical meningitis and cause symptoms such as headaches, seizures, and vasospasms.
CT shows
-hypoattenuating primary lesion (fat density due to sebum).
-typically, not exclusively, in midline location.
-sometimes rim calcification of the primary lesion.
-smaller similar hypoattenuating lesions in the subarachnoid space in case of rupture.

MRI shows
-generally T1-hyperintense signal (sebum).
-scattered T1-hyperintense droplets in the subarachnoid space and intraventricular. Fat-fluid level within the ventricles.
-variable T2 signal.
-generally no enhancement of the lesion. Leptomeningeal enhancement in case of chemical meningitis.

References

https://radiopaedia.org/articles/intracranial-dermoid-cyst-1

Neuroradiology #36

Clinical Information

A young adult male presents with progressive limb numbness and gait disturbances. Medical history was unremarkable.
MRI brain was performed and showed no intracranial abnormalities.
The neurologist ordered an MRI scan of the cervical spinal cord.

Showing MRI images:

What do you see?

A long segment T2-hyperintense lesion in the posterior part of the cervical myelum, specifically in the dorsal columns (‘inverted V-sign’). There is no perilesional oedema, mass effect, or enhancement.

What is the differential diagnosis based on the MRI findings?

Subacute Combined Degeneration due to Vitamin B12 deficiency or inactivation
Intrathecal MTX-induced myelopathy
Vitamin E deficiency
Copper deficiency
Tabes dorsalis (neurosyphilis)
HIV vacuolar myelopathy

More information
The laboratory values of Vitamine B12 were normal, as well as Copper and Vitamin E values.
HIV and Syphilis screening were negative.

The patient finally confirmed recreational (ab)use of nitrous oxide.

What is the most likely diagnosis?

Subacute Combined Degeneration due to nitrous oxide-induced Vitamin B12 inactivation.

Subacute Combined Degeneration

SCD is a neurological complication of vitamin B12 deficiency or inactivation. Several drugs can inactivate vitamin B12 such as metformin and nitrous oxide. Abuse of nitrous oxide inactivates vitamin B12 by oxidizing Cobalt-ion. In case of nitrous oxide abuse, vitamin B12 serum levels can appear normal.
Clinical symptoms include loss of vibration and proprioception in hands and feet and sensory gait ataxia. In severe cases, muscle weakness especially in the distal extremities can be seen.
MRI shows bilateral T2 high signal in the dorsal columns (inverted V sign) which explain the sensory deficits (paraesthesia, propriocepsis, and fine touch). In severe or untreated cases, the lateral columns may be involved leading to motor deficits such as limb weakness, spasticity, and paraplegia. The lesions typically involve a long segment in the cervical and higher thoracic spinal cord and show no enhancement or cord expansion.
It is crucial to promptly identify this disease and treat the vitamin B12 deficiency and/or discontinue the inactivating drug to prevent serious complications.

Neuroradiology #35

What do you see in the following images?

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Polymicrogyria
Bilateral cortical thickening with numerous small gyri with signal characteristics similar to normal grey matter.
Dilated bilateral perivascular spaces in the subjacent white matter.

Neuroradiology #34

54-year-old woman:
– Known breast cancer
– Arm paresis and soft-tissue lump

What are the salient findings?

Left: NECT, bone algorithm. Aggressive-like bone lesion with permeative pattern and hair on end periosteal reaction

Right: MRI T1 post-Gd. Associated trans-diploic soft-tissue mass with extracranial and intracranial-extraaxial components. Solid, homogeneous and avidly enhancing. Contiguous dural thickening and enhancement.

What is the differential diagnosis?
DIFFERENTIAL DIAGNOSIS FOR TRANS-DIPLOIC SKULL VAULT LESION WITH AGGRESSIVE-LIKE BONE AFFECTATION

1- Metastasis
2 – Myeloma/Plasmocytoma
3 – Lymphoma
4 – Primary Bone Tumour (Osteosarcoma)
5 – Dural Lesion (Meningioma+++, Hemangiopericytoma)

METASTASES
METASTASES

– Always consider in older patients
– Multiplicity and known primary

Imaging
Varies depending on tumor type and aggressiveness

– Lytic: Most tumor types
– Permeative: Highly cellular and small-round cell tumors (PNET, small cell lung, lymphoma)
– Sclerotic/mixed: Prostate, breast. Less frequently: Transitional cell, neuroendocrine, PNET
– Hypervascular: Renal cell, melanoma, thyroid, hepatocarcinoma, lung, neuroendocrine

Possible soft-tissue components

LYTIC AGGRESSIVE BONE LESION/S IN PATIENT >40 years old. METASTASES vs MYELOMA

MULTIPLE MYELOMA (MM)/SOLITARY PLASMOCYTOMA
MULTIPLE MYELOMA (MM)/SOLITARY PLASMOCYTOMA

– Affects older patients (median 68-70 years). Very rare under 40 years (<10%) Imaging
MM 4 patterns of bone involvement
– Diffuse lytic bone infiltration simulating osteopenia
– Multiple focal lytic well-defined lesions
– Solitary plasmacytoma
– Sclerotic bone lesions (exclusively associated with POEMS sd)

Solitary plasmacytoma in the skull: lytic, aggressive trans-diploic, soft tissues, and hypervascular aspect

CLASSIC APPEARANCE OF MM
CLASSIC APPEARANCE OF SOLITARY PLASMOCYTOMA OF THE SKULL
LYMPHOMA
LYMPHOMA

– 7% of all bone malignancy; 5% of extranodal lymphoma
– All ages; predominates in adults (peak 50-60 years); men/women 1.5:1
– Secondary dissemination >>> primary bone lymphoma
– Imaging characteristics of a hypercellular small round cell tumour

Imaging
– Trans-diploic permeative bone pattern and abundant of tissue components (small round blue cells spread through Haversian canals conditioning a striking relatively little bone destruction in comparison to important soft-tissue lesions)
Hyperdensity on NECT, T2 hypodensity and striking diffusion restriction on DWI (all signs related to hypercellularity)
– Homogenous enhancement
– No or little necrosis

CHARACTERISTIC IMAGING FINDINGS FOR LYMPHOMA
OSTEOSARCOMA
OSTEOSARCOMA

– Most common primary high-grade bone sarcoma
– Bimodal distribution: 10-14 and >40 years old
Extremely rare in the skull in adults, and much more frequently arising from coexisting Paget’s disease> >previously irradiated bone> or bone infarction
– Clinically, quickly growing painful mass

Imaging
– Destructive, aggressive lesion, with periosteal reaction, soft tissue-mixed lytic-blastic component. May show “fluffy”, “cloud-like” osteoid matrix.

Secondary osteosarcoma arising in a Pagetic skull. See the globally aggressive pattern and the deep hypointensities inside the soft-tissue components probably transducing osteoid matrix (usually easily depicted on CT, non-available in this case)

MENINGIOMA
MENINGIOMA

– Most common brain tumor (36% of all brain tumors)
– Predilection for middle-aged females
– Can produce neurologic symptoms due to compression
– Most do not infiltrate bone, but when they do it, the hyperostosis is very specific, virtually pathognomonic
– Intra-diploic or trans-diploic meningiomas are less frequent

Imaging
Key signs:
Calcifications
“Dural tail” and extra-axial semiology
Hyperostosis (very specific)
– Hypervascular with intense homogenous enhancement

*Even the great specificity of the hyperostosis, bone involvement can be VERY VARIABLE including aggressive-like lysis and periosteal reactions that do not exclude or go against the diagnostic

Ddx: Hemangiopericytoma (Solitary Fibrous Tumor New WHO 2016 classification). Younger, frequently male patients. Osteolysis possible, but NO hyperostosis. NO calcifications. The rest of imaging features identical to meningioma, differentiation is very difficult and challenging

EXAMPLES OF THE MULTIPLE FACES OF MENINGIOMAS AND THEIR BONE INVOLVEMENT. REMEMBER, POLYMORPHISM IS AN IMPORTANT FEATURE OF THIS ENTITY

With all the information mentioned above:

Could meningiomas condition aggress periosteal reaction? Does it go against its diagnosis

Meningiomas are very frequent, specially in middle-aged woman, if all or the vast majority of features favour this diagnosis, a relatively atypical bone affectation (lysis, periosteal reaction instead of the virtually pathognomonic hyperostosis) may not change the diagnostic orientation.

Bonus clues and some advance imaging pearls

Diffusion: Striking restriction in lymphomas
Perfusion: Striking high rCBV in meningiomas
Spectroscopy: Alanine (and GLX) in meningiomas. Striking high Cho in lymphoma and plasmacytoma. Striking high lipids in metastases

Back to the case:

ARE THE ADVANCED IMAGING TECHNIQUES HELPFUL?

FINAL DIAGNOSIS: MENINGIOMA (WHO GRADE 2)

TAKE HOME MESSAGE REGARDING MENINGIOMA

– Very frequent, specially middle-aged women
– Important to know the classic characteristic features, some of them are very specific; but recognize the great polymorphism/many faces of this entity
– Advanced imaging can be helpful
– Not all the lesions in a neoplastic patient are metastases

Neuroradiology #33

72-year-old male:
– With known pulmonary neuroendocrine tumor
– New onset dorsal pain

What do you see?

Vertebral blastic metastasis from pulmonary neuroendocrine origin presenting as an ivory vertebra.

IVORY VERTEBRAE (differential)

– Paget
– Lymphoma
– Metastasis on men: prostate
– Matastesis on women: breast

Do not forget: transitional cell carcinomas, neuroendocrine tumours, medullary thyroid carcinoma and osteosarcoma.

Neuroradiology #28

A 24-year-old female patient with headache. What do you see?

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Multinodular and vacuolating neuronal tumor (MVNT): Cortical ribbon-juxtacortical T2 hyperintense (a-b) round to oval nodular lesions, not suppressed on FLAIR images (c) and usually no enhancement (d) may show fair enhancement rarely, without diffusion restriction (not shown)

Neuroradiology #24 – Flashcard

89-year-old female patient with aplastic anemia. Showing CT images without contrast media. What do you see?

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CT images without contrast media: Subacute isodense right subdural hematoma, revealed with narrowing of right cerebral hemispheric sulci and right lateral ventricle and minimal midline shift (red arrows), acute left subdural hematoma (blue arrow)

Neuroradiology #22 – Flashcard

What do you see on these images?

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Oligodendroglioma

CT scan shows a large calcified lesion. MRI shows a large cortical-based high T2 lesion with cystic component and dark T2 foci corresponding to the calcifications. Post-contrast images show patchy enhancing areas.  

Differential Diagnosis

DNET (usually may calcify) ganglioglioma (cystic areas, enhancing solid component, may calcify).