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Training Collections
Library Memberships
On-demand course library with video lectures, expert case reviews, and more
Fellowship Certificate™ Programs
Practice-focused training programs designed to help you gain experience in a specific subspecialty area.
Ultimate Learning Pass
Unlock access to our full Course Library and all self-paced Fellowships.
Continuing Medical Education (State CME)
Complete all of your state CME requirements in one convenient place.
Noon Conference (Free)
Get access to free live lectures, every week, from top radiologists.
Case of the Week (Free)
Get a free weekly case delivered right to your inbox.
Case Crunch: Rapid Case Review (Free)
Register for free live board reviews.
Dr. Resnick's MSK Conference
Learn directly from the MSK Master himself.
Lower Extremities MRI Conference
Musculoskeletal Imaging
Emergency Imaging
PET Imaging
Pediatric Imaging
For Training Programs
Supplement your training program with case-based learning for residents, registrars, fellows, and more.
For Private Practices
Upskill in high growth, advanced imaging areas.
Compliance
NewTrack, fulfill, and report on all your radiologists' credentialing and licensing requirements.
Emergency Call Prep
Prepare trainees to be on call for the emergency department with this specialized training series.
1 topic,
15 topics, 59 min.
Case: Assessing Lesion Position
4 m.Intra-Axial vs. Extra-Axial Lesions
3 m.Case: Typical Locations of Meningiomas
3 m.Case: Defining Meningioma
2 m.Case: Meningioma Appearance on MRI
6 m.Case: Meningioma Enhancement
3 m.Case: Meningioma vs. Schwannoma
5 m.Case: Meningiomas in the Posterior Fossa
5 m.Case: Planum Sphenoidale Meningioma with Orbital Apex Extension
4 m.Case: Suprasellar Meningioma
7 m.Case: Optic Nerve Meningioma
6 m.Case: Vascular Encasement of Meningioma With Absent Vasogenic Edema
3 m.Case: Parafalcine Meningioma
6 m.Case: Meningiomatosis
5 m.Case: Solitary Fibrous Tumor
6 m.9 topics, 38 min.
Case: Hemangioblastoma and Von Hippel-Lindau Syndrome
7 m.Case: Recurrent Hemangioblastoma
3 m.Case: Spinal Hemangioblastoma
4 m.Case: VHL Renal Lesions
6 m.Case: Endolymphatic Sac Tumor
3 m.Case: Central Neurocytoma
6 m.Case: Lhermitte-Duclos Disease/Dysplastic Cerebellar Gangliocytoma
6 m.Case: Epidermoid Cyst
4 m.Case: Rhabdomyosarcoma
4 m.10 topics, 44 min.
Introduction to Glioma Imaging
1 m.Introduction to the 2021 WHO CNS Tumor Classification
5 m.Neuroimaging Techniques For CNS Tumors
13 m.Pediatric Brain Tumors Based on Molecular Genetics: Medulloblastomas
2 m.Pediatric Brain Tumors Based on Molecular Genetics: Ependymomas
6 m.Pediatric Brain Tumors Based on Molecular Genetics: Diffuse Midline Gliomas
4 m.Adult Brain Tumors Based on Molecular Genetics: Solitary Fibrous Tumors and Hemangiopericytoma
2 m.Adult Brain Tumors Based on Molecular Genetics: Circumscribed Gliomas
2 m.Adult Brain Tumors Based on Molecular Genetics: Glioblastomas
3 m.Adult Brain Tumors Based on Molecular Genetics: Diffuse Gliomas
9 m.21 topics, 1 hr. 32 min.
IDH-Wildtype Gliomas
8 m.Case: Primary IDH-Wildtype Glioma
3 m.Case: IDH-Wildtype Glioma
6 m.Case: IDH-Wildtype Gliobastoma with Epedymal Extension
7 m.IDH-Mutant Gliomas
9 m.Case: IDH-Mutant Astrocytoma, FLAIR Mismatch, Grade 2
5 m.Case: IDH-Mutant Astrocytoma, Grade 2
3 m.Case: IDH-Mutant Oligodendroglioma, Grade 2
2 m.Case: Oligodendroglioma, Grade 3
3 m.Case: CNS Lymphoma
4 m.H3 and BRAF Gliomas
9 m.Case: H3K27M Midline Glioma, Grade 4
3 m.Case: H3K27 Glioma
3 m.Case: BRAF V600E Tumor
5 m.T2 FLAIR Mismatch Sign of IDH-Mutant Astrocytomas
8 m.Case: T2 FLAIR Mismatch Sign, Astrocytoma – 31 y/o Female
2 m.Case: T2 FLAIR Mismatch Sign, Astrocytoma – 28 y/o Male
1 m.Case: IDH Mutant Astrocytoma, No Mismatch Sign
2 m.Approach to Intra-Axial Tumors: Tumor Mimics, Non-Neoplastic Lesions
12 m.Final Pearls, Pediatric Non-Gliomas
5 m.Summary
2 m.17 topics, 26 min.
Case: Typical Medulloblastoma
2 m.Case: WNT-activated Medulloblastoma
1 m.Case: SHH-activated Medulloblastoma
2 m.Case: Ependymoma
2 m.Case: Posterior Fossa Ependymoma Type B
2 m.Case: Pilocytic Astrocytoma
2 m.Case: Solid Pilocytic Astrocytoma With No Discernible Cyctic Component
3 m.Case: Pilocytic Astrocytoma Within the Fourth Ventricle
2 m.Case: H3K27M Diffuse Midline Glioma With a DIPG Pattern, Grade 4
3 m.Case: Diffuse Midline Glioma With a DIPG Pattern
2 m.Case: Pilocytic Astrocytoma Masked as DIPG
2 m.Case: Embryonal Tumor With Multilayered Rosettes
2 m.Case: Diffuse Midline Glioma With a Bi-thalamic Pattern
2 m.Case: Pilocytic Astrocytoma Arising From the Thalamus
2 m.Case: Diffuse Astrocytoma
1 m.Case: Diffuse Astrocytoma With Apparent Discrete Margins
2 m.Case: Diffuse Astrocytoma With Gliomatosis Cerebri Pattern of Spread
2 m.0:00
I'd like to talk to you about this next case,
0:05
which is often in the differential diagnosis
0:09
of patients who have a glial tumor.
0:13
This was a patient who had behavioral
0:17
changes and aphasia and agitation.
0:22
The FLAIR imaging shows a mass which has
0:27
low signal intensity on the FLAIR scan
0:32
compared to the surrounding edema.
0:35
And on the ADC map which was also performed,
0:41
one can see the relatively low values of the ADC.
0:46
If we do a region of interest for
0:49
those ADC values of the mass,
0:53
you can see that the numbers on average are about 756,
0:59
but the low range is down at 588.
1:03
This mass showed avid contrast enhancement,
1:08
as you can see,
1:09
and the lesion was crossing the midline and there
1:12
was abnormal signal extending
1:13
into the corpus callosum.
1:16
On the perfusion imaging,
1:19
which was done without color coding,
1:22
you can see that as compared to the gray
1:24
matter which has this darker area,
1:27
the tumor is hypoperfused compared
1:31
to the gray matter,
1:32
but slightly greater perfusion than
1:35
that of the white matter.
1:37
When you have a mass that has low ADC values and
1:42
is not showing very avid perfusion and shows
1:48
homogeneous contrast enhancement and darker signal
1:53
on FLAIR or T2-weighted scanning.
1:56
Let me see whether I have a T2-weighted.
1:58
This is more classic T2-weighted scanning.
2:01
You can see how dark the lesion is.
2:03
You would include in your differential diagnosis
2:06
a lymphoma, as opposed to the glial tumors
2:11
such as glioblastoma.
2:13
So, we usually think of tumors that cross the
2:16
corpus callosum are going to be confined to high
2:20
grade astrocytomas and glioblastomas
2:23
and lymphomas. In this case,
2:25
it has many of the important features of lymphoma
2:29
with the dark on T2, low on ADC,
2:33
kind of intermediate in perfusion
2:37
cerebral blood volume
2:38
and avid contrast enhancement.
2:41
Now, for making this diagnosis,
2:44
if the lesion does go to the dural surface
2:46
or the subarachnoid space, or if you see,
2:49
as in this area over here,
2:52
a small area of ependymal enhancement,
2:56
you might recommend CSF sampling
2:59
as a way to make the diagnosis without having to
3:03
go through a biopsy or craniotomy.
3:06
The importance here is that glioblastomas
3:09
generally are treated with attempts
3:12
at complete resection,
3:14
whereas lymphoma is usually treated with
3:18
chemotherapy and radiation therapy
3:20
and is quite effective.
Interactive Transcript
0:00
I'd like to talk to you about this next case,
0:05
which is often in the differential diagnosis
0:09
of patients who have a glial tumor.
0:13
This was a patient who had behavioral
0:17
changes and aphasia and agitation.
0:22
The FLAIR imaging shows a mass which has
0:27
low signal intensity on the FLAIR scan
0:32
compared to the surrounding edema.
0:35
And on the ADC map which was also performed,
0:41
one can see the relatively low values of the ADC.
0:46
If we do a region of interest for
0:49
those ADC values of the mass,
0:53
you can see that the numbers on average are about 756,
0:59
but the low range is down at 588.
1:03
This mass showed avid contrast enhancement,
1:08
as you can see,
1:09
and the lesion was crossing the midline and there
1:12
was abnormal signal extending
1:13
into the corpus callosum.
1:16
On the perfusion imaging,
1:19
which was done without color coding,
1:22
you can see that as compared to the gray
1:24
matter which has this darker area,
1:27
the tumor is hypoperfused compared
1:31
to the gray matter,
1:32
but slightly greater perfusion than
1:35
that of the white matter.
1:37
When you have a mass that has low ADC values and
1:42
is not showing very avid perfusion and shows
1:48
homogeneous contrast enhancement and darker signal
1:53
on FLAIR or T2-weighted scanning.
1:56
Let me see whether I have a T2-weighted.
1:58
This is more classic T2-weighted scanning.
2:01
You can see how dark the lesion is.
2:03
You would include in your differential diagnosis
2:06
a lymphoma, as opposed to the glial tumors
2:11
such as glioblastoma.
2:13
So, we usually think of tumors that cross the
2:16
corpus callosum are going to be confined to high
2:20
grade astrocytomas and glioblastomas
2:23
and lymphomas. In this case,
2:25
it has many of the important features of lymphoma
2:29
with the dark on T2, low on ADC,
2:33
kind of intermediate in perfusion
2:37
cerebral blood volume
2:38
and avid contrast enhancement.
2:41
Now, for making this diagnosis,
2:44
if the lesion does go to the dural surface
2:46
or the subarachnoid space, or if you see,
2:49
as in this area over here,
2:52
a small area of ependymal enhancement,
2:56
you might recommend CSF sampling
2:59
as a way to make the diagnosis without having to
3:03
go through a biopsy or craniotomy.
3:06
The importance here is that glioblastomas
3:09
generally are treated with attempts
3:12
at complete resection,
3:14
whereas lymphoma is usually treated with
3:18
chemotherapy and radiation therapy
3:20
and is quite effective.
Report
Faculty
David M Yousem, MD, MBA
Professor of Radiology, Vice Chairman and Associate Dean
Johns Hopkins University
Tags
Oncologic Imaging
Neuroradiology
MRI
Brain
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