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Saturday, June 5, 2010




Cervical spinal cord MRI in the sagittal plane of a 28-year-old woman with polyphasic neuromyelitis optica. (A) T1-weighted image showing thickening of the cord from C7 to T2 with patchy areas of subtle intraparenchymal hyperintensity. (B) T1-weighted image, post gadolinium contrast administration, showing several enhancing lesions from C7 to T2. (C) T2-weighted image showing a contingous area of increased signal intensity spanning from C6 to T3.









MRI (Magnetic Resonance Imaging) is the leading diagnostic tool used in determining SM. The MR imager takes pictures of body structures, such as the brain and spinal cord, in vivid detail. MRI Testing will show the syrinx in the spine or any other conditions, such as the presence of a tumor. MRI is safe, painless, and informative and has greatly improved the diagnosis of syringomyelia.
What is syringomyelia?

Syringomyelia is a disorder in which a cyst forms within the spinal cord This cyst called a syrinx expands and elongates over time destroying the center of the cord Since the spinal cord connects the brain to the nerves in the extremities this damage may result in pain weakness and stiffness in the back shoulders arms or legs Other symptoms may include headaches and loss of the ability to feel extremes of hot or cold especially in the hands and disruption in body temperature SM may also adversely affect sweating sexual function and bladder and bowel control.

What causes Syringomyelia?

• Trauma to the spinal cord or congenital developmental problems of the brain and/or spinal cord may result in SM

o Spinal cord trauma such as a car accident or serious fall may manifest years later as SM

- OR -

o Congenital developmental problems, sometimes undetectable may result in syringomyelia

In either case the condition may lie dormant and undetected for months or years until a symptom or variety of symptoms become bothersome enough to warrant medical attention. Many people with SM are not diagnosed until mid-life.


What are the different forms of Syringomyelia?

Generally, there are two forms of SM. The disorder may be related to a congenital abnormality of the brain called Arnold Chiari malformation. A syrinx may then develop in the cervical region of the spinal cord; this is referred to as communicating syringomyelia. Some people with this form of the disorder also have hydrocephalus (water on the brain), a condition in which CSF accumulates in the skull, or arachnoiditis, in which a covering of the spinal cord is inflamed.

The second major form of SM occurs as a complication of trauma, meningitis, hemmorrhage or tumor. Here, the cyst or syrinx develops in a segment of the spinal cord damaged by one or more of these conditions. The syrinx may start to expand; this is sometimes referred to as noncommunicating syringomyelia.

Presumed spinal cord metastasis in a female patient known to have breast cancer. MRI shows:
- Focal cord expansion with intramedullary enhancing mass,
- Thin enhancing rim along lower anterior cord surface and,
- Enhancing metastatic foci in the bone marrow.
Spinal cord metastases can be:
1-Intramedullary (within the cord): rare.
2-Pial (Superficial, along pial surface): in most of the cases.
Common primary CNS tumors: PNET/medulloblastoma and glioblastoma.
Common primary malignancy outside CNS: lung (70%), breast (11%), melanoma, kidney, lymphoma and leukemia.


Post contrast MRI demonstrates so called “sugar coating” or zuckerguss (German for sugar icing) of the lower portions of the spinal cord in keeping with leptomeningeal metastases.
MR findings in all intramedullary gliomas may be similar. T1WI typically demonstrates fusiform widening of the cord over one or several segments by a soft tissue mass that is iso or slightly hypointense to normal cord. T2WI demonstrates focal areas of increased signal within the enlarged cord segments that represents the tumor and surrounding edema. There is a frequent association of both intratumoral cysts and an adjacent syrinx with astrocytomas (38%) and ependymomas (46%). It is difficult to differentiate cystic tumor from a benign or adjacent syrinx on standard spin-echo sequences, since the signal may vary depending on the fluid characteristics. Gadolinium may help in this regard, as nearly all gliomas can be expected to enhance.

1-moderate spinal cord expansion from T9 to conus.
2-tumor are hypertense in T1&T2.
3-tumor enhances in certain manner in serpentine fashion.

Thursday, June 3, 2010




lipoma with agenesis of corpus callosum







partially thrombosed berry aneurysm.
Required description on a radiology report
size : ideally 3 axis maximum size meansurements.
neck : maximal width of the neck of the aneurysm.
shape and lobulation.
orientation : the direction in which the aneurysm points is often important in both endovascularand surgical planning.
Diagnosis: Arachnoid Cyst. For complete description of case, please visit http://www.radsWiki.net (sponsor of this image)

















Fetal Acrania. (A) Gray scale ultrasound of the fetus (3.5 MHz probe) in sagittal plane. Gestational age 30 weeks. White arrows = Normal looking spine. Fetal brain is seen floating in the amniotic fluid now placed posterior to the cervical spine without covering skull. Asterisk denotes craniocervical junction. (B) Coronal gray scale ultrasound scan showing normal orbits. No skull is seen around the brain. Small Arrows = Inferior Interhemispheric Fissure. Arrows = Orbits, Arrowheads = Fetal brain lacking covering skull.

http://www.google.com.eg/imgres?imgurl=http://www.radiologycases.com/casereports/getimage.cgi%3Fr%3D400%26id%3D271%26i%3D271-10&imgrefurl=http://www.radiologycases.com/index.php/radiologycases/article/viewArticle/271/html&usg=__GWQIL5mtCkGyx49W-9bR1zOaEm4=&h=371&w=400&sz=27&hl=en&start=15&itbs=1&tbnid=2zdFMH-HTUmtyM:&tbnh=115&tbnw=124&prev=/images%3Fq%3Dacrania,us%26hl%3Den%26sa%3DG%26gbv%3D2%26tbs%3Disch:1
This sagittal T1-weighted MR image demonstrates some of the features found in the skull in achondroplasia. Click on the image for arrows. There is a relatively large cranial vault with small skull base. There is a prominent forehead with depressed nasal bridge (blue arrow). The foramen magnum is narrowed (red arrowheads), and there is a cervicomedullary kink (red line).

Relative elevation of the brainstem gives rise to a large suprasellar cistern (yellow arrow) and a vertically-oriented straight sinus (green arrows).

There was moderate enlargement of ventricles and surface CSF spaces consistent with communicating hydrocephalus. CSF flow studies demonstrated flow around the craniocervical junction. MR venography demonstrated restricted flow in the sigmoid sinuses and jugular bulbs, which probably contributed to the hydrocephalus.

Craniocervical junction constriction can give rise to problems in achondroplasia including sleep apneoa, sudden apneoas, sudden death, and myelomalacia. Surgical decompression may be helpful in selected cases.

References:eMedicine June 2006

Sunday, May 30, 2010

s=superior mesenteric artery

T1MRI image
A=Aortic aneurysm
arrow=mural thrombus.



Reference:BiblioMed Textbook-Computed Body Tomography

-bilateral ureteric obstruction(long white arrow).
-fibrous band of fibrosis.
Reference:BiblioMed Textbook-Computed Body Tomography
band of fibrous tissue encasing aorta
Reference:BiblioMed Textbook-Computed Body Tomography
could be idiopathic or due to:
-ruptured aortic aneurysm.
-malignant etiology(cause moderate enhancement).
Reference:BiblioMed Textbook-Computed Body Tomography
right posterior para renal hyperdense,heterogenous
mass suggestive of retro peritoneal hemorrhage,pushing
right kidney anteriorly.
this case due to anti coagulant intake.

left psoas muscle hemorrhage due to ruptured
aortic aneurysm.
Reference:BiblioMed Textbook-Computed Body Tomography

arrow=inter aorto caval lymph adenopathy
this site is the first site to show metastases
from ovarian and testicular carcinoma.
Reference:BiblioMed Textbook-Computed Body Tomography
Benign and malignant lymphadenopathy may exhibit mild (mean, +6 HU) to pronounced (mean, +61 HU) enhancement after intravenous administration of iodinated contrast material with maximal enhancement occurring 1 to 2 minutes after injection.

long black arrow=rim enhancement.
short black arrow=heterogenous enhancement.
this case is renal cell carcinoma.
Reference:BiblioMed Textbook-Computed Body Tomography

R= retro caval lymph adenopathy.
note anterior displacement of aorta.
Reference:BiblioMed Textbook-Computed Body Tomography
low density lymph adenopathy
causes:
1-whipple disease.
2-AIDS disease.
Reference:BiblioMed Textbook-Computed Body Tomography
black arrow=retro peritoneal lymph adenopathy.
white arrow=mesenteric lymph adenopathy.
curved arrow=thickened jejunum.
Reference:BiblioMed Textbook-Computed Body Tomography
arrrow=L.N.enlargement.
arrows=L.N. enlargement forming soft
tissue masses.

big retro peritoneal mass obscuring
great vessels.

Reference:BiblioMed Textbook-Computed Body Tomography


different radiological appearances in different patients with lymphoma.
p=para-aortic L.N.
AC=inter aorto-caval L.N.
RC=retro-caval L.N.
M=mesenteric L.N.
Reference:BiblioMed Textbook-Computed Body Tomography

Reference:BiblioMed Textbook-Computed Body Tomography
arrow head=retro peritoneal lymph nodes
seen in patient after lymph angiography.
Reference:BiblioMed Textbook-Computed Body Tomography


Reference:BiblioMed Textbook-Computed Body Tomography