Wednesday, February 28, 2007

Esthesioneuroblastoma (Olfactory neuroblastoma)








Findings

Large enhancing mass with epicenter at the level of the cribriform plate with postobstructive non-inflammatory mucosal disease. Mass invades left orbit, anterior ethmoidal air cells, medial aspect of the left maxillary sinus and frontal sinuses bilaterally. Intracranial, extradural extension with bifrontal mass effect and moderate dural enhancement. Edema or infiltration of the subcutaneous soft tissues of the frontal scalp.

Differential diagnosis:
- Esthesioneuroblastoma
- Squamous cell carcinoma of the nasal cavity
- Lymphoma
- Ewing sarcoma
- Embryonal rhabdomyosarcoma


Diagnosis: Esthesioneuroblastoma (Olfactory neuroblastoma)


Key points

Rare, highly malignant tumors composed of small round cells encircled by vascularized connective tissue.
Usually occurs in young men with second occurrence peak at ~50-60 years.
Most commonly arise superolaterally in the nasal cavity (between the middle turbinate and cribriform plate) from neuroendocrine cells within the olfactory mucosa.
Locally invasive within the nasal cavity and paranasal sinuses with frequent intraorbital and intracranial extension (squamous cell carcinoma and lymphoma often demonstrate less aggressive pattern of bony destruction).
Non-inflammatory sinusitis often accompanies disease due to obstruction.
Distant metastases in approximately 20% of cases.


Radiology

MRI:
- Hypointense to brain on T1-weighted images.
- Hyperintense to brain on T2-weighted images.
- Heavily T2-weighted images help to differentiate mass from associated obstructed sinus secretions, which usually appear brighter than the tumor.

CT: Enhancing mass with associated bony expansion and destruction.

The Radiology Blogosphere

Here is an attempt to compile the complete of interesting Radiology Blogs, all good ones. I suggest all Radiology Sites should keep a link these to keep a track of latest in the world of radiology blogs. If you know any more Radiology related blogs, kindly suggest in the comment section.


The Radiology Blogosphere (in no particular order)-

Sumer's Radiology Site

Dalai's PACS Blog

Americans For Responsible Imaging

Film Jacket.com

Nuclear Vision

Spot Diagnosis
Radiology Grand Rounds

Cochin Blogs

MidEssex Ray

Scanman's Notes

Radiology Indications

Inner Visions

Codeblue Blog

Radiology Picture of the Day

Radiology.ro

Information for the Patients

Cool MRI stuff

Clinical Cases and Images

Desert Imaging

Radfiles

Tuesday, February 27, 2007

Ruptured intracranial dermoid









Findings

Non-contrast series demonstrates multiple areas of low attenuation in the subarachnoid space (Figure 1 and Figure 2).
The second CT series demonstrates a heterogeneous, predominantly fatty lesion in the left aspect of the middle cranial fossa extending toward the orbital apex extending across the tentorial notch (3). Focus of fat is seen extending into the region of the internal audiory canal (IAC) (Figure 3).
Sagittal T1 image demonstrates multiple punctuate areas of high signal, consistent with fat droplets (Figure 4). Axial T1 post gadolinium image demonstrates a lesion with fatty and cystic components extending into the left internal auditory canal, (Figure 5). Axial T1 post gad fat sat images demonstrate the extensive fatty component, which saturates on this sequence, (Figure 6).


Diagnosis: Ruptured intracranial dermoid


Intracranial dermoids are rare, accounting for less than 1% of brain “tumors” in the US. They are more common in men than women. Unlike teratomas, they are not true neoplasms. Histologically, dermoid cysts are inclusion cysts lined by epithelium. They are caused by displaced ectodermal elements during development around the time when the neural tube closes at midline. This explains their usual near-midline location. Dermoid and epidermoid cysts are often discussed together due to their similar appearance and origin. In contrast to epidermoids, dermoids have an epithelial lining further differentiated into hair, sebaceous glands, and sweat glands. The two can be differentiated radiographically based on their typical locations and imaging characteristics. Click here for a quick comparison of the two.

Dermoid cysts are benign and slow growing, and are usually located near midline within the posterior cranial fossa, parasellar, and sub frontal areas. Symptoms depend on the size, location, and mass effect on adjacent structures. Patients may present with visual disturbances, seizures, diabetes insipidus, or headache. Intraventricular dermoids are most commonly in the fourth ventricle and rarely cause hydrocephalus. Spontaneous rupture, as in this case, can incite a chemical meningitis, resulting in recurrent headaches or seizures. Although rare, the resultant meningeal inflammation can cause vasospasm, and even stroke and death. Traumatic rupture has also been reported. In addition to intracranial involvement, dermoid cysts may also be seen in the scalp, skull, orbit, spine, nasal/oral cavity, and neck. Ovarian (abdominal) dermoids are actually well-differentiated and organized teratomas.

On CT, dermoid cysts are low attenuation, well-circumscribed, and cystic. Wall calcifications may be seen (about 20% calcify) and enhancement is rare. Fat in the subarachnoid and ventricular spaces suggests rupture, and occasionally fat/fluid levels may be seen. The resorption of subarachnoid fat is variable, and may be present up to 6 years following surgery.

On MR, dermoids typically have signal characteristics of fat – hyperintense on T1 weighted images, and hypointense on T2. Fat suppression sequences may be helpful. On both CT and MR, calcification, follicles, and debris can give dermoids a heterogeneous appearance. Dermoids are never associated with vasogenic edema, and as mentioned above, rarely cause hydrocephalus.

Treatment usually consists of complete surgical resection, depending on the size, location, and effects on local nerves and vessels. There is a risk of causing chemical meningitis during removal of the dermoid cyst if its contents spill into the subarachnoid or ventricular spaces. Recurrence is rare.

Monday, February 26, 2007

Radiology Grand Rounds-IX

Dear Readers the ninth edition of the Radiology Grand Rounds is up at cochin blogs, a blog by Dr Joe Anthony, Radiologist. Check it here-
If you want to check out the previous issue they are available here-

Saturday, February 24, 2007

About Telesonography

According to a recent article in AJR-The Feasibility of Real-Time Transmission of Sonographic Images from a Remote Location over Low-Bandwidth Internet Links: A Pilot Study. AJR 2007; 188:W219-W222
"Authors sought to show that sonography can be performed in teleconference settings, "telesonography," in which a remotely located sonography interpreter can monitor the examination in real-time and guide the examiner with voice commands while the patient simultaneously undergoes imaging, albeit at low resolution, thus helping to overcome the lack of trained operators in certain areas. According to them, this system of image transfer offers the potential for sonography to be performed at a remote underdeveloped region and interpreted in real-time at a distant site by trained radiologists, thereby extending the presence of physicians in virtual space. "

Friday, February 23, 2007

Epidermoid




Findings

Axial T1W image without contrast showed a small, rounded mass lesion in the right half of the quadrigeminal plate cistern that is minimally hyper intense to adjacent CSF. Minimal mass effect. Axial post contrast T1W shows no enhancement of the mass lesion. Axial T2W shows the same mass as the T1 image. On T2 images it is minimally hypo intense to CSF. Coronal post contrast T1W shows the lesion in the region of the quadrigeminal plate cistern. Mass is slightly hyper intense to CSF, but does not show post contrast enhancement. Diffusion weighted images show the mass to be markedly hyper intense.

Differential diagnosis:
- Epidermoid
- Arachnoid Cyst
- Parasitic infection (e.g. Cysticercosis)
- Craniopharyngioma
- Dermoid


Diagnosis: Epidermoid (presumed diagnosis)


Key points

Intracranial epidermoid represents up to 1.8% of all primary intracranial tumors. They are the most common congenital intracranial tumor. They represent the third most common CPA/IAC mass after schwannoma and meningioma.

They most commonly present with headaches and possibly with cranial nerve palsies, typically of the 5th, 7th, and 8th nerves. They may remain clinically silent for many years. There is no gender predilection. Their presentation peaks at age 40 and has a range of 20 – 60 years of age.

As the have epithelia components they grow slowly. They can cause chemical meningitis if they leak and rarely have been reported to undergo malignant transformation to squamous cell carcinoma.

Treatment involves microsurgical resection which can be complicated by encasement of surrounding structures. Recurrence is common if they are not completely resected and seeding of the subarachnoid space has been reported.


Radiology

Epidermoid typically follow CSF density and may encase surrounding structures. Most commonly they are found in the CP angle (40-50%). They can also commonly be found in the fourth ventricle and middle cranial fossa, typically para-sellar. Occasionally they can be found within the skull and spine.

CT findings: Most are hypo dense, although 10-25% will have calcifications. They typically do not show post contrast enhancement however may have minimal enhancement at the margin. There is a rare variant which may be dense secondary to hemorrhage or high protein.

MRI findings: Again they are similar to CSF on T1 and T2 pulse sequences. On T1 they are slightly hyper intense to CSF and on T2 they are isointense to slightly hyper intense to CSF. Intensity will be altered depending on the cyst contents. Minimal enhancement can be seen at the margins. They key distinguishing feature is the appearance on diffusion weighted images which is markedly intense, "light bulb bright". On ADC mapping they are isointense to brain parenchyma.

The differential diagnosis includes arachnoid cyst, which follow CSF signal on all sequences and does not show restricted diffusion. Arachnoid cysts typically displace adjacent structures whereas epidermoid lesions encase them. Cystic neoplasm's often enhance and do not follow CSF signal. Dermoid cysts are typically heterogeneous on MR and more closely follow fat signal characteristics. Additionally dermoid are typically midline. Inflammatory cysts typically enhance and have surrounding edema and/or gliosis.

Wednesday, February 21, 2007

Tunneled Coronary Artery

"Tunneled coronary arteries are clinically relevant due to their association with myocardial ischemia.The coronary arteries may dip into the myocardium for varying lengths and then reappear on the heart surface. The muscle overlying the intramyocardial segment of the epicardial coronary artery is termed as myocardial bridge and the artery coursing within the myocardium in called a tunneled artery."
One of the conditions where CT coronary angiography can give mor einformation than angiography.
Reference-
Garde PS, Karandikar AA, Tavri OJ, Patkar DP, Dalal AK. Tunneled coronary artery: Case report. Indian J Radiol Imaging [serial online] 2006 [cited 2007 Feb 21];16:283-284.

Tuesday, February 20, 2007

Increasing work load leaves Radiologists fatigued

"Today's radiologist is a multitasking technology wizard, responding to pages, phone calls and personal consults with clinicians while reviewing plain films, MRIs and CTs and editing their voice recognition-developed dictations.This is a far cry from the early 1990s when we didn't even carry pagers.Not only has the demand for imaging increased in the past decade – producing a definite increase in volume of studies to be performed and interpreted – imaging plays an increasingly pivotal role in the diagnosis, triage and management of patients, resulting in a greater sense of urgency and stress for radiologists during the workday and on call."
Read the interesting full article entitled "Fatigued radiology departments secretly starve bottom lines" By Amy Storer---

Lancet-Top Ten Free Software for Doctors

"Computers and the internet have an increasingly important role in medicine, and have become integral to modern care. For instance, it has been suggested that search engines can help doctors diagnose difficult cases. The internet is not only a font of factual knowledge but also a source of useful software, much of it free (freeware). These are our “top ten” free utilities for computers running the Windows operating system. They are small programs that facilitate common computing tasks and which we use regularly to supplement standard commercial software."
Full article here-

Monday, February 19, 2007

Optic nerve sheath dural ectasia in neurofibromatosis type I





Findings

Figure 1: Axial contrast enhanced CT scan of the orbits reveals dilated, tortuous optic nerve sheath with no abnormal enhancement of the nerve.
Figure 2: Coronal reconstructed CT image again depicts the significant optic nerve sheath dilatation with absent enhancement.


Diagnosis: Optic nerve sheath dural ectasia in neurofibromatosis type I


The optic pathway lesions in NF-1 include glioma, meningioma, nerve sheath dural ectasia, perioptic gliosis and optic hydrops. Dural ectasia is a benign, unusual feature of NF-1 that causes nerve sheath expansion with no abnormal enhancement. The nerve can be identified separately within the dilated sheath in contrast to gliomas and meningiomas which reveal variable contrast enhancement with obliteration of the nerve itself, and homogeneous contrast enhancement around a non-enhancing nerve respectively. The differential diagnosis for optic nerve sheath dilatation includes other conditions like acute optic neuritis, intracranial hypertension and osteopetrosis, which have distinct clinical features.

While there are no pathognomonic symptoms, this entity may present with visual blurring and headaches, and rarely with proptosis and optic disc shunt vessels. Most patients have a benign clinical course and surgical intervention (nerve sheath fenestration) is reserved for patients with progressive optic nerve dysfunction. While contrast enhanced CT scan can reliably demonstrate the entity, MRI is considered the imaging modality of choice due to its high contrast resolution and multiplanar acquisition.

Sunday, February 18, 2007

Submissions requested for the next Radiology Grand Rounds

Next Radiology Grand Rounds will be hosted on last sunday of this month 25-2-07 at Cochin Blogs by Dr Joe Anthony, so hurry send all your Radiology Related submissions to me at sumerdoc@yahoo.com or to Dr Joe at drjoea@gmail.com. If you are not familiar with the concept of the Radiology Grand Rounds check out the archive and concept here-

Thursday, February 15, 2007

Benign lymphoepithelial cysts of parotid glands in HIV






Findings


Figure 1: Lateral scout image of CT scan showing the large soft tissue mass in the neck.
Figure 2 and Figure 3: Showing multiple variable sized thin walled cystic lesions in both parotid glands. Mild lymphoid hypertrophy at the base of the tongue is seen.

Differential diagnosis:
- Benign lymphoepithelial cysts of parotid glands in HIV
- Bilateral Warthin’s tumors
- Sjogren’s syndrome
- Bilateral cystic pleomorphic adenomas
- Necrotic intraparotid lymph nodes or lymphoma post-treatment
- Bilateral first branchial cleft cysts (intraparotid)


Diagnosis: Benign lymphoepithelial cysts of parotid glands in HIV


Benign lymphoepithelial cysts (BLC) of the parotid gland have been reported to occur in up to 5% of patients infected with HIV. HIV testing is recommended in patients with BLC since this can often be the initial presentation of the patient’s HIV status. A point of note is that BLC can occur before seroconversion so patients who initially test negative with BLC should be re-tested after 6-8 weeks. The exact pathogenesis of BLC is unclear but it is hypothesized that the cystic dilation and squamous metaplasia is caused by obstruction of the small intraparotid ducts by hyperplastic lymphoid tissue of the parotid lymph nodes. BLC are similar histologically to salivary duct cysts with the exception that BLC have dense lymphoid tissue within the cystic wall.

When present in patients without HIV, BLC usually presents as a unilateral cystic mass in patients in the 4th or 5th decade. In HIV positive patients the lesions are usually bilateral with associated findings of diffuse cervical lymphadenopathy and prominent adenoid and tonsillar tissue. The differential diagnosis in these patients includes bilateral Warthin’s tumors, Sjogren’s syndrome, bilateral cystic pleomorphic adenomas, necrotic intraparotid lymph nodes or lymphoma post-treatment and bilateral first branchial cleft cysts (intraparotid). BLC display characteristics of thin-walled cysts by CT and follow CSF signal characteristics on MR imaging.

The lesions of BLC are usually self-limited but surgical resection is an option in BLC for cosmetic purposes. Alternate methods of treatment include: cyst enucleation, low-dose radiation, sclerotherapy with doxycycline, antiretroviral therapy although all of these methods are associated with recurrence. There is a small risk of malignant transformation of benign lymphoepithelial cysts to lymphoma.

Wednesday, February 14, 2007

Cochrane Library now freely available in India

The Cochrane Library is now freely available to all residents of India with internet access thanks to funding from the Indian Council of Medical Research (ICMR). Through several provisions and funding schemas, the Cochrane Library is currently freely available in many geographic areas of the world including Australia, Norway, Ireland, parts of Canada and many other countries, regions and territories. For a full list, look under "Access to Cochrane" on the Cochrane Library's homepage via John Wiley & Sons. From 29 January 2007 the Cochrane Library will be freely available to all residents of India with internet access thanks to funding from the Indian Council of Medical Research (ICMR) (www.icmr.nic.in), and work of the South Asia Cochrane Netork (www.cochrane-sacn.org). More than a thousand million people will now have the opportunity to access the high-quality, independent evidence for healthcare decision-making found in the Cochrane Library. Here is a link to an article in the Indian newspaper,

Monday, February 12, 2007

MRI better than CT for initial evaluation of stroke

"A multicenter prospective trial involving 1210 patients in Europe has found that the odds of a favorable clinical outcome were one-third higher for acute stroke patients who received diffusion-perfusion MRI to determine the appropriateness of tPA thrombolysis than patients assessed with conventional noncontrast CT. Results drawn from the Safe Implementation of Thrombolysis in Stroke trial were presented at International Stroke Conference in San Francisco."
Report from International Stroke Conference: MRI outperforms CT for initial stroke evaluation
Reference

Friday, February 9, 2007

Radiology Search Engine-Yottalook


Yottalook is a free radiology-centric search engine based on Google's indexing technology with proprietary relevance algorithm by iVirtuoso.
Check out-

Star Wars IV: The Force Takes Chewbacca

Another fun trivia question for Washington Redskins fans. In 1974, the Washington Redskins offered a professional wrestler a contract to play professional football. The wrestler turned down the football contract to make far more money as a wrestler. Which wrestler was offered a contract by the Redskins?

As you walk the Hollywood Walk of Fame, you pass by the beautiful and historic Grauman's Chinese Theater. Every day, you can walk by the theater and see panhandlers dressed up as stars such as Marilyn Monroe and Superman, offering to pose with tourists for a nominal fee.

Well, sometimes the panhandlers can be a bit aggressive. In probably the best news story ever, a 6-foot 4-inch tall man, dressed in a hairy Chewbacca costume was aggressively offering to pose for a picture with two asian tourists on a guided tour. The tour guide did not appreciate Chewbacca bothering his customers, so he yelled "Stop bothering the tourists!"

Infuriated by the tour guide's comment, Chewbacca screamed "NOBODY TELLS THIS WOOKIEE WHAT TO DO!" and proceeded to headbutt the tour guide. Chewbacca was then arrested by police and taken away in his giant hairiness.

Well, that news story was a great segue into the answer to the trivia question. Both Chewbacca and the wrestler were hairy, large and had very little grasp of the english language. Nobody got this one, huh? Oh well, the answer is Andre the Giant. And for those of you who still don't know who he is, he's the big guy from "The Princess Bride" movie.

Developmental venous anomaly







Findings

Initial noncontrast head CT (Figure 1) shows abnormal hyperdensities within the right Sylvian fissure and adjacent insular cortex, raising the possibility of a vascular malformation.
Follow-up T2-weighted MR image (Figure 2) shows multiple linear increased signal intensity foci in the deep white matter converging near the ventricular surface. These represent dilated medullary veins of the caput medusa.
Cerebral angiography during the arterial phase (Figure 3) is normal while the venous phase (Figure 4) shows umbrella-like medullary veins converging on two collector veins (red arrows in Figure 4) which then empty into a normal venous system.


Diagnosis: Developmental venous anomaly


Developmental venous anomaly (DVA), also known as venous malformation or venous angioma, refers to aberrant venous development and is composed of a network of dilated medullary veins converging in a radial or umbrella-like fashion onto a large collector vein. The collector vein follows an aberrant course to empty into normal superficial or deep veins. A DVA can occur in the cerebrum, cerebellum, or brainstem and is characterized by normal intervening parenchyma. As it is a normal variant, clinically significant hemorrhage is unusual and should raise the possibility of a concomitant cavernous angioma or other vascular malformation.

On CT, a small DVA may not be visualized; however, a large DVA may be seen as a hyperdense lesion.

Blood flow within DVAs is slow, which produces fluid-like signal intensity rather than flow void on MR imaging. Strong contrast enhancement is typical; the lack thereof should raise doubt about the diagnosis of DVA.

On cerebral angiography, the classic “Medusa head” appearance is visualized on the venous phase, with the arterial and capillary phases normal.

Thursday, February 8, 2007

Myeloma with cord compression






Findings

Sagittal T1-image (Figure 1) in a patient with multiple myeloma shows a large epidural mass in the midthoracic region with associated cord deformity. The mass displaces the epidural fat. Postsurgical changes are seen in the lower spine consistent with repair of a prior compression deformity. Marrow signal is heterogeneous throughout.
Sagittal T2 image (Figure 2) in a patient with multiple myeloma shows a large epidural mass in the mid-thoracic region with associated cord deformity. The normal CSF signal is completely displaced by the mass. Post-surgical changes are seen in the lower spine consistent with repair of a prior compression deformity. Marrow signal is heterogeneous throughout
Post-contrast T1 axial image (Figure 3) demonstrates compression of the cord anteriorly by a large epidural mass.


Diagnosis: Myeloma with cord compression


Myeloma patients with abnormal neurological findings suggesting cord compression should be evaluated by MRI when available. Imaging exam should be primarily targeted, based on the results of motor and reflex tests, rather than pain or sensory level.
Spinal cord compression is a neurological emergency that may be diagnosed by the presence of a mass lesion abutting the cord with cord deformity, or abnormal cord T2-signal.

Acute spinal cord compression is a potentially devastating neurological emergency that requires both prompt diagnosis and intervention to prevent permanent impairment. The frequency of metastatic cord compression is increasing as cancer prevalence rises and new treatment modalities prolong patient survival. Close cooperation between clinical services and diagnostic radiologists is essential for patient triage. This is especially true in cases where patients cannot be fully examined neurologically. Magnetic resonance imaging is the study of choice in evaluating these patients; it is noninvasive, does not involve radiation, and provides for investigation of both osseous and soft tissue lesions.

Many etiologies can result in acute spinal cord compression. These include trauma, infection, neoplasm, degenerative disc disease, and others. Differentiation between these various causes of acute cord compression relies on a combination of clinical history, neurological exam, and imaging findings. However, the constellation of imaging findings indicative of cord compression are similar, regardless of the causative process.

In evaluating the patient, close cooperation between clinical staff and the diagnostic radiologist is essential. Information from the neurological exam is critical for localization of the lesion and optimization of the imaging protocol. Whole spine imaging is generally undesirable as it is more time-consuming, expensive, and difficult for patients who are often in considerable pain. It further lowers resolution on exams that are often suboptimal, secondary to severe patient pain and patient movement. Spinal sensory levels on neurological examination may be up to several segments below the anatomic level of cord compression. Evaluation of motor function and reflexes is very useful for lesion localization.

There has been considerable debate within the literature on the precise radiological definition of cord compression. Animal models suggest that both direct mass effect on the cord and impingement on the epidural venous plexus contribute to pathology. Spinal cord compression may be defined as the presence of a mass lesion abutting the cord with the complete loss of intervening CSF. This must be accompanied by deformation of the spinal cord, or the presence of signal changes within the cord. The findings are best visualized on T2-weighted images. If the patient is concurrently symptomatic, acute intervention is mandated with the specific type of intervention determined by the underlying disease process.

Supraclinoid Aneurysm- A Case Report


Case Submitted by Dr MGK Murthy Sr Consultant Teleradiology Providers

Case Details and Discussion
55 yr old lady complains of chronic headache of 10 yrs duration with increasing severity
she is normotensive and has no neurological deficit Routine MRI shows well defined regular heterogenous altered signal intensity extraaxial lesion in left paracavernous and supraclinoid locations with an intensely enhancing nodule within on contrast as well as hypointense periphery with no significant perilesional oedema- likely to be partially thrombosed internal carotid giant aneurysm with thrombus within. DSA is the solution. At times Meningimas which are cystic, haemangioblstomas and pilocytic astrocytomas could present a diagnostic difficulty. However intense nodular enhancement, lack of perilesional oedema, chronic headache of long duration with no deficit are supportive of aneurysm. Supraclinoid component is suggested as intracavernous ICA appears compressed and shows normal flow void.




Monday, February 5, 2007

MRI features in Placental Invasion

The value of specific MRI features in the evaluation of suspected placental invasion by Lax A et al in Magn Reson Imaging 2007 Jan;25(1):87-93. Epub 2006 Nov 14 points out that MRI can be a useful adjunct to ultrasound in diagnosing placenta accreta prenatally. Three features that are seen on MRI in patients with placental invasion appear to be useful for diagnosis: uterine bulging; heterogeneous signal intensity within the placenta; and the presence of dark intraplacental bands on T2W imaging.

Friday, February 2, 2007

Craniopharyngioma








Findings

There is a well-circumscribed suprasellar mass that is predominantly cystic with focal rim calcifications (Figure 1).
The pituitary gland appears normal (Figure 2). Fluid-fluid level is noted with bright signal on T1-WI (Figure 3), T2-WI and FLAIR (Figure 4 and Figure 5). Post contrast image show minimal enhancement along the periphery of the lesion with no enhancement of the lesion itself.


Diagnosis: Craniopharyngioma


Key points

Craniopharyngiomas are benign dysodontogenic epithelial tumors derived from Rathke pouch epithelium. These tumors are mostly suprasellar (75%), with intrasellar extension seen in 20% of cases.

Two types of Craniopharyngioma are classically described:
1) Childhood form- Peak 5-15 years. Has cyst formation and calcification. Has an adamantinomatous microscopic pattern and carries poor prognosis.
2) Adult form- Peaks in sixth decade. Shows papillary squamous epithelium. Symptoms are usually due to mass effect-headache, visual disturbances, behavioral changes, hydrocephalus, and endocrine dysfunction.

Craniopharyngiomas are WHO Grade I lesions. These are multilobulated, multicystic masses. The cyst may contain variations of highly proteinaceous fluid, cholesterol, and blood products.

On CT, these appear as large, lobulated heterogeneous suprasellar masses. Intrasellar extension may enlarge the sella and cause erosion of dorsum sellae. Cysts may vary in density, depending on contents. Calcification may be peripheral or irregular and nodular.

High-signal intensity within a suprasellar mass should raise suspicion of craniopharyngioma. Cyst contents are typically hyperintense on T2 and FLAIR images. Enhancement is heterogeneous in the solid portion of the tumor, with the cyst walls enhancing strongly. Cyst contents show a broad lipid spectrum on MRS (0.9 ppm to 1.5 ppm). Infiltration is common, making complete surgical resection difficult.