Wednesday, January 17, 2007
IUCD and MRI
Are CXR in preemployment check up justified?
CT Angiography and Cancer Risk
Reference and full article on Diagnostic Imaging, Study finds measurable cancer risk with CTA
Warthin's tumor
Findings
Figure 1: Contrast enhanced axial CT scan image showing the predominantly cystic left intraparotid mass, with enhancing eccentric nodule and minimal wall thickening. Right parotid gland is normal. No cervical lymphadenopathy was seen on the study.
Differential diagnosis:
- Pleomorphic adenoma
- Warthin’s tumor
- Lymphoma
- Lymphoepithelial cyst
- Mucoepidermoid carcinoma
- Adenoid cystic carcinoma
- Metastasis
Diagnosis: Warthin's tumor
Also known as papillary cystadenoma lymphomatosum, Warthin’s tumors exhibit a slight male predominence and most commonly occur in patients older than 50. The majority of cases are seen in patients in their seventh to eighth decade of life. They are the second most common benign parotid tumor next to pleomorphic adenoma (approximately 75% to 80% of benign parotid tumors are pleomorphic adenoma). Smokers have an eightfold increased risk of developing this tumor, which likely accounts for the historic male predominance. Warthin's tumors are the most common bilateral parotid tumors. About 6% to 10% of patients will have bilateral tumors. They most commonly arise in the tail of the parotid gland, usually presenting as painless and slow-growing masses. There is a very low incidence of malignant transformation.
Typical CT characteristics include a small, ovoid, well-circumscribed, smoothly marginated mass of the posterior parotid gland. The tumor can be cystic or lymphoma-like in appearance. Warthin’s tumors often present as homogeneous soft tissue densities. Cyst formation is common, and the classic appearance is of a cystic lesion with focal tumor nodule(s). On T1-weighted MR, the mass contrasts to the hyperintense signal of the normal parotid gland. On T2WI, Warthin’s tumors are often heterogeneous, with variable signal intensity. Warthin’s tumors show significant uptake of Technetium 99m pertechnetate, as does oncocytoma.
Warthin’s tumor is usually treated by surgical excision. Facial nerve involvement is rare and the facial nerve can usually be spared. Conservative management with close follow-up is acceptable, particularly in poor surgical candidates.
Saturday, January 13, 2007
Polyorchidism-A Case Report

The presence of more than 2 testes is called polyorchidism. It is rare and less than 100 cases are reported in medical literature.Dr Joe presents a case of polyorchidism. The patient presented with a small, painless mass in the left scrotum. Physical examination revealed a small, non-tender lump below the left testes. Sonography revealed a well-defined, solid ovoid mass of less than 2 cms., just below the left testes. It shows same echogencity and echotexture as the testes. This is a very important point that clearly identifies the mass as a supernumerary testes.
D/d: this includes bilobate testes; other differentials include solid masses like fibroma, lipoma and neurofibroma.
Prognosis: polyorchidism is associated with higher risk of malignancy and torsion of the supernumerary testes. Normal spermatogenesis has been reported in the extra testes. Careful follow up examination of the testes is usually sufficient.
Case submitted by-
DR. JOE ANTONY, MD,
Consultant Radiologist.
free to view ultrasound gallery
http://drjoea.googlepages.com
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Thursday, January 11, 2007
Trigeminal schwannoma
Findings
CT postcontrast reveals an unenhancing soft tissue mass centered at Meckel's cave on the left (Figure 1)
CT bone window (Figure 2) reveals a markedly enlarged foramen ovale on the left, with smooth, corticated margins.
Axial T1-WI (Figure 3) demonstrates a well-circumscribed extraaxial mass in the region of left Meckel’s cave that is mildly hypointense to brain parenchyma. The mass shows heterogeneous signal intensity on FLAIR (Figure 3). Postcontrast images show moderately intense enhancement, extending into the cisternal segment of cranial nerve V (Figure 4). The mass is seen to extend through a widened foramen ovale into left infratemporal fossa and present as masticator mass (Figure 4).
Diagnosis: Trigeminal schwannoma
Schwannomas account for 6% to 8% of intracranial neoplasms. Vestibular schwannomas are the most common cranial nerve schwannomas, followed by trigeminal and facial schwannomas.
The trigeminal nerve (CN V) exits the brainstem at the level of the mid pons, and its three divisions—the ophthalmic (CN V1), maxillary (CN V2), and mandibular (CN V3) branches—together proceed anteriorly toward the trigeminal ganglion in the Meckel’s cave. From here, the mandibular division exits inferiorly via the foramen ovale. The maxillary and ophthalmic divisions continue anteriorly along the lateral aspect of the cavernous sinus. Eventually, the ophthalmic division enters the orbit via the superior orbital fissure, while the maxillary division exits the cranial vault through the foramen rotundum.
Trigeminal schwannomas are encapsulated tumors of Schwann cells displace rather than infiltrate fascicles of CN V3.
Trigeminal schwannomas usually present in the third to fourth decade with sensory disturbances. Mastication muscles weakness or facial pain is less common.
Trigeminal schwannomas may arise along any segment of CN V, but the majority develop at the level of trigeminal ganglion. They may then extend posteriorly into the posterior fossa, or anteriorly through the skull base foramina, and often have a “dumbbell” configuration.
On nonenhanced CT scans, most schwannomas are isodense relative to brain parenchyma. Calcification or areas of hemorrhage are rare. On contrast-enhanced CT scans, the enhancement pattern is typically homogeneous. Foramen ovale is most commonly enlarged by CN V3 schwannoma.
Schwannomas typically are isointense or slightly hypointense relative to gray matter on T1-weighted images and hyperintense on T2-weighted images. Gadolinium enhancement typically is homogeneous, although larger schwannomas can show areas of cystic degeneration and heterogeneous signal intensity. Atrophy of masticator muscles may be seen as high signal fatty infiltration on T1-weighted images with volume loss.
Surgical resection is the treatment of choice.
Trigeminal schwannoma may be associated with Neurofibromatosis type 2, especially if it occurs in younger patients.
Tuesday, January 9, 2007
Ika-400 Taon na Kapistahan ng Kiyapo
A devotee's collection of Nazareno statuettes in various sizes
A sleeping "pulubi" in front of the Quiapo Church. This pulubi is unmindful of the massive crowd surrounding her.
George Tapan and me, (with two friends) chat while waiting for the procession to start
The crowd gathers in front of Quiapo Church hoping to catch a glimpse of the Nazareno
Devotees wave their towels to greet the Black Nazarene amidst shouts of "Viva!"
The mass prior to the procession
Devotees form themselves into a brigade to surround the Nazarene and touch their white towels to him.
The massive crowd surround the Black nazarene to get their towels touch the holy image.