PubMed Health⌕ Search

Biomedical subjects

J Alwatban

Publications and source records attributed to J Alwatban.

8 recordsLinked to original sources
PubMed2001

Extra-axial cavernous hemangioma: two case reports.

Two patients with extra-axial cavernous hemangioma who presented with headache and oculovisual disturbances were investigated with computed tomography and magnetic resonance imaging. The lesions masqueraded as basal meningioma, but this diagnosis was not supported by magnetic resonance spectroscopy in one patient. Cerebral angiography with embolization was indicated in one patient, but embolization was not justified in the other. Both patients underwent a pterional craniotomy. The lesions were extradural and highly vascular, necessitating excessive transfusion in one patient in whom gross total resection was achieved, and precluding satisfactory removal in the other. There was no mortality. Transient ophthalmoplegia, the only complication in one patient, was due to surgical manipulation of the cavernous sinus; it resolved progressively over 3 months. Extra-axial skull base cavernous hemangiomas are distinct entities with clinical and radiological characteristics that differ from those of intraparenchymal cavernous malformations. They can mimic meningiomas or pituitary tumors. In some cases, magnetic resonance spectroscopy may narrow the differential diagnoses. Surgical resection remains the treatment of choice, facilitated by preoperative embolization to reduce intraoperative bleeding and by the application of the principles of skull base surgery. Fractionated radiotherapy is an alternative in partial or difficult resections and in high-risk and elderly patients.

Case Reports↗
PubMed1999

Aneurysmal bone cyst involving the skull base: report of three cases.

Aneurysmal bone cyst is a bening, non-neoplastic lesion that present most frequently under the age of 20 years. The metaphysis of long bones is the usual site of origin. The involvement of the skull is rare. In the 2.5 to 6% of such cases reported in the literature, the skull vault is more often the site than the skull base. Three cases of aneurysmal bone cyst involving the skull base have been managed at King Faisal Specialist Hospital and Research Center. Two females and one male, all 10 years of age and younger, presented with a painless, progressive swelling. The preoperative radiological studies showed characteristic findings and were highly suggestive of the diagnosis. Angiography also gave characteristic findings. Preoperative endovascular embolization of the arterial feeders to the tumor was performed in two patients who had a significant decrease in intraoperative bleeding from the tumor. All cases underwent surgical excision with a good outcome.

Case Reports↗
PubMed1998

Sphenoid sinus brown tumor of secondary hyperparathyroidism: case report.

OBJECTIVE AND IMPORTANCE: Brown tumor is a misnomer for a reparative cellular process caused by primary or, less commonly, secondary or tertiary hyperparathyroidism. Atypical involvement of the base of the cranium in the area of the sphenoid sinus and the orbit is exceedingly rare and may produce a neurological deficit as a primary clinical presentation. Those neurosurgeons dealing with cranial base and pituitary lesions should be aware of this disease entity, and it should be listed in the differential diagnosis. CLINICAL PRESENTATION: A 21-year-old woman with end-stage renal failure on chronic dialysis was referred to the Department of Neurosciences at King Faisal Specialist Hospital and Research Centre with a 4-month history of progressive impairment of vision, associated with headache and nausea. Computed tomography and magnetic resonance imaging demonstrated an expansive mass lesion in the sphenoid sinus with erosion of the sellar floor and posterior medial wall of the orbit causing compression of the optic nerves. The biochemical laboratory studies showed elevation of parathyroid hormone and confirmed the diagnosis of hyperparathyroidism. INTERVENTION: The transnasal-transsphenoidal approach was used for extensive microsurgical removal of the lesion. The postoperative course was uneventful, and the improvement in vision was dramatic. CONCLUSION: Brown tumor, although rare, should be listed in the differential diagnosis of expansive mass lesions in the area of the sphenoid sinus and cranial base. The management is multidisciplinary, and therapeutic options should target the underlying cause.

Adult↗
PubMed1997

Cerebral manifestation of Erdheim-Chester disease: clinical and radiologic findings.

A 33-year-old woman presented with a 3-year history of progressive numbness in the hand, cerebellar ataxia, limb weakness, nystagmus, and dysarthria. T2-weighted MRI revealed abnormal foci of increased signal intensity mimicking demyelinating plaques in the periventricular white matter, and brain 18FDG-PET scan showed increased uptake in the pons. Biopsy from a tibial lesion showed aggregates of foamy histiocytes in the intertrabecular spaces replacing the bone marrow, characteristic of Erdheim-Chester disease. The patient was treated with craniospinal radiation. After 6 months, the clinical picture was stable and the MRI was unchanged.

Adult↗
PubMed1995

Intramedullary schwannoma.

OBJECTIVE: To present the imaging findings for two cases of intramedullary schwannoma involving the thoracic cord and the conus medullaris. PATIENTS AND METHODS: a 34-year-old man and a 53-year-old woman presented with symptoms of weakness and pain in the lower limbs. Myelography and magnetic resonance imaging as well as other examinations, were performed. RESULTS: The imaging failed to indicate the correct diagnosis in either patient. However, intramedullary schwannoma was confirmed pathologically in both patients. Subtotal excision resulted in local tumour recurrence at 5 and 3 years, respectively. CONCLUSIONS: Intramedullary schwannoma should be considered in the differential diagnosis of spinal cord tumours. The importance of accurate diagnosis from frozen sections at surgical biopsy is emphasized .

Adult↗
PubMed1994

Transcranial Doppler ultrasonographic changes after embolization of cerebral arteriovenous malformations.

The authors assessed the potential role of transcranial Doppler ultrasonography (US) in monitoring hemodynamic changes induced by embolization of cerebral arteriovenous malformations. Transcranial Doppler US was performed in eight patients with such lesions before and after embolization with n-butyl cyanoacrylate [corrected]. Changes in mean flow velocity and pulsatility index were analysed in all feeding and nonfeeding arteries. Anatomic and hemodynamic observations were also correlated with the results of digital subtraction angiography. A consistent trend was observed in all treated feeding arteries after embolization: the flow velocity decreased by a mean of 26% or 33 cm/s (p = 0.01, paired t-test), and the pulsatility index increased by a mean of 27% or 0.15 (p = 0.005). Although these changes did not correlate with the degree of angiographic reduction of the nidus (r = -0.31), they were most marked in malformations with a lower Spetzler grade or a higher degree of shunt obliteration. After embolization, recruitment of untreated feeding arteries was documented in two cases and a decrease in the "steal effect" from contralateral nonfeeding arteries in three. Changes in the nonfeeding arteries ipsilateral and contralateral to the malformation were variable. The authors conclude that transcranial Doppler US is a convenient and reliable method to evaluate quantitatively the hemodynamic effects of embolization of cerebral arteriovenous malformations.

Adult↗