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At least 37 records · Page 2Linked to original sources

Giant cell tumors of the sphenoid bone.

Giant cell tumors of the sphenoid are rare; there are 36 previously reported cases. We report two cases of these tumors in women in their thirties, both associated with pregnancy. In the first patient, the tumor was removed via a transnasal transsphenoidal approach. In the second patient, a Le Fort maxillotomy was required. In these cases, an interoperative diagnosis was made, and in both, this diagnosis directed surgical tactics towards a more radical excision. Reported experience with the outcome of giant cell tumors in other sites suggest that total removal by curettage is the ideal treatment; the main principle is to prevent local recurrence because the metastatic potential of this tumor is low. A combination of surgery and radiotherapy is essential for giant cell tumors occurring in sites where access is difficult, such as the sphenoid bone. Previous objections to radiotherapy have included poor response rate and malignant change. Recent studies suggest that neither of these problems is significant when modern therapeutic techniques are employed.

Adult↗

[Changes in the sphenoid bone in the upper third of the carotid groove].

The article discusses the changes of the bone plate of the sphenoid bone in the upper third of the carotid groove; the plate separates the siphon of the internal carotid artery from the cavity of the sphenoid sinus. Both carotid grooves were examined on blocks removed from the base of the skull of 65 cadavers and on 45 macerated skulls. Two types of bone changes were found in the upper third of the carotid groove, namely, osteoporosis and perforating defects. Osteoporosis was revealed in 50 grooves and defects only in the upper third in 45 grooves. Osteoporosis and defects were encountered about five times more frequently between the ages of 41 and 60 than till the age of 40 and 10 times more frequently after the age of 60. The same relations were found when osteoporosis was combined with a defect. These bone defects are an anatomical precondition for profuse nasal bleeding because the wall of the internal carotid artery ruptures during a craniocerebral trauma and blood flows freely from it into the sphenoid sinus and then into the nasopharynx.

Adolescent↗

Imaging the sphenoid bone and basiocciput: pathological considerations.

Many diverse pathologic processes can involve the sphenoid bone because of its complex embryologic origin. In addition to primary neoplasia, the central location of the sphenoid predisposes it to involvement by many intracranial and extracranial lesions. The presence of multiple foramina and fissures offer "paths of least resistance" that allow the spread of pathology across the skull base. Sphenoid sinus disease also accounts for a number of pathologic entities occurring in this vicinity. This article reviews the more common lesions affecting the sphenoid bone as well as their CT and MR appearance.

Bone Diseases↗

Radiation-induced osteosarcoma of the sphenoid bone.

The case of a patient who developed osteosarcoma in the sphenoid bone 15 years after radiation therapy for a craniopharyngioma is reported. Radiation-induced osteosarcoma of the sphenoid bone has not been reported previously. Reported cases of radiation-induced osteosarcomas are reviewed.

Bone Neoplasms↗

Osteogenic sarcoma of sphenoid bone: an extended lateral skull base approach.

Osteogenic sarcoma involving the sphenoid bone is an extremely rare condition. The rarity of the disease and the close proximity of the sphenoid bone to the various important intracranial structures poses a real challenge in diagnosis and surgical management of these lesions. An extended lateral craniofacial resection by a multidisciplinary approach was carried out in one such case to attempt en bloc resection. This case is presented and also a review of the relevant literature.

Adult↗

[Leiomyosarcoma metastatizing to the sphenoid bone presenting exophthalmos: a case report].

A rare subcutaneous leiomyosarcoma metastatizing to the sphenoid bone and presenting exophthalmos is reported. A 56-year-old female presented with protrusion of the right eye and a slowly growing lump on the right temporal region. Six years previously, she had undergone removal of a subcutaneous mass in the back, which was histologically diagnosed in another hospital as leiomyosarcoma. She had undergone four other operations, including removal of local recurrences and a right renal metastasis. On admission, physical examination showed no neurological deficits. Craniogram revealed an osteolytic lesion without marginal sclerosis in the right sphenoid bone. CT showed an inhomogeneously enhanced mass with irregular expansion of the diploic space, which was partly invading the right orbit. MRI demonstrated an extradural mass in the right sphenoid region, which was slightly low-intense in T1-weighted image, high-intense in T2-weighted image, and inhomogeneously enhanced by Gd-DTPA. Right external carotid angiogram showed a highly vascular stain fed by meningeal arteries. Radionuclide bone scintigram showed multiple high-uptake areas in the left femoral head, the ribs, and the sphenoid bone. Preoperative embolization of the tumor vessels fed by the external carotid artery was performed. Following this procedure, the tumor stain disappeared completely. The tumor was totally excised with minimal bleeding through an orbitozygomatic approach. The tumor was loosely adherent to the dura and periorbit. The bone defect was covered with a methylmethacrylate resin plate. the histological examination demonstrated fascicular arrangement of the spindle shaped cells with mitotic figures. Immunohistochemical studies showed that most tumor cells were positive for actin and myosin, but negative for desmin.(ABSTRACT TRUNCATED AT 250 WORDS)

Exophthalmos↗

Postirradiation sarcoma of the sphenoid bone--a case report.

INTRODUCTION: The development of secondary tumours as a result of radiation therapy is a rare but serious complication. CLINICAL PICTURE: This is a case report of a 45-year-old Chinese male who developed postirradiation sarcoma of the sphenoid bone in less than 5 years after radiation therapy for Stage T3N1M0 nasopharyngeal carcinoma. DISCUSSION: In the literature, the only case of postirradiation osteosarcoma of the sphenoid bone was after radiation therapy for craniopharyngioma. There was no previously reported case of postirradiation sarcoma of the sphenoid bone after radiation therapy for nasopharyngeal carcinoma. CONCLUSION: This is the first case of postirradiation malignant fibrous histiocytoma of the sphenoid to be reported. Of about 3000 patients treated with radiotherapy for nasopharyngeal carcinoma over a 10-year period in Singapore, only 1 patient developed postirradiation tumour of the sphenoid bone.

Bone Neoplasms↗

Microsurgical anatomy and dissection of the sphenoid bone, cavernous sinus and sellar region.

The topographic and internal anatomy of the sphenoid bone is reviewed with an emphasis on the relationships important to the transcranial and subcranial surgical approaches to the sphenoid sinus, sella turcica and cavernous sinus. A stepwise method of study and dissection is outlined. The equipment and materials needed for sphenoid bone dissection in the laboratory are reviewed.

Cavernous Sinus↗

Giant cell tumor of the sphenoid bone.

A case of giant cell tumor of the sphenoid bone is reported, the first case in which a computed tomogram is available. The radiologic features of the neoplasm resembled both pituitary adenoma and parasellar meningioma, but with more bone destruction. It is appropriate to consider this lesion in the differential diagnosis of a parasellar mass in a teenage or young adult patient when extensive bone destruction is present.

Adolescent↗

Giant-cell tumor of the sphenoid bone: case report and review of the literature.

We report the case of a 23-year-old man with a giant-cell tumor of the sphenoid bone. The radiologic manifestations consisted of an expansile mass arising from the sphenoid bone with extension into the cranial cavity and the nasopharynx. The findings with computed tomography and magnetic resonance imaging best reflected respectively the osseous and soft-tissue extent of the disease.

Adult↗

Capillary hemangioma of the sphenoid bone.

A capillary hemangioma in the body of the sphenoid bone produced unilateral optic atrophy in a 13-year-old boy. The typical reticulated appearance of an osseous hemangioma was clearly demonstrated only on direct magnification radiographs. At angiography, patchy filling occurred through vessels arising from the internal carotid and internal maxillary arteries bilaterally. The few other reports of sphenoid hemangiomas are reviewed.

Adolescent↗

Venous occlusions of the cavernous area--a complication of crushing fractures of the sphenoid bone.

Four patients who sustained crushing fractures of the sphenoidal bone had angiographic evidence of venous occlusions of the cavernous area. Signs depended upon the type of basal venous and cavernous anatomy. The diagnosis can be made by demonstrating abrupt cutoff of veins in the cavernous region, preferred retrograde flow of the anterior cavernous sinus, direct venous hemorrhage, and venous stasis.

Adolescent↗

Ocular findings and sphenoid bone morphology in tuberous sclerosis.

The aim of the study was to focus on the correlation between the ocular findings and the morphology of the sphenoid bone supporting the optic nerve in patients with tuberous sclerosis. Ten patients participated in the investigation. The sphenoid bone morphology was analyzed from existing radiographs of the cranium. The results were compared to the individual ophthalmologic diagnosis. Changes in the midline osseous structure, the sella turcica and optic sulcus seem to be correlated with the severity of the ocular findings.

Adolescent↗

Primary osteosarcoma of the sphenoid bone with extensive periosteal extension--case report.

A 28-year-old male presented with a primary osteosarcoma of the sphenoid bone with extensive periosteal extension manifesting as severe headache and right exophthalmos. Computed tomography (CT) and magnetic resonance imaging revealed an anterior middle cranial fossa tumor extending into both the orbit and the extracranial space. However, roentgenography and CT with bone windows showed no marked osteolytic changes of the sphenoid bone. Total removal of the tumor was performed via the orbitozygomatic approach. Surgery revealed that the tumor had extended periosteally without macroscopic bone destruction, but no obvious abnormalities of the skull. The histological diagnosis was osteosarcoma. The patient was treated with chemotherapy and radiation therapy, but died of tumor recurrence 10 months after the surgery.

Adult↗

[A case of pyocele in the sphenoid bone cavity].

A case is reported where the clinical symptomatology as well as the ophthalmological, radiological, endocrinological, and scintigraphic results offered significant evidence in favor of the presence of a tumor in the sellar region. The diagnosis of a pyocele originating in the sphenoid bone could be established intraoperatively only. Cysts originating in the sphenoid bone are described as what is usually called an "orbital inlet syndrome" from which the present case differs in some respects.

Aged↗

Effects of pulsed ultrasound on sphenoid bone temperature and the heart rate in guinea-pig foetuses.

Temperature increase induced by exposure to unscanned pulsed ultrasound at an intensity (I(SPTA)) 2.82 W/cm2 was measured in the brain adjacent to the sphenoid bone of foetal guinea-pigs in late gestation under in vitro and in vivo (in utero) conditions. After 120 s exposure a mean temperature increase of 2.6 degrees C was measured in vitro. Removal of the overlying parietal bones increased this value to 5.2 degrees C. Mean temperature increases at the sphenoid bone recorded in utero were 1.5 degrees C live and 2.0 degrees C post mortem. Measurement of foetal ECG showed that ultrasound-induced heating of the hypothalamic region did not significantly alter foetal heart rate.

Animals↗