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2.
Pathologica ; 99(3): 71-5, 2007 Jun.
Article de Anglais | MEDLINE | ID: mdl-17987726

RÉSUMÉ

Primary melanocytic neoplasms of the central nervous system consist of a spectrum of lesions ranging from well-differentiated melanocytoma to its overtly malignant counterpart, melanoma. Clinicopathologic features of 5 cases of primary central nervous system malignant melanoma were studied to define histologic appearances, diagnostic criteria, and the clinical behavior of lesions along this spectrum. There were three women and two men (mean age was 35 years) with symptoms of increased intracranial pressure. Radiological findings showed a solitary intra parenchymal lesion with variable enhancement after gadolinium administration. All patients underwent surgical treatment. Histologic examination revealed primary melanoma.


Sujet(s)
Tumeurs du système nerveux central/anatomopathologie , Mélanome/anatomopathologie , Adulte , Tumeurs du cerveau/anatomopathologie , Tumeurs du système nerveux central/complications , Tumeurs du système nerveux central/chirurgie , Diagnostic différentiel , Femelle , Humains , Hypertension intracrânienne/étiologie , Imagerie par résonance magnétique , Mâle , Mélanome/complications , Mélanome/chirurgie , Tumeurs de la moelle épinière/anatomopathologie
3.
Pathologica ; 98(2): 153-5, 2006 Apr.
Article de Anglais | MEDLINE | ID: mdl-16929789

RÉSUMÉ

Secretory meningiomas are rare histological subtypes of meningiomas with benign biological behaviour. In this study, the authors describe the first case of secretory meningioma with many mitotic figures and brain invasion, and discuss the clinicopathologic features including immunohistochemical staining profile and ultrastructural appearance of this tumour. A case of a 54-year-old man diagnosed with an intracranial tumour located in the left frontal lobe is presented. On pre-contrast CT scans, the tumour was hypodense and the contrast enhancement was marked in the pseudo membrane. The tumour was partially removed. The histological diagnosis was secretory meningioma with many mitotic figures, a high MIB-1 labeling index and a brain invasion.


Sujet(s)
Lobe frontal/anatomopathologie , Tumeurs des méninges/anatomopathologie , Méningiome/anatomopathologie , Antigène carcinoembryonnaire/analyse , Association thérapeutique , Irradiation crânienne , Lobe frontal/chirurgie , Humains , Kératines/analyse , Antigène KI-67/analyse , Mâle , Tumeurs des méninges/composition chimique , Tumeurs des méninges/radiothérapie , Tumeurs des méninges/chirurgie , Méningiome/composition chimique , Méningiome/radiothérapie , Méningiome/chirurgie , Adulte d'âge moyen , Index mitotique , Mucine-1/analyse , Invasion tumorale , Protéines tumorales/analyse , Récidive tumorale locale/radiothérapie , Radiothérapie adjuvante
4.
AJNR Am J Neuroradiol ; 27(5): 1098-100, 2006 May.
Article de Anglais | MEDLINE | ID: mdl-16687551

RÉSUMÉ

Symptomatic Rathke cleft cysts (RCC) are reported in the sellar and suprasellar regions, but no case of sphenoidal RCC has been reported. We report a case of sphenoidal RCC in a 41-year-old man. The lesion was revealed by headaches and diplopia. Symptoms disappeared transiently after a spontaneous rhinorrhea but relapsed 4 months later. MR imaging showed a cystic sphenoidal lesion, isointense on T1-weighted images (WI) with peripheral gadolinium enhancement and hyperintense on T2 WI. The patient underwent surgery through a transrhinoseptal approach. The wall of the sphenoid sinus was paper-thin. The cyst contained a motor-oil-like fluid and communicated widely with the nasal fossa. Its wall was partially extracted. Symptoms and signs ceased after surgery. MR imaging performed 1 year later showed the disappearance of the sphenoidal cyst. Embryological origin of RCCs is discussed. The hypothesis of a continuum between the different epithelial cystic lesions of the sellar and parasellar region is discussed. Imaging has an important impact on the diagnosis; nevertheless, the specific characterization remains difficult.


Sujet(s)
Kystes du système nerveux central , Tumeurs des sinus de la face , Sinus sphénoïdal , Adulte , Kystes du système nerveux central/diagnostic , Kystes du système nerveux central/chirurgie , Humains , Imagerie par résonance magnétique , Mâle , Tumeurs des sinus de la face/diagnostic , Tumeurs des sinus de la face/chirurgie
5.
Tunis Med ; 77(12): 631-7, 1999 Dec.
Article de Français | MEDLINE | ID: mdl-10730154

RÉSUMÉ

OBJECTIVE: To report the results of the use of the stereotactic techniques in the management of intra cranial lesions. MATERIALS AND METHODS: Between july 1994 and march 1998, we carried out 117 stereotactic procedures of whom only 100 cases were analyzed. All the procedures were achieved after a CT scan. Patients were separated in two groups: (A) stereotactic biopsy (91 patients), (B) surgery with laser guidance (9 patients). The mean age in group A was 38 years (2-75 years) versus 27 years (11-66 years) in group B. The sex-ratio was 1.3. RESULTS: In the group A, the correct pathological diagnosis was obtained in 91.2% of cases. Glial tumors was the frequent histopathological variety of tumor (67.47%). Only one patient was operated after biopsy for a bilateral meningioma of the anterior 1/3 of the falx. There was only one death (1.09%) and 3.29% of transitory complications. In the group B, all patients were operated with laser guidance. Thirty seven per cent of patients underwent radiotherapy after the stereotactic biopsy or surgery. CONCLUSION: Stereotactic biopsy is a reliable method for the histopathological diagnosis of deep-seated brain lesions. Surgery with laser guidance is a useful alternative for the management of small deep-seated lesions or lesions located in functional areas.


Sujet(s)
Tumeurs du cerveau/chirurgie , Gliome/chirurgie , Méningiome/chirurgie , Techniques stéréotaxiques , Adolescent , Adulte , Sujet âgé , Biopsie/méthodes , Encéphale/anatomopathologie , Tumeurs du cerveau/anatomopathologie , Enfant , Enfant d'âge préscolaire , Femelle , Gliome/anatomopathologie , Humains , Mâle , Méningiome/anatomopathologie , Adulte d'âge moyen , Résultat thérapeutique
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