Status: Bibliographieeintrag
Standort: ---
Exemplare:
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| Online-Ressource |
Verfasst von: | Tüttenberg, Jochen [VerfasserIn]  |
| Back, Walter [VerfasserIn]  |
| Wenz, Frederik [VerfasserIn]  |
| Schadendorf, Dirk [VerfasserIn]  |
Titel: | A rare case of primary sellar melanoma |
Titelzusatz: | Case report |
Verf.angabe: | Jochen Tüttenberg, Wolfram Fink, Walter Back, Frederik Wenz, Dirk Schadendorf, and Claudius Thomé |
E-Jahr: | 2004 |
Jahr: | May 2004 |
Umfang: | 4 S. |
Fussnoten: | Gesehen am 25.11.2020 |
Titel Quelle: | Enthalten in: Journal of neurosurgery |
Ort Quelle: | Charlottesville, Va. : American Assoc. of Neurological Surgeons, 1944 |
Jahr Quelle: | 2004 |
Band/Heft Quelle: | 100(2004), 5, Seite 931-934 |
ISSN Quelle: | 1933-0693 |
Abstract: | The authors report on the case of a 37-year-old woman in whom a primary sellar malignant melanoma mimicking a hemorrhagic pituitary macroadenoma was treated. This entity is exceedingly rare; only five cases are described in the literature. The patient presented with rapid deterioration of vision within a 2-week period. After an ophthalmological diagnosis of chiasmal syndrome was made, magnetic resonance (MR) imaging of the head revealed an intra- and suprasellar mass that was elevating and compressing the optic chiasm. Because of the signal heterogeneity of the lesion a hemorrhagic pituitary macroadenoma was assumed; the lesion was transsphenoidally resected. Histological examination of the specimen showed a malignant melanocytic tumor with immunopositivity for S100 protein and HMB-45. Despite extensive staging no other primary melanotic tumor was found. Thus, a primary sellar melanoma was diagnosed. Postoperative MR images demonstrated no residual tumor. For adjuvant therapy the region around the sella turcica received 40.4 Gy stereotactically guided radiation. A 24-month follow-up examination revealed no tumor recurrence.</p><p>This represents the sixth case of such a lesion reported in the literature, the third case evaluated using MR imaging, and the first case with a progression-free survival of 24 months. Thus, the authors advocate that management of primary sellar melanoma should include gross-total removal and postoperative stereotactic radiotherapy. |
DOI: | doi:10.3171/jns.2004.100.5.0931 |
URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
Volltext: https://doi.org/10.3171/jns.2004.100.5.0931 |
| Volltext: https://thejns.org/view/journals/j-neurosurg/100/5/article-p931.xml |
| DOI: https://doi.org/10.3171/jns.2004.100.5.0931 |
Datenträger: | Online-Ressource |
Sprache: | eng |
K10plus-PPN: | 1741073839 |
Verknüpfungen: | → Zeitschrift |
A rare case of primary sellar melanoma / Tüttenberg, Jochen [VerfasserIn]; May 2004 (Online-Ressource)
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