2004
DOI: 10.1055/s-2004-832358
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Differential Diagnosis of Suprasellar Tumors in Children

Abstract: In contrary to the adult age the most common suprasellar tumors in children are with decreasing frequency craniopharyngiomas, chiasmatic/hypothalamic low-grade gliomas, germinomas and lesions attributable to a Langerhans cell histiocytosis. For differential diagnostic purposes also the rare hypothalamic hamartoma and meningeal metastases in the infundibular recess of the third ventricle are included. The typical aspects of the various tumors on computed tomography (CT) and magnetic resonance imaging (MRI) toge… Show more

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Cited by 84 publications
(63 citation statements)
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References 25 publications
(32 reference statements)
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“…These results are in accordance with the previous observation that the occurrence of fluid-fluid levels within hemorrhagic pituitary tumors ranges from 48.1-55.8% (10,14). Additionally, hemorrhage within pituitary adenomas is common in patients with non-functioning adenomas and prolactinomas (9,(16)(17)(18)(19)(20)(21); although an earlier study suggests that GH-and ACTH-secreting pituitary adenomas are more likely to present apoplexy than others (22). This immunological variation may be due to the lack of specific clinical markers for non-functioning and FSH/LH tumors, which may remain undetected for many years until they become large enough to induce tumor ischemia (13,21).…”
Section: Discussionsupporting
confidence: 82%
“…These results are in accordance with the previous observation that the occurrence of fluid-fluid levels within hemorrhagic pituitary tumors ranges from 48.1-55.8% (10,14). Additionally, hemorrhage within pituitary adenomas is common in patients with non-functioning adenomas and prolactinomas (9,(16)(17)(18)(19)(20)(21); although an earlier study suggests that GH-and ACTH-secreting pituitary adenomas are more likely to present apoplexy than others (22). This immunological variation may be due to the lack of specific clinical markers for non-functioning and FSH/LH tumors, which may remain undetected for many years until they become large enough to induce tumor ischemia (13,21).…”
Section: Discussionsupporting
confidence: 82%
“…Cranial magnetic resonance imaging (MRI) was prospectively performed according to the recommendations as part of the trial protocol KRANIOPHARYNGEOM 2000 (19,22) at diagnosis and at 3-month intervals during follow-up. The assessment of progression or recurrence was based on MRI and prospectively confirmed by reference panel in all cases.…”
Section: Neuroimagingmentioning
confidence: 99%
“…If this occurs while the tumor contracts, it can be unclear whether the tumor involves the optic nerve or is a new mass formation in front of the neurohypophseal germinoma without infiltrating the pituitary stalk. There is no difference in treatment according to the region of occurrence of the germinoma, but differentiation with craniophalyngioma, chiasmatic/hypothalamic low-grade gliomas, Langerhans cell histiocytosis and lymphocytic hypophysitis is needed when a tumor is large [13]. Also, it is necessary to differentiate optic nerve germinoma as well as optic sheath meningioma, infectious or granulomatous neuritis, orbital pseudotumor, lymphoma, medulloepithetlioma of the optic nerve and metastasis even if the mass is limited to the optic nerve [10].…”
Section: Discussionmentioning
confidence: 99%