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Paragangliome im Kopf-Hals-Bereich
Paragangliomas represent a heterogeneous group of rare neuroendocrine tumors with marked variability in symptoms and disease course. Due to the close...
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Paragangliome der A. carotis
Paraganglioma of the head and neck region are rare tumors that occur both sporadically and as a hereditary predisposition. They may represent a...
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Nuklearmedizin bei endokrinen Erkrankungen Diagnose und Therapie
Dieses Buch enthält aktuelle Informationen über die allgemeinen Grundsätze der diagnostischen und therapeutischen Nuklearmedizin im Kontext der...
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Das Paragangliom der Harnblase – eine seltene, aber relevante Differentialdiagnose
A paranglioma is a rare, extra-adrenal neuroendocrine tumour. Paraganglioma of the urinary bladder is very rare, accounting for < 1% of all...
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Hereditäre neuroendokrine Tumoren im Kindesalter
Childhood neuroendocrine tumors in childhood are usually associated with genetic tumor predisposition syndromes. Therefore, predictive genetic...
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Personalisierte Therapie des Phäochromozytoms
BackgroundPheochromocytoma is a rare but severe disease of the adrenal glands. The aim of this study is to present and discuss recent developments in...
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Phäochromozytom und Paragangliom im Kindes- und Jugendalter
BackgroundPheochromocytoma and paraganglioma belong to the group of rare catecholamine-producing tumours during childhood and adolescence. They occur...
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Minimal-invasive Chirurgie retroperitonealer Paragangliome
Retroperitoneal paragangliomas are rare tumors with the characteristics of adrenal pheochromocytomas. They may occur sporadically or in conjunction...
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Exokrin trifft neuroendokrin: Mimickers neuroendokriner Neoplasien des Pankreas
Neuroendocrine neoplasms (NENs) originate from various epithelial or neuroectodermal tissues, can occur in any organ, including the pancreas, and are...
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Zufallsbefunde: submuköser Tumor bei der Gastroskopie
Submucosal tumors are usually asymptomatic and are generally an incidental finding during gastroscopy. However, submucosal tumors can also become...
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Neurofibromatose Typ 1: Vorsorgebogen für Kinder und Jugendliche in Österreich
BackgroundNeurofibromatosis type 1 (NF1) manifests in childhood with a variety of potential symptoms. Besides the development of tumours (primarily...
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Läsionen des viszeralen Mediastinums
BackgroundThe visceral or middle mediastinum contains nonvascular (trachea, carina, esophagus, and lymph nodes) and vascular structures (heart,...
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Gastrointestinale Stromatumoren
For more than 20 years gastrointestinal stromal tumors (GIST) have been a paradigm for a targeted treatment with tyrosine kinase inhibitors....
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Nebennierentumoren – aktuelle Standards im klinischen Management
Adrenal tumors are among the most common tumors in humans. They are most frequently discovered incidentally during abdominal imaging for other...
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Neue WHO-Klassifikation 2022: Harnblasenkarzinom
The new World Health Organization (WHO) classification of urogenital tumors is still primarily based on anatomic location, but is also a hierarchical...
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Primäre maligne Gefäßtumoren
The involvement of vessels in nonvascular tumors is always an indication of advanced local tumor growth. In principle, however, functional...
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