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Primary Spinal Anaplastic Ganglioglioma
Pediatric Neurosurgery, 2006Gangliogliomas of the spinal cord are very unusual and the anaplastic variant of these tumors is extremely rare. In spinal anaplastic gangliogliomas, malignant changes (hypercellularity, vascular proliferation, necrosis, high numbers of mitotic figures) are typically evident in the glial element of the tumor. Gangliogliomas can arise in any part of the
Karabekir, Hamit Selim +2 more
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Current Treatment Options in Oncology, 2000
Anaplastic thyroid carcinoma (ATC) is a rare, highly aggressive tumor characterized by rapid growth that causes death soon after diagnosis. Optimal treatment is debatable because of inherent difficulties investigating a rare malignancy associated with a survival of only months. Nevertheless, there is evidence that a multimodality approach consisting of
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Anaplastic thyroid carcinoma (ATC) is a rare, highly aggressive tumor characterized by rapid growth that causes death soon after diagnosis. Optimal treatment is debatable because of inherent difficulties investigating a rare malignancy associated with a survival of only months. Nevertheless, there is evidence that a multimodality approach consisting of
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2009
Although the majority of thyroid cancer patients presenting to our surgical endocrinology clinics present with resectable and often curable disease, patients may rarely present with a history and physical findings suggestive of an anaplastic thyroid cancer.
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Although the majority of thyroid cancer patients presenting to our surgical endocrinology clinics present with resectable and often curable disease, patients may rarely present with a history and physical findings suggestive of an anaplastic thyroid cancer.
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2021
Clinical History: A previously healthy 55-year-old man was admitted in the hospital because of a focal-onset seizure that evolved into a generalized tonic-clonic seizure. Prodromal or premonitory symptoms were absent. He had no history of epilepsy. On examination, he was conscious and oriented, without any focal neurologic deficit.
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Clinical History: A previously healthy 55-year-old man was admitted in the hospital because of a focal-onset seizure that evolved into a generalized tonic-clonic seizure. Prodromal or premonitory symptoms were absent. He had no history of epilepsy. On examination, he was conscious and oriented, without any focal neurologic deficit.
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Head & Neck, 2005
A 48-year-old woman is seen for evaluation of a slowly enlarging lower neck mass. Three months previously, she had symptoms consistent with an upper respiratory tract infection that resolved within 3 to 4 days, then noticed a lump in her lower neck just to the left of midline.
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A 48-year-old woman is seen for evaluation of a slowly enlarging lower neck mass. Three months previously, she had symptoms consistent with an upper respiratory tract infection that resolved within 3 to 4 days, then noticed a lump in her lower neck just to the left of midline.
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Anaplastic Oligodendroglioma and Oligoastrocytoma
Neurologic Clinics, 2007Until approximately 15 years ago, the diagnosis of an oligodendroglioma (OD) was merely as a pathologic entity. The only clinical relevant meaning of this histologic diagnosis was the observation that the prognosis of OD was in general better than that of astrocytic tumors of similar grade. This changed with the recognition of the marked sensitivity to
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Congenital Anaplastic Astrocytoma
Journal of Neurosurgery, 1990R, Schober, N, Roosen
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