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carcinoid tumor/seizures
Linkki tallennetaan leikepöydälle
14 tuloksia
Single Subcutaneous Nodule as Initial Presentation of Atypical Lung Carcinoid.
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We report a 50-year-old woman whose atypical lung carcinoid presented as a single subcutaneous nodule. Biopsy of the nodule revealed neuroendocrine carcinoma likely from the lungs. Imaging studies revealed masses in lungs, pelvis and right axilla, and a seizure a few months later lead to discovery
[Multiple brain metastasis of bronchial atypical carcinoid: unusual MR imaging, case report].
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We reported a case of a 76-year-old male who suffered from gait disturbance. His first MR image showed multiple masses in the cerebellum and cerebrum. After 50Gy of whole brain irradiation the masses downsized, but, after 8 months the patient was readmitted because of general convulsions. MRI on his
Malignant carcinoid tumor metastatic to the dura mater simulating a meningioma.
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A 50-year-old man, transferred from another hospital, was admitted because of adult onset seizures. Nine months earlier, he had undergone an esophagogastrectomy; the lesion was confirmed to be a carcinoid tumor. Laboratory tests, chest x-rays, and electrocardiogram were normal. A second liver and
Primary midgut carcinoid, a rare cause of paraneoplastic limbic encephalitis: a case report.
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A 60-year-old male presented with an unexplained seizure whose aetiology could not be demonstrated. After 8 weeks, patient on evaluation for abdominal pain was detected to have primary midgut carcinoid with nodal and hepatic metastasis. Patient underwent cytoreductive surgery and metastatectomy with
Paraneoplastic limbic encephalitis due to thymic carcinoid.
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Limbic encephalitis is a multifocal inflammatory disorder characterized by personality changes, irritability, memory loss, seizures, and, in some cases, dementia. In many cases, it may occur as a paraneoplastic syndrome and therefore the diagnosis of limbic encephalitis should raise the possibility
Multicystic metastatic carcinoid to brain: case report.
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Symptomatic intraparenchymal brain metastases from carcinoid tumors are unusual, and neurological deficits are rarely the first symptom of underlying carcinoid primaries. We report a patient with multiple cystic metastases to the brain from a lung primary who first presented with headaches and
Fatal carcinoid crisis after percutaneous fine-needle biopsy of hepatic metastasis: case report and literature review.
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Immediately after a fine-needle aspiration biopsy (FNAB) was performed of a carcinoid liver metastasis, a patient had severe flushing, nausea, and faintness, followed by generalized seizure activity, profound hypotension, and cardiopulmonary arrest refractory to resuscitative efforts. This was
The protean manifestations of pheochromocytoma.
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The treacherous and deceptive nature of pheochromocytoma makes it crucial to detect and treat it promptly; otherwise it will almost certainly be fatal from cardiovascular complications or metastases. Hypertension occurring in patients with pheochromocytomas is sustained in about 50% and paroxysmal
[Diverse expression of multiple endocrine neoplasia type 1].
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MEN-1 is an autosomal dominantly inherited disorder, characterised by the occurrence of multiple tumours, particularly in the parathyroid glands, the pancreatic islets, the pituitary gland and the adrenal glands, as well as by neuroendocrine carcinoid tumours. Various clinical manifestations are
[Clinical spectrum of digestive neuroendocrine tumors].
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Digestive neuro-endocrine tumours have a broad and initially misleading clinical spectrum. Tumours from the duodenopancreatic area should be distinguished from digestive carcinoid tumours. In the first group, insulinomas, gastrinomas, and non-functioning tumours are the most frequent. Insulinoma is
Simultaneous diagnosis of glioblastoma, cervical schwannoma, adrenal masses and growth hormone-secreting adenoma in a previously healthy patient.
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A constellation of newly diagnosed benign tumours and glioblastoma is an uncommon occurrence in a single individual. We present a case of a patient with a history of skin lipomas who presented with seizures and was found to have a left frontotemporal multifocal enhancing mass on MRI. Work-up for
Central diabetes insipidus due to herpes simplex in a patient immunosuppressed by Cushing's syndrome.
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OBJECTIVE
To describe a patient immunocompromised by Cushing's syndrome in whom central diabetes insipidus developed as a complication of herpes simplex involvement of the hypothalamus.
METHODS
We present a case, including results of laboratory and histopathologic studies, in which herpes simplex
Neoplastic lesions in CADASIL syndrome: report of an autopsied Japanese case.
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is one of the most common heritable causes of stroke and dementia in adults. The gene involved in the pathogenesis of CADASIL is Notch3; in which mutations affect the number of cysteine residues in
Neuron-Specific Enolase as a Biomarker: Biochemical and Clinical Aspects.
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Neuron-specific enolase (NSE) is known to be a cell specific isoenzyme of the glycolytic enzyme enolase. In vertebrate organisms three isozymes of enolase, expressed by different genes, are present: enolase α is ubiquitous; enolase β is muscle-specific and enolase γ is neuron-specific. The
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