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paraneoplastic syndromes/kopfschmerz
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Seite 1 von 21 Ergebnisse
[A rarely diagnosed paraneoplastic syndrome: cerebral venous thrombosis].
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Cerebral venous thromboses are uncommon in cancer, and rarely presents as a paraneoplastic syndrome. A 42-year-old patient presented with headache and a bilateral papillar edema. Cerebral computed tomographic (CT) scan did not find a tumoral process. Biological tests disclosed increased acute phase
Facial pain as first manifestation of lung cancer: a case of lung cancer-related cluster headache and a review of the literature.
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Facial pain can, on rare occasions, be the presenting symptom of lung cancer. This report describes a patient with non-metastatic lung cancer, which was associated with attacks of debilitating facial pain, presenting as cluster headache. Moreover, 32 reported cases of lung cancer-related facial pain
Brain paraneoplastic syndromes in a patient with mediastinal ganglioneuroma
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Paraneoplastic neurologic syndromes are a rare and heterogeneous group of immune-mediated syndromes caused by underlying solid and nonsolid tumors. We present a case of 8-year-old female with long history of mild headaches and central instability who presented multiple poorly defined signal
Paraneoplastic syndromes in olfactory neuroblastoma.
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Olfactory neuroblastoma (ONB) is a rare malignant neoplasm of sinonasal tract, derived from olfactory epithelium. Unilateral nasal obstruction, epistaxis, sinusitis, and headaches are common symptoms. Olfactory neuroblastoma shows neuroendocrine differentiation and similarly to other neuroendocrine
Primary adrenal lymphoma with paraneoplastic syndrome.
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BACKGROUND
The adrenal gland is a common site for neoplastic diseases and primary adrenal lymphoma (PAL) is a rare tumor with around 120 cases reported so far.
METHODS
We present a rare case of 76-year-old male who presented with headache, confusion, inappropriate body movements and abdominal pain.
Intrahepatic cholestasis as a paraneoplastic syndrome associated with pheochromocytoma.
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Pheochromocytoma is a rare tumor of chromaffin cells that secrete catecholamines and several cytokines. The clinical manifestations are protean and may include hypertension, weight loss, sweating, palpitation, headache, anxiety, tremor, nausea, vomiting, and hypercalcemia. The tumor can mimic many
Neurologic complications of ovarian carcinoma.
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BACKGROUND
Neurologic complications of ovarian carcinoma are uncommon and to the authors' knowledge the full spectrum has not been delineated previously.
METHODS
The authors reviewed the findings of 121 neurologic consultations on 83 ovarian carcinoma patients between 1993 and 1996; this represents
Application of the 2016 diagnostic approach for autoimmune encephalitis from Lancet Neurology to Chinese patients.
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BACKGROUND
A unified clinical approach to diagnose autoimmune encephalitis was published in Lancet Neurology in 2016. Purpose of our study is to examine the feasibility and reasonability of the 2016 "A clinical approach to diagnosis of autoimmune encephalitis" in China with a retrospective
Early Dorsal Midbrain Syndrome Mimicking an Adie's Tonic Pupil.
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BACKGROUND
While tonic pupils have been attributed to various diseases, including syphilis, herpes zoster, orbital trauma, temporal arteritis, endometriosis, and paraneoplastic syndromes, obstructive hydrocephalus has not been implicated.
METHODS
A 36-year-old woman visited a neurology department
18F-FDG PET/CT of Generalized Arteritis.
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A 75-year-old man presented with significant weight loss, persistent cough, single episode of frontotemporal pulsatile headache, and leg weakness. A paraneoplastic syndrome was suspected, and F-FDG PET/CT was performed. Diffuse, moderate-to-intense tracer symmetrical uptake of many large and medium
Cochlear Impairment and Autoimmune Ear Disorder in a Patient with Breast Cancer.
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The purpose of this study was to consider the possible role of autoimmune diseases and paraneoplastic syndrome in the genesis of tinnitus. The incidence of autoimmune inner ear disease (AIED) is rare, accounting for <1% of all cases of hearing impairment and dizziness. In presence of auditory and
Glazed (vision) and confused.
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A 60-year-old man presented with vitritis and optic neuropathy in the setting of headaches and behavioral changes. MRI brain revealed bilateral temporal lobe inflammation consistent with limbic encephalitis. He was subsequently diagnosed with small cell lung cancer with a paraneoplastic syndrome
Anti-Ma-1 and Anti-Ma-2 Antibodies in Isolated Fatal Hypothalamitis.
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Lymphocytic hypothalamitis (LHT) is a rare disease characterized by pituitary dysfunction, autonomic instability, metabolic disturbances, and neuropsychiatric disorders. We report the case of a 30-year-old man found to have LHT that progressed despite treatment with methylprednisolone and
Reversible postvaccination paraneoplastic encephalomyelitis in a patient with lung adenocarcinoma.
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Encephalomyelitis occurs in paraneoplastic syndrome and acute disseminated encephalomyelitis through different autoimmune mechanisms. No postvaccinal encephalomyelitis other than acute disseminated encephalomyelitis has been reported in patients with malignancy. A 68-year-old woman was admitted
[A young patient with endometrioid adenocarcinoma who suffered Trousseau's syndrome associated with vasculitis].
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A 27-year-old woman was admitted to our hospital because of headache, fever and right neck pain. Neurological examination revealed mild meningeal signs, and hyper-reflexia in all extremities. In the laboratory tests, white-cell count was 13,000/mm3, rheumatoid factor(RF) and C-reactive protein(CRP)
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