sarcoidosis/peavalu

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Systemic Sarcoidosis Presenting with Headache and Stroke-Like Episodes.

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Sarcoidosis is a multisystem granulomatous disorder. Neurological manifestations as a presenting symptom are relatively rare. A 26-year-old male presented with a five-week history of headache suggestive of raised intracranial pressure. He subsequently developed transient episodes of mild right-sided

Cluster-like headache and a cystic hypothalamic tumour as first presentation of sarcoidosis.

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BACKGROUND Sarcoidosis is a granulomatous, multisystem inflammatory disease of unknown cause, which presents with a wide variety of symptoms. We describe a rare case of a newly diagnosed sarcoidosis, with cluster-like headache as a presenting symptom. METHODS A 31-year-old man presented with cluster

Headache with Midline Shift: An Uncommon Presentation of Sarcoidosis.

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Childhood osseous sarcoidosis presenting with headache and lytic skull lesions.

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July 2004: 40-year-old man with headaches and dyspnea.

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A 40-year-old man had a 6-week history of severe frontal headaches and dry cough. Chest x-ray showed hilar adenopathy with bilateral parenchymal infiltrates. A diagnosis of atypical pneumonia was made. Four weeks later he was admitted with persistent headache. Infectious screen was negative. Brain

[A case of isolated sarcoidosis of the cerebral falx].

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A 28 year-old man complaining of intermittent headaches for a month following an episode of general convulsions was admitted to the Department of Neurosurgery of our hospital. His brain CT scan showed a well-enhanced mass growing symmetrically along the anterior cerebral falx in a manner compatible

A sarcoidosis-lymphoma syndrome revealed by hypopituitarism.

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A 26-year-old woman presented with persistent headache and tiredness. Biological investigations disclosed a moderate inflammatory syndrome, low PTH-hypercalcemia and complete anterior hypopituitarism. A magnetic resonance imaging (MRI) of the pituitary gland was performed and revealed

[Chronic polyarthritis in a patient affected by sarcoidosis and chronic HCV infection. Case report and review of the literature].

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Sarcoidosis is a systemic granulomatous disease of unknown etiology that has a wide variety of clinical manifestation. Lung involvement may slowly undergo pulmonary fibrosis. Chronic sarcoid arthritis is a rare, usually non destructive arthropathy; may be a mono, oligo or polyarthritis. Knees,

[A case of primary acute pulmonary cavitation in sarcoidosis complicated by multiple nodular lesions in the central nervous system].

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A 20-year-old man visited our hospital complaining of headache and a dry cough. Chest X-ray and chest CT showed bilateral hilar and mediastinal lymphadenopathy, multiple cavitations with thin, smooth walls, and diffuse granular shadows. A transbronchial biopsy specimen revealed sarcoid granuloma.

[A case of CNS sarcoidosis -case report of hydrocephalus due to mechanical obstruction secondary to sarcoid granulomata at the outlet of the fourth ventricle (author's transl)].

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A 28-year old male was admitted to Musashino Red Cross Hospital on June 21, 1975, because of symptoms of increased intracranial pressure and cerebellar dysfunction. Thirteen months prior to admission he had a mild fever, tremor of right arm, headache, nausea and unsteady gait, but made a gradual

[A case of meningeal disseminated sarcoidosis with marked hypoglycorrhachia in the CSF].

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A 29-year-old man diagnosed as having pulmonary sarcoidosis in 2008, and hypothyroidism secondary to thyroidectomy for Basedow's disease was admitted to our hospital with pustular psoriasis in November 2010. He experienced high fever (38°C) and headache in late October 2010. Gadolinium-enhanced

Sarcoidosis in an athlete.

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BACKGROUND Sarcoidosis is a multisystem granulomatous disorder of unknown etiology, characterized by "noncaseating granulomas" in different organs. Clinical signs are variable and dependent on the organ involved. Although it is often asymptomatic in athletes, considering the high level of athletic

Isolated neurosarcoidosis: case series in 2 sarcoidosis centers.

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BACKGROUND Neurosarcoidosis occurs in the central or peripheral nervous system and is usually associated with other sarcoidosis organ involvement. However, when sarcoidosis develops exclusively in the nervous system, its diagnosis is problematic. METHODS Retrospective analysis of patients who were

Intradural, extramedullary spinal sarcoidosis: report of a rare case and review of the literature.

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BACKGROUND Spinal sarcoidosis represents a rare subgroup of neurosarcoidosis. Most spinal sarcoid lesions are intramedullary, and only eight cases of intradural, extramedullary sarcoid lesions have been reported hitherto. We describe the complete entity of intradural, extramedullary spinal

Interferon-alpha-induced sarcoidosis in a patient being treated for hepatitis C.

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METHODS Female, 43 FINAL DIAGNOSIS: - METHODS Diarrhea • generalized weakness • headache • lightheadedness • nausea • rash • short of breath • vomiting METHODS - Clinical Procedure: - Specialty: Pulmonology. OBJECTIVE Rare diseae. BACKGROUND IFN-alpha-2b in combination with ribavirin is now the

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