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BACKGROUND Sarcoidosis is a systemic disease that can affect any organ, including the liver. It is manifested by the presence of non-caseating granulomas within involved organs, most commonly the pulmonary, lymphatic, and hepatic system. Unlike pulmonary or lymphatic involvement, hepatic involvement
Sarcoidosis is a multisystemic disease of unknown etiology characterized by formation of non-caseificating epithelioid cell granulomas in affected organs. The clinically manifest involvement of the gastrointestinal tract (GIT) in the pathological process is documented in less than 1% of the
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
OBJECTIVE
To report a case of drug-induced fever associated with azathioprine treatment in a patient with sarcoidosis.
METHODS
A 52-year-old man with pulmonary sarcoidosis presented to the emergency department with a 1-day history of fever (temperature 39.9 °C), chills, nausea, and vomiting. One
BACKGROUND Sarcoidosis is a systemic inflammatory disorder characterized by a classic pathologic feature of non-caseating granulomas involving any organ system. Hemophagocytic lymphohistiocytosis (HLH) is a catastrophic cytokine surge characterized by dysregulation of the macrophage response, which
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
Sarcoidosis is a granulomatous disease of unknown etiology. Over 90% of patients with sarcoidosis present with pulmonary findings at the time of diagnosis. Extrapulmonary involvement is common, including the liver, eyes, central nervous system, lymph nodes, and joints. However, isolated
A case of hydrocephalus is described which developed as a late complication of sarcoidosis. In a female patient aged 37 years manifestations of sarcoidosis in the form of Löfgren's syndrome developed 13 years earlier and the diagnosis was confirmed with histological examination of lymph node and
In a 26-year-old patient admitted to the emergency ward with acute abdomen, all the symptoms--nausea, vomiting, indeterminate abdominal pain, constipation, renal failure, polyuria and polydipsia--could be explained by calcium intoxication syndrome. Investigation revealed generalized sarcoidosis.
A patient, whose symptoms included epigastric pain, nausea and vomiting relieved with antacids but with no history of diarrhea or constipation, was found to have generalized sarcoidosis involving his lungs, liver, lymph nodes, skin, stomach and rectum. Because sarcoidosis rarely involves the
We present a case of isolated granulomatous gastritis in a 21-year-old woman. Initial symptoms included nausea, vomiting and inability to tolerate oral intake. An upper oesophagogastroduodenoscopy revealed nodular and thickened mucosa with histological findings of granulomatous gastritis.
Five patients with persistent or progressive pulmonary shadowing due to sarcoidosis were treated with 150 mg levamisole daily and one patient with 150 mg twice weekly. Only the latter patient completed a 12-week course without unwanted side-effects. One of the remaining five patients on full dose
Eleven patients with chronic sarcoidosis resistant to high-dose corticosteroids and other immunosuppressive treatments were treated with cyclosporine A at the initial daily dose of 5 mg per kg body weight (ideal weight in the case of overweight subjects) combined with flucortolone and methotrexate.
Sarcoidosis is a systemic granulomatous disease of unknown etiology, characterized by an immunological disorder with accumulation of activated lymphocytes and macrophages in all the organs and apparatus. The intrathoracic lymphnodes and the lung remain the most common sites of such disease. The
A 32-year-old black man had a two-year history of malaise, nausea, and vomiting, and a weight loss of 75 lb. Four months before his first clinic visit, a fine papular eruption developed on the torso and ichthyotic lesions found on the arms and legs. Medical evaluation revealed sarcoidosis involving