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protein-losing enteropathies/треска
Врската е зачувана во таблата со исечоци
Страница 1 од 217 резултати
Familial Mediteranean fever with protein-losing enteropathy due to constrictive pericarditis.
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BACKGROUND
Constrictive pericarditis (CP) represents a rare cause of protein-losing enteropathy (PLE) resulting from intestinal lymphangiectasia (IL). In this report, we describe an 8-year-old Turkish boy with IL and PLE secondary to CP.
METHODS
The boy was introduced to our clinic due to bilateral
Primary amyloidosis with pulmonary involvement which presented exudative pleural effusion and high fever.
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We describe here an extremely rare case of primary amyloidosis which presented moderate pleural effusion and high fever. A 71-year-old man was admitted to our hospital because of exertional dyspnea, fatigue and fever. A chest X-ray showed right-sided moderate pleural effusion. A thoracocentesis
Neutropenic enteropathy: a 10-year review.
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OBJECTIVE
With the advent of more aggressive chemotherapy, the incidence of neutropenic enteropathy is increasing. This review was performed to (1) determine which children are affected, (2) identify predisposing factors, and (3) assess efficacy of treatment.
METHODS
A 10-year (1988 to 1997) review
Celiac disease presenting as Fever of unknown origin.
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Celiac disease (CD) is a common autoimmune enteropathy that occurs, in affected individuals, with exposure to gluten in the diet and improves with removal of dietary gluten. Although CD is readily considered in patients with classical presentations of the disease, atypical manifestations may be the
Enteropathy-associated T-cell lymphoma type II complicated by autoimmune hemolytic anemia.
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A 74-year-old man was admitted to hospital because of persistent fever, diarrhea, and abdominal pain. CT scanning showed extensive wall thickening of the colon. He was transferred to our hospital because he further developed ascites and paraaortic lymph node swelling. On presentation, he was
Unilateral lymphocytic pleuritis as a manifestation of familial Mediterranean fever.
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Familial Mediterranean fever (FMF) is an autosomal recessive disease affecting predominantly populations surrounding the Mediterranean basin. It is the most prevalent hereditary periodic fever syndrome characterized mainly by recurrent and short attacks of fever and serositis (pleuritis, arthritis,
Enteropathy-associated T-cell lymphoma (type II): a Brazilian case report.
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Enteropathy-associated T-cell Lymphoma (EATL) is a rare form of aggressive T-cell lymphoma. It is more prevalent in men over 60 years and the prognosis is very poor. EATL is classified into two groups based on morphology, immunohistochemistry, and genetic profile. EATL type I is highly associated
Methods of predicting pale, soft, exudative pork and their application in breeding programmes-A review.
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The condition of pale, soft, exudative (PSE) pork has long been considered to be mainly a post mortem phenomenon. There is now substantial evidence that such pigs are suffering from a kind of myopathy, which predisposes them to an abnormal post mortem metabolism. Genetic studies on PSE muscle
The Exudative-Constrictive Tuberculosis Pericarditis Diagnosed by Toracoscopic Biopsy
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Purpose: To present the problems and possibilities of diagnostic and treatment in a patient with resistant exudative-constrictive pericarditis.
Methods: The male patient 31 y. was admitted to the clinic due to exudative
Lawsonia intracellularis associated equine proliferative enteropathy in Danish weanling foals.
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Staphylococcal enterotoxins G and I, a cause of severe but reversible neonatal enteropathy.
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OBJECTIVE
Staphylococcus aureus is recognized to produce toxins A-E and toxic shock syndrome toxin-1 associated with food poisoning and toxic shock syndrome. Enterotoxins G and I co-exist in the same S aureus strains (staphylococcal enterotoxin G and staphylococcal enterotoxin I) and are implicated
[Eosinophilic exudative pleurisy as a manifestation of drug allergy].
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The paper is concerned with a study in which eosinophilic exudative pleuritis was the first sign of drug allergy (penicillin, streptomycin, claphoran), also manifesting itself in fever, hemorrhagic eruption, eosinophilia in the blood. Fast recovery was achieved after discontinuation of antibacterial
Hemophagocytic Lymphohistiocytic Syndrome and Enteropathy-Associated T-cell Lymphoma in a Patient with Refractory Celiac Disease.
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A 70-year-old woman with celiac disease presented with weight loss and diarrhea unresponsive to gluten-free diet (GFD) and prednisone. Diagnosis of type 2 refractory celiac disease (RCD) was made by small intestinal biopsies showing severe villous blunting and intraepithelial lymphocytosis. She was
[Type II enteropathy-associated T-cell lymphoma: a clinicopathologic study].
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OBJECTIVE
To study the clinicopathologic features, immunohistochemical findings, differential diagnosis and prognosis of type II enteropathy-associated T-cell lymphoma (EATL).
METHODS
Fourteen cases of type II EATL encountered in Department of Pathology, Nanjing General Hospital were retrospectively
Encephalopathy due to carnitine deficiency in an adult patient with gluten enteropathy.
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A 48-year-old male patient had two episodes of fever, headache, confusion and seizures following an upper respiratory tract infection. Electroencephalography (EEG) revealed diffuse slowing of background activity. Plasma free carnitine and serum lipid levels were low; fecal fat content and serum
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