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retroperitoneal fibrosis/треска
Линкът е запазен в клипборда
Страница 1 от 84 резултата
Association between familial mediterranean fever and retroperitoneal fibrosis: retroperitoneal fibrosis regression after colchicine therapy.
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Retroperitoneal fibrosis (RPF) is a disease characterized by inflammatory fibrotic processes affecting the retroperitoneal structures. Familial Mediterranean Fever (FMF) is an autosomal recessive disorder, characterized by fever and attacks of sterile serositis. Colchicine is the only suitable drug
Retroperitoneal fibrosis as a cause of fever of undetermined origin.
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Idiopathic retroperitoneal fibrosis: a rare onset of the illness caused by haemorrhagic fever with renal syndrome.
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The differential diagnosis of two cases of chronic periaortitis.
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The imaging features of chronic periaortitis resemble those of infected aneurysms. Two illustrative cases of chronic periaortitis, in which the etiologies were caused by IgG4-related disease, are presented. The first case involved a 68-year-old man who presented with vague discomfort in his lower
[A case of intrathoracic extension of retroperitoneal fibrosis].
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A 70-year-old man was diagnosed as having retroperitoneal fibrosis 12 years ago. The patient was admitted to our hospital with complaints of fever and left chest pain. On admission, chest radiography revealed left pleural effusion and left pleural thickening. Percutaneous pleural biopsy was
Chronic periaortitis (retroperitoneal fibrosis) concurrent with giant cell arteritis: a case report.
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BACKGROUND
Giant cell arteritis is the most common form of large-vessel vasculitides. However, it is probable that extracranial involvement is underdiagnosed in patients with classical giant cell arteritis. In the recent literature most cases of giant cell arteritis have been described in
A case of uveitis associated with idiopathic retroperitoneal fibrosis.
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We treated a patient with nongranulomatous panuveitis associated with idiopathic retroperitoneal fibrosis who had symptoms of abdominal pain, severe fever, leg edema, and blurred vision. A high C-reactive protein level, a high erythrocyte sedimentation rate, anemia, and abnormalities of the immune
[Retroperitoneal fibrosis in children].
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A 13 year-old boy was hospitalized because of persisted fever had pallor for three months. Abdominal ultrasound, intravenous pyelogram, and abdominal computerized axial tomography scan disclosed a space occupying lesion located postero-superior to the bladder. Biopsies of the above lesion disclosed
IgG4-related Disease Involving Multiple Organs with Elevated Serum Interleukin-6 Levels.
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A 63-year-old woman presented to our hospital with elevated levels of serum IgG4, marked wall thickening of the gallbladder, hepatomegaly, and abdominal lymphadenopathy. She experienced a recurrent fever and leg edema. Her laboratory data demonstrated anemia, hypoalbuminemia, and elevated serum
[Retroperitoneal fibrosis: a clinical analysis of 18 cases].
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OBJECTIVE
To investigate the clinical features and outcomes of 18 patients with retroperitoneal fibrosis (RPF).
METHODS
We retrospectively analyzed the clinical data of 18 RPF patients who received treatment in Peking Union Medical College Hospital from 1988 to 2004.
RESULTS
The initial symptoms
Prognostic factors in retroperitoneal fibrosis.
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The aim of this study is to evaluate effective prognostic factors in the evolution of patients with retroperitoneal fibrosis and to establish the validity of fractal analysis in determining the disease severity in these patients.
METHODS
This study included 19 patients (M/F: 5/14) treated for
Filariasis an Unusual Cause of Retroperitoneal Fibrosis, Hydronephrosis, and Infertility in a Young Adult Male
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Background: Filariasis is a tropical disease caused by infection with nematode parasites of the Filarioidea family. Filariasis is an endemic disease in parts of India, Sub-Saharan Africa, and Southeast Asia. Filariasis is a progressive disease predominantly affecting the
Chronic Tubulo-interstitial Pyelonephritis with Retroperitoneal Fibrosis.
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A large proportion of patients with retroperitoneal fibrosis (RPF) have been labelled as having idiopathic RPF historically. Recent reports of a subset of these patients having a fibro-inflammatory condition with characteristic histology and good response to therapy has helped in renewed
IgG4-Related disease simulating paraneoplastic syndrome: Role of 18FDG PET/CT imaging.
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Immunoglobulin G4 (IgG4)-related systemic disease (IgG4-RSD) is a new systemic entity associated with autoimmune pancreatitis (AIP). Other organ involvements take the form of sclerosing cholangitis, sclerosing cholecystitis, sclerosing sialadenitis, retroperitoneal fibrosis, and interstitial
[A 22 year old woman with fever, night sweats, weight loss and hepatomegaly].
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A 22 year old female patient presented with fever, night sweats, weight loss and hepatomegaly associated with elevated inflammatory parameters and liver enzymes. Computer tomography revealed a mass located between the inferior vena cava and the psoas muscle as well as enlarged celiac,
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