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Diagnostic Criteria for Idiopathic Multicentric Castleman Disease (iMCD)

Human herpesvirus-8 (HHV-8)–negative, idiopathic multicentric Castleman disease (iMCD) is a rare and life-threatening disorder involving systemic inflammatory symptoms, polyclonal lymphoproliferation, cytopenias, and multiple organ system dysfunction caused by a cytokine storm often including interleukin-6. Accurate diagnosis is challenging, because no standard diagnostic criteria or diagnostic biomarkers currently exist, and there is significant overlap with malignant, autoimmune, and infectious disorders. Continue reading “Diagnostic Criteria for Idiopathic Multicentric Castleman Disease (iMCD)”

Diagnostic Criteria for Idiopathic Intracranial Hypertension (IIH)

The combination of raised intracranial pressure, without hydrocephalus or mass lesion, normal cerebrospinal fluid (CSF) composition and where no underlying aetiology is found are accepted criteria for the diagnosis of IIH. Continue reading “Diagnostic Criteria for Idiopathic Intracranial Hypertension (IIH)”

Diagnostic Criteria for Idiopathic Pulmonary Fibrosis (IPF)

In 2000, IPF was defined as a specific form of chronic, progressive, fibrosing interstitial pneumonia of unknown cause, occurring primarily in older adults and limited to the lungs. Usual interstitial pneumonia (UIP) is the histopathological pattern of IPF. IPF is characterized by progressive worsening of dyspnea and lung function and is associated with a poor prognosis. Continue reading “Diagnostic Criteria for Idiopathic Pulmonary Fibrosis (IPF)”

ILAR Classification Criteria for Juvenile Idiopathic Arthritis (JIA)

Juvenile idiopathic arthritis is a heterogeneous group of diseases characterised by arthritis of unknown origin with onset before age of 16 years.
Continue reading “ILAR Classification Criteria for Juvenile Idiopathic Arthritis (JIA)”

Diagnostic Criteria for Idiopathic Hypereosinophilic Syndrome (HES)

Diagnostic Criteria for Idiopathic Hypereosinophilic Syndrome (HES) are:

1. Persistent eosinophilia of over 1500/cubic millimeter for longer than 6 month;

2. Lack of evidence of other known causes of secondary hypereosinophilia (SH);

3. Multiple organ involvement.

Continue reading “Diagnostic Criteria for Idiopathic Hypereosinophilic Syndrome (HES)”

ATS/ERS Criteria for Diagnosis of Idiopathic Pulmonary Fibrosis (IPF)

Idiopathic interstitial pneumonias (IIPs) are part of a broad, heterogeneous group of interstitial lung diseases that encompasses more than 200 acute or chronic diseases with varying degrees of inflammation or fibrosis. Continue reading “ATS/ERS Criteria for Diagnosis of Idiopathic Pulmonary Fibrosis (IPF)”

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