syndrome

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Related to Churg-Strauss syndrome: sarcoidosis, polyarteritis nodosa, Wegener's granulomatosis, Goodpasture's syndrome, Microscopic polyangiitis
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Acute coronary syndrome associated with Churg-Strauss syndrome.
A case of Churg-Strauss syndrome with necrotizing crescentic glomerulonephritis accompanied by acute coronary syndrome due to vasospasm.
Chronic eosinophilic pneumonia followed by Churg-Strauss syndrome.
infestation Larva migrans syndrome Strongyloides stercoralis infection Associated with systemic disease Churg-Strauss syndrome Hypereosinophilic syndromes Associated with drugs, toxic agents and radiation Associated with miscellaneous lung diseases Asthma and eosinophilic bronchitis Idiopathic interstitial pneumonias Langerhans cell granulomatosis Sarcoidosis Paraneoplastic syndrome Idiopathic eosinophilic lung disease Idiopathic chronic eosinophilic pneumonia Idiopathic acute eosinophilic pneumonia Table 2.
Each patient with Churg-Strauss syndrome was then matched with 100 controls for age, sex, health plan region, and year of cohort entry.
Prevalence and clinical significance of antineutrophil cytoplasmic antibodies in Churg-Strauss syndrome.
Differentiation of Wegener granulomatosis from Churg-Strauss syndrome is discussed in the following section.
Immunophenotype of Large Cells in Hodgkin Disease and Limited Lymphadenopathic Churg-Strauss Syndrome(*) Classic RS NLP Hodgkin Antibodies cells Cells CSS Large Cells L26 (CD20) Usually Positive Positive negative perifollicular UCHL-1 (CD45RO) Negative Negative Negative Leu-M1 (CD15) Usually Usually Negative positive negative Ber-H2 (CD30) Positive Weak or Positive negative perifollicular KP1 (CD68) Negative Negative Negative LN2 (CD74, B cells) Positive Positive Negative S100 (Langerhans) Negative Negative Positive in granulomas (*) RS indicates Reed-Sternberg cells; NLP, nodular lymphocyte-predominant; and CSS, Churg-Strauss syndrome.
Symptoms can also be caused by numerous uncommon inflammatory conditions, including sarcoidosis, Wegener's granulomatosis, Churg-Strauss syndrome, lupus, other collagen diseases, and Sjogren's s syndrome.
Microscopic polyangiitis (MPA) is a systemic vasculitis that involves small vessels, as is the case with Wegener granulomatosis and Churg-Strauss syndrome.
A sural nerve biopsy showed vasculitis consistent with Churg-Strauss syndrome.
Adu D, Bacon PA: Classical polyarteritis nodosa, microscopic polyarteritis, and Churg-Strauss syndrome.
Churg-Strauss syndrome does not typically present with clinical ALI/ARDS but may arise in the histologic differential of EP.
International Vasculitis Patient Groups: Churg-Strauss Syndrome Association: http://www.
1) ANCA-associated vasculitis includes a spectrum of entities, including Wegener granulomatosis, Churg-Strauss syndrome, microscopic polyangiitis, as well as pauciimmune glomerulonephritis (2)