granulomatosis


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gran·u·lo·ma·to·sis

n. granulomatosis, granuloma múltiple.

granulomatosis

n granulomatosis f; — with polyangiitis, Wegener’s — (ant) granulomatosis con poliangeítis, granulomatosis de Wegener (ant)
References in periodicals archive ?
Rituxan was initially developed for the treatment of non-Hodgkin's lymphoma and subsequently gained marketing approvals for use in RA, chronic lymphocytic leukemia (CLL) and granulomatosis (Roche, 2013).
The mother-of-two suffers with Wegener's granulomatosis, a rare auto immune illness that causes the capillary vessels to become inflamed and burst, meaning the main organs don't get fed and can die off.
Correlating the clinical & histopatholgy, a final diagnosis of Orofacial granulomatosis has been etablished.
Retrospective Histopathological Study of Nine Cases of Mycotic Granulomatosis in the Digestive Tract of Canines
Literature baktigimizda akcigerde multiple kaviteler lezyonlara yol acabilecek hastaliklar arasinda Wegener granulomatosis, lenfoma, Tuberkuloz, fungal enfeksiyonlar, perfore kist hidatik ve anaerob bakteri enfeksiyonlarinin oldugu goruldu (6-9).
Granulomatosis with polyangiitis in children: report of a case with kidney-lung syndrome
Another diagnosis that is commonly entertained in these groups of patients is orofacial granulomatosis (OFG).
Jonny, of Leeds, was eventually diagnosed with Wagner's granulomatosis, which causes the body's immune system to attack itself and can result in kidney failure.
Key words: Hereditary gingival fibromatosis; Plasma cell gingivitis, Oro-facial granulomatosis, Drug induced gingival hyperplasia
Orofacial granulomatosis (OFG) This is the occurrence of persistent diffuse facial swelling affecting the lips and cheeks with the key histopathological feature of deep non-necrotising/non-caseating granulomas [Wiesenfeld et al.
The text opens with an historical overview, followed by physiological and radiological features of common ILDs, such as idiopathic interstitial pneumonia, non-specific interstitial pneumonitis, and sarcoidosis, and uncommon ILDs, such as lymphangioleiomyomatosis, Langerhans cell granulomatosis, drug-induced lung disease, eosinophilic lung disease, alveolar proteinosis, and alveolar michrolithiasis.
The 29-year-old who lives with James in Clayton West, suffers from Wegener's Granulomatosis - an incurable disease in which blood vessels become inflamed, making it hard for blood to flow.

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