IgG4-related disease associated with renal microaneurysms and polycythaemia
نویسندگان
چکیده
منابع مشابه
Anaemia and polycythaemia with renal disease.
Red Cell Morphology in Renal Anemia In early studies by Ashe (1929) and Parsons and Ekola-Strolberg (I933) the anlemia was found to be associated with erythrocytes normal both in size and haemoglobin content. A striking feature was the absence of any disturbance of white cells or platelets. Studies of bone marrow morphology by Dameshek (I935) and Nordenson (1938) revealed the same pattern. Eryt...
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While autoimmune pancreatitis (AIP) has been recognized since the first description by Sarles et al in 1961, its involvement of other organs has been recognized more recently. Now, some form of IgG4-related systemic disease (IgG4-RSD) has been described in nearly every organ system, including the liver, gallbladder, other gastrointestinal sites, kidney, salivary and lacrimal glands, orbit, brea...
متن کاملSecondary polycythaemia associated with bilateral renal lymphocoeles.
A patient with a 15 year history of secondary polycythaemia due to renal erythropoietin hypersecretion is presented. Subsequent spontaneous development of bilateral renal lymphocoeles, which contained high erythropoietin levels, was shown by computerized tomography. The lymphocoeles were successfully treated by bilateral peritoneal marsupialization. No cause for the persistent polycythaemia or ...
متن کاملSecondary polycythaemia associated with bilateral renal
A patient with a 15 year history of secondary polycythaemia due to renal erythropoietin hypersecretion is presented. Subsequent spontaneous development of bilateral renal lymphocoeles, which contained high erythropoietin levels, was shown by computerized tomography. The lymphocoeles were successfully treated by bilateral peritoneal marsupialization. No cause for the persistent polycythaemia or ...
متن کاملAcute tubulointerstitial nephritis with severe renal impairment associated with multisystem IgG4-related disease.
The IgG4-related disease has a wide clinical spectrum where multiple organs can be affected, and the diagnosis depends on typical histopathological findings and an elevated IgG4 expression in plasma cells in the affected tissue. We describe the clinical presentation and evolution of a patient with acute tubulointerstitial nephritis, severe kidney failure and systemic manifestations such as lymp...
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ژورنال
عنوان ژورنال: Rheumatology
سال: 2015
ISSN: 1462-0324,1462-0332
DOI: 10.1093/rheumatology/kev365