Results 61 to 70 of about 8,073,410 (232)

An Elderly Patient with Diabetic Nephropathy Complicated by ANCA-associated Nephritis [PDF]

, 2012
A 67-year-old man, on oral therapy for type 2 diabetes mellitus since 1990, had sustained proteinuria since 2005. When hematuria was first discovered in 2008, renal dysfunction [creatinine (Cr), 1.2 mg/dL], inflammation [C-reactive protein (CRP), 12 mg ...
Uramatsu, Tadashi, Taguchi, Takashi, Nishino, Tomoya, Kohno, Shigeru, Sakamoto, Noriho, Minami, Kana, Arai, Hideyuki, Obata, Yoko   +7 more
core   +1 more source

A clinical case of ANCA-associated systemic vasculitis in a nine-yearold Sakha child

Якутский медицинский журнал
ANCA-associated vasculitis (AAV) is a group of diseases characterized by chronic immune inflammation of the wall of small vessels, a polymorphic clinical picture with frequent involvement of the lungs and kidneys, and the presence of circulating ...
O. N. Ivanova, V. M. Argunova, P. A. Sleptsova, M. V. Afonskaya, S. I. Innokentyeva, I. S. Ivanova, T. A. Argunova, T. E. Burtseva, O. L. Kolobova, I. A. Chikova, A. V. Santimov, M. M. Kostik   +11 more
doaj   +1 more source

Hydralazine-induced pauci-immune glomerulonephritis: intriguing case series with misleading diagnoses [PDF]

Journal of Community Hospital Internal Medicine Perspectives, 2016
Hydralazine has been used since the 1950s for the management of hypertension. Evidence for hydralazine-associated vasculitis dates to pre-ANCA (antineutrophil cytoplasmic antibodies) era.
Faizan Babar, Jeffery N. Posner, Eugene A. Obah   +2 more
doaj   +1 more source

Case report: Testicular manifestation of ANCA vasculitis

Urology Case Reports
ANCA-associated vasculitis is a rare autoimmune disorder affecting small to medium-sized vessels, often targeting the respiratory tract and kidneys. Testicular involvement is rare and can resemble malignancy, leading to unnecessary surgery. A 36-year-old
Noah J. Sandel, Henry Wielzen
doaj   +1 more source

The pathogenesis of ANCA-associated vasculitis

Japanese Journal of Clinical Immunology, 2016
ANCA-associated vasculitis is characterized by the presence of anti-neutrophil cytoplasmic antibody (ANCA) in the serum. ANCA is a pathogenic autoantibody as well as the disease marker. It has been realized that ANCA-cytokine sequence is involved in the pathogenesis of ANCA-associated vasculitis.
openaire   +3 more sources

Tattoo Inflammation With Uveitis: From Recognition to Definition

Clinical &Experimental Ophthalmology, EarlyView.
ABSTRACT Tattoo inflammation with uveitis (TIU) is increasingly recognised but growing case numbers have revealed substantial heterogeneity. Patients currently classified as TIU appear to include those with overt or evolving systemic sarcoidosis as well as those with isolated, pigment‐associated ocular inflammation.
Anthea Anantharajah, Nicolas Kluger, Anthony J. H. Hall, Michelle Sharp, Jennifer E. Thorne, Lyndell L. Lim   +5 more
wiley   +1 more source

Genetically distinct subsets within ANCA-associated vasculitis

, 2012
BACKGROUND: Antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis is a severe condition encompassing two major syndromes: granulomatosis with polyangiitis (formerly known as Wegener's granulomatosis) and microscopic polyangiitis.
Holle, Julia U,, Chaudhry, A.N., Holle, Julia U., Brenchley, Paul; id_orcid, Feighery, C., Rayner, Tim F, Baslund, Bo,, Clayton, David G., Sanders, Jan-Stephan F,, Sanders, Jan-Stephan F., Lyons, Paul A., Baslund, B., Lyons, Paul A,, Ohlsson, Sophie, Rees, Andrew J, Clayton, David G,, Martorana, D., Smith, K., Vaglio, A., Padmanabhan, Sandosh,, Jayne, David R W, Guillevin, L., Lyons, P.A., Zwerina, J., Hruskova, Zdenka,, Holle, J.U., Feighery, Conleth,, Rayner, Tim F,, Smith, Kenneth G C,, Tesar, Vladimir,, Lund University., Rayner, Tim F., Sanders, Jan-Stephan F, Little, Mark A,, Wieczorek, Stefan, Little, Mark A., Neumann, T., Little, Mark A, Holle, Julia U, Hrušková, Z., Tervaert, Jan Willem Cohen,, Martorana, Davide, Neumann, Thomas, Brenchley, Paul, Deloukas, Panos,, Rees, A.J., Deloukas, P., Gunnarsson, I., Baslund, Bo, Trivedi, S., Pusey, Charles D, Cohen Tervaert, Jan Willem, Salama, Alan D, Ohlsson, S., Gunnarsson, Iva,, Pusey, C.D., Sanders, J.F., Pusey, Charles D,, Gross, Wolfgang L, Stegeman, Coen A,, Stegeman, Coen A., Pusey, Charles D., Segelmark, Mårten, Jayne, David R. W., Lyons, Paul A, Wieczorek, S., Stegeman, Coen A, Neumann, Thomas,, Bruchfeld, Annette, Brenchley, Paul,, Rayner, T.F., Guillevin, Loic, Cohen Tervaert, J., Harper, L., Gross, Wolfgang L,, Gross, W.L., Vaglio, Augusto, Sanders, Jan-Stephan F.; id_orcid, Feighery, Conleth, Gross, Wolfgang L., Stegeman, Coen A.; id_orcid, Segelmark, Mrten, Martorana, Davide,, Segelmark, Mårten,, Salama, A.D., Brenchley, P., Chaudhry, Afzal N., Vaglio, Augusto,, Watts, R.A., Deloukas, Panos, Watts, Richard A,, Zwerina, Jochen, Watts, Richard A., Clayton, David G, Padmanabhan, S., Wilde, Benjamin, Bruchfeld, A., Bruchfeld, Annette,, Hrušková, Zdenka, Salama, Alan D,, Chaudhry, Afzal N,, Salama, Alan D., Guillevin, Loic,, Smith, Kenneth G. C., Padmanabhan, Sandosh, Trivedi, Sapna, Chaudhry, Afzal N, Wieczorek, Stefan,, Zwerina, Jochen,, Trivedi, Sapna,, Tervaert, Jan Willem Cohen, Segelmark, M., Smith, Kenneth G C, Savage, Caroline O, Wilde, Benjamin,, Savage, C.O., Jayne, David R W,, Wilde, B., Gunnarsson, Iva, Tesař, Vladimir, Rees, Andrew J., Jayne, D.R.W., Rees, Andrew J,, Savage, Caroline O., Watts, Richard A, Harper, Lorraine,, Savage, Caroline O,, Stegeman, C.A., Clayton, D.G., Tesař, V., Sanders, Jan Stephan F, Little, M.A., Ohlsson, Sophie,, Harper, Lorraine, Chaudhry, AN, Rayner, TF, Lyons, PA, Vaglio, A, Brenchley, P, Baslund, B, Trivedi, S, Jayne, DRW, Bruchfeld, A,, Watts, RA, Holle, JU   +144 more
core   +1 more source

Immune-Complex Allergic Vasculitis in Association with the Immune-Complex Allergic Vasculitis in Association with the Development of Transverse Myelitis: A Case Report [PDF]

, 1996
A severe vasculitis, probably therapy related, in a sixty-four-year-old man being treated for possible subacute bacterial endocarditis, was associated with the development of transverse myelitis.
Huehns, Tanya Y., Nikol, Sigrid, Pilz, Günter, Scheidt, Wolfgang von, Günter Pilz, Wolfgang von Scheidt, Sigrid Nikol, Tanya Y. Huehns   +7 more
core   +1 more source

Update on eosinophilic granulomatosis with polyangiitis

Allergology International, 2019
Eosinophilic granulomatosis with polyangiitis (EGPA) (formerly Churg-Strauss syndrome) is a rare form of anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitis characterized by eosinophil-rich granulomatous inflammation and small to medium-size ...
Shunsuke Furuta, Taro Iwamoto, Hiroshi Nakajima   +2 more
doaj   +1 more source

An Atypical Skin Presentation of Adult‐Onset Still's Disease With Histological Description: A Case Report

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Adult‐onset Still's disease (AOSD) is an auto inflammatory disorder with a variable clinical presentation, and without a pathognomonic diagnostic test, characterized by high spiking fever, arthralgia/arthritis, a suggestive skin rash, elevated white blood cell count 10 G/L (> 80% neutrophils), elevated ferritin, with glycosylated ferritin < 20%
M. Nordmann, T. Mazza, S. Menzinger, G. Kaya, S. Bogiatzi, S. Vandenberghe‐Dürr, M. Blanchard, J. Stirnemann   +7 more
wiley   +1 more source