Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Rajib K. Gupta"'
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background Coronavirus disease-2019 (COVID-19) is an ongoing pandemic which has affected over 12 million people across the globe. Manifestations in different organs systems are being reported regularly. Renal biopsy findings in hospitalized
Externí odkaz:
https://doaj.org/article/76f457cf543f40e7a4f748035365e426
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Crystalglobulin-associated nephropathy (CAN), a rare subtype of monoclonal gammopathy, usually associated with multiple myeloma and occasionally monoclonal gammopathy of uncertain significance (MGUS), is characterized by occluding
Externí odkaz:
https://doaj.org/article/c18a19375c8b41269caf9b898d2982ef
Publikováno v:
Journal of Community Hospital Internal Medicine Perspectives, Vol 6, Iss 6, Pp 1-3 (2016)
Medications, especially non-steroidal anti-inflammatory drugs and antimicrobials, have been most commonly associated with acute interstitial nephritis (AIN); antiepileptic drugs (AEDs) are rarely known to cause AIN. This is a case of a 27-year-old ma
Externí odkaz:
https://doaj.org/article/a7d2febdd9494912bb31523f3c4050ac
Autor:
Brigid K Ellis, Rajib K Gupta
Publikováno v:
Kidney International Reports
Publikováno v:
Arthritisrheumatology (Hoboken, N.J.). 72(1)
Renal crystal-storing histiocytosis involving glomeruli - A comprehensive clinicopathologic analysis
Publikováno v:
Annals of diagnostic pathology. 43
Crystal-storing histiocytosis (CSH) is a rare manifestation of monoclonal gammopathy in which histiocytes containing monoclonal proteins in their cytoplasm are found in various organs of the body including the kidney. Within the kidney, these monoclo
Autor:
Abhijit Chougule, Carlos Fernandez-del Castillo, Masayuki Akita, Yoh Zen, Vikram Deshpande, Azfar Neyaz, David G. Forcione, Rajib K Gupta, Cristina R. Ferrone
Publikováno v:
The American journal of surgical pathology. 43(7)
Autoimmune pancreatitis (AIP) encompasses a heterogenous disease group that includes IgG4-related type 1 AIP and non-IgG4-related type 2 AIP. Clinically and on imaging, type 2 AIP mimics type 1 AIP, other forms of chronic pancreatitis and pancreatic
Autor:
Vikram Deshpande, Rajib K Gupta
Publikováno v:
Diagnostic Histopathology. 22:211-218
Autoimmune pancreatitis (AIP), an inflammatory disease of the pancreas first described in Japan, is characterized by a tumefactive lesion in the pancreas, thus clinically resembling pancreatic cancer. Currently, it is classified into two variants –
Autor:
Vikram Deshpande, David S. Klimstra, Rajib K Gupta, Mikhail Lisovsky, Bill H. Xie, Kurt T. Patton, Eric J. Burks, Stephen W. Behrman
Publikováno v:
Human Pathology. 48:154-162
Follicular pancreatitis is a recently described variant of chronic pancreatitis characterized clinically by the formation of a discrete pancreatic mass and histologically by the presence of florid lymphoid aggregates with reactive germinal centers. O
Autor:
Shweta Shinagare, Rajib K Gupta, Carlos D. Fernandez, Arezou Khosroshahi, John H. Stone, Cristina R. Ferrone, Vikram Deshpande, Gregory Y. Lauwers
Publikováno v:
Pancreas. 42:506-510
To estimate the risk of malignancy in autoimmune pancreatitis (AIP).We examined resected pancreata to compare the prevalence of pancreatic intraepithelial neoplasia (PanIN) in 28 cases of AIP and 30 cases of chronic pancreatitis not otherwise specifi