Publication Cover
Amyloid
The Journal of Protein Folding Disorders
Volume 18, 2011 - Issue 4
118
Views
5
CrossRef citations to date
0
Altmetric
Case Reports

Renal transplantation in AA amyloidosis associated with Whipple’s disease

, , , , , & show all
Pages 240-244 | Received 26 Jun 2011, Accepted 11 Aug 2011, Published online: 13 Oct 2011

References

  • Whipple GH. A hitherto undescribed disease characterized anatomically by deposits of fat and fatty acids in the intestinal and mesenteric lymphatic tissues. Bull John Hopkins Hosp 1907; 18:382–391.
  • Raoult D, Birg ML, La Scola B, Fournier PE, Enea M, Lepidi H, Roux V, et al. Cultivation of the bacillus of Whipple’s disease. N Engl J Med 2000;342:620–625.
  • Fenollar F, Puéchal X, Raoult D. Whipple’s disease. N Engl J Med 2007;356:55–66.
  • Famularo G, Minisola G, De Simone C. A patient with cerebral Whipple’s disease and a stroke-like syndrome. Scand J Gastroenterol 2005;40:607–609.
  • Dearment MC, Woodward TA, Menke DM, Brazis PW, Bancroft LW, Persellin ST. Whipple’s disease with destructive arthritis, abdominal lymphadenopathy, and central nervous system involvement. J Rheumatol 2003;30:1347–1350.
  • James TN, Bulkley BH. Abnormalities of the coronary arteries in Whipple’s disease. Am Heart J 1983;105:481–491.
  • Biernat S, Kozlowski W. [Case of Whipple’s disease complicated by amyloidosis]. Pol Tyg Lek 1975;30:113–114.
  • Cruz I, Oliveira AP, Lopes JM, Ricardo JL, de Freitas J. Whipple’s disease and renal amyloidosis. Am J Gastroenterol 1993;88:1954–1956.
  • Leidig P, Stolte M, Krakamp B, Störkel S. [Whipple’s disease – a rare cause of secondary amyloidosis]. Z Gastroenterol 1994;32:109–112.
  • Kramer LC, Manschot TAJM, Barendregt JNM, Smit JM. Whipple’s disease: often a late diagnosis and a rare cause of nephropathy. Nephrol Dial Transplant Plus 2009; 2: 55–58.
  • Niemczyk S, Filipowicz E, Wozniacki L, Grochowski J, Zaleski L, Grzejszczak A, Ptasinska AP, et al. Renal amyloidosis in Whipple disease: a case report. Cases J 2009;2:8444.
  • Stoll T, Keusch G, Jost R, Burger H, Oelz O. IgA nephropathy and hypercalcemia in Whipple’s disease. Nephron 1993;63:222–225.
  • Evrenkaya R, Basak M, Cosansel S, Cankir Z, Güney Y, Kurtoglu S, Yildirim S, et al. A case of Whipple’s disease associated with acute Ebstein Barr virus hepatitis and Berger’s disease. Nephrol Dial Transplant 1999;14:241–242.
  • Schlumpf A, Marbet UA, Stöcklin E, Wegmann W, Lämmle B, Mujagic M, Jösch W, et al. Chronic interstitial nephritis in Whipple’s disease. Klin Wochenschr 1983;61:25–33.
  • Marie I, Lecomte F, Levesque H. Granulomatous nephritis as the first manifestation of Whipple disease. Ann Intern Med 2000;132:94–95.
  • Sander S. Whipple’s disease associated with amyloidosis. Acta Pathol Microbiol Scand 1964;61:530–536.
  • Fleming JL, Wiesner RH, Shorter RG. Whipple’s disease: clinical, biochemical, and histopathologic features and assessment of treatment in 29 patients. Mayo Clin Proc 1988;63:539–551.
  • Kleine G. Weight loss, renal insufficiency, aortal stenosis and arthralgies. Der Internist 2005; 46: 575–579.
  • Pasternack A, Ahonen J, Kuhlbäck B. Renal transplantation in 45 patients with amyloidosis. Transplantation 1986;42:598–601.
  • Haq A, Hussain S, Meskat B, Mohan P, Conlon P, Hickey DP. Complications of renal transplantation in patients with amyloidosis. Transplant Proc 2007;39:120–124.
  • Sherif AM, Refaie AF, Sobh MA, Mohamed NA, Sheashaa HA, Ghoneim MA. Long-term outcome of live donor kidney transplantation for renal amyloidosis. Am J Kidney Dis 2003;42:370–375.
  • Sobh M, Refaie A, Moustafa F, Shokeir A, Hassan N, Sally S, Ghoneim M. Study of live donor kidney transplantation outcome in recipients with renal amyloidosis. Nephrol Dial Transplant 1994;9:704–708.
  • Razonable RR, Pulido JS, Deziel PJ, Dev S, Salomão DR, Walker RC. Chorioretinitis and vitreitis due to Tropheryma whipplei after transplantation: case report and review. Transpl Infect Dis 2008;10:413–418.
  • Mahnel R, Kalt A, Ring S, Stallmach A, Strober W, Marth T. Immunosuppressive therapy in Whipple’s disease patients is associated with the appearance of gastrointestinal manifestations. Am J Gastroenterol 2005;100:1167–1173.
  • Marth T, Roux M, von Herbay A, Meuer SC, Feurle GE. Persistent reduction of complement receptor 3 alpha-chain expressing mononuclear blood cells and transient inhibitory serum factors in Whipple’s disease. Clin Immunol Immunopathol 1994;72:217–226.
  • Bjerknes R, Odegaard S, Bjerkvig R, Børkje B, Laerum OD. Whipple’s disease. Demonstration of a persisting monocyte and macrophage dysfunction. Scand J Gastroenterol 1988;23:611–619.
  • Marth T, Kleen N, Stallmach A, Ring S, Aziz S, Schmidt C, Strober W, et al. Dysregulated peripheral and mucosal Th1/Th2 response in Whipple’s disease. Gastroenterology 2002;123:1468–1477.
  • Migita K, Yamasaki S, Shibatomi K, Ida H, Kita M, Kawakami A, Eguchi K. Impaired degradation of serum amyloid A (SAA) protein by cytokine-stimulated monocytes. Clin Exp Immunol 2001;123:408–411.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.