scholarly journals Acquired von Willebrand Syndrome associated to secondary IgM MGUS emerging after Autologous Stem Cell Transplantation for AL Amyloidosis

2017 ◽  
Vol 9 (1) ◽  
pp. e2017034 ◽  
Author(s):  
Victor H Jimenez-Zepeda ◽  
Hina Qamar ◽  
Adrienne Lee ◽  
Karen Valentine ◽  
Leslie Skeith

Acquired von Willebrand syndrome (AVWS) is a rare hemorrhagic disorder that occurs in patients with no prior personal or family history of bleeding. Here, we describe a case of AVWS occurring after autologous stem cell transplantation (ASCT). Interestingly, AVWS developed after bortezomib-based induction and conditioning regimens. Recent evidence suggests that the proximity of the bortezomib therapy to the collection of stem cells with consequent depletion of regulatory T cells after the conditioning regimen could explain some of the unusual autoimmune complications reported in patients receiving bortezomib prior to ASCT. In addition, this patient developed a secondary MGUS post-ASCT, which may have also contributed to the AVWS. To the best of our knowledge, this is the first case of post-ASCT AVWS reported. Prospective data is needed to better elucidate the mechanisms by which these unusual complications occur in patients receiving bortezomib prior to ASCT.

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 4078-4078
Author(s):  
Cynthia A. Kos ◽  
Jennifer E. Ward ◽  
Karim Malek ◽  
Vaishali Sanchorawala ◽  
Daniel G. Wright ◽  
...  

Abstract Easy bruising is a common clinical symptom in primary (AL) amyloidosis, and can occur through multiple mechanisms. Infiltration of amyloid fibrils into thin-walled capillaries leads to mechanical fragility predisposing to petechiae and purpura, with periorbital “raccoon-eye” purpura being pathognomonic of AL amyloidosis. Another mechanism predisposing to bleeding in AL amyloidosis is adsorption of coagulation factors to amyloid fibrils. In 1977, Furie et al. reported (New England Journal of Medicine) that elevation of the clotting times is most commonly due to deficiency of factor X, and other investigators have since reported deficiencies of factors II, V, IX, or XIII. We have demonstrated that remission of the underlying plasma cell dyscrasia after high dose melphalan chemotherapy and autologous stem cell transplantation can lead to remission of the acquired factor X deficiency (Choufani et al., Blood 2001). From 2000–2004, four amyloidosis patients presented to Boston University Medical Center with bleeding and a prolonged activated partial thromboplastin time (aPTT), but with no such factor deficiency. Instead, they were found to have abnormal von Willebrand ristocetin cofactor (vWF:RCo) and/or factor VIII (FVIII:C) activities, with normal vWF antigen (vWF:Ag), consistent with a functional defect in von Willebrand factor (vWF). None of the patients had a prior history or family history consistent with congenital von Willebrand’s disease, thus they were diagnosed with acquired von Willebrand syndrome (AvWS). AvWS has most often been reported in association with other lymphoproliferative or myeloproliferative disorders. The aPTT was prolonged in three out of the four cases. Loss of high molecular weight multimers (HMWM) was observed in two of the four cases. Two of the patients were treated with high-dose intravenous melphalan followed by autologous stem cell transplantation and achieved remission of their underlying plasma cell disease; in addition, the bleeding diathesis ceased and the coagulation parameters normalized, indicating reversal of the AvWS with effective treatment of AL amyloidosis.


2019 ◽  
Vol 98 (5) ◽  
pp. 1259-1266 ◽  
Author(s):  
Haiwen Huang ◽  
Lihong Zhang ◽  
Yibin Jiang ◽  
Shuo Liu ◽  
Zhengming Jin ◽  
...  

2015 ◽  
Vol 15 ◽  
pp. e173
Author(s):  
S.K. Toprak ◽  
P. Ataca ◽  
E. Atilla ◽  
S.C. Bozdag ◽  
M.K. Yuksel ◽  
...  

2018 ◽  
Vol 8 (11) ◽  
Author(s):  
Richa Manwani ◽  
Ute Hegenbart ◽  
Shameem Mahmood ◽  
Sajitha Sachchithanantham ◽  
Charalampia Kyriakou ◽  
...  

2014 ◽  
Vol 100 (6) ◽  
pp. 554-558 ◽  
Author(s):  
Toshiaki Hayashi ◽  
Hiroshi Ikeda ◽  
Tetsuyuki Igarashi ◽  
Yumiko Maruyama ◽  
Yuka Aoki ◽  
...  

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