1.
Leuk Lymphoma
; 63(8): 1771-1773, 2022 08.
Article
in English
| MEDLINE
| ID: mdl-35703117
2.
Lancet Oncol
; 23(6): 699-701, 2022 06.
Article
in English
| MEDLINE
| ID: mdl-35654051
3.
Am J Hematol
; 97(5): E168-E171, 2022 05.
Article
in English
| MEDLINE
| ID: mdl-35108412
4.
Case Rep Hematol
; 2013: 837906, 2013.
Article
in English
| MEDLINE
| ID: mdl-23431487
ABSTRACT
Type 2N Von Willebrand's disease (2N VWD) is a rare, recessively inherited bleeding disorder, comprising 1-2% of all VWD patients, usually manifesting as a mild bleeding diathesis. Treatment includes desmopressin (DDAVP) or intermediate purity plasma-derived FVIII concentrates containing residual VWF. We present a case of a 75-year-old gentleman, incidentally diagnosed with type 2N VWD in 2002 on routine blood testing before surgery with an ISTH bleeding score of 1-2, who was treated with recombinant FVIII preoperatively.