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| ORIGINAL ARTICLE |
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| Year : 2013 | Volume
: 59
| Issue : 2 | Page : 98-101 |
Acquired von Willebrand syndrome: A rare disorder of heterogeneous etiology
P Kasatkar, K Ghosh, S Shetty
Department of Hemostasis, National Institute of Immunohaematology (ICMR), KEM Hospital, Parel, Mumbai, Maharashtra, India
Correspondence Address:
S Shetty
Department of Hemostasis, National Institute of Immunohaematology (ICMR), KEM Hospital, Parel, Mumbai, Maharashtra
India
 Source of Support: The authors gratefully acknowledge the partial financial
assistance received from Lady Tata contingency Grant in carrying out this
work, Conflict of Interest: None  | Check |
DOI: 10.4103/0022-3859.113816
Context: Acquired von Willebrand syndrome (AVWS) is a rare bleeding disorder that mimics the inherited form of von Willebrand disease (VWD) in terms of laboratory findings and clinical presentation. Aims: To study the etiology of acquired VWD. Settings and Design: The patients referred from various hospitals in and out of Mumbai were included in the study. Materials and Methods: Six patients with AVWS diagnosed at this center over the last 10 years were analyzed against 171 patients with inherited VWD. The differential diagnosis of AVWS was made based on reduced levels of von Willebrand antigen and von Willebrand ristocetin cofactor, decrease in ristocetin induced platelet aggregation, absence of correction in mixing studies with no prior history of bleeding problems and a negative family history for bleeding disorders. Results: In three patients, the disease was associated with systematic lupus erythematosus, out of which one was also associated with Kikuchi lymphadenitis and second with autoimmune hemolytic anemia. Fourth case was associated with hypothyroidism and fifth was a case of dermatitis and vitiligo. The last patient was a case of hemophilia A with Burkitts lymphoma, who developed autoantibodies to von Willebrand factor. Except two patients, all other patients responded to immune suppressive therapy with corticosteroids, while the patient with hypothyroidism responded to oral thyroxine. Conclusion: AVWS is a rare condition and may often be missed or diagnosed as inherited disease associated with heterogeneous disease conditions.
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