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Revista Médica del Uruguay

versión On-line ISSN 1688-0390

Resumen

MORO, Isabel et al. Enfermedad de Von Willebrand adquirida en un linfoma linfoplasmocitario/Macroglobulinemia de Waldenström: reporte de caso. Rev. Méd. Urug. [online]. 2010, vol.26, n.4, pp.246-252. ISSN 1688-0390.

Summary Acquired Von Willebrand disease is an unusual situation arising within the context of self-immune diseases, lymphoproliferative and mieloproliferative disorders. The study presents the clinical case of a patient carrier of a lymphoplasmocitary lymphoma with Waldenström's disease which presented with a hemorrhagic syndrome and alterations of the blood crasis in the intrinsic way. Monoclonal gammopathies such as Waldenström's macroglobulinemia usually appear with varied IgM dosifications, being it 11 g/dl in the case described. Clinical symptoms may be very proteiform, affecting several systems, and in this case it presented complications resulting from tumor adsorption: acquired Von Willebrand disease. Chemotherapy with thalidomide, cyclophosphamide and dexamethasone was indicated for the base disease and there was favourable evolution, the hemorrhagic syndrome remitted and there was a tendency to crasis normalization, the same as globular and platelets values ongoing normalization after six series of treatment. Other therapeutic measures aiming to reverse coagulopathy, such as plasmapheresis, are short-acting, and they are not exempt from risks, and they are considered as options upon obvious acute hyperviscosity with a risk of life. Multidisciplinary patient assessment enabled the best diagnosis and therapeutic approach.

Palabras clave : VON WILLEBRAND DISEASES; WALDENSTROM MACROGLOBULINEMIA.

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