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Rarity of IgH translocations in Waldenström macroglobulinemia.
Ackroyd, Sam; O'Connor, Sheila J M; Owen, Roger G.
Afiliación
  • Ackroyd S; HMDS Laboratory, The Leeds Teaching Hospitals NHS Trust, Leeds LSI 3EX, United Kingdom.
Cancer Genet Cytogenet ; 163(1): 77-80, 2005 Nov.
Article en En | MEDLINE | ID: mdl-16271961
ABSTRACT
Comparatively little is known of the cytogenetics of Waldenström macroglobulinemia (WM). This is primarily due to the low proliferation of the clonal B cells, which precludes conventional karyotyping in many cases. Translocations involving the immunoglobulin heavy chain (IGH) gene at 14q32 are characteristic of many B-cell lymphomas and myelomas. Initial reports suggested that the t(9;14) was characteristic of lymphoplasmacytic lymphoma (the underlying pathological diagnosis in WM), but subsequent studies have failed to confirm the uniqueness of the translocation. To clarify this, we examined 69 cases of WM with interphase fluorescence in situ hybridization and failed to demonstrate an IgH translocation in 67 (97%). We conclude that IGH translocations are not a feature of WM, and the implications of this finding are discussed.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Translocación Genética / Cromosomas Humanos Par 14 / Cadenas Pesadas de Inmunoglobulina / Macroglobulinemia de Waldenström Límite: Aged / Female / Humans / Male Idioma: En Revista: Cancer Genet Cytogenet Año: 2005 Tipo del documento: Article País de afiliación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Translocación Genética / Cromosomas Humanos Par 14 / Cadenas Pesadas de Inmunoglobulina / Macroglobulinemia de Waldenström Límite: Aged / Female / Humans / Male Idioma: En Revista: Cancer Genet Cytogenet Año: 2005 Tipo del documento: Article País de afiliación: Reino Unido