Congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary report
<p>Abstract</p> <p>Background</p> <p>Congenital thrombotic risk factors, oncological diseases and its therapies have been related to an increased occurrence of upper extremities deep venous thrombosis (UEDVT).</p> <p>Patients and methods</p> <p>W...
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doaj-92c6d54f14c74f5886eb7d47f35eadcc2020-11-24T21:09:45ZengBMCJournal of Translational Medicine1479-58762004-03-0121710.1186/1479-5876-2-7Congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary reportScudiero OlgaDi Fiore RosannaLucania AnnaDe Renzo AmaliaNiglio AlferioDi Micco PierpaoloCastaldo Giuseppe<p>Abstract</p> <p>Background</p> <p>Congenital thrombotic risk factors, oncological diseases and its therapies have been related to an increased occurrence of upper extremities deep venous thrombosis (UEDVT).</p> <p>Patients and methods</p> <p>We studied seven patients bearing lymphoma (one Hodgkin's and six non-Hodgkin's) who developed UEDVT, one at diagnosis and six during chemotherapy (two of these six cases had implantation of a central venous catheter and four received Growth Colony Stimulating Factors in addition to chemotherapy). Patients were screened for: factor V G1691A (Leiden), prothrombin G20210A, methylene tetrahydrofolate reductase (MTHFR) C677T mutations and antithrombin III, proteins C and S plasma activity.</p> <p>Results</p> <p>All patients were wild-type homozygotes for G20210A. One was heterozygote for factor V G1691A, the other 6 were wild-type homozygotes. Three of the 7 patients were homozygotes and 2 heterozygotes for the MTHFR mutation; the remaining 2 were wild-type homozygotes. Clotting inhibitor levels were normal in all patients.</p> <p>Conclusions</p> <p>UEDVT in patients bearing haematological malignancies can occur irrespective of congenital thrombophilic alterations. However, in a subgroup of patients UEDVT could also depend on congenital thrombophilic alterations. A screening for inherited thrombophilia can identify high risk patients that could be specifically treated to prevent thrombotic complications.</p> http://www.translational-medicine.com/content/2/1/7inherited thrombophiliaacquired thrombophiliamalignancymolecular markers UEDVTLEDVTnon-Hodgkin lymphomaHodgkin's diseaseMTHFR<sub>C677T</sub>FVLPTHRA<sub>20210</sub>Gcentral venous cathetersG-CSF |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Scudiero Olga Di Fiore Rosanna Lucania Anna De Renzo Amalia Niglio Alferio Di Micco Pierpaolo Castaldo Giuseppe |
spellingShingle |
Scudiero Olga Di Fiore Rosanna Lucania Anna De Renzo Amalia Niglio Alferio Di Micco Pierpaolo Castaldo Giuseppe Congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary report Journal of Translational Medicine inherited thrombophilia acquired thrombophilia malignancy molecular markers UEDVT LEDVT non-Hodgkin lymphoma Hodgkin's disease MTHFR<sub>C677T</sub> FVL PTHRA<sub>20210</sub>G central venous catheters G-CSF |
author_facet |
Scudiero Olga Di Fiore Rosanna Lucania Anna De Renzo Amalia Niglio Alferio Di Micco Pierpaolo Castaldo Giuseppe |
author_sort |
Scudiero Olga |
title |
Congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary report |
title_short |
Congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary report |
title_full |
Congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary report |
title_fullStr |
Congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary report |
title_full_unstemmed |
Congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary report |
title_sort |
congenital and acquired thrombotic risk factors in lymphoma patients bearing upper extremities deep venous thrombosis: a preliminary report |
publisher |
BMC |
series |
Journal of Translational Medicine |
issn |
1479-5876 |
publishDate |
2004-03-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Congenital thrombotic risk factors, oncological diseases and its therapies have been related to an increased occurrence of upper extremities deep venous thrombosis (UEDVT).</p> <p>Patients and methods</p> <p>We studied seven patients bearing lymphoma (one Hodgkin's and six non-Hodgkin's) who developed UEDVT, one at diagnosis and six during chemotherapy (two of these six cases had implantation of a central venous catheter and four received Growth Colony Stimulating Factors in addition to chemotherapy). Patients were screened for: factor V G1691A (Leiden), prothrombin G20210A, methylene tetrahydrofolate reductase (MTHFR) C677T mutations and antithrombin III, proteins C and S plasma activity.</p> <p>Results</p> <p>All patients were wild-type homozygotes for G20210A. One was heterozygote for factor V G1691A, the other 6 were wild-type homozygotes. Three of the 7 patients were homozygotes and 2 heterozygotes for the MTHFR mutation; the remaining 2 were wild-type homozygotes. Clotting inhibitor levels were normal in all patients.</p> <p>Conclusions</p> <p>UEDVT in patients bearing haematological malignancies can occur irrespective of congenital thrombophilic alterations. However, in a subgroup of patients UEDVT could also depend on congenital thrombophilic alterations. A screening for inherited thrombophilia can identify high risk patients that could be specifically treated to prevent thrombotic complications.</p> |
topic |
inherited thrombophilia acquired thrombophilia malignancy molecular markers UEDVT LEDVT non-Hodgkin lymphoma Hodgkin's disease MTHFR<sub>C677T</sub> FVL PTHRA<sub>20210</sub>G central venous catheters G-CSF |
url |
http://www.translational-medicine.com/content/2/1/7 |
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