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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Main Authors: Scudiero Olga, Di Fiore Rosanna, Lucania Anna, De Renzo Amalia, Niglio Alferio, Di Micco Pierpaolo, Castaldo Giuseppe
Format: Article
Language:English
Published: BMC 2004-03-01
Series:Journal of Translational Medicine
Subjects:
FVL
Online Access:http://www.translational-medicine.com/content/2/1/7
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spelling 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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