TY - JOUR
T1 - Abdominal vein thrombosis in essential thrombocythemia
T2 - Prevalence, clinical correlates, and prognostic implications
AU - Gangat, Naseema
AU - Wolanskyj, Alexandra P.
AU - Tefferi, Ayalew
PY - 2006/10/1
Y1 - 2006/10/1
N2 - Among 460 consecutive patients with essential thrombocythemia (ET) seen at our institution, 19 cases (4%) of abdominal vein thrombosis (AVT) were documented either at (n = 9) or after (n = 10) diagnosis. Women (P = 0.03) and the young (P = 0.002) were preferentially affected. Accordingly, clinical comparisons were performed among three groups of female patients: those with AVT (group A; n = 17), a control group without AVT but closely matched to group A in terms of age and year of diagnosis (group B; n = 34), and all female patients without AVT (group C; n = 288). As expected from the consequences of AVT-associated portal hypertension and anticoagulant therapy, patients in group A experienced significantly higher rates of hemorrhage, palpable splenomegaly, and anemia. Unexpectedly, however, compared with group B, group A displayed both a higher conversion rate into myelofibrosis/acute leukemia (P = 0.0008) and a shorter median survival (116 vs. 156 months; P = 0.0012). Multivariable analysis including all female patients with ET identified AVT, along with advanced age, leukocytosis, and tobacco use, as an independent risk factor for inferior survival. Groups A, B, and C did not differ in either JAK2V617F mutational frequency or incidence of non-abdominal thrombosis. We conclude that AVT in ET is a marker of aggressive disease biology.
AB - Among 460 consecutive patients with essential thrombocythemia (ET) seen at our institution, 19 cases (4%) of abdominal vein thrombosis (AVT) were documented either at (n = 9) or after (n = 10) diagnosis. Women (P = 0.03) and the young (P = 0.002) were preferentially affected. Accordingly, clinical comparisons were performed among three groups of female patients: those with AVT (group A; n = 17), a control group without AVT but closely matched to group A in terms of age and year of diagnosis (group B; n = 34), and all female patients without AVT (group C; n = 288). As expected from the consequences of AVT-associated portal hypertension and anticoagulant therapy, patients in group A experienced significantly higher rates of hemorrhage, palpable splenomegaly, and anemia. Unexpectedly, however, compared with group B, group A displayed both a higher conversion rate into myelofibrosis/acute leukemia (P = 0.0008) and a shorter median survival (116 vs. 156 months; P = 0.0012). Multivariable analysis including all female patients with ET identified AVT, along with advanced age, leukocytosis, and tobacco use, as an independent risk factor for inferior survival. Groups A, B, and C did not differ in either JAK2V617F mutational frequency or incidence of non-abdominal thrombosis. We conclude that AVT in ET is a marker of aggressive disease biology.
KW - Budd-Chiari syndrome
KW - Hepatic vein thrombosis
KW - Leukemic transformation
KW - Portal vein thrombosis
KW - Prognosis
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=33748355823&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33748355823&partnerID=8YFLogxK
U2 - 10.1111/j.1600-0609.2006.00715.x
DO - 10.1111/j.1600-0609.2006.00715.x
M3 - Article
C2 - 16856928
AN - SCOPUS:33748355823
SN - 0902-4441
VL - 77
SP - 327
EP - 333
JO - European Journal of Haematology
JF - European Journal of Haematology
IS - 4
ER -