Thromb Haemost 1992; 67(03): 297-301
DOI: 10.1055/s-0038-1648435
Original Articles
Schattauer GmbH Stuttgart

Hematological Causes of Venous Thrombosis in Young People: High Incidence of Myeloproliferative Disorder as Underlying Disease in Patients with Splanchnic Venous Thrombosis

Luciana Teofili
Istituto di Semeiotica Medica, Università Cattolica del Sacro Cuore, Roma, Italy
,
Valerio De Stefano
Istituto di Semeiotica Medica, Università Cattolica del Sacro Cuore, Roma, Italy
,
Giuseppe Leone
Istituto di Semeiotica Medica, Università Cattolica del Sacro Cuore, Roma, Italy
,
Paola Micalizzi
Istituto di Semeiotica Medica, Università Cattolica del Sacro Cuore, Roma, Italy
,
Michela Stefania lovino
Istituto di Semeiotica Medica, Università Cattolica del Sacro Cuore, Roma, Italy
,
Generoso Alfano
Istituto di Semeiotica Medica, Università Cattolica del Sacro Cuore, Roma, Italy
,
Bruno Bizzi
Istituto di Semeiotica Medica, Università Cattolica del Sacro Cuore, Roma, Italy
› Author Affiliations
Further Information

Publication History

Received 13 May 1991

Accepted after revision 12 September 1991

Publication Date:
03 July 2018 (online)

Summary

Thrombotic events occur frequently in myeloproliferative disorders, namely polycythaemia vera and essential throm-bocythaemia. Standard diagnostic criteria are designed quite stringent, so that a number of patients could be underdiagnosed. Spontaneous erythroid colonies formation from bone marrow or peripheral blood in the absence of exogenous erythropoietin is considered a reliable index of myeloproliferative disorder even at early stages. Endogenous erythroid colonies (EECs) formation was assessed in 43 patients having recently suffered from venous thrombosis prior to 45 years and without a previous diagnosis of hematological disease favouring thrombosis. A screening for coagulative abnormalities associated with thrombophilia was also carried out: in 5 patients (11.6%) a plasmatic thrombogenic defect was found (quantitative deficiency of antithrombin III, 1 case, protein C, 2 cases, protein S, 1 case, and plasminogen, 1 case). In 10 patients (2 males and 8 females) (23.2%) EECs assay was positive, allowing diagnosis of myeloproliferative disease even though 7 of them did not fulfill standard diagnostic criteria. In the other 3 patients who met the criteria for diagnosis of overt myeloproliferative disease the thrombotic event was the inaugural manifestation. In all these EECs-positive patients thrombosis involved mesenteric and portal veins (n = 4), hepatic veins (n = 3), portal vein (n = 2), mesenteric vein (n = 1). One of them was simultaneously affected from congenital protein C deficiency. Thus latent or atypical forms of myeloproliferative disease as well as the overt stages were the most frequent recognized cause of splanchnic venous thrombosis, accounting for 55% of the cases of our series. On the contrary no EECs-positive subject was found among the 25 patients with other sites of thrombosis. It is concluded that a myeloproliferative disorder should be carefully considered in young patients with splanchnic venous thrombosis and a thorough investigation should include evaluation of EECs.

 
  • References

  • 1 Schafer AI. Bleeding and thrombosis in the myeloproliferative disorders. Blood 1984; 64: 1-12
  • 2 Anger B, Haugh U, Seidler R, Heimpel H. Polycythaemia vera. A clinical study on 141 patients. Blut 1989; 59: 493-500
  • 3 Cortelazzo S, Viero P, Finazzi G, D’Emilio A, Rodeghiero F, Barbui T. Incidence and risk factors for thrombotic complications in a historical cohort of 100 patients with essential thrombocythaemia. J Clin Oncol 1990; 8: 556-562
  • 4 Fenaux P, Simon M, Caulier MT, Lai JL, Goudemand J, Bauters F. Clinical course of essential thrombocythemia in 147 cases. Cancer 1990; 66: 549-556
  • 5 Eaves CJ, Eaves AC. Erythropoietin (Ep) dose-response curves for three classes of erythroid progenitors in normal human marrow and in patients with polycythaemia vera. Blood 1978; 52: 1196-1210
  • 6 Lacombe C, Casadevall N, Varet B. Polycythaemia vera: in vitro studies of circulating erythroid progenitors. Br J Haematol 1980; 44: 189-199
  • 7 Eaves C, Eaves CJ. Abnormalities in the erythroid progenitor compartment in patients with chronic myelogenous leukemia (CML). Exp Hematol 1979; 7 Suppl (05) 65-75
  • 8 Lutton JD, Levere RD. Endogenous erythroid colony formation by peripheral blood mononuclear cells from patients with myelofibrosis and polycythaemia vera. Acta Haematol 1979; 62: 94-99
  • 9 Eridani S, Batten E, Sawyer B. Erythroid colony formation in primary thrombocythaemia: evidence of hypersensitivity to erythropoietin. Br J Haematol 1983; 55: 157-161
  • 10 Reid C, Chanarin I, Lewis J. Formes frustes in myeloproliferative disorders. Identification by the growth of an endogenous erythroid clone in vitro in patients with arterial vascular disease. Lancet 1982; i: 14-16
  • 11 Lemoine F, Najman A, Baillou C, Stachowiak J, Boffa G, Aegerter P, Douay L, Laporte JP, Gorin NC, Duhamel G. A prospective study of the value of bone marrow progenitor cultures in polycythemia. Blood 1986; 68: 996-1002
  • 12 Casadevall N, Vainchenker W, Lacombe C, Vinci G, Chapman J, Breton-Gorius J, Varet B. Erythroid progenitors in polycythaemia vera: demonstration of their hypersensitivity to erythropoietin using serum-free cultures. Blood 1982; 59: 447-451
  • 13 Valla D, Casadevall N, Lacombe C, Varet B, Goldwasser E, Franco D, Maillard J-N, Parente EA, Leporrier M, Rueff B, Muller O, Benhamou J-P. Primary myeloproliferative disorder and hepatic vein thrombosis. A prospective study of erythroid colony formation in vitro in 20 patients with Budd-Chiari syndrome. Ann Intern Med 1985; 103: 329-334
  • 14 Valla D, Casadevall N, Huisse MG, Tulliez M, Grange JD, Muller O, Binda T, Varet B, Rueff B, Benhamou J-P. Etiology of portal vein thrombosis in adults. A prospective evaluation of primary myeloproliferative disorders. Gastroenterology 1988; 94: 1063-1069
  • 15 Pagliuca A, Mufti GJ, Janossa-Thaernia M, Eridani S, Westwood NB, Thumpston J, Sawyer B, Sturgess R, Williams R. In vitro colony culture and chromosomal studies in hepatic and portal vein thrombosis. Possible evidence of an occult myeloproliferative state. Quart J Med 1990; 281: 981-989
  • 16 Leone G, De Stefano V, Di Donfrancesco A, Ferrelli R, Traisci G, Bizzi B. Antithrombin III Pescara: a defective AT III variant with no alterations of plasma crossed immunoelectrophoresis but with an abnormal crossed immunoelectrofocusing pattern. Br J Haematol 1987; 65: 187-191
  • 17 De Stefano V, Leone G, Teofili L, Ferrelli R, Pollari G, Antonini V, Bizzi B. Transient ischemic attack in a patient with protein C congenital deficiency during treatment with stanazolol. Am J Haematol 1988; 29: 120-121
  • 18 De Stefano V, Leone G, Ferrelli R, Hassan HJ, Macioce G, Bizzi B. Factor X Roma: a congenital factor X variant defective at different degrees in the intrinsic and the extrinsic activation. Br J Haematol 1988; 69: 387-391
  • 19 De Stefano V, Leone G, Teofili L, Micalizzi P, Netri G, Bizzi B. Mesenteric vein thrombosis in protein S congenital deficiency. Thromb Res 1990; 57: 935-944
  • 20 Alving BM, Baldwin PE, Richards RL, Jackson BJ. The diluted phospholipid aPTT : a sensitive assay for verification of lupus anticoagulant. Thromb Haemostas 1985; 54: 709-712
  • 21 Exner T, Rickard KA, Kronenberg H. A sensitive test demonstrating lupus anticoagulant and its behavioural patterns. Br J Haematol 1978; 40: 143-151
  • 22 Schleider MA, Nachman RL, Jaffe EA, Coleman M. A clinical study of the lupus anticoagulant. Blood 1976; 48: 499-509
  • 23 Aye MT, Niho Y, Till JE, McCulloch EA. Studies of leukemic cell populations in culture. Blood 1974; 44: 205-219
  • 24 Wasserman LR. The management of polycythaemia vera. Br J Haematol 1971; 21: 371-376
  • 25 De Stefano V, Teofili L, Rocca B, Nicoletti G, Leone G, Bizzi B. Association of congenital protein C deficiency and latent myeloproliferative disease as cause of splanchnic venous thrombosis in a 34-year-old woman. Br J Haematol 1989; 73: 565-566
  • 26 Stoll DB, Peterson P, Exten R, Laszlo J, Pisciotta AV, Ellis JT, White P, Vaidya K, Bozdech M, Murphy S. Clinical presentation and natural history of patients with essential thrombocythaemia and the Philadelphia chromosome. Am J Hematol 1988; 27: 77-83
  • 27 Najean Y, Mugnier P, Dresch C, Rain J-D. Polycythaemia vera in young people: an analysis of 58 cases diagnosed before 40 years. Br J Haematol 1987; 67: 285-291
  • 28 Mannucci PM, Tripodi A. Laboratory screening of inherited thrombotic syndromes. Thromb Haemostas 1987; 57: 247-251
  • 29 Gladson CL, Scharrer I, Hach V, Beck KH, Griffin JH. The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis. Thromb Haemostas 1988; 59: 18-22
  • 30 Boughton BJ. Hepatic and portal vein thrombosis. Closely associated with chronic myeloproliferative disorders. Br Med J 1991; 302: 192-193