Thrombo-embolic disease after splenectomy for hereditary stomatocytosis

British Journal of Haematology

Volumn 93, Issue 2, 1996, Pages 303-310

  Stewart, Gordon W ^a   Amess, John A L ^b   Eber, Stefan W ^c   Kingswood, Christopher ^d   Lane, Peter A ^e   Smith, Brian D ^f   Mentzer, William C ^g  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^b ST BARTHOLOMEW S HOSPITAL   (United Kingdom)

^c UNIVERSITY MEDICAL CENTER GÖTTINGEN   (Germany)

^d ROYAL SUSSEX COUNTY HOSPITAL   (United Kingdom)

^e UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

^f Highland Hospital Rochester   (United States)

^g UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

haemolysis; iron overload; splenectomy; stomatocytosis; thrombosis

Indexed keywords

ANTICOAGULANT AGENT; HEPARIN; WARFARIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; FEMALE; GENETIC DISORDER; HEMOLYTIC ANEMIA; HUMAN; IRON OVERLOAD; MALE; PRIORITY JOURNAL; SPLENECTOMY; THROMBOSIS;

EID: 0029872495     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1996.4881033.x     Document Type: Article

References (41)

1. Barosi, G., Ambrosetti, A., Buratti, A., Finelli, C., Liberato, N., Quaglini, S., Ricetti, M., Visani, G., Tura, S. & Ascari, E. (1993) Splenectomy for patients with myeoloid metaplasia: pretreatment variables and outcome prediction. Leukemia, 7, 200-206.
2. Bertina, R.M., Koeleman, B.P., Koster, T., Rosendaal, F.R., de Dirven, R.J., van der Velden, P.A. & Reitsma, P.H. (1994) Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature, 369, 64-6.
3. Bienzle, U., Niethammer, D., Kleegerg, U., Ungelfehr, K., Kohne, E. & Kleihauer, E. (1975) Congenital stomatocytosis and chronic haemolytic anaemia. Scandinavian Journal of Haematology, 15, 339-346.
4. Bridges, K. & Seligman, P. (1995) Disorders of iron metabolism. Blood: Principles and Practice of Hematology (ed. by R. Handin, S. Lux and T. Stossel), pp. 1433-1472. Lippincott, Philadelphia.
5. Clark, M.R., Shohet, S.B. & Gottfried, E.L. (1993) Hereditary hemolytic disease with increased red blood cell phosphatidylcholine and dehydration: one, two, or many disorders? American Journal of Hematology, 42, 25-30.
6. Dacie, J.V. (1985) The Haemolytic Anaemias, Volume 1. The Hereditary Haemolytic Anaemias, Part 1, 2nd edn, pp. 259-281. Churchill, Edinburgh.
7. Eber, S.W., Lande, W.M., Iarocci, T.A., Mentzer, W.M., Hohn, P., Wiley, J.S. & Schroter, W. (1989) Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency. British Journal of Haematology, 72, 452-455.
8. Eldor, A., Lellouche, F., Goldfarb, A., Rachmilewitz, E.A. & Maclouf, J. (1991) In vivo platelet activation in beta-thalassemia major reflected by increased platelet-thromboxane urinary metabolites. Blood, 77, 1749-53.
9. Fargion, S., Cappellini, M.D., Piperno, A., Panajotopoulos, N., Ronchi, G. & Fiorelli, G. (1986) Association of hereditary spherocytosis and idiopathic hemochromatosis: a synergistic effect in determining iron overload. American Journal of Clinical Pathology, 86, 645-649.
10. Forget, B. & Pearson, H. (1995) Hemoglobin synthesis and the thalassemias. Blood: Principles and Practice of Hematology (ed. by R. Handin, S. Lux and T. Stossel), pp. 1525-1590. Lippincott, Philadelphia.
11. Hirsh, J. & Dacie, J.V. (1966a) Persistent post-splenectomy thrombocytosis and thrombo-embolism: a consequence of continuing anaemia. British Journal of Haematology, 12, 44-53.
12. Hirsh, J., McBride, S.A. & Dacie, J.V. (1966b) Thrombo-embolism and increased platelet adhesiveness in post-splenectomy thrombocytosis. Australian Annals of Medicine, 15, 122-128.
13. Jaffe, E.R. & Gottfried, E.L. (1968) Hereditary nonspherocytic hemolytic disease associated with an altered phospholipid composition of the erythrocytes. Journal of Clinical Investigation, 47, 1375-1388.
14. Lande, W.M. & Mentzer, W.C. (1985) Haemolytic anemia associated with increased cation permeability. Clinical Hematology, 14, 89-103.
15. Lande, W.M., Thiemann, P.W. & Mentzer, W.M. (1982) Missing band 7 membrane protein in two patients with high Na. low K erythrocytes. Journal of Clinical Investigation, 70, 1273-1280.
16. Lane, P.A., Kuypers, F.A., Clark, M.R., Andrews, D.A., Wagner, G.M., Butikofer, P., Shapiro, A.D., Chiu, D.T.Y., Lubin, B.H. & Mentzer, W.C. (1990) Excess of red cell membrane proteins in hereditary high-phosphatidylcholine hemolytic anemia. American Journal of Hematology, 34, 186-192.
17. Lind, S. (1995) The hemostatic system. Blood: Principles and Practice of Hematology (ed. by R. Handin, S. Lux and T. Stossel), pp. 949-972. Lippincott, Philadelphia.
18. Lock, S.P., Sephton Smith, R. & Hardisty, R.M. (1961) Stomatocytosis: a hereditary haemolytic anomaly associated with haemolytic anaemia. British Journal of Haematology, 7, 303-314.
19. Mabin, D.C. & Chowdhury, V. (1990) Aplastic crisis caused by human parvovirus in two patients with hereditary stomatocytosis. British Journal of Haematology, 76, 153-154.
20. Meadow, S.R. (1967) Stomatocytosis. Proceedings of the Royal Society of Medicine, 60, 13-15.
21. Mentzer, W.C., Smith, W.B., Goldstone, J. & Shohet, S.B. (1975) Hereditary stomatocytosis: membrane and metabolism studies. Blood, 46, 659-669.
22. Miller, D.R., Rickles, F.R., Lichtman, M.A., La Celle, P.L., Bates, J. & Weed, R.I. (1971) A new variant of hereditary hemolytic anemia with stomatocytosis and erythrocyte cation abnormality. Blood, 38, 184-203.
23. -1) cotransport in a case of congenital stomatocytosis. British Journal of Haematology, 71, 141-146.
24. Otsuka, A., Sugihara, T. & Yawata, Y. (1990) No beneficial effect of splenectomy in hereditary high red cell membrane phosphatidylcholine hemolytic anemia: clinical and membrane studies of 20 patients. American Journal of Hematology, 34, 8-14.
25. Porter, J., Young, L., Mackie, L. Marshall, L. & Machin, S. (1993) Sickle cell disorders and chronic intravascular haemolysis are associated with low plasma heparin cofactor II. British Journal of Haematology, 83, 459-465.
26. Rattner, D., Ellman, L. & Warshaw, A. (1993) Portal vein thrombosis after elective splenectomy: an underappreciated. potentially lethal syndrome. Archives of Surgery, 128, 565-570.
27. Schroter, W., Ungefehr, K. & Tillman, W. (1981) Role of the spleen in congenital stomatocytosis associated with high sodium low potassium erythrocytes. Klinische Wochenschrift, 59, 173-179.
28. Seligsohn, U. (1995) Disseminated intravascular coagulation. Blood: Principles and Practice of Hematology (ed. by R. Handin, S. Lux and T. Stossel), pp. 1289-1317. Lippincott, Philadelphia.
29. Shirahata, A., Funahara, Y., Opartkiattikul, N., Fucharoen, S., Laosombat, V. & Yamada, K. (1992) Protein C and protein S deficiency in thalassaemic patients. Southeast Asian Journal of Tropical Medicine and Public Health. 23, 65-73.
30. Shurin, S. (1995) Disorders of the spleen. Blood: Principles and Practice of Hematoloyy (ed. by R. Handin, S. Lux and T. Stossel), pp. 1359-1380. Lippincott, Philadelphia.
31. Sonakul, D. & Fucharoen, S. (1992) Pulmonary thromboembolism in thalassaemic patients. South-East Asian Journal of Tropical Medicine and Public Health, 23, (Suppl. 2), 25-28.
32. Stewart, G.W. (1993) The membrane defect in hereditary stomatocytosis. Red Cell Membrane Antigens (ed. by M. J. A. Tanner and D. J. Anstee), pp. 371-400. Bailliere-Tyndall, London.
33. Stewart, G.W. & Argent, A.C. (1992) The integral band 7 membrane protein of the human erythrocyte membrane. Biochemical Society Transactions, 20, 785-790.
34. Stewart, G.W. & Ellory, J.C. (1985) A family with mild xerocytosis showing increased cation permeability at low temperatures. Clinical Science, 69, 309-319.
35. Stewart, G.W., Hepworth-Jones, B.E., Keen, J.N., Dash, B.C.J., Argent, A.C. & Casimir, C.M. (1992) Isolation of cDNA coding for a ubiquitous membrane protein deficien: in high Na, low K stomatocytic erythrocytes. Blood, 79, 1593-1601.
36. Stuart, M.J. (1979) Platelet dysfunction in homozygous beta-thalassemia. Pediatric Research, 13, 1345-1349.
37. Tso, S., Chan, T. & Todd, D. (1982) Venous thrombosis in haemoglobin H disease after splenectomy. Australian and New Zealand Journal of Medicine, 12, 635-638.
38. Wang, D., Turetsky, T., Perrine, S., Johnson R. & Mentzer, W. (1992) Further studies on RBC membrane protein 7.2b deficiency in hereditary stomatocytosis. Blood, 80, (Suppl. 1), 275a.
39. Wiley, J.S. (1984) Inherited red cell dehydration: a hemolytic syndrome in search of a name. Pathology, 16, 115-116.
40. Wiley, J.S., Ellory, J.C., Shuman, M.A., Shaller, C.C. & Cooper, R.A. (1975) Characteristics of the membrane defect in the hereditary stomatocytosis syndrome. Blood, 46, 337-356.
41. Zanella, A., Berzuini, A., Colombo, M., Guffanti, A., Lecchi, L., Poli, F., Cappellini, D. & Barosi, G. (1993) Iron status in red cell pyruvate kinase deficiency: study of Italian cases. British Journal of Haematology, 83, 485-490.