Natural history of paroxysmal nocturnal haemoglobinuria in adolescents, adults and children: The Mexican experience;Historia natural de la hemoglobinuria paroxística nocturna en adolescentes, adultos y en la edad pediátrica: La experiencia mexicana

Sangre

Volumn 42, Issue 3, 1997, Pages 171-177

  Góngora Biachi, Renán A ^a,d   González Martínez, Pedro ^a   Sosa Muñoz, Jorge ^b   Castrosansores, Carlos ^a   Delgado Lamas, José Luis ^b   Vázquez Villegas, Vicente ^b   Rico Balzadua, Guadalupe ^b   Herrera Sánchez, Pascual ^b   Selva Pallares, Julio ^c   González Llaven, José ^d  

^a UNIVERSIDAD AUTÓNOMA DE YUCATÁN   (Mexico)

^b INSTITUTO MEXICANO DEL SEGURO SOCIAL   (Mexico)

^c U de Hematol y Transfusión   (Mexico)

^d Invest Cie en Hematol AC   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE DISEASE; ADOLESCENT; ADULT; ANEMIA; BLEEDING; BONE MARROW; CHILD; CLASSIFICATION; CLINICAL TRIAL; DIFFERENTIAL DIAGNOSIS; FEMALE; HUMAN; IDIOPATHIC THROMBOCYTOPENIC PURPURA; INCIDENCE; INFANT; LIFE TABLE; MALE; MEXICO; MULTICENTER STUDY; MYELOID LEUKEMIA; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PATHOLOGY; PRESCHOOL CHILD; PROGNOSIS; REFRACTORY ANEMIA WITH EXCESS BLASTS; RETROSPECTIVE STUDY; REVIEW; SURVIVAL; THROMBOSIS;

ACUTE DISEASE; ADOLESCENT; ADULT; ANEMIA; ANEMIA, REFRACTORY, WITH EXCESS OF BLASTS; BONE MARROW; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FEMALE; HEMOGLOBINURIA, PAROXYSMAL; HEMORRHAGE; HUMANS; INCIDENCE; INFANT; LEUKEMIA, MYELOID; LIFE TABLES; MALE; MEXICO; PROGNOSIS; PURPURA, THROMBOCYTOPENIC, IDIOPATHIC; RETROSPECTIVE STUDIES; SURVIVAL ANALYSIS; THROMBOSIS;

EID: 0031155597     PISSN: 00364355     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (27)

1. Rotoli B, Luzzatto L. Paroxysmal nocturnal hemoglobinuria. Semin Hematol 1989; 26: 201-207.
2. Pangburn NK, Scheiber RD, Millar-Eberhard HJ. Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria. Proc Natl Acad Sci 1983; 80: 5430-5434.
3. Moore JG, Humpies RK, Frank MM, Young N Characterization of the haemopoietic defect in paroxysmal nocturnal haemoglobinuria. Exp Haematol 1986; 14: 222-229.
4. Norris J, Hall S, Ware RE, Kamitani T, Chang HM, Yeh E, et al. Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal noctural hemoglobinuria: partial or complete defect in an early step. Blood 1994; 83: 816-821.
5. Yomtovian R, Prince GM, Medof ME. The molecular basis for paroxysmal nocturnal hemoglobinuria. Transfusion 1993; 33: 852-873.
6. Takeda J, Miyata T, Kawagoe K, Iida Y, Enoo Y, Fujita T, et al. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal haemoglobinuria Cell 1983; 73: 703-711.
7. Ware RE, Rosse WF, Howard TA. Mutations within the PIG-A gene in patients with paroxysmal nocturnal hemoglobinuria. Blood 1994; 83: 2418-2422.
8. Bessler M, Mason P, Hillmen P, Luzzatto L. Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria. Lancet 1994; 343: 951-953.
9. Gaither JC. Paroxysmal nocturnal hemoglobinuria. A successful imposter. N Engl J Med 1961; 265: 421-426.
10. Góngora-Biachi RA, González-Martínez P Hemoglobinuria paroxística nocturna: conceptos y controversias actuates. Rev Clin Esp 1987; 180: 438-43.
11. Góngora-Biachi RA, González-Martínez P, Aguilar-Ortega M, Achach-Asaf J, Lara-Perera D. Hemoglobinuria paroxística nocturna en edad pediátrica: observaciones en siete casos. Bol Med Hosp Infant Mex 1987; 44: 222-227.
12. Ware RE, Hall SE, Rosse WF. Paroxysmal nocturnal hemoglobinuria with onset in childhood and adolescence. N Engl J Med 1991; 325: 991-996.
13. Brubaker LH, Schaberg DR, Jefferson DH, Mengel C. A potencial screening test for PHN. N Engl J Med 1975; 268: 1059.
14. Beutler E. Sucrose hemolysis and acidified-serum lysis test. En: Beutler E, Lichtman MA, Coller BS, Kipps TJ ed. Hematology. Fith Edition. New York: Mc Grawhill, 1995; L48-L49.
15. Dacie JV. Paroxysmal nocturnal haemoglobinuria. Proc R Soc Med 1963; 56: 87-96.
16. Forman K, Sokol RJ, Hewitt S, Stamps BK. Paroxysmal nocturnal haemoglobinuria. A clinicopathological study of 26 cases. Acta Haematol 1984; 71: 217-226
17. Kruatrachue M, Wasi P, Nakorn N. Paroxysmal nocturnal haemoglobinuria in Thailand with special reference to an association with aplastic anaemia. Br J Haematol 1978; 39: 267-276
18. Góngora-Biachi RA, Sosa-Muñoz J, Duarte-Zapata L, Pinto-Escalante D, González-Martínez P, Achach-Asaf J. Hemoglobinuria paroxística nocturna: Análisis de 36 casos. Sangre 1987; 32. 27-37.
19. Tianying L, Linsheng Q. Clinical study of 78 cases of aplastic anemiaparoxysmal nocturnal hemoglobinuria syndrome. Blood 1994; 84 (Suppl. 1): 564a.
20. Fujioka S, Asai T Prognostic fetaures of paroxysmal nocturnal hemoglobinuria in Japan. Acta Haematol Jpn 1989; 52: 1386-1394.
21. Hertenstein B, Wagner B, Bunjes D, Duncker C, Raghavachar A, Arnold R. Emergence of CD52, phosphatidylinositolglycan-anchordeficient T lymphocytes after in vivo application of Carnpath-1H for refractory B-cell non Hodgkin lymphoma. Blood 1995; 86: 1487-1492.
22. Tudela M, Jarque I, Pérez-Sirvent ML, Palau J, Sanz MA. Perfil clínico y evolutive de la hemoglobinuria paroxística nocturna. Sangre 1993; 38: 301-307.
23. Hillmen P, Lewis SM, Bessler M Luzzatto L, Dacie JV. Natural history of paroxysmal nocturnal hemoglobinuria. N Engl J Med 1995; 333: 1253-1258.
24. Yamada N, Miyata T, Maeda K, Kitani T, Takeda J. Somatics mutations of the PIG-A gene found in Japanese patients with paroxysmal nocturnal hemoglobinuria. Blood 1995; 85: 885-892.
25. Pramoonjago P, Wanachiwanawin W, Chinprasertsak S, Pattanapanayasat K, Takeda J, Kinoshita T. Somatic mutations of PIG-A in Thai patients with paroxysmal nocturnal hemoglobinuria. Blood 1995; 86: 1736-1739.
26. Stafford HA, Nagarajan S, Weinberg JB, MedofME. PIG-A,DAF and proto-oncogene expression in paroxysmal nocturnal haemoglobinuria-associated acute myelogenous leukaemia blast. Br J Haematol 1995; 89: 72-78.
27. Van Kamp H, Smith JW, Van den Berg E, Halie MR, Vallienga E. Myelodysplasia following paroxysmal nocturnal haemoglobinuria: evidence for the emergence of a separate clone. Br J Haematol 1994; 87: 399-400.