Extramedullary hematopoiesis in hereditary spherocytosis deficient in Ankyrin: A case report

International Journal of Hematology

Volumn 76, Issue 2, 2002, Pages 153-156

  Granjo, E ^a,b   Bauerle, R ^c   Sampaio, R ^d   Manata, P ^e   Torres, N ^a   Quintanilha, A ^a,f  

^a UNIVERSITY OF PORTO   (Portugal)

^b HOSPITAL DE SÃO JOÃO   (Portugal)

^c Hospital de Santa Luzia   (Portugal)

^d Diagnóstico Por Imagem   (Portugal)

^e CENTRO HOSPITALAR E UNIVERSITÁRIO DE COIMBRA   (Portugal)

^f UNIVERSITY OF PORTO   (Portugal)

Author keywords

Ankyrin deficiency; Erythropoietin production; Extramedullary hematopoiesis; Hereditary spherocytosis; Hypoxia

Indexed keywords

ANKYRIN; ERYTHROPOIETIN;

AGED; ARTICLE; CASE REPORT; CLINICAL FEATURE; ERYTHROID CELL; EXTRAMEDULLARY HEMATOPOIESIS; HEREDITARY SPHEROCYTOSIS; HUMAN; HYPOXIA; MALE; RESPIRATORY TRACT INFECTION; BLOOD; NUCLEAR MAGNETIC RESONANCE IMAGING; THORAX;

AGED; ANKYRINS; ERYTHROPOIETIN; HEMATOPOIESIS, EXTRAMEDULLARY; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; RESPIRATORY TRACT INFECTIONS; SPHEROCYTOSIS, HEREDITARY; THORAX;

EID: 1842868527     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02982578     Document Type: Article

References (29)

1. Delaunay J, Alloisio N, Morlé L, Carré G. La sphérocytose héreditaire en 1995: l'apport de la génétique moléculaire. Hématologie. 1995;2:115-122.
2. McLellan NJ, Rutter N. Hereditary spherocytosis in sisters unmasked by parvovirus infection. Postgrad Med J. 1987;63:49-50.
3. Brown KE, Young NS. Parvovirus B19 in human disease. Annu Rev Med. 1997;48:59-67.
4. Miraglia del Giudice E, Francese M, Nobili B, et al. High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis. J Pediatr. 1998;132:117-120.
5. Miraglia del Giudice E, Lombardi C, Francese M, et al. Frequent de novo monoallelic expression of β-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency. Br J Haematol. 1998;101:251-254.
6. Gallagher PG, Forget BG. Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis. Blood Cells Mol Dis. 1998;24:539-543.
7. Gallagher PG, Forget B. Hematologically important mutations: band 3 and protein 4.2 in hereditary spherocytosis. Blood Cells Mol Dis. 1997;23:417-421.
8. Bastion Y, Coiffier B, Felman P, et al. Massive intestinal extramedullary hematopoiesis in hereditary spherocytosis: a case report. Am J Hematol. 1990;35:263-265.
9. Cobas A, Gomez E, Lago CF, Torres JP. Hereditary spherocytosis and a paravertebral mass. Med Clin (Barc). 1995;104:237.
10. Coventry WD, LaBree RH. Heterotopia of bone marrow simulating mediastinal tumor. Ann Intern Med. 1960;53:1042-1052.
11. Hanford RB, Schneider GF, MacCarthy JD. Massive thoracic extramedullary hemopoiesis. N Engl J Med. 1960;263:120-123.
12. Herait P, Janvier M, Bernard J, et al. Focus of intrathoracic extramedullary hematopoiesis: a little known cause of posterior mediastinal tumor. Presse Med. 1984;13:1513-1514.
13. Vetrani A, Cecere C, Fulciniti F, Ferrante G. Intrathoracic extramedullary hemopoiesis: report of a case in a patient with hereditary spherocytosis. Pathologica. 1984;76:733-736.
14. Kalina P, Hillstrom MM. MR of extramedullary hematopoiesis causing cord compression in β-thalassemia. AJNR Am J Neuroradiol. 1992;13:1407-1409.
15. Martin J, Palacio A, Petit J, Martin C. Fatty transformation of thoracic extramedullary hematopoiesis following splenectomy: CT features. J Comput Assist Tomogr. 1990;14:477-478.
16. Nastri G, Cappelletti M, Cappellini MD, Bonelli N, Balzani A, Fiorelli G. Localizzazioni toraciche dell' eritropoiesi extramidollare. Radiol Med Torino. 1992;84:576-581.
17. Savader SJ, Otero RR, Savader BL. MR imaging of intrathroracic extramedullary hematopoiesis. J Comput Assist Tomog. 1988;12:878-880.
18. Siegelman ES, Mitchell DG, Rubin R, et al. Parenchymal versus reticuloendothelial iron overload in the liver: distinction with MR imaging. Radiology. 1991;179:361-366.
19. Soler R, Pombo F, Rodriguez E, Cobas A, Lago CF, Torres JP. MR findings in hereditary spherocytosis. Comput Med Imaging Graph. 1995;19:247-250.
20. Steiner RM, Mitchell DG, Rao VM, Schweitzer ME. Magnetic resonance imaging of diffuse bone marrow disease. Radiol Clin North Am. 1993;31:383-409.
21. Warshauer DM, Schiebler ML. Intrahepatic extramedullary hematopoiesis: MR, CT and sonographic appearance. J Comput Assist Tomogr. 1991;15:683-685.
22. Yamato M, Fuhrman CR. Computed tomography of fatty replacement in extramedullary hematopoiesis. J Comput Assist Tomogr. 1987;11:541-542.
23. Abe T, Yachi A, Ishii Y, et al. Thoracic extramedullary hematopoiesis associated with hereditary spherocytosis. Intern Med. 1992;341:1151-1154.
24. Papavaciliou C, Sandillos P. Effect of radiotherapy on symptoms due to heterotopic marrow in β-thalassemia. Lancet. 1987;i:13-14.
25. Pulsoni A, Ferrazza G, Malagnino F. Mediastinal extramedullary haematopoiesis as first manifestation of hereditary spherocytosis. Ann Haematol. 1992;65:196-198.
26. Reman O, Carre G, Belloy F, Galateau F, Cheze S, Macro M. Extramedullary hematopoiesis in hereditary spherocytosis simulating mediastinal tumour. Eur J Haematol. 1997;58:124-126.
27. Guarnone R, Centenar E, Zappa M, Zanella A, Barosi G. Erythropoietin production and erythropoiesis in compensated and anaemic of hereditary spherocytosis. Br J Haematol. 1996;92:150-154.
28. Granjo E, Rocha S, Rocha P, et al. Serum erythropoietin levels in hereditary spherocytosis pre and post splenectomy [abstract]. Acta Haematol. 2000;103(suppl 1):18.
29. Granjo E, Baüerle R, Manata P, et al. Hereditary spherocytosis associated to extramedullary hematopoietic tumor [abstract]. Int J Hematol. 2000;72(suppl 1):122.