A to O bone marrow transplantation in severe aplastic anaemia: dynamics of blood group conversion and demonstration of early dyserythropoiesis in the engrafted marrow

A. M. Marmont; E. E. Damasio; A. Bacigalupo; D. Giordano; E. Rossi; G. Reali; A. Gay; F. Dagna-Bricarelli; F. Brema; A. M. Carella; G. Santini

A to O bone marrow transplantation in severe aplastic anaemia: dynamics of blood group conversion and demonstration of early dyserythropoiesis in the engrafted marrow

A. M. Marmont, E. E. Damasio, A. Bacigalupo, D. Giordano, E. Rossi, G. Reali, A. Gay, F. Dagna-Bricarelli, F. Brema, A. M. Carella, G. Santini

IRCCS Casa Sollievo della Sofferenza

Research output: Contribution to journal › Article › peer-review

Abstract

A to O bone marrow transplantation was performed in a 25 yr old male affected with severe aplastic anemia, the donor being an HLA compatible brother. Three plasma exchanges had to be performed with an Aminco separator to remove the original and recurring anti A isohemagglutinins. The dynamics of O to A blood group conversion were followed by means of differential agglutination. An early wave of marked dyserythropoiesis was observed in the engrafted marrow. Mild to moderate GvHD was treated successfully with MTX, bolus high dosage 6 methylprednisolone and, at relapse, with intravenous ALG.

Original language	English
Pages (from-to)	511-518
Number of pages	8
Journal	British Journal of Haematology
Volume	36
Issue number	4
Publication status	Published - 1977

ASJC Scopus subject areas

Hematology

Access to Document

Fingerprint Dive into the research topics of 'A to O bone marrow transplantation in severe aplastic anaemia: dynamics of blood group conversion and demonstration of early dyserythropoiesis in the engrafted marrow'. Together they form a unique fingerprint.

Cite this

Marmont, A. M., Damasio, E. E., Bacigalupo, A., Giordano, D., Rossi, E., Reali, G., Gay, A., Dagna-Bricarelli, F., Brema, F., Carella, A. M., & Santini, G. (1977). A to O bone marrow transplantation in severe aplastic anaemia: dynamics of blood group conversion and demonstration of early dyserythropoiesis in the engrafted marrow. British Journal of Haematology, 36(4), 511-518.

A to O bone marrow transplantation in severe aplastic anaemia : dynamics of blood group conversion and demonstration of early dyserythropoiesis in the engrafted marrow. / Marmont, A. M.; Damasio, E. E.; Bacigalupo, A.; Giordano, D.; Rossi, E.; Reali, G.; Gay, A.; Dagna-Bricarelli, F.; Brema, F.; Carella, A. M.; Santini, G.

In: British Journal of Haematology, Vol. 36, No. 4, 1977, p. 511-518.

Research output: Contribution to journal › Article › peer-review

Marmont, AM, Damasio, EE, Bacigalupo, A, Giordano, D, Rossi, E, Reali, G, Gay, A, Dagna-Bricarelli, F, Brema, F, Carella, AM & Santini, G 1977, 'A to O bone marrow transplantation in severe aplastic anaemia: dynamics of blood group conversion and demonstration of early dyserythropoiesis in the engrafted marrow', British Journal of Haematology, vol. 36, no. 4, pp. 511-518.

Marmont, A. M. ; Damasio, E. E. ; Bacigalupo, A. ; Giordano, D. ; Rossi, E. ; Reali, G. ; Gay, A. ; Dagna-Bricarelli, F. ; Brema, F. ; Carella, A. M. ; Santini, G. / A to O bone marrow transplantation in severe aplastic anaemia : dynamics of blood group conversion and demonstration of early dyserythropoiesis in the engrafted marrow. In: British Journal of Haematology. 1977 ; Vol. 36, No. 4. pp. 511-518.

@article{f280deda01cc4bbdae7a747cd85938ce,

title = "A to O bone marrow transplantation in severe aplastic anaemia: dynamics of blood group conversion and demonstration of early dyserythropoiesis in the engrafted marrow",

abstract = "A to O bone marrow transplantation was performed in a 25 yr old male affected with severe aplastic anemia, the donor being an HLA compatible brother. Three plasma exchanges had to be performed with an Aminco separator to remove the original and recurring anti A isohemagglutinins. The dynamics of O to A blood group conversion were followed by means of differential agglutination. An early wave of marked dyserythropoiesis was observed in the engrafted marrow. Mild to moderate GvHD was treated successfully with MTX, bolus high dosage 6 methylprednisolone and, at relapse, with intravenous ALG.",

author = "Marmont, {A. M.} and Damasio, {E. E.} and A. Bacigalupo and D. Giordano and E. Rossi and G. Reali and A. Gay and F. Dagna-Bricarelli and F. Brema and Carella, {A. M.} and G. Santini",

year = "1977",

language = "English",

volume = "36",

pages = "511--518",

journal = "British Journal of Haematology",

issn = "0007-1048",

publisher = "John Wiley & Sons, Ltd (10.1111)",

number = "4",

}

TY - JOUR

T1 - A to O bone marrow transplantation in severe aplastic anaemia

T2 - dynamics of blood group conversion and demonstration of early dyserythropoiesis in the engrafted marrow

AU - Marmont, A. M.

AU - Damasio, E. E.

AU - Bacigalupo, A.

AU - Giordano, D.

AU - Rossi, E.

AU - Reali, G.

AU - Gay, A.

AU - Dagna-Bricarelli, F.

AU - Brema, F.

AU - Carella, A. M.

AU - Santini, G.

PY - 1977

Y1 - 1977

N2 - A to O bone marrow transplantation was performed in a 25 yr old male affected with severe aplastic anemia, the donor being an HLA compatible brother. Three plasma exchanges had to be performed with an Aminco separator to remove the original and recurring anti A isohemagglutinins. The dynamics of O to A blood group conversion were followed by means of differential agglutination. An early wave of marked dyserythropoiesis was observed in the engrafted marrow. Mild to moderate GvHD was treated successfully with MTX, bolus high dosage 6 methylprednisolone and, at relapse, with intravenous ALG.

AB - A to O bone marrow transplantation was performed in a 25 yr old male affected with severe aplastic anemia, the donor being an HLA compatible brother. Three plasma exchanges had to be performed with an Aminco separator to remove the original and recurring anti A isohemagglutinins. The dynamics of O to A blood group conversion were followed by means of differential agglutination. An early wave of marked dyserythropoiesis was observed in the engrafted marrow. Mild to moderate GvHD was treated successfully with MTX, bolus high dosage 6 methylprednisolone and, at relapse, with intravenous ALG.

UR - http://www.scopus.com/inward/record.url?scp=0017644080&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0017644080&partnerID=8YFLogxK

M3 - Article

C2 - 19032

AN - SCOPUS:0017644080

VL - 36

SP - 511

EP - 518

JO - British Journal of Haematology

JF - British Journal of Haematology

SN - 0007-1048

IS - 4

ER -