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1.
Medicina (B Aires) ; 57(3): 323-6, 1997.
Article de Espagnol | MEDLINE | ID: mdl-9640767

RÉSUMÉ

The case of a 33 year old woman with a large granular lymphocytic leukemia is presented. The main symptoms were neutropenia and recurrent respiratory bacterial infections. No enlargement of the liver, spleen or lymph nodes was noted. Circulating lymphocytes averaged 3000/microliter with 35% of large granular cells. The bone marrow biopsy showed lymphatic infiltration with both nodular and interstitial pattern. Lymphocytes bore the T suppressor phenotype (CD8+, CD45 RO+, CD20-, kappa-, lambda-). Cytogenetic studies revealed a low expression clone with 7q-: del (7)(q36). Gene rearrangements for immunoglobulins or T-cell receptors could not be demonstrated by Southern Blot. Bone marrow cultures grew normally while both normal and patient bone marrow showed marked inhibition when incubated with patients serum. Normalization of the peripheral granulocytic count was obtained with prednisone, while granulocytic-stimulating factors, chlorambucil, and cyclosporine A were partially active or inactive. We suggest that this case represents a form of the lymphoproliferative disease of granular lymphocytes. To our knowledge, the deletion of the long arm of chromosome 7 has not been described in this disease.


Sujet(s)
Leucémie lymphoïde/sang , Leucémie lymphoïde/physiopathologie , Adulte , Femelle , Humains
2.
Leuk Lymphoma ; 21(1-2): 169-72, 1996 Mar.
Article de Anglais | MEDLINE | ID: mdl-8907285

RÉSUMÉ

Occasional cases with the chromosomal translocations that juxtapose the c-myc oncogene to Ig genes have been reported in large cell, small lymphocytic, immunoblastic, and follicular lymphomas. In this report, we present a 20 year-old female with lymphoblastic lymphoma of B-cell type and a translocation t(8;22), in which cytogenetic, immunologic, and molecular studies were performed. To the best of our knowledge this is the first report of this association.


Sujet(s)
Chromosomes humains de la paire 22 , Chromosomes humains de la paire 8 , Leucémie-lymphome lymphoblastique à précurseurs B et T/génétique , Translocation génétique , Adulte , ADN tumoral/analyse , ADN tumoral/génétique , Femelle , Humains , Immunophénotypage , Caryotypage , Leucémie-lymphome lymphoblastique à précurseurs B et T/immunologie , Leucémie-lymphome lymphoblastique à précurseurs B et T/anatomopathologie
3.
Haematologica ; 79(1): 40-5, 1994.
Article de Anglais | MEDLINE | ID: mdl-15378947

RÉSUMÉ

BACKGROUND AND METHODS: Consistent and specific chromosomal aberrations have been observed in an increasing number of neoplasias. In the present report, we describe the cytogenetic findings from 50 cases of de novo ANLL in Argentina, South America, studied at diagnosis. In addition, their relation with the FAB classification is analyzed. Children with Down's syndrome and secondary ANLL were excluded from this analysis. RESULTS AND CONCLUSIONS: Out of 50 banded cases studied, 11 (22%) had normal karyotype, while the remaining 39 (78%) presented abnormal metaphases with structural alterations in the majority of them. Chromosomes 7 and 22 were most frequently involved in numerical alterations in children, while chromosomes 6, 8, 14 and 16 were the ones most often involved in adults. Consistent chromosome rearrangements were observed and they were linked to specific cytomorphologic subsets. The translocations t(8;21) and t(15;17) were seen only in M2 and M3, respectively. The inversion of chromosome 16, inv(16), was a typical finding in M4, but was not restricted to this subtype. Translocation t(2;3) was observed in three cases, all M4, each with a variable chromosome pattern. These results are in accordance with cytogenetic findings in Western Europe and the USA.


Sujet(s)
Aberrations des chromosomes , Leucémie aigüe myéloïde/génétique , Leucémie aigüe myélomonocytaire/génétique , Adolescent , Adulte , Sujet âgé , Aneuploïdie , Argentine/épidémiologie , Enfant , Enfant d'âge préscolaire , Zébrage chromosomique , Femelle , Humains , Nourrisson , Caryotypage , Leucémie aigüe myéloïde/épidémiologie , Leucémie aigüe myéloïde/anatomopathologie , Leucémie aigüe myélomonocytaire/épidémiologie , Leucémie aigüe myélomonocytaire/anatomopathologie , Mâle , Adulte d'âge moyen , Translocation génétique
4.
Cir. Urug ; 61(3/4): 138-9, mayo-ago. 1991.
Article de Espagnol | LILACS | ID: lil-126994

RÉSUMÉ

Los autores realizaron un estudio prospectivo y pareado de la reacción plástico adherencial frente a dos mallas protésicas intraperitoneales. Se utilizó como animal de experimentación, 20 perros mestizos que se abordaron por laparotomía mediana y se colocó una malla de polipropileno a la derecha y una de poliglactina 910 a la izquierda, en la cara profunda del peritoneo parietal anterior. Se analizó la presencia y firmeza de adherencias viscerales frente a ambas mallas. Los resultados, analizados mediante el test de x2 mostraron diferencias significativas en cuanto a la formación y firmeza de las adherencias frente a cada una de las mallas, siendo éstas más frecuentes y firmes frente a la de polipropileno


Sujet(s)
Chiens , Polyglactine 910 , Polypropylènes , Filet chirurgical
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