INVESTIGADORES
PRECIADO Maria Victoria
artículos
Título:
Epstein Barr virus associated Hodgkin's disease in a HIV-positive child presenting with a hemophagocytic syndrome
Autor/es:
MARIA VICTORIA PRECIADO; DE MATTEO, E.; FALLO, A.; CHABAY, P.; DRELICHMAN, G.; GRISNTEIN, S.
Revista:
LEUKEMIA AND LYMPHOMA
Editorial:
TAYLOR & FRANCIS LTD
Referencias:
Año: 2001 vol. 42 p. 231 - 234
ISSN:
1042-8194
Resumen:
An 8-years-old boy was admitted with fever of unknown origin, cervical lymphadenopathy
and hepatosplenomegaly and weight loss. His mothers HIV infection was diagnosed two
weeks before his hospitalization, so he was diagnosed as perinatally acquired AIDS. Serology
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
weeks before his hospitalization, so he was diagnosed as perinatally acquired AIDS. Serology
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
weeks before his hospitalization, so he was diagnosed as perinatally acquired AIDS. Serology
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
HIV infection was diagnosed two
weeks before his hospitalization, so he was diagnosed as perinatally acquired AIDS. Serology
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
as perinatally acquired AIDS. Serology
and serial cultures were negative for viral infections, toxoplasmosis, chagas, tuberculosis and
atypical mycobacterium. The patient met clinical and laboratory criteria for hemophagocytic
syndrome (HS) that was confiied on bone marrow aspirate and biopsy. A cervical lymph
node biopsy was performed which was diagnosed as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistry
as Hodgkins disease (HD) diffuse fibrosis
lymphocyte depletion subtype. EBERs in situ hybridization and LMP-1 immunohistochemistryEBERs in situ hybridization and LMP-1 immunohistochemistry
on the lymph node biopsy established the EBV association. On the basis of a sequence of
appearance of the clinical, laboratory and histological signs, HIV, EBV or HD may have triggered
HS as the last fatal event in this pediatric patient.
HS as the last fatal event in this pediatric patient.
HS as the last fatal event in this pediatric patient.
appearance of the clinical, laboratory and histological signs, HIV, EBV or HD may have triggered
HS as the last fatal event in this pediatric patient.
HS as the last fatal event in this pediatric patient.
HS as the last fatal event in this pediatric patient.
appearance of the clinical, laboratory and histological signs, HIV, EBV or HD may have triggered
HS as the last fatal event in this pediatric patient.
HS as the last fatal event in this pediatric patient.
HS as the last fatal event in this pediatric patient.
EBV association. On the basis of a sequence of
appearance of the clinical, laboratory and histological signs, HIV, EBV or HD may have triggered
HS as the last fatal event in this pediatric patient.
HS as the last fatal event in this pediatric patient.
HS as the last fatal event in this pediatric patient.
HIV, EBV or HD may have triggered
HS as the last fatal event in this pediatric patient.as the last fatal event in this pediatric patient.