Síndrome Hemofagocítico
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Transcript of Síndrome Hemofagocítico
A PROPOSITO DE UN CASO
Ernesto Garciacutea Ureta
httpwwwgarciauretacomXXIV Congreso de la SEAP
Varoacuten de 11 antildeos
Linfoma no Hodgkin de alto grado de celulas Brico en celulas T
Asociado al virus de Epstein Barr
Diagnostico de Proceso Hemofagociticoen biopsia de Medula Osea
Ascitis
CD-68
S-100
1979 Sep44(3)993-1002
AbstractNineteen patients whose bone marrow smears showed histiocytic hyperplasia with prominent hemophagocytosis were found to have a clinicopathologic syndrome associated with active viral infection High fever constitutional symptoms liver function and coagulation abnormalities and peripheral blood cytopenias were characteristic findings Hepatosplenomegaly lymphadenopathy bilateral pulmonary infiltrates and skin rash were often present Fourteen of the patients were immunosuppressed Active infection by herpes group viruses was documented in 14 patients and by adenovirus in 1 The bone marrow of most patients also showed decreased granulopoiesis and erythropoiesis with normal to increased numbers of megakaryocytes Treatment generally consisted of supportive therapy and withdrawal of immunosuppressive drugs Thirteen patients recovered Lymph node biopsy and autopsy material showed generalized histiocytichyperplasia with hemophagocytosis The relationship of this disorder to familial hemophagocytic reticulosis familial erythrophagocytic lymphohistiocytosis histiocyticmedullary reticulosis and malignant histiocytosis is discussed Immunosuppressive and cytotoxic therapy may be contraindicated in the treatment of this virus-associated syndrome
Kimura S
Hemophagocytic Symdrome
Intern Med 205 44 278- 280
FIN
httpwwwgarciauretacom
Varoacuten de 11 antildeos
Linfoma no Hodgkin de alto grado de celulas Brico en celulas T
Asociado al virus de Epstein Barr
Diagnostico de Proceso Hemofagociticoen biopsia de Medula Osea
Ascitis
CD-68
S-100
1979 Sep44(3)993-1002
AbstractNineteen patients whose bone marrow smears showed histiocytic hyperplasia with prominent hemophagocytosis were found to have a clinicopathologic syndrome associated with active viral infection High fever constitutional symptoms liver function and coagulation abnormalities and peripheral blood cytopenias were characteristic findings Hepatosplenomegaly lymphadenopathy bilateral pulmonary infiltrates and skin rash were often present Fourteen of the patients were immunosuppressed Active infection by herpes group viruses was documented in 14 patients and by adenovirus in 1 The bone marrow of most patients also showed decreased granulopoiesis and erythropoiesis with normal to increased numbers of megakaryocytes Treatment generally consisted of supportive therapy and withdrawal of immunosuppressive drugs Thirteen patients recovered Lymph node biopsy and autopsy material showed generalized histiocytichyperplasia with hemophagocytosis The relationship of this disorder to familial hemophagocytic reticulosis familial erythrophagocytic lymphohistiocytosis histiocyticmedullary reticulosis and malignant histiocytosis is discussed Immunosuppressive and cytotoxic therapy may be contraindicated in the treatment of this virus-associated syndrome
Kimura S
Hemophagocytic Symdrome
Intern Med 205 44 278- 280
FIN
httpwwwgarciauretacom
CD-68
S-100
1979 Sep44(3)993-1002
AbstractNineteen patients whose bone marrow smears showed histiocytic hyperplasia with prominent hemophagocytosis were found to have a clinicopathologic syndrome associated with active viral infection High fever constitutional symptoms liver function and coagulation abnormalities and peripheral blood cytopenias were characteristic findings Hepatosplenomegaly lymphadenopathy bilateral pulmonary infiltrates and skin rash were often present Fourteen of the patients were immunosuppressed Active infection by herpes group viruses was documented in 14 patients and by adenovirus in 1 The bone marrow of most patients also showed decreased granulopoiesis and erythropoiesis with normal to increased numbers of megakaryocytes Treatment generally consisted of supportive therapy and withdrawal of immunosuppressive drugs Thirteen patients recovered Lymph node biopsy and autopsy material showed generalized histiocytichyperplasia with hemophagocytosis The relationship of this disorder to familial hemophagocytic reticulosis familial erythrophagocytic lymphohistiocytosis histiocyticmedullary reticulosis and malignant histiocytosis is discussed Immunosuppressive and cytotoxic therapy may be contraindicated in the treatment of this virus-associated syndrome
Kimura S
Hemophagocytic Symdrome
Intern Med 205 44 278- 280
FIN
httpwwwgarciauretacom
S-100
1979 Sep44(3)993-1002
AbstractNineteen patients whose bone marrow smears showed histiocytic hyperplasia with prominent hemophagocytosis were found to have a clinicopathologic syndrome associated with active viral infection High fever constitutional symptoms liver function and coagulation abnormalities and peripheral blood cytopenias were characteristic findings Hepatosplenomegaly lymphadenopathy bilateral pulmonary infiltrates and skin rash were often present Fourteen of the patients were immunosuppressed Active infection by herpes group viruses was documented in 14 patients and by adenovirus in 1 The bone marrow of most patients also showed decreased granulopoiesis and erythropoiesis with normal to increased numbers of megakaryocytes Treatment generally consisted of supportive therapy and withdrawal of immunosuppressive drugs Thirteen patients recovered Lymph node biopsy and autopsy material showed generalized histiocytichyperplasia with hemophagocytosis The relationship of this disorder to familial hemophagocytic reticulosis familial erythrophagocytic lymphohistiocytosis histiocyticmedullary reticulosis and malignant histiocytosis is discussed Immunosuppressive and cytotoxic therapy may be contraindicated in the treatment of this virus-associated syndrome
Kimura S
Hemophagocytic Symdrome
Intern Med 205 44 278- 280
FIN
httpwwwgarciauretacom
1979 Sep44(3)993-1002
AbstractNineteen patients whose bone marrow smears showed histiocytic hyperplasia with prominent hemophagocytosis were found to have a clinicopathologic syndrome associated with active viral infection High fever constitutional symptoms liver function and coagulation abnormalities and peripheral blood cytopenias were characteristic findings Hepatosplenomegaly lymphadenopathy bilateral pulmonary infiltrates and skin rash were often present Fourteen of the patients were immunosuppressed Active infection by herpes group viruses was documented in 14 patients and by adenovirus in 1 The bone marrow of most patients also showed decreased granulopoiesis and erythropoiesis with normal to increased numbers of megakaryocytes Treatment generally consisted of supportive therapy and withdrawal of immunosuppressive drugs Thirteen patients recovered Lymph node biopsy and autopsy material showed generalized histiocytichyperplasia with hemophagocytosis The relationship of this disorder to familial hemophagocytic reticulosis familial erythrophagocytic lymphohistiocytosis histiocyticmedullary reticulosis and malignant histiocytosis is discussed Immunosuppressive and cytotoxic therapy may be contraindicated in the treatment of this virus-associated syndrome
Kimura S
Hemophagocytic Symdrome
Intern Med 205 44 278- 280
FIN
httpwwwgarciauretacom
Kimura S
Hemophagocytic Symdrome
Intern Med 205 44 278- 280
FIN
httpwwwgarciauretacom
FIN
httpwwwgarciauretacom