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1.
Rev Med Interne ; 30(3): 274-6, 2009 Mar.
Artículo en Francés | MEDLINE | ID: mdl-18584920

RESUMEN

We report a case of dengue fever with plasma cells in the blood (3980 per cubic millimeter) and bone marrow (30%) in a 55-year-old woman hospitalized for fever, arthralgias and thrombocytopenia (66,000 per cubic millimeter) on returning from the West Indies. Serological testing confirmed the diagnosis. Plasmacytosis is rare in dengue fever and its frequency and correlation with the different forms of the disease remain to be determined.


Asunto(s)
Médula Ósea , Dengue , Células Plasmáticas , Médula Ósea/patología , Examen de la Médula Ósea , Dengue/sangre , Dengue/complicaciones , Dengue/diagnóstico , Dengue/patología , Femenino , Estudios de Seguimiento , Humanos , Persona de Mediana Edad , Células Plasmáticas/patología , Trombocitopenia/diagnóstico , Trombocitopenia/etiología , Factores de Tiempo
2.
Rev Med Interne ; 30(10): 886-9, 2009 Oct.
Artículo en Francés | MEDLINE | ID: mdl-19748163

RESUMEN

INTRODUCTION: Fever during a myelodysplastic syndrome can be due to infectious complications, systemic disease or acute transformation with clonal evolution. CASE REPORT: A 51-year-old woman, with a 5q- syndrome and neutropenia, presented with a several week fever duration. Infectious work-up was negative and therapy with antibiotics had no influence on the clinical course. Neither bone marrow nor blood blasts were detected, but liver biopsy demonstrated significant blast infiltration compatible with the diagnosis of acute myeloid leukaemia (AML). CONCLUSION: The absence of blasts in blood or bone marrow does not exclude the malignant transformation of a myelodysplastic syndrome to AML. Tissue biopsy may be necessary to confirm the leukaemic progression.


Asunto(s)
Fiebre/etiología , Leucemia Mieloide Aguda/diagnóstico , Síndromes Mielodisplásicos/complicaciones , Femenino , Humanos , Infiltración Leucémica , Hígado/patología , Persona de Mediana Edad
3.
Rev Med Interne ; 34(3): 168-70, 2013 Mar.
Artículo en Francés | MEDLINE | ID: mdl-23182291

RESUMEN

INTRODUCTION: Adult-onset Still's disease is characterized by non-specific polymorphic features. The efficacy of anakinra, an IL-1 receptor antagonist, has been shown in several studies. This medication is well-tolerated, and only one case of severe hepatitis has been previously reported. CASE REPORT: A 22-year-old woman presented with fever, rash, arthritis, and pericarditis, associated with systemic inflammatory response syndrome and elevated ferritin serum level with low glycosylated ferritin. Adult-onset Still's disease was diagnosed, but treatment with steroids did not achieve remission. The patient was then treated with anakinra, which resulted in spectacular improvement, but 3 weeks after the initiation of the treatment she experienced severe hepatitis that resolved after the discontinuation of anakinra. CONCLUSION: Hepatitis is a rare side effect of anakinra and the monitoring of liver tests should be recommended during anakinra therapy.


Asunto(s)
Antirreumáticos/efectos adversos , Enfermedad Hepática Inducida por Sustancias y Drogas/etiología , Proteína Antagonista del Receptor de Interleucina 1/efectos adversos , Enfermedad de Still del Adulto/tratamiento farmacológico , Antirreumáticos/administración & dosificación , Femenino , Humanos , Proteína Antagonista del Receptor de Interleucina 1/administración & dosificación , Enfermedad de Still del Adulto/diagnóstico , Adulto Joven
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