anomalias de la serie rojaecaths1.s3.amazonaws.com/hematologiaclinicafacena/1647291698.serie...
TRANSCRIPT
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ANOMALIAS DE LA SERIE ROJA
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CLASIFICACION
1-ALTERACIONES DE TAMAÑO 2-ALTERACIONES DE LA FORMA 3-ALTERACIONES EN LA
COLORACION DE LA Hb 4-INCLUSIONES ERITROCITARIAS
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1-ALTERACIONES DE TAMAÑO ANISOCITOSIS MICROCITOSIS: predominio de hematíes
con Ø < 6 µm y volumen < 80 fL MACROCITOSIS: predominio de hematíes
con Ø entre 8-11 µm y volumen > 100 fL
MEGALOCITOSIS: predominio de hematíes con Ø ≥ 12 µm y volumen > 110 fL
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ANISOCITOSIS
INESPECIFICO POLITRANSFUNDIDOS ANEMIA EN RECUPERACION
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MICROCITOSIS ANEMIA FERROPENICA TALASEMIA ANEMIA DE ENFERME-DADES CRONICAS DEFICIT DE PK HIPERTIROIDISMO HIPOTIROIDISMO
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MACROCITOSIS DEFICIT DE FACTORESMADURATIVOS HEPATOPATIAS CRONICAS SMD EBF ASPLENIA RECUPERACION DEHEMORRAGIAS HIV - SIDA
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MEGALOCITOSIS ANEMIA MEGALO-BLASTICA (ANEMIA PERNICIOSA) CELIAQUEZ BY PASS GASTRICO VEGETARIANOS ESTRICTOS
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2-ALTERACIONES DE LA FORMA (POIQUILOCITOSIS) ESQUISTOCITOS DACRIOCITOS ESFEROCITOS ELIPTOCITOS DREPANOCITOS TARGET CELLS ESTOMATOCITOS EQUINOCITOS ACANTOCITOS EXCENTROCITOS BITED CELLS KNOCITOS
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ESQUISTOCITOS CID SUH PROTESIS VALVULARES IRA AH MICROANGIPATICA HEMOGLOBINURIA DELA MARCHA CARCINOMAS
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DACRIOCITOS ANEMIA GRAVE METAPLASIA MIE-LOIDE AGNOGENICA SUFRIMIENTO ME-DULAR ASPLENIA
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ESFEROCITOS ESFEROCITOSIS HEREDI-TARIA ASPLENIA AHAI QUEMADURAS GRAVES ALTERACIONES DE MEM-BRANA (VERTICALES) INCOMPATIBILIDAD ABO
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ELIPTOCITOS INESPECIFICO ELIPTOCITOSIS HERE-DITARIA ANEMIA MEGALO-BLASTICAS ANEMIAS FERROPE-NICAS TALASEMIAS
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DREPANOCITOS HEMOGLOBINA S HEMOGLOBINA S-C
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TARGET CELL - CODOCITOS
TALASEMIA (Enf. Cooley) HEMOGLOBINOPATIA C HEPATOPATIAS DEFICIT DE LCAT FARMACOS CON ELEVADOMETABOLISMO HEPATICO
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ESTOMATOCITOS ESTOMATOCITOSISHEREDITARIA CIRROSIS HEPATICA HEPATOPATIAALCOHOLICA ANEMIAS HEMOLITICADE ORIGEN INMUNE
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EQUINOCITOS
DEFICIT DE PK UREMIA HEPATOPATIAS NEONATALES CARCINOMAS GASTRICOS SANGRE CONSERVADA PORTA – EXTENSORMOJADOS O SUCIOS
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ACANTOCITOS – SPUR CELLS
ALFA/BETA LIPO-PROTEINEMIA CONGENITA HEPATOPATIAS ASPLENIA TRAT. CON HEPARINA MIELOFIBROSIS
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EXCENTROCITOS
DEFICIT DE G-6-PDH
AH
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BITED CELLS
DEFICIT DEG-6-PDH
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KNOCITOS DEFICIT DE G-6PDH
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La combinación de una o más de estas formas se informa como POIQUILOCITOSIS
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3-ALTERACIONES EN LA COLORACION DE LA Hb HIPOCROMIA PSEUDO HIPERCROMIA POLICROMATOFILIA /
POLICROMASIA / ANISOCROMIA
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HIPOCROMIA
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ANULOCITO
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PSEUDO HIPERCROMIA
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POLICROMATOFILIA
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4-INCLUSIONES
CUERPOS DE HOWELL-JOLLY ANILLOS DE CABOT PUNTEADO BASOFILO CUERPOS DE PAPPENHEIMER CUERPOS DE HEINZ PARASITOS
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CUERPOS DE HOWELL JOLLY
ASPLENIA AH ANEMIA MEGALOBLASTICA SATURNISMO ASPLENIA FUNCIONAL
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ANILLOS DE CABOT
CARECEN DEESPECIFICIDAD AUNQUESU PRESENCIA INDICASEVERO TRASTORNO EN LAERITROPOYESIS DISERITROPOYESIS
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PUNTEADO BASOFILO SATURNISMO ANEMIA HEMOLITICAS BETA TALASEMIA DEFICIT DE P5’N SMD LEUCEMIAS FARMACOS
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CUERPOS DE PAPPENHEIMER
SOBRECARGA DE Fe
TALASEMIAS
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CUERPOS DE HEINZ ALFA TALASEMIA AH POR ENZIMOPATIA Hb INESTABLES REGENERACION MEDULAR FARMACOS Y TOXINASOXIDANTES ASPLENIA
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ABC
Azul Nilo
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PARASITOS
Plasmodiumfalciparum
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PARASITOS T. cruzi
T. rhodiense
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PARASITOS
Babesia microti
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OTROS ROULEAUX
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OTROS AGLUTINACION
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Y esto???
ARTEFACTOS DE FIJACION YCOLORACION
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FIN