Hematología Clínica Integral

24/02/2026

13/02/2026

Es momento de llevar tu práctica profesional al siguiente nivel

🚨 Registro abierto hasta el 15 de febrero a las 12:00 horas
⏳ Cupo limitado
📩 Inscríbete en el enlace: https://es.research.net/r/8B5RCGR

05/06/2025

XXVI Congreso Nacional de Hemofilia 2025

03/06/2025

🩺 ¡Personal de salud!

Tu formación continua es clave para brindar una mejor atención en Hematología.

Las instituciones que Avalan:
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Capacítate y adquiere los conocimientos necesarios para comprender a fondo el comportamiento de las enfermedades en la sangre.

📚 Inscríbete hoy:
👉 https://unidoscapacitacion.org.mx

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22/10/2024

21/11/2023

El 🩸sangrado abundante puede ser reflejo de una o no diagnosticada.

🔴 El riesgo trombótico de la persona requiere una valoración multidisciplinar
🔴 Estamos viviendo el potencial del factor XI como nueva diana terapéutica

➡ Nota de prensa: https://seth.es/sangrado-menstrual-abundante-puede-ser-reflejo-de-una-coagulopatia-o-trombocitopatia-no-diagnosticada/

29/09/2023

Las plaquetas son células de la sangre. Si sangras, ayudan a formar coágulos para frenar el sangrado y a cicatrizar las heridas. Si tienes cáncer, es importante saber si tienes pocas o demasiadas plaquetas. Algunos tratamientos de cáncer, como la quimioterapia o la radioterapia, disminuyen la cantidad de plaquetas. Busca este y otros términos en nuestro Diccionario de cáncer. https://www.cancer.gov/espanol/publicaciones/diccionarios/diccionario-cancer/def/plaqueta

28/09/2023

For today's , we are going over a group of extrinsic hemolytic anemias called autoimmune hemolytic anemia.

Logically, in autoimmune hemolytic anemias, antibodies are directed against RBCs, leading to their destruction. You can imagine it as an RBC equivalent of immune thrombocytopenic purpura. In fact, some patients develop both conditions together, and that’s called Evan syndrome.

Based on the type of antibodies produced, autoimmune hemolytic anemia can be further divided into IgG, also called warm antibody hemolytic anemia, and IgM hemolytic anemia, also known as cold agglutinin disease.

Warm antibody hemolytic anemia is typically seen in chronic lymphocytic leukemia, or CLL; systemic lupus erythematosus, or SLE; and with the use of antibiotics like penicillins and cephalosporins, sulfa drugs, and the antihypertensive drug, methyldopa.

Cold agglutinin disease is often seen in CLL; Waldenstrom macroglobulinemia, a rare type of malignant lymphoma; and infections such as infectious mononucleosis and mycoplasma pneumoniae infections.

Symptoms of autoimmune hemolytic anemia include symptoms of anemia in general, such as fatigue, pallor, and shortness of breath, as well as symptoms of hemolysis, like jaundice, dark or tea-colored urine, and back pain due to kidney damage.

Sometimes there are more specific symptoms that can help you identify the cause of anemia. For example, in cold agglutinin disease, when individuals are exposed to cold temperatures, IgM antibodies react with RBC antigens and make them agglutinate, or clot.

Learn more about all types of extrinsic hemolytic anemia on Osmosis: https://osms.it/pathology-auto-hemo-anemia-fb

29/07/2023

Auer rod–like inclusions in chronic lymphocytic leukemia

A 64-year-old man presented with leukocytosis with absolute abnormal lymphocytosis. The lymphocytes were small to medium in size with mature chromatin and variably prominent nucleoli (with 20% prolymphocytes noted), with a few demonstrating needle-shaped azurophilic cytoplasmic inclusions resembling Auer rods (panels A-C, 100× objective; Wright-Giemsa stained peripheral blood smear). Flow cytometry analysis revealed a mature CD5+ surface λ light chain–restricted B-cell population expressing CD23 and CD200 and negative for FMC7 (panels D-F). Cytogenetic karyotype revealed an abnormal male karyotype: 46,XY,del(7)(q22q32),del(13)(q12q14)add(13)(q34),del(14)(q11.2q24)[20]. The patient was diagnosed with chronic lymphocytic leukemia.
Auer rods are a morphologic hallmark of myeloid differentiation in neoplastic blasts. However, Auer rod–like inclusions do not always indicate a high-grade myeloid neoplasm and can rarely be found in B-cell lymphoproliferative disorders. The composition of these inclusions is uncertain with some proposing a lysosomal origin and others hypothesizing they are abnormal immunoglobulin precipitates. Considering the difference in therapy and prognosis for myeloid versus lymphoid malignancies, it is important to make the distinction, and additional studies are essential to arrive at a correct diagnosis. In general, cases with Auer rod–like inclusions can be diagnostically challenging and require the correlation of morphology, cytochemistry, immunophenotype, and sometimes cytogenetic or molecular studies to confirm the lineage of the neoplastic cells and establish the correct pathologic diagnosis.
https://ashpublications.org/blood/article/142/4/397/496886/Auer-rod-like-inclusions-in-chronic-lymphocytic

18/05/2023

Welcome to EHA . Our schema today is on the diagnosis of : can you fill in the missing parts A, B and C?

For details, check the recent European guidelines on Diagnosis and Management of Neutropenia:
https://eha.fyi/EHA_EuNet-INNOCHRON_Neutropenias

12/08/2022

La Coordinación de Formación y Capacitación del Personal de Salud les hace la más cordial invitación a la sesión de lanzamiento del curso "Bases de hematología para el personal de salud" el día 12 de agosto a las 12:00 h (hora CDMX) a través del Facebook Live de Insabi Educación, o desde la liga de videoconferencia:
https://videoconferencia.telmex.com/j/1238416124