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Majito30
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Majito30
@majopito
Médico🇪🇨/Hematóloga en proceso🩸🇪🇦 Dios 💓/soñando 🌄
Katılım Kasım 2010
1K Takip Edilen367 Takipçiler
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Muy orgullos@s de nuestro residente @jburgos_tovar por el premio a la
👏🏻👏🏻mejor comunicación oral 👏🏻👏🏻
en el congreso #46SEMI
“Descripción clínica y microbiológica de una serie de casos de Micobacterias No Tuberculosas entre 2018 y 2024”
Enhorabuena 💥💥



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ELEVATED VITAMIN B12
High vitamin B12? 🧪 Unlike deficiency, elevated B12 usually isn’t about diet or supplements. It’s often a marker of disease.
... but no consensus on whether/how to investigate!
See: thebloodproject.com/elevated-vitam…

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Excited to share our paper on Frailty Dynamics & QoL in MM patients undergoing auto-HCT a @GETH_info study is now out in @BrJHaem
Thank you @QueraltSalas for your support, advices and ideas!
FRAILTY MATTERS! #MultipleMyeloma #HCT #Frailty #QOL
onlinelibrary.wiley.com/doi/10.1111/bj…
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🔬 AML Classification: WHO 5th vs ICC 🩸🧵
1️⃣ WHO 5th Edition:
✅ AML with defining genetic abnormalities (no blast threshold):
•🧬 Fusion: RUNX1::RUNX1T1, CBFB::MYH11, DEK::NUP214, BCR::ABL1, etc.
•🧬 Rearrangements: KMT2A, MECOM, NUP98
•🧬 Molecular: NPM1, CEBPA
⚠️ If none:
➡️ AML defined by differentiation (blasts ≥20%):
•AML M0, M1, M2, M4, M5, M6, M7, etc.
🩺 Separate group:
•Post-cytotoxic therapy
•Germline predisposition
📄 Ref:
•WHO Classification of Haematolymphoid Tumours 5th Ed
⸻
2️⃣ ICC Classification:
✅ AML with recurrent genetic abnormalities (blasts ≥10%):
•RUNX1::RUNX1T1, CBFB::MYH11, DEK::NUP214, NPM1, BCR::ABL1, in-frame bZIP CEBPA
➡️ If no:
✅ AML with TP53 mutation (VAF >10%)
➡️ If no:
✅ AML with myelodysplasia-related gene mutation
➡️ If no:
✅ AML with myelodysplasia-related cytogenetic abnormality
➡️ If no:
✅ AML – NOS
⚠️ Appended qualifiers:
•💉 Therapy-related
•📈 Prior MDS
•📈 Prior MDS/MPN
•🧬 Germline predisposition
⚠️ Blast %:
•10–19%: MDS/AML
•≥20%: AML
📄 Ref:
•ICC 2022 Haematological Malignancies Classification
⸻
🩺 Key takeaways:
✅ ICC lowers blast threshold to 10% if recurrent genetic abnormality present.
✅ WHO retains 20% threshold unless defining genetics.
✅ Emphasis on genetics > morphology.
✅ Clear approach to therapy-related and germline AML.
⸻
🔗 Save for #Hematology #Boards
🔗 Share with your #Pathology team
🔗 Use during #AML discussions and teaching

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Te invitamos a las Jornadas Regionales de Linfoma Cutáneo en Barcelona y Madrid @geltamo
🗓️ 22 y 29 de septiembre 2025
📝Formato presencial
ℹ️ geltamo.com/noticias/233-j…
@DrBastosOreiroM @EvaEvagbarca
Plazas limitadas!
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🆕Nuevo documento "Manejo del Síndrome Antifosfolipídico (SAF)" de los GT de Enfermedades Autoinmunes Sistémicas (@gtgeassemi) y Enfermedad Tromboembólica (@GT_Trombo) de @Sociedad_SEMI🩺
👉Disponible en la web de SEMI y en la webapp "Algoritmos y protocolos de SEMI".
🔹Web SEMI (Publicaciones): fesemi.org/publicaciones/…
🔹Webapp (GT GEAS y Enf. Tromboembólica): protocolos.fesemi.org/#/
#MedicinaInterna @JavierPagan1988 @mmartinasenjo @DrGlezGarcia @gabi_puchepalao @LuisSaezComet @gerardespinosa5

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📢¡No te puedes perder el I Curso #SETH JOVEN: #Hemostasia para tod@s 4.0!
📚Formación dirigida a R4 y adjuntos/as de reciente incorporación👩⚕️👨⚕️
📅29 de abril |📍Sede #SETH, Madrid
🔗Inscripción gratuita: seth.es/i-curso-seth-j…
#FormaciónSETH #hemostasia #trombosis #hematólogos #HematoEnRed @HematoCAUSA

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🎙️ Avui, a les 11 h, la Dra. Elisenda Solé, adjunta al servei de Pediatria de l’Hospital Universitari #MútuaTerrassa, intervindrà al magazín “Faves comptades” de @cugatmedia.
🗣️ Parlarà de la iniciativa “Llegir ens fa créixer!”.
cugat.cat/directe/index.…
Català
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Waldenström Macroglobulinemia: 2025 Update on Diagnosis, Risk Stratification, and Management |American Journal of Hematology | Blood Research Journal | Wiley Online Library onlinelibrary.wiley.com/doi/full/10.10…

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¡Ya tenemos programa de H-ONCOBARNA! Curso Multidisciplinar de Patología Hematológica y Oncológica Crítica, 7-9 mayo 2025 en @vallhebron (Barcelona). Formato teórico-práctico, presencial y online.
+info e inscripciones⬇️
aula.vallhebron.com/?go=info_curso…
¡Os esperamos en H-ONCOBARNA!




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📢 Myelodysplastic/Myeloproliferative Neoplasms (MDS/MPN) Comprehensive Review 🔬🩸
📄 Guideline-Based Approach 🎯 WHO 2022 / NCCN / BSH / ELN
🔗 Reference: WHO 5th Ed (2022), NCCN, BSH, ELN
🆘 MDS/MPN is a group of overlapping hematologic disorders with features of both myelodysplasia & myeloproliferation 🚨.
Key Subtypes:
🔹 Chronic Myelomonocytic Leukemia (CMML) 🟤
🔹 Atypical Chronic Myeloid Leukemia (aCML) ⚪
🔹 MDS/MPN with Ring Sideroblasts and Thrombocytosis (MDS/MPN-RS-T) 🟣
🔹 MDS/MPN Unclassifiable (MDS/MPN-U) 🔘
⸻
🟥 Clinical Manifestations 🏥
🔹 CMML 🟤
✅ Monocytosis (>1 × 10⁹/L, Monocytes ≥10% WBC)
✅ Splenomegaly 🫛, Constitutional symptoms (weight loss, fever) 🌡️
✅ Cytopenias (Anemia, thrombocytopenia) & Dysplastic BM features 🔬
✅ Increased risk of AML progression (15-30%) 🚨
🔹 aCML ⚪
✅ Marked Leukocytosis (>13 × 10⁹/L), Dysplastic Neutrophils 🩸
✅ NO BCR-ABL fusion gene 🚫
✅ Splenomegaly 🫛
✅ High risk of AML transformation 🚨
🔹 MDS/MPN-RS-T 🟣
✅ Ring sideroblasts ≥15% in BM 🔬
✅ Thrombocytosis (PLT >450 × 10⁹/L) 📊
✅ SF3B1 mutation (~90%) 🧬
✅ Lower risk of transformation to AML 🚨
🔹 MDS/MPN-U 🔘
✅ Mixed features of MDS & MPN but doesn’t fit other categories
✅ Highly variable prognosis & therapy 🤷♂️
⸻
🟦 Diagnostic Criteria (WHO 2022) 🔍
✅ Overlap of dysplastic (MDS) & proliferative (MPN) features
✅ Absence of BCR-ABL1 fusion gene (excludes CML) 🚫
✅ Absence of rearrangements in PDGFRA, PDGFRB, FGFR1, PCM1-JAK2 🚫
✅ No previous MPN, MDS, or AML history
✅ Cytopenias (anemia, neutropenia, thrombocytopenia)
✅ Dysplastic bone marrow 🔬
🧪 Key Biomarkers:
🔹 CMML → TET2, ASXL1, SRSF2 🧬
🔹 aCML → SETBP1, ASXL1, NRAS 🧬
🔹 MDS/MPN-RS-T → SF3B1 🧬
📌 Cytogenetics:
✅ Normal or complex karyotype
✅ Del(7q), Del(5q), Trisomy 8 seen in CMML
⸻
🟡 Differential Diagnosis ❓
🔹 CML 🚨
🔸 BCR-ABL1+ (CML) vs. BCR-ABL1- (aCML)
🔹 MDS 🩸
🔸 More cytopenias, fewer proliferative features
🔹 MPNs (PV, ET, PMF)
🔸 No significant dysplasia
📌 Key Tests to Differentiate:
— BCR-ABL1 (CML vs. aCML) 🧬
— JAK2, CALR, MPL (ET, PMF, PV vs. MDS/MPN)
— SF3B1 (MDS/MPN-RS-T)
⸻
🟢 Risk Stratification (CMML Prognostic Models - CPSS, CPSS-Mol) 🎯
✅ Low Risk: 🎯
— WBC <13 × 10⁹/L
— No ASXL1 mutation
— Good cytogenetics
✅ High Risk: 🚨
— WBC >13 × 10⁹/L
— ASXL1 mutation 🧬
— Complex karyotype
⸻
🟠 Management 💊🩸
🔹 Supportive Therapy (All Patients)
✅ Transfusions for anemia (RBC) 💉
✅ Erythropoiesis-Stimulating Agents (ESA) if low EPO 💊
✅ Hydroxyurea for proliferative disease 💊
🔹 Disease-Modifying Therapy 🎯
✅ Hypomethylating Agents (HMA) (Azacitidine, Decitabine) 🔬
✅ Lenalidomide in MDS/MPN-RS-T (SF3B1-mutated cases) 💊
✅ Ruxolitinib for JAK2+ proliferative CMML 🎯
🔹 Curative Option 🚨
✅ Allogeneic Stem Cell Transplant (SCT) for high-risk cases 🏥
📌 Special Considerations:
— CMML with high WBC → Hydroxyurea to control count
— MDS/MPN-RS-T → Avoid cytoreduction unless symptomatic
— Transplant in young/high-risk patients
⸻
🔴 Complications & Monitoring 🔍
⚠️ Thrombosis & Bleeding (MDS/MPN-RS-T) 🚨
⚠️ Progression to AML (Highest in aCML & CMML) 🧬
⚠️ Splenomegaly & Constitutional Symptoms 🫛
⚠️ Cytopenias & Infections 🦠
📆 Follow-Up:
— CBC & BM monitoring every 3-6 months 📊
— Mutation tracking (ASXL1, SF3B1, TET2) 🧬
— Assess splenomegaly & thrombosis risk
⸻
📌 Key Takeaways
✅ MDS/MPN overlaps dysplastic & proliferative features 🔬
✅ CMML = Monocytosis + Cytopenia + AML risk 🟤
✅ aCML = Neutrophilia + Dysplasia, BCR-ABL- ⚪
✅ MDS/MPN-RS-T = Ring sideroblasts + Thrombocytosis (SF3B1+) 🟣
✅ Risk-based management (HMA, Hydroxyurea, SCT for high-risk) 🎯
🔬 MDS/MPN syndromes require careful risk stratification & personalized treatment!
#Hematology #MDSMPN #CMML #aCML #Myeloproliferative #Leukemia #BloodCancer
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Com cada dissabte podeu recuperar els continguts destacats de la setmana. Avui #8M parlem dels 15 anys del SIAD #ElPrat. També coneixerem la campanya "Llegir ens fa créixer!" @Mutua_Terrassa i la proposta literària de la psicoterapeuta Verónica Portillo.
open.spotify.com/episode/3JH3sA…
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🚨 ABRIL 2025 🚨 Reunión Presencial!🚨
@ICO_oncologia @HematICO_Hosp @HematoCanRuti @Hemato_Vhebron @hematosantpau @hematoclinicbcn
#CARTalunya

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