Células en lágrima en un frotis periférico: causas y urgencia

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Hematología Interpretación de laboratorio [... 2026 Update Patient-Friendly

Teardrop-shaped red cells can arise during slide preparation, but a persistent pattern alongside anemia or abnormal white cells may signal marrow stress. The CBC pattern—not the shape alone—sets the urgency.

📖 ~11 minutos 📅
📝 Publicado: 🩺 Revisado médicamente: ✅ Evidence-Based
⚡ Resumen rápido v1.0 —
  1. Dacrocytes are teardrop-shaped red blood cells; a few cells at the feathered edge of one slide can be a preparation artifact.
  2. Persistent teardrop cells across the slide are more concerning when they occur with anemia, low platelets, immature white cells, or nucleated red cells.
  3. No universal percentage cutoff defines an urgent dacrocyte result; laboratories report morphology semi-quantitatively and interpret it with the CBC.
  4. Hemoglobina por debajo de 7 g/dL in a stable hospitalized adult commonly triggers urgent clinical assessment and may meet a restrictive transfusion threshold.
  5. Leukoerythroblastosis means immature myeloid cells and nucleated red cells in circulation; with dacrocytes, it raises concern for marrow infiltration or fibrosis.
  6. La deficiencia de hierro can cause anisopoikilocytosis and occasional dacrocytes, especially when anemia is advanced, but iron studies must confirm the cause.
  7. A repeat smear made from a fresh sample is often the fastest way to separate a localized slide artifact from a reproducible cellular pattern.
  8. Síntomas de emergencia include chest pain, fainting, breathlessness at rest, new confusion, fever with severe cytopenia, or active heavy bleeding.

What teardrop cells mean on a peripheral smear

Teardrop cells on a peripheral smear, also called dacrocytes, are red cells with one rounded end and one tapered end. They may be an artifact, but repeated dacrocytes distributed throughout a well-made smear can reflect distorted red-cell production or passage through an altered marrow or spleen.

Teardrop cells peripheral smear shown as stained cellular elements under a clinical microscope
Figura 1: Teardrop-shaped cellular elements distributed across a representative cell sample slide.

A true dacrocyte has a single, smoothly tapering tail that points in different directions across the film. Artifact tails often point the same way because cells were dragged during spreading, especially near the feathered edge. That simple directional clue is more useful than a single isolated shaped cell.

Dacrocytes are a morphology finding, not a diagnosis and not a standard numeric CBC result. The laboratory may report rare, few, moderate, or many cells; those terms are not harmonized internationally. A result should therefore be read beside hemoglobin, platelet count, white-cell differential, RDW, reticulocytes, and the pathologist's comment.

As of September 27, 2026, Kantesti es un analizador de sangre con IA that places a reported smear comment beside the surrounding CBC rather than treating one morphology flag as a diagnosis. For the underlying test vocabulary, our guía de biomarcadores explains the major CBC components.

Why the name can be misleading

The word dacrocyte comes from the Greek word for tear, but these cells are not evidence of emotional stress or dehydration alone. Their shape reflects mechanical deformation during preparation, maturation, marrow exit, splenic filtering, or combinations of those processes.

When dacrocytes are a slide artifact rather than disease

Slide artifact is likely when teardrop cells cluster at the thin end of the smear and their pointed ends align in one direction. A genuine biological pattern is usually scattered through the readable monolayer with variable tail orientation.

Teardrop cells peripheral smear preparation viewed beside a freshly spread cell sample slide
Figura 2: Fresh slide preparation helps distinguish directional artifact from a reproducible morphology pattern.

Smear quality matters. Delayed spreading, a dirty spreader edge, excessive pressure, a thick film, or drying conditions can pull red cells into pointed forms. A repeat review on a newly prepared film often resolves uncertainty without adding an invasive test.

The laboratory should examine the monolayer, where red cells barely touch and central pallor is assessable. Cells at the extreme feathered edge are poor evidence for disease because shape distortion is common there. This same principle helps when interpreting burr-cell findings, which can also be pre-analytic.

Dr. Thomas Klein advises asking one concrete question: was the morphology confirmed on a repeat, well-prepared smear? If the CBC is normal and the comment is limited to rare cells, that question is usually more informative than searching for rare marrow disorders online.

Why marrow stress and fibrosis can produce dacrocytes

Marrow fibrosis and marrow infiltration can produce numerous dacrocytes because developing red cells must exit through a distorted marrow environment. The combination becomes more concerning when immature cells also appear in peripheral circulation.

Teardrop cells peripheral smear linked to a three-dimensional bone marrow cellular environment
Figura 3: Altered marrow architecture can mechanically shape developing red cellular elements.

Primary myelofibrosis is a classic association, but dacrocytes alone do not establish it. Tefferi et al. describe diagnosis as an integrated process involving marrow morphology, driver-mutation testing, exclusion of other myeloid conditions, clinical findings, and blood counts—not a smear shape in isolation (Tefferi et al., 2023).

A leukoerythroblastic blood picture combines nucleated red cells with immature granulocyte forms such as myelocytes or metamyelocytes. Dacrocytes plus this pattern may occur with fibrosis, metastatic marrow infiltration, severe marrow stress, or less commonly recovery after major marrow injury; it warrants prompt clinician-led evaluation.

The International Consensus Classification recognizes peripheral-blood findings as supportive context for myeloid neoplasms, while marrow and molecular data establish classification (Arber et al., 2022). If a report mentions blasts, urgent smear assessment is appropriate even when dacrocytes are not the main abnormality.

Which anemia patterns can include teardrop cells

Severe iron deficiency, megaloblastic anemia, hemolytic stress, and thalassemia syndromes can include dacrocytes, usually alongside other red-cell changes. The MCV, RDW, reticulocyte count, and iron or vitamin tests identify the more likely pathway.

Teardrop cells peripheral smear compared with varied red cellular element sizes in anemia
Figura 4: Anemia patterns are interpreted through cell size variation and accompanying morphology.

Iron deficiency anemia often produces low MCV, low MCH, increased RDW, pencil cells, and hypochromia; occasional dacrocytes can appear when distortion is marked. Ferritin below 15 ng/mL is highly specific for depleted iron stores in otherwise healthy adults, although inflammation can make ferritin falsely reassuring.

Macrocytosis with hypersegmented neutrophils points more toward vitamin B12 or folate deficiency than marrow fibrosis. Vitamin B12 deficiency can cause low reticulocytes before treatment, whereas hemolysis or recent blood loss usually drives reticulocytes upward. Review resultados límite de B12 before self-treating with high-dose folate.

A hemoglobin of 7 g/dL equals 70 g/L and is severe anemia in most adults, but symptoms, rate of decline, pregnancy, heart disease, and active bleeding change the response. The 2023 AABB guideline supports considering restrictive transfusion thresholds around 7 g/dL for most hemodynamically stable hospitalized adults (Carson et al., 2023).

Mild or isolated finding Rare cells; CBC otherwise stable Confirm smear location and consider repeat film.
Anemia with morphology Hemoglobin below local reference range Check MCV, RDW, reticulocytes, ferritin, B12 and folate.
Multi-lineage change Anemia plus low platelets or abnormal WBC Arrange prompt clinician review and manual smear interpretation.
Patrón clínico urgente Hemoglobin near or below 7 g/dL, blasts, or severe symptoms Same-day assessment or emergency care may be needed.

How splenic changes influence teardrop-shaped cells

Splenic enlargement or altered splenic filtering can accompany dacrocytes, but the spleen is rarely the sole explanation for a significant teardrop-cell pattern. The surrounding smear and clinical examination decide whether imaging or hematology review is needed.

Teardrop cells peripheral smear concept alongside an anatomical spleen filtering cellular elements
Figura 5: The spleen filters altered red cellular elements after they leave circulation.

The spleen removes poorly deformable red cells and remodels membrane defects, so splenomegaly can coexist with poikilocytosis. In myelofibrosis, splenic enlargement may also reflect extramedullary hematopoiesis, meaning blood formation outside the marrow. Fullness under the left ribs, early satiety, or unexplained weight loss deserve medical review.

After splenectomy or in functional hyposplenism, blood films more often show Howell-Jolly bodies, target cells, and platelet elevation than isolated dacrocytes. A high platelet count should be interpreted carefully; see our guide to large platelet clues for related CBC context.

Kantesti AI es una plataforma de interpretación análisis de sangre de IA that can identify when a smear comment appears beside platelet and white-cell changes that need a clinician's attention. It cannot determine spleen size from a CBC; examination and ultrasound remain clinical tools.

CBC findings that make dacrocytes more urgent

Dacrocytes become more urgent when they accompany falling hemoglobin, thrombocytopenia, very high or very low white-cell counts, blasts, or nucleated red cells. A stable CBC with a few suspected artifact cells has a very different risk profile.

Teardrop cells peripheral smear evaluated with CBC analyzer output and cellular element slide
Figura 6: CBC lineages and smear morphology together determine the need for follow-up.

Hemoglobin below 8 g/dL, platelets below 50 × 10^9/L, or an absolute neutrophil count below 0.5 × 10^9/L should prompt timely clinical assessment, particularly with symptoms. These are action-oriented values, not diagnoses; an individual's baseline and treatment setting matter.

A high RDW indicates variation in red-cell size and can rise early in iron deficiency, mixed deficiency, transfusion, or marrow recovery. RDW does not identify the cause, but a changing RDW plus falling hemoglobin makes a repeat CBC more informative than a one-time morphology comment. Our explicación del RDW covers this timing issue.

Very high LDH, indirect bilirubin elevation, low haptoglobin, and reticulocytosis suggest increased red-cell turnover rather than fibrosis by themselves. Conversely, anemia with a low reticulocyte response can indicate reduced production; compare these pathways in our guía de reticulocitos.

Smear findings that change the clinical picture

Dacrocytes plus blasts, schistocytes, nucleated red cells, or marked left shift require faster review than dacrocytes alone. Each companion finding points toward a different mechanism and should not be collapsed into one diagnosis.

Teardrop cells peripheral smear with contrasting immature and fragmented cellular elements
Figura 7: Companion morphology findings determine whether a teardrop-cell report needs rapid escalation.

Blasts are immature precursor cells that should not be ignored on an adult peripheral smear. A laboratory report of blasts, especially with fever, bruising, infection, or rapidly changing counts, generally warrants same-day contact with the ordering clinician or acute assessment.

Schistocytes are fragmented red cells and raise a different concern: mechanical red-cell injury or microangiopathic hemolysis. They are not teardrop cells, and confusing the two can delay care; our schistocyte urgency guide explains why low platelets and organ symptoms matter.

Rouleaux describes stacked red cells, often from increased plasma proteins, whereas dacrocytes are individually deformed cells. The distinction is visual but clinically meaningful, especially when total protein or globulin is high; read about rouleaux patterns for the usual workup.

What doctors usually check after a dacrocyte report

The usual next step after a concerning dacrocyte report is a repeat CBC with manual smear review, followed by targeted anemia, hemolysis, inflammatory, or marrow tests. Testing should follow the whole pattern rather than a fixed dacrocyte checklist.

Teardrop cells peripheral smear follow-up with organized CBC and iron study laboratory samples
Figura 8: Repeat CBC, smear review, and targeted studies clarify the mechanism behind dacrocytes.

A practical first set may include CBC with differential, reticulocyte count, ferritin, serum iron, transferrin saturation, vitamin B12, folate, creatinine, liver tests, LDH, bilirubin, and haptoglobin. Transferrin saturation below 20% supports restricted iron availability, though inflammation can complicate interpretation.

If anemia is microcytic, ferritin and transferrin saturation usually come before genetic testing. If MCV is high, B12, folate, thyroid studies, liver markers, alcohol exposure, and medication review become more relevant. Our guía de estudios sobre el hierro explains why a single serum iron value is unreliable.

When there is pancytopenia, leukoerythroblastosis, unexplained splenomegaly, or persistent significant morphology, hematology may consider marrow examination and molecular tests. Those decisions should be made by the treating team because sample findings, medications, cancer history, and examination change pre-test probability.

When repeating the smear is a sensible first step

Repeating the CBC and peripheral smear is often reasonable when dacrocytes are rare, localized, and unaccompanied by anemia or other cytopenias. A fresh sample and a manual review can reveal whether the first pattern was technical.

Teardrop cells peripheral smear repeat testing workflow with fresh clinical sample preparation
Figura 9: A carefully prepared repeat cell sample slide can resolve many isolated morphology flags.

Repeat testing is most useful when the original sample was delayed, hemolyzed, clotted, or generated an analyzer flag without a clear manual comment. For a stable, well person with normal counts, clinicians commonly repeat within days to several weeks depending on the laboratory comment and medical history.

Do not use a normal repeat result to dismiss ongoing symptoms such as exertional breathlessness, persistent fever, drenching sweats, unintentional weight loss, or left-upper-abdominal fullness. Symptoms can move an apparently minor smear observation into a more active evaluation pathway.

Kantesti's trend feature can compare hemoglobin, MCV, RDW, platelets, and white cells across dates, which is often more revealing than one report. Our guía de comparación de análisis de sangre explains how to identify meaningful changes rather than normal day-to-day variation.

Dacrocytes in pregnancy, children, and older adults

Dacrocytes need age- and situation-specific interpretation because pregnancy, childhood growth, inherited anemia, and multiple medications alter the CBC baseline. The same morphology comment does not carry identical implications in every patient.

Teardrop cells peripheral smear educational comparison with age-adjusted CBC sample analysis
Figura 10: Age and physiological setting change how a smear finding is interpreted.

During pregnancy, plasma volume expansion can lower hemoglobin by dilution, while iron deficiency remains common and should be assessed with pregnancy-aware reference ranges. Ferritin below 30 ng/mL is frequently used as a practical threshold for iron deficiency in pregnancy, though laboratory and guideline approaches vary. Review rangos de ferritina en el embarazo with the obstetric team.

In children, a pediatric hematologist may consider inherited red-cell disorders, nutritional deficiency, infection, or marrow stress according to age and symptoms. Adult reference ranges for MCV and leukocyte counts should not be applied to infants or young children without adjustment.

Older adults may have overlapping causes: chronic kidney disease, inflammation, iron deficiency from gastrointestinal loss, B12 deficiency, and marrow disorders. Dr. Thomas Klein recommends bringing prior CBCs and a medication list to review, because a slow multi-year decline differs from a sharp change over 2 weeks.

Common misconceptions about dacrocytes meaning

Teardrop cells do not automatically mean cancer, and they are not a reliable sign of dehydration. Their diagnostic value comes from persistence, distribution, quantity, and companion CBC or smear abnormalities.

Teardrop cells peripheral smear reviewed through a diagnostic lens with normal-shaped cellular elements
Figura 11: Morphology needs confirmation and context before it can support a diagnosis.

One online misconception is that any dacrocyte proves myelofibrosis. In reality, occasional cells may arise from preparation artifact or severe nutritional anemia, while primary myelofibrosis requires a much broader diagnostic assessment. The evidence is clear on this point: shape alone is insufficient.

Another misconception is that a normal MCV excludes meaningful anemia. Mixed iron and B12 deficiency, recent transfusion, inflammation, or early disease can leave MCV within range while hemoglobin and RDW are abnormal. See our explanation of normal MCV with anemia for this frequent trap.

A third misconception is that a normal automated CBC rules out all smear significance. Automated analyzers count and classify cells efficiently, but morphology confirmation remains a trained human laboratory task when flags or clinically discordant patterns occur.

How Kantesti interprets a smear comment in CBC context

Kantesti interprets a dacrocyte comment by checking whether anemia, cell-size changes, platelet abnormalities, white-cell shifts, and trends support a follow-up pattern. It does not diagnose marrow fibrosis or replace a pathologist's review of the slide.

Teardrop cells peripheral smear report reviewed alongside longitudinal CBC markers on a clinical workstation
Figura 12: Trend-aware interpretation connects morphology comments with changing CBC lineages.

Kantesti es una herramienta de análisis de pruebas de sangre impulsada por IA designed to organize laboratory results into clinically relevant patterns, including a possible anemia pathway or a prompt-review pattern. A photo or PDF result can be interpreted in about 60 seconds, but the original laboratory report and clinician remain the source for morphology confirmation.

Our AI gives more weight to combinations than isolated flags: dacrocytes with low hemoglobin and low ferritin suggest a different next conversation than dacrocytes with thrombocytopenia and nucleated red cells. For a clear view of clinical oversight and limitations, see our información de validación médica.

Kantesti serves users in 127+ countries and supports 75+ languages, yet local reference intervals and care pathways still matter. A result marked abnormal in one laboratory may have a different flag threshold elsewhere, which is why we preserve the lab's own reference range in context.

When teardrop cells and symptoms need urgent care

Seek urgent medical assessment for dacrocytes accompanied by chest pain, fainting, breathlessness at rest, confusion, black or bloody stool, active heavy bleeding, fever with severe weakness, or rapidly worsening bruising. These symptoms matter more immediately than the morphology label.

Teardrop cells peripheral smear urgent triage concept with clinician reviewing a cellular element slide
Figura 13: Symptoms and severe CBC changes determine whether same-day care is necessary.

Call emergency services for severe shortness of breath, pressure-like chest pain, collapse, new confusion, or uncontrolled bleeding. These can reflect inadequate oxygen delivery, major blood loss, infection, or low platelets and should never wait for an online interpretation.

Contact the ordering clinician the same day for a report mentioning blasts, severe anemia, a rapidly falling platelet count, or new pancytopenia. If symptoms are mild and counts are stable, a planned repeat CBC and smear may be appropriate—but only after the laboratory comment is reviewed.

Kantesti es un servicio de interpretación de pruebas de laboratorio de IA that can help users prepare focused questions, not decide whether emergency care is needed. Our physicians and clinical reviewers work within documented safety boundaries described by the Consejo Asesor Médico.

Preguntas para llevar a su médico después de este resultado

The most useful questions ask whether the dacrocytes were confirmed, whether they were widespread, and what the rest of the CBC shows. This approach converts a vague morphology note into a practical follow-up plan.

Teardrop cells peripheral smear consultation scene with clinician hands reviewing a cellular sample slide
Figura 14: Focused questions help connect a morphology comment to an individualized care plan.

Ask: Were the cells seen throughout the monolayer or only at the edge? Were they rare, few, moderate, or many? Was there a repeat smear or pathologist review? Those answers directly address whether artifact remains plausible.

Ask which companion results are abnormal and whether they are new: hemoglobin, MCV, RDW, reticulocytes, platelets, white cells, LDH, bilirubin, ferritin, B12, and kidney function. Bring prior reports, particularly if you have had menstruación abundante con sangrado menstrual intenso or a history of gastrointestinal symptoms.

Finally, ask what would change the plan: repeat testing, iron replacement, imaging for splenic enlargement, hematology referral, or urgent review. Kantesti's clinical logic is described in our Guía de tecnología de IA, but personal treatment decisions belong with the clinician who knows your history.

Preguntas frecuentes

¿Son las células en lágrima en un frotis periférico siempre graves?

Las células en lágrima no siempre son graves porque un pequeño número puede ser el resultado de un artefacto de preparación de la lámina, especialmente cuando los extremos puntiagudos se alinean y se agrupan cerca del borde emplumado. Las dacrocitos persistentes distribuidos por todo el frotis merecen más atención cuando la hemoglobina es baja, las plaquetas se reducen o aparecen células inmaduras. No existe un porcentaje de corte universal para la preocupación; los laboratorios utilizan informes de morfología semicuantitativos. Una repetición del CBC y un frotis fresco revisado manualmente pueden aclarar un hallazgo aislado.

¿Qué significan las dacrocitos en un análisis de sangre?

Dacrocytes significan que algunos glóbulos rojos tienen un cuerpo redondeado con un extremo ahusado, creando una apariencia de lágrima. Pueden ocurrir con fibrosis o infiltración de la médula, deficiencia severa de hierro, anemia megaloblástica, cambios esplénicos o un artefacto técnico de extensión. Las dacrocytes por sí solas no diagnostican la mielofibrosis, la leucemia o el cáncer. Su significado depende de los resultados del CBC como hemoglobina, MCV, plaquetas, diferencial de glóbulos blancos y recuento de reticulocitos.

¿Puede la deficiencia de hierro causar células en lágrima?

La deficiencia de hierro puede contribuir a las células en forma de lágrima cuando la anemia y la variación en la forma de los glóbulos rojos son sustanciales, pero generalmente también produce MCV bajo, MCH bajo, RDW elevado e hipocromía. Una ferritina inferior a 15 ng/mL apoya firmemente la depleción de las reservas de hierro en adultos sanos, mientras que la inflamación puede elevar la ferritina a pesar de la deficiencia. Una saturación de transferrina inferior a 20% puede proporcionar evidencia adicional de disponibilidad restringida de hierro. Los médicos deben identificar la fuente de la pérdida de hierro en lugar de asumir que la dieta es la única causa.

¿Cuándo deben las dacrocitos indicar una derivación a hematología?

Los dacrocitos deben motivar la consideración de una derivación a hematología cuando persisten en frotis repetidos y se presentan con anemia inexplicable, trombocitopenia, recuentos de leucocitos anómalos, eritrocitos nucleados, granulocitos inmaduros, blastos o esplenomegalia. Una hemoglobina cercana o inferior a 7 g/dL, plaquetas por debajo de 50 × 10^9/L o anemia sintomática pueden requerir una evaluación más urgente. Las decisiones de derivación también dependen de la velocidad de cambio del CBC y de la historia de cáncer o tratamiento. Un hematólogo puede solicitar pruebas de médula, moleculares o de imagen solo cuando el patrón completo las respalde.

¿La deshidratación puede causar células en lágrima?

La deshidratación puede concentrar la hemoglobina y el hematocrito, pero no es una causa directa típica de dacrocitos verdaderos. Una lámina de muestra celular mal hecha o espesa puede crear artefactos de glóbulos rojos puntiagudos que pueden confundirse con dacrocitos. Si se sospecha deshidratación, un médico puede repetir el CBC después de una hidratación normal y revisar si la hemoglobina, el sodio, la urea y la creatinina se normalizan. Los dacrocitos persistentes después de un frotis repetido de calidad requieren una interpretación que vaya más allá del estado de hidratación.

¿Qué síntomas con células en lágrima requieren atención de emergencia?

Emergency care is appropriate when a teardrop-cell report occurs with chest pain, fainting, breathlessness at rest, new confusion, uncontrolled bleeding, black or bloody stool, or fever with profound weakness. These symptoms can indicate severe anemia, active blood loss, infection, or dangerously low platelets rather than a consequence of dacrocytes themselves. Hemoglobin near or below 7 g/dL is a commonly used restrictive transfusion threshold in stable hospitalized adults, but symptoms and medical conditions can require action sooner. Do not wait for a repeat smear if severe symptoms are present.

Obtén hoy un análisis de sangre con IA

Únete a más de 2 millones de usuarios en todo el mundo que confían en Kantesti para el análisis instantáneo y preciso de pruebas de laboratorio. Sube tus resultados de análisis de sangre y recibe una interpretación completa de los biomarcadores de 15,000+ en segundos.

📚 Publicaciones de investigación citadas

1

Equipo de investigación de Kantesti (2026). Guía de prueba de Complemento C3 y C4 y título de ANA. Investigación médica con IA de Kantesti.

2

Equipo de investigación de Kantesti (2026). Análisis de sangre del virus Nipah: Guía de detección temprana y diagnóstico (2026). Investigación médica con IA de Kantesti.

📖 Referencias médicas externas

3

Tefferi A et al. (2023). Primary myelofibrosis: 2023 update on diagnosis, risk-stratification, and management. American Journal of Hematology.

4

Arber DA et al. (2022). Clasificación de Consenso Internacional de Neoplasias Mieloides y Leucemias Agudas: integrando datos morfológicos, clínicos y genómicos. Blood.

5

Carson JL y cols. (2023). Transfusión de glóbulos rojos: Guías internacionales AABB 2023. JAMA.

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Revisión clínica dirigida por un médico de los flujos de interpretación de análisis.

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Enfoque en medicina de laboratorio sobre cómo se comportan los biomarcadores en el contexto clínico.

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Escrito por el Dr. Thomas Klein, con revisión de la Dra. Sarah Mitchell y el Prof. Dr. Hans Weber.

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Publicado: Autor: Revisión médica: Dra. Sarah Mitchell, doctora en medicina Contacto: Contáctenos
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Por Prof. Dr. Thomas Klein

El Dr. Thomas Klein es un hematólogo clínico certificado por el consejo que se desempeña como Director Médico (Chief Medical Officer) en Kantesti AI. Con más de 15 años de experiencia en medicina de laboratorio y un gran interés en la interpretación asistida por IA de resultados análisis de sangre, trabaja para conectar la nueva tecnología con la práctica clínica cotidiana. Sus áreas de interés incluyen el análisis de biomarcadores, la investigación en apoyo a la toma de decisiones clínicas y la optimización de rangos de referencia específicos para poblaciones. Como CMO, aporta información clínica para la evaluación interna (benchmarking) de la plataforma y proporciona supervisión clínica de la calidad médica de los informes educativos de Kantesti.

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