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1.
Ann Pathol ; 39(2): 144-150, 2019 Apr.
Artículo en Francés | MEDLINE | ID: mdl-30711337

RESUMEN

Medical education is currently facing great changes that affect all medical specialties, including anatomical pathology. Due to rapidly increasing medical knowledge and diagnostic complexity, we are living an era of teaching resources mutualization. We present different tools that allow large numbers of students to access courses, self-evaluations, and competencies assessments. MOOC platforms and e-learning platforms are central to these new online tools, which include the French National Platform of Medical Specialties, dedicated to the teaching of 50,000 medical residents in France. We also discuss "serious games" and the use of images and virtual slides in anatomical pathology teaching. These new modalities can deliver essential knowledge to large student populations, but they must be used in conjunction with adapted teacher-led courses focusing on competencies and professional skills in order to be fully effective.


Asunto(s)
Patología Clínica/educación , Educación a Distancia , Educación de Postgrado en Medicina/organización & administración , Educación de Postgrado en Medicina/estadística & datos numéricos , Francia
2.
J Clin Pathol ; 72(7): 453-459, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-31164443

RESUMEN

Clonal haematopoiesis (CH) is defined by the presence of acquired mutations and/or cytogenetic abnormalities in haematopoietic cells. By definition, these premalignant clones do not meet criteria for haematopoietic neoplasms listed in the Revised Fourth Edition of the WHO classification. CH is fairly common in elderly individuals and is associated with higher risks for haematological cancers, in particular myelodysplastic syndrome and acute myeloid leukaemia (AML), as well as cardiovascular events. Similar small clones have also been detected during follow-up in patients with AML in morphological remission, in individuals with aplastic anaemia, and in pre-chemotherapy blood samples from patients with other types of cancers. In each of these contexts, the presence of mutations carries different clinical implications, and sometimes demonstrates unique genetic profiles. Emerging research suggests that the number and identity of mutations, the size of the mutant clones and various other factors, including age, immune status and history of exogenous drugs/toxins, are important for disease biology and progression. This review focuses specifically on the subset of CH with gene mutations detected by sequencing, and includes discussions of nomenclature and molecular technologies that detect and quantify gene mutations.


Asunto(s)
Aberraciones Cromosómicas , Hematopoyesis/genética , Leucemia Mieloide Aguda/genética , Síndromes Mielodisplásicos/genética , Células Clonales , Humanos , Mutación
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