Faculty/Authors
CME or CMLE Credit: 2.0 Estimated Completion Time: 2 hoursFormat: Online Educational Activity and Post Exam Physician Competencies: Patient Care, Medical KnowledgeEligibility for CME/CMLE credit: Max three attempts. You will have a maximum of three attempts to meet the following criteria:
Default Credit Type: None (You must meet the eligibility requirements in order to obtain CME credit.) Accreditation Statement: The American Society for Clinical Pathology (ASCP) is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education (CME) for physicians. This activity has been planned and implemented in accordance with the Essential Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME).Credit Designation Statement: The American Society for Clinical Pathology (ASCP) designates this enduring material for a maximum of 2 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Instructions
To claim CME credit for the exercise, do the following:
To claim CMLE credit for the exercise, do the following:
Faculty Disclosures
Technical ConsiderationsRelease Date: 2/28/2025 Review Date:Expiration Date: 12/31/2027
understand the rationale and importance for including the new entity of myeloid neoplasms (MNs) with germline predisposition in the revised 4th edition WHO Classification of Myeloid Neoplasms and Acute Leukemia and the update on this entity in the 5th edition WHO and the 2022 ICC classifications;
be familiar with the unique clinicopathologic features of DDX41 germline predisposition syndrome;
understand the importance of distinguishing between premalignant DDX41 germline predisposition syndrome and neoplastic myelodysplastic syndrome (MDS) with DDX41 germline predisposition;
recognize the diagnostic challenges and pitfalls in the diagnosis of MDS with deleterious DDX41 germline variants and their consequential impact on clinical management;
know how to avoid over- and under-diagnosing MDS in patients with deleterious DDX41 germline variants by using the diagnostic algorithm and pearls provided by this article; and
suggest and/or conduct molecular/genetic tests on appropriate samples for DDX41 and other germline predispositions based on their practical considerations and available information and resources.