One of the difficult aspects of #hemepath training is time management in a high-paced/demanding environment & the ability to multitask effectively while learning a difficult discipline. Every yr I offer our fellows helpful tips I’ve learned so far 🧵👇🏻More tips welcome,pls add 1/
Get rid of paper…
Don’t do anything twice
Take ownership of your cases… they are just as much yours as they are your faculty’s
Bookmark your frequently visited websites… saves you a lot of time over the year… here are some of mine! Shoutout to @hematogones for his awesome BM diff calculator
Use social media… it will accelerate your learning, networking opportunities and will expand your professional circle
Your time is your most valuable commodity! I realize you don’t make a lot of money as a trainee but invest in yourself… use your time wisely… it’s ok to accumulate some debt!
Aim for perfection…. Your definition of perfection will evolve with time… don’t shortchange yourself!! This is your opportunity to learn!!
And finally…. Appreciate the opportunity you have as a trainee… this is your only time to make mistakes that are mostly inconsequential….the goal is to learn from your mistakes!! Give yourself the time and freedom to learn and enjoy yourself…. Happy learning all!!!
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Just another ordinary day at #hemepathMDA … 🤯
60-70 y/o woman
To all brave #hemepath aficionados how would you classify this case?
Poll and individual high quality images below. Pls comment if you’re feeling particularly brave today, let’s talk new #WHO 😎
The story of 1 day in the life of a #hematopathologist… I’m too exhausted to make a fancy educational thread but here are some amazing 🔬 pics for your viewing pleasure. I diagnosed all cases in one day 🤯 only at @MDAndersonNews Happy almost weekend people 🥂 #hemepath 🧵 1/n
Myeloproliferative neoplasm w/ concurrent BCR::ABL1 and JAK2 V617F ..the megekaryocyte morphology is clue to something beyond CML #mpnsm#PathOutPic 2/
BPDCN with perfect so-called “hand mirror” (red) and “pearl necklace” (black) morphology #BPDCN#PathOutPic 3/
WT1 mutations are present in ~7% of de novo AML, are typically Lof mutation involving exons 7-9 of the gene. They frequently (~15%) co-occur w/ NPM1mut & have detrimental impact in this setting, shown by @AkEisfeld and colleagues in bit.ly/3eWQtXw@LeukemiaJnl
We studies a cohort of de novo NPM1-mut AML. 7% had concurrent WT1 mutations at baseline. 22% (15/67) relapsed; 4 (27%) with newly acquired Lof WT1-mut. Illustrated by @furudateken