""Diagnostic Flow Cytometry: Case-Based Problem Solving" as presented at the 2022 WASPaLM Meeting, Punta del Este, Uruguay, October 1, 2022"
Learning Objectives:
Define the basis of NGS.
Explain the difference between whole-genome sequencing, whole exome sequencing and hot spot panels and identify the best option for clinical application.
Below is a list of questions received from the live webinar attendees. Click on any question to reveal the speaker's response.
NEW QUESTION/ANSWER
It is common to see necrosis in cHL, hard to put a number on it offhand.
NEW QUESTION/ANSWER
Classic in the 2017 WHO
NEW QUESTION/ANSWER
It can be expressed in both CHL and ALCL so it may not be reliable.
NEW QUESTION/ANSWER
CD15, CD30, CD20, PAX5, OCT2, BOB1 and CD45 can be helpful.
NEW QUESTION/ANSWER
I have never seen this.
NEW QUESTION/ANSWER
No, there is no clinical role for this at present.
NEW QUESTION/ANSWER
This would be highly unusual
NEW QUESTION/ANSWER
I don’t have any experience with J chain but is usually negative in RS-cells. MUM1 is typically positive but not specific.
NEW QUESTION/ANSWER
No
NEW QUESTION/ANSWER
Yes. J-chain and MEF2B have been reported to be useful as well. PMID: 28851661
NEW QUESTION/ANSWER
I don’t think it is particularly helpful, some cases of cHL may have rearranged IGH
NEW QUESTION/ANSWER
No
NEW QUESTION/ANSWER
I don’t find it that helpful
NEW QUESTION/ANSWER
There has been some data to suggest it is prognostic.
NEW QUESTION/ANSWER
It does not appear to commonly result in loss of CD30 expression in follow-up biopsy but I don’t believe this has been extensively studied.
NEW QUESTION/ANSWER
Yes, for T-cell lymphomas including cutaneous T-cell lymphomas it is reasonable to report the % positive tumor cells because some trials that resulted in the approval of brentuximab used specific cutoffs.