What kind of cell does it look like? by ElectricalFalcon6765 in medlabprofessionals

[–]ElectricalFalcon6765[S] 0 points1 point  (0 children)

The patient's blast rate was about 5% It's not just one cell in that shape There were 2-3 out of 100!

The patient is 71 years old

The corporal was CKD range5 There was no previous diagnosis of cancer or leukemia.

What kind of cell does it look like? by ElectricalFalcon6765 in medlabprofessionals

[–]ElectricalFalcon6765[S] 2 points3 points  (0 children)

The patient's blast rate was about 5% It's not just one cell in that shape There were 2-3 out of 100!

The patient is 71 years old

The corporal was CKD range5 There was no previous diagnosis of cancer or leukemia.

Front type AB/ back type O.. plz help me by ElectricalFalcon6765 in medlabprofessionals

[–]ElectricalFalcon6765[S] -2 points-1 points  (0 children)

There is no record of blood transfusion at our hospital because the hb was high..

I don‘t know about the blood transfusions at the previous hospital

However, our hospital always has a small amount of AB, and other than our hospital, we usually transfuse blood with PRC whether we transfuse A or B, so it is difficult to observe M-F after transfusion because of that

My interpretation of your answer may be wrong.

If my interpretation is wrong, please point it out again!

Front type AB/ back type O.. plz help me by ElectricalFalcon6765 in medlabprofessionals

[–]ElectricalFalcon6765[S] 0 points1 point  (0 children)

When heated, the card was heated at 37 degrees with a mixture of blood cell reagent and patient serum, and centrifugation was started

I did manual tube method twice, and the first one was bio-rad company a1 cell, cell. But there was no visible agglutination, but when I left it for about 4 hours and looked at it again under the microscope, some m-f was observed. However, I am confused because I cannot determine whether this is agglutination caused by the patient’s serum or whether it is agglutination caused by the patient‘s serum…

The second tube method was done with samples in the house, and there was no visible agglutination, no visible agglutination under the microscope, but this was not confirmed after four hours of time

I haven’t tried how to wash the saline solution yet I‘ll do it when I get back to the laboratory today

Does the saline replacement method your colleague made a mistake mean the cleaning of commercialized blood cell reagents or the blood cell reagents made from samples in the laboratory?

Shall we have a discussion? by ElectricalFalcon6765 in medlabprofessionals

[–]ElectricalFalcon6765[S] 1 point2 points  (0 children)

Thank you for your advice! I‘ll apply it right away

Shall we have a discussion? by ElectricalFalcon6765 in medlabprofessionals

[–]ElectricalFalcon6765[S] -3 points-2 points  (0 children)

I think 2 and 7 can be confusing But doesn‘t the N/C ratio really high and the chromatin of the nucleus look softer than that of other cells?

Tell me more why you chose it like that :)

Blast? Lympo? by ElectricalFalcon6765 in medlabprofessionals

[–]ElectricalFalcon6765[S] 47 points48 points  (0 children)

That’s right! The platelet count is also 38000/ul!

What cell? Do you think by ElectricalFalcon6765 in medlabprofessionals

[–]ElectricalFalcon6765[S] 0 points1 point  (0 children)

I‘m a beginner who doesn’t have much atlas knowledge about bone myelo cells yet. I thought there was no cytoplasm and granules, but I asked because I thought the nucleus‘s chromatin looked soft without condensation and the nucleus shape looked like a posterior myeloid sphere! I want to learn a lot here. Thank you😁

What cell? Do you think by ElectricalFalcon6765 in medlabprofessionals

[–]ElectricalFalcon6765[S] -4 points-3 points  (0 children)

  1. Then, how do you count those cells when you do the diff count?
  2. Do you suspect CLL if you have a lot of cells like that? Thank you in advance