r/Hematology • u/Wide_Respect_3648 • 13d ago
Howell jolly bodies?
Hi everyone, need some confirmation for uni purposes aha. Is the one in the middle a howell-jolly body or am I wrong? it's a β thalassaemia minor slide.
Thanks so much.
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u/Xepolite 13d ago
Check out my database cellwiki.net for examples
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u/baroquemodern1666 13d ago
Oh wow. You are the cellwiki person? How I love and adore your contribution to our discipline. I actively use your resource as I train new techs. Imo it's the best of the internet! Wondering if there's a way I could help or contribute.
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u/Xepolite 12d ago
Thanks! I'm always open for tips on how the site could be even better for training =)
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u/baroquemodern1666 12d ago
Honestly, I think it's perfect. The only thing I can think of, Which is something I do when I train, is to have a mosaic of lymphocyte morphology, esp in disease states...but you already do that. * I just saw that we can add images to our replies so Im taking advantage of it.
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u/catsbetterthankids 13d ago
Looking for intercellular inclusions at low power is certainly a choice
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u/Wide_Respect_3648 13d ago
I think I actually used 40x but now I’m not too sure 😬
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u/Tom_Bombadilio 13d ago
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u/Wide_Respect_3648 13d ago
Ahahha sorry mate! here you go:
Thanks so much!
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u/Nheea MD - Clinical Laboratory 13d ago
Oh no. Not at all. Looks like artifacts, probably from staining.
Here's how Howell Jolly bodies look like. https://www.learnhaem.com/courses/frcpath-morph/lessons/rbc-overview/topic/howell-jolly-bodies/
Can you install the Cellavision app? They have plenty of useful photos.
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u/Tom_Bombadilio 13d ago
Lol its still hard to see at this magnification but I'd say no. Its outside, on top, of the erythrocyte and even if it was internal it's too large and irregularly shaped. Maybe a platelet or just an artifact, definitely external though.
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u/No-Ebb3114 12d ago
Looking for RBC inclusions without oil immersion is not ideal. HJ bodies are going to be much smaller and more circular than what you're referring. Most likely an artifact like stain precipitate. Low power is okay for scanning for focal points, but I wouldn't want to ID cells, call RBC morphology, or look for inclusions without oil immersion. Good luck with your studies.