LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Fry blood smear -- help me understand it?

 - UBBFriend: Email this page to someone!    
Author Topic: Fry blood smear -- help me understand it?
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Can anyone explain to me why bartonella in a lot of blood smears seems to exist outside of the red blood cell, as in these Dr. JS pictures:
http://www.personalconsult.com/articles/bartonellabloodsmears.html

Whereas in mine (below) it seems to be fully inside the cell? What does it all mean?


Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
jamescase20
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
How can you tell there fully inside the cell, if they are fully inside the cell, you CANT see them. There sitting on the outside, attached to the cells outter wall.
IP: Logged | Report this post to a Moderator
painted turtle
LymeNet Contributor
Member # 7801

Icon 1 posted      Profile for painted turtle   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
What does the text underneath the picture say?

You can always call the lab and ask questions if you need to.

--------------------
www.lymefire.blogspot.com

Posts: 855 | From United States of Mind | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Those are bizarre. I've never seen it clustered like that.

Usually, with babesia, there is a circle or X shape in the blood cell.

What does it say on the blood slide?

You can call the lab and ask.

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
disturbedme
Frequent Contributor (1K+ posts)
Member # 12346

Icon 1 posted      Profile for disturbedme   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yeah, I'd call and ask Fry Labs about it. I'm sure they'll be very helpful.

Mine's like the ones you saw that are on the outside of the cell:

 -

Also, if you call them and ask Fry about it, please tell us what they say! [Smile]

--------------------
One can never consent to creep when one feels an impulse to soar.
~ Helen Keller

My Lyme Story

Posts: 2965 | From Land of Confusion (bitten in KS, moved to PA, now living in MD) | Registered: Jun 2007  |  IP: Logged | Report this post to a Moderator
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
The text next to the slide says:
"Many coccobacilli adherent to erythrocytes indicated with arrows. This is suggestive of bartonella spp."

My bartonella IgG was 1:64 (B. quintana & hensalae). I was negative at Fry for babs, ehrlichia, ANA, and anaplasma.

Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
painted turtle
LymeNet Contributor
Member # 7801

Icon 1 posted      Profile for painted turtle   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hmmmmm....I'd call the lab ASAP if I were you and inquire about it.

--------------------
www.lymefire.blogspot.com

Posts: 855 | From United States of Mind | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
Gabrielle
LymeNet Contributor
Member # 5329

Icon 1 posted      Profile for Gabrielle     Send New Private Message       Edit/Delete Post   Reply With Quote 
Did you notice that in Disturbed's blood smear Fry says: "This is consistent with Bartonella ssp." and in LymeCFIDSMCS's picture they say: "This is suggestive of bartonella spp."?

In my picture there was only 1 coccobacillus and they also said: "This is suggestive of bartonella spp."

Does that mean they are not sure which kind of bacilli one can see in LymeCFIDSMCS's and my blood?

Gabrielle

Posts: 767 | From Germany | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Okay I just talked to a lab tech and Fry and this is what he said:

He said that since a slide is a 2-dimensional representation of a 3-dimensional object, cells may just be facing away, so the bartonella may actually be on the outside and not the inside, just on the outside facing the viewer.

I said well it's kind of weird that all six of the marked cells on my slide would be facing the same direction. . . He also said it could be a species of bartonella that likes to lodge in the concave part of the red blood cells. I asked if he knew what species of bart. do that and he said the research isn't out yet.

Now I really want to talk to anyone else who has a slide similar to mine, because perhaps we have a similar species?

Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
aiden424
LymeNet Contributor
Member # 7633

Icon 1 posted      Profile for aiden424     Send New Private Message       Edit/Delete Post   Reply With Quote 
It seems like there have been several people who have had Bart IgG 1:64 results from the Fry Bart test. Is that unusual, or maybe I'm mistaken?

Kathy

--------------------
You never know how strong you are until being strong is the only choice you have.

Posts: 807 | From South Dakota | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Am I nuts or does my blood smear kind of resemble this one of bartonella bacilliformis:

http://web.mst.edu/~microbio/BIO221_2004/B_bacilliformis.htm

I'm not saying I have this strain (I've never been to S. America, for one, so it makes no sense), just that this type of bartonella seems to behave more as the lab tech suggested.

This article notes that "B. bacilliformis can adhere to and enter red blood cells and its continued interaction leads to extensive deformation of the red cell surface, as pits and invaginations develop."

Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
WOW, that's very interesting.

Every bart slide I've seen have them sticking to the side of the cell.

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
mikej2323
LymeNet Contributor
Member # 8913

Icon 1 posted      Profile for mikej2323     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yeah, that is strange...every other time I've followed a Fry smear thread, it always states "adherent".

Our "text" said exactly the same thing...same titer result, too.

How did you get a copy of the slide? We only got a fax and it's not very clear.


Mike
[email protected]

www.caringbridge.com/visit/angelsforalex

Posts: 252 | From Iowa | Registered: Mar 2006  |  IP: Logged | Report this post to a Moderator
Tumble weed
Junior Member
Member # 15362

Icon 1 posted      Profile for Tumble weed     Send New Private Message       Edit/Delete Post   Reply With Quote 
[IMG]  - [/IMG]

Here is my pic

moderate number of coccobacilli adherent to erythrocytes this is suggestive of bartonella spp.

Posts: 9 | From Myerstown Pa | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
That last slide looks a lot more like mine -- maybe we have the same strain? What are your main bart symptoms?

I got the copy of the slide from my doctor.

Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
jamescase20
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
NO, it MAKES perfect sense. YOU PROBLY DO HAVE THE STRAIN from s. america. My cat had, MANY years ago, classic signs of Bart 1, carrions disease, which said to exist ONLY in the mountains in s. america. Dont forget, airplanes fly, bring people, alliens cross our boarders. Etc. The doctors just dont know it yet.
IP: Logged | Report this post to a Moderator
jamescase20
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
BART 23, the new discovered bart found in someone who flew back from s america in 2006, looked exactly like bart no 1, but it turned out to be a new discovered strain, the lady infected lived in San Fran. I have a strong hunch, this is the new bart most of us have. But this bart, no rash, just the sores. Purple wort, LATER in infection, sometimes no sore, or 1 sore. Weak imunne sys has MANY sores. This is what adis victims broke out with in the early 90s
IP: Logged | Report this post to a Moderator
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
So the purple sores look like Kaposi's Sarcoma? Is that what you're saying? Wow. I have had the crimson crescents typical of CFIDS (back of throat) that some postulate have a relationship to Kaposi's Sarcoma sores.

I think my bart symptoms most closely match accounts I have read of bartonella vinsonii, which is in dogs and coyotes and causes a lot of cardiac problems. It has been written up in at least one or two human cases as well.

Can someone explain why they can test for these species in coyotes but not in me though? Do I have to see a veterinarian?

Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
Tumble weed
Junior Member
Member # 15362

Icon 1 posted      Profile for Tumble weed     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi my main problem is tired ,very tired what is your main problem lymecfidsmcs ??
Posts: 9 | From Myerstown Pa | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've got epic tiredness too, different from the CFIDS I had before bart. But my main problems are cardiac and neurological. The tired is really bad though: I feel in a total fog most of the time.
Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
christinelyme2
Member
Member # 15028

Icon 1 posted      Profile for christinelyme2     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi! I was wondering if anyone else has

the numbness and tinglyness on different parts

of their body? I also have spots on my MRI's

and doctors think I have MS. I was diagnosed

with lyme two years ago. Now I'm going to see a

specialist for the first time next week. What

questions are good to ask? [confused]

Posts: 27 | From pa | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
mikej2323
LymeNet Contributor
Member # 8913

Icon 1 posted      Profile for mikej2323     Send New Private Message       Edit/Delete Post   Reply With Quote 
LymeCFIDSMCS-

Those crimson crescents are a commonplace with mycoplasma. Don't know if you have looked into that much.

How did you go about getting a quality slide on your computer? Did you scan it? Ours was faxed and it's not clear.

Mike
[email protected]

www.caringbridge.com/visit/angelsforalex

Posts: 252 | From Iowa | Registered: Mar 2006  |  IP: Logged | Report this post to a Moderator
Tumble weed
Junior Member
Member # 15362

Icon 1 posted      Profile for Tumble weed     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi the doc will get the pics / my pic took 2-3wks after the fax I scand them i'm not sure that it is bart the levaquin is not working??? What kind of( what )is in cells

[ 05. May 2008, 01:52 PM: Message edited by: Tumble weed ]

Posts: 9 | From Myerstown Pa | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
That's interesting about the mycoplasma/crimson crescents connection. I had read that the crescents could be a manifestation of the herpes virus (HHV-7? 8?) that causes Kaposi's Sarcoma in AIDS patients.

I did test for mycoplasma many years ago with Garth Nicolson's lab when he was finding high percentages of CFIDS patients and Gulf War vets with mycoplasma in their blood and treating with long-term antibiotic. My tests then were negative.

I had a really clear picture that my doc sent me and scanned it -- I'm sure you'll be able to get one.

Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
tickbattler
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Hi there,

I just wanted to mention that my husband's Fry lab smear looked exactly like yours and he tested positive for bart quintana at 1:64. They wrote the same description on the smear as yours.

My husband also has lyme and babesia. The babesia came back at 1:64, but they did not mention seeing it in the smear.

We think he has had lyme since summer of 06 and started treatment in Sept 07. His current symptoms are headache, fatigue, brain fog and motion sickness. He is able to function and work but it is hard for him. He used to have many more symptoms such as insomnia, muscle pain, head buzzing, frequent urination, nausea.

Hope this helps,

tickbattler

IP: Logged | Report this post to a Moderator
Aligondo Bruce
LymeNet Contributor
Member # 6219

Icon 1 posted      Profile for Aligondo Bruce     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am wondering if someone can tell me HOW to get the good photos of the slides from FRY. All they sent me was a crappy xerox (from my docs office) and you can't tell anything, at all. I want the actual photos.

I found the people at fry to be very unhelpful.

Posts: 523 | From Stillwater,OK,USA | Registered: Sep 2004  |  IP: Logged | Report this post to a Moderator
skigal
LymeNet Contributor
Member # 7443

Icon 1 posted      Profile for skigal     Send New Private Message       Edit/Delete Post   Reply With Quote 
Bruce, since YOU paid for the test, ask your doc for the original color picture. Doc's office can keep the xerox copy.
Posts: 269 | From VA | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.