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Lab results - looking for opinions [PLEASE READ 1ST POST]

Started by vividsailor7 · · 👁 76 views · 3.9K replies

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Participants vividsailor7redcrane22Sandra Rivera37swiftbear86melloworca6Dana Martin87ironskipper80mellowgardener15goldenmarlin6analogbison13Nicholas Myersstormygardener34Roger RodriguezDonna Mitchell3Kenneth Vaughn2Laura Ward98briskseal32Susan Vaughn46Zachary Lewis4driftingmason52rustyheron55Laura Chavez47vividstag24lonecanyon8 …
Hannah Kelly Hannah Kelly Member
18 messages
joined Jan 2013
#681 ·
Maria Fisher46 said:Unfortunately, that isn't an option right now.

Aside from the facial flushing and capillary breakage, how would you actually describe the rest of the skin issues? I mean, is it just redness, or are we talking blisters, acne-like bumps, or maybe rough plaques? And do they pop up on a schedule based on sun exposure? Like, does it happen minutes or hours after being out in the sun, then vanish once you're back inside?

Excessive capillary breakage might just be a sign of fragile vessel walls. It could be hereditary, too—especially in women, if there’s a family history of this kind of thing. If that's the case, there isn't really a specific treatment.

Given the skin changes you're describing, it probably wouldn't hurt to get checked out at a dermatology clinic, maybe specifically at an autoimmune specialty clinic.

You should definitely mention these changes to your immunologist. It would also be useful to verify the level of dryness in your eyes (via an ophthalmology exam, Schirmer test, BUT test, or Rose Bengal test) and your mouth.

In rare cases—though it's possible—an ANA test can come back negative even if the anti-Ro/SSA and anti-LA/SSB antibodies are positive.

I should also tell you that plenty of patients don't meet the full criteria for a systemic autoimmune disease yet, so they end up on a "waiting list."

In those situations, it's better not to rush a diagnosis. Waiting until all the criteria are met can sometimes take years.


Thank you so much, Nicholas Myers, for your patience and your time. I'm sorry I can't make it to see you, but I managed to book an appointment with Dr. Markeljevic for late November. The wait is long, but I know she's just as thorough as you are. 😉

Thanks again from the bottom of my heart. 🙂you're wonderful
darkcanyon17 darkcanyon17 Newcomer
1 message
joined Jun 2013
#682 ·
Hey,
so I have a question because I'm honestly just confused. I went in for some hepatitis testing and got these results back:
this part is reactive:
HBeAg - 1218.282
HBsAgQ2 - 926.64

The doctor says my results show I don't have any antibodies, which apparently I should have given my age.
She asked if I’d ever had hepatitis before, and I told her no—I've never even had jaundice or anything, I feel perfectly fine.
So now she's sent me off for more tests.

It just confuses me how these numbers look so bad when I actually feel fine. 🙂 🙂

I guess I'm just wondering what could be going on here. 😲
nimblegull23 nimblegull23 Member
16 messages
joined Oct 2006
#683 ·
Carotid Doppler:

Transcranial Color Doppler:
PSV ADV -20, AVS -20 cm/s

Conclusion: Bilateral insufficiency in PSV values.
Neck issues. See a physiatrist.

Anyone know how risky this actually is?

I work on a computer all day, so obviously my neck is killing me. Can a physiatrist actually do anything about these results?
tnx.
Nicholas Myers Nicholas Myers Active Member
163 messages
joined Jan 2012
#684 ·
darkcanyon17 said:Hi there,
I have a question because I’m a bit confused. I just had some hepatitis testing done and got these results:
The reactive markers are:
HBeAg - 1218.282
HBsAgQ2 - 926.64

My doctor mentioned that based on these labs, I lack the antibodies I should have given my age.
She asked if I’d ever had hepatitis before. I told her no—I’ve never had jaundice or anything else. I feel perfectly fine.
She sent me for more follow-up tests.

It’s confusing to me that the numbers look bad when I feel so good. 🙂 🙂

So, I'm wondering what this might mean. 😲

Hello,

Having both positive HBsAg and HBeAg could indicate an active Hepatitis B infection. It suggests you might be in the early stages where the virus is replicating heavily, meaning you are likely infectious.

Further testing will be conducted to confirm this.

To provide some perspective, the clinical presentation of Hepatitis B is incredibly varied. Some people experience very mild symptoms—or perhaps none at all—even when their serology clearly shows they are infected.

Consequently, how a person feels (whether good or bad) isn't a reliable way to rule in or rule out an infection.

Best regards. 🙂
Nicholas Myers Nicholas Myers Active Member
163 messages
joined Jan 2012
#685 ·
Marko1976 and Zlatko99, your posts have been moved to the cholesterol thread.
Nicholas Myers Nicholas Myers Active Member
163 messages
joined Jan 2012
#686 ·
ironseal78 said:Here are my results. My doctor is out on vacation. 🙂

Ferritin. 9.53 (15-150)

IgG 9.12 (Normal range: 7–16). Within limits.

IgA 2.45 (Range: 0.7–4.0)

IgM. 3.03 (0,4-2,3)

EMA (IIF) negative titer (
The tTG test wasn't performed (
Fibrinogen 2.9 (Ref range: 1.8–4.1). Within normal limits.

Lactate dehydrogenase 155 (normal range
Calcium. Totaling 2.57 (range: 2.14 - 2.53).

Phosphorus. Anorganic 1.42 (range: 0.79 - 1.42). Right at the edge.

Female, 24. For the last decade, I’ve been dealing with recurring keratitis of unknown origin—always sterile cultures. About six or seven years ago, Dr. Sentić sent me on an absolute marathon of testing. Blood work, X-rays, dentist, dermatologist, OBGYN, thyroid, rheumatologist... basically everyone under the sun. She theorized about a laundry list of diseases and predicted some pretty grim outcomes, but nothing ever stuck. Every single test came back perfect, except for being HLA B27 positive and having elevated IgM. Otherwise, I was the picture of health—almost never even catch a cold. Doctors were actually puzzled by my iron surplus, though apparently, that isn't the case anymore. After a brief experimental stint on Decortina, the consensus was that this is likely immunological, though local corticosteroid eye drops yield the same result. At that point, the doctor and I went our separate ways. It only affects my right eye, and it follows a strange pattern: one year is a total disaster, the next is calm. No one can explain the cycle. My only trigger seems to be summer—the heat, the beach, the sun. My eye and the outdoors just don't get along. Allergies have been ruled out, so I just stick with my ophthalmologist.

I was referred for these tests because I dealt with two bouts of "pyoderma" last year—once in the summer and again in the fall. It actually flared up a few years back too, but my doctor just dismissed it as acne. Since I deal with breakouts regularly, I didn't think much of it at the time. However, once it resurfaced last year, things changed. It wasn't just a breakout; it was this intense, inflamed, hot sensation concentrated entirely around my chin area. It lasted about two months from start to finish. The rest of my face felt completely fine—almost like it belonged to a different person. That’s when I decided to seek a second opinion from another dermatologist. 🙂All my swabs came back negative. My OBGYN says everything looks normal there, too. However, the dermatology clinic thinks this is part of a much larger puzzle given my keratitis, so they've sent me down this diagnostic rabbit hole. They’re looking into Celiac or maybe Crohn’s disease and want me to see a gastroenterologist. Celiac is on the table because it runs in my family—apparently, that’s a common diagnosis these days—and Crohn’s is a possibility since I deal with occasional stomach cramps and bouts of diarrhea. I avoid the sun like a vampire, so I'm guessing my Vitamin D levels are low. No issues with my kidneys so far. I don't eat much dairy, but I go heavy on the nuts.

Thanks for the input and the help. My apologies if I went on a bit too long or dumped too much info on you all at once. 🙂

To whom it may concern,

If you're dealing with recurring keratitis—specifically cases where you see corneal ulceration, thinning at the edges of the cornea, or significant inflammation—you need to look deeper. These symptoms often point toward systemic autoimmune issues. Rheumatoid arthritis is the most frequent culprit, followed less often by systemic lupus erythematosus or Sjögren's syndrome. Other possibilities include polyarteritis nodosa or Wegener granulomatosis. Furthermore, modern medical literature increasingly suggests screening for Hepatitis C as a standard precaution. There is also the phenomenon known as a Moore ulcer, where corneal damage occurs without an identifiable cause.

Given you mentioned pyoderma gangrenosum alongside digestive issues, it makes sense to consider inflammatory bowel disease (more commonly ulcerative colitis). Usually, IBD presents with uveitis—inflammation of the middle layer of the eye—rather than direct corneal involvement.

Even though you followed all the tests suggested by Dr. Sentić and they came back clear, keep in mind that systemic autoimmune diseases are notoriously unpredictable. Often, lab results don't turn positive right away, leaving patients in a diagnostic limbo. You shouldn't have abandoned the idea of a follow-up or a consultation with Dr. Sentić just because those specific markers were normal at the time.

Looking at the results you posted, there's a drop in iron stores (low ferritin). This suggests iron loss somewhere in the body. When paired with digestive complaints, a visit to a gastroenterologist—which you've already been referred to—is necessary. Of course, in younger women, low ferritin and related anemia are most frequently just the result of heavy menstrual cycles.

Your IgM levels are also somewhat elevated, which can happen with autoimmune conditions, but it occurs in many other illnesses too. A protein electrophoresis would be a useful next step to determine if we're looking at monoclonal or polyclonal IgM (essentially checking for the presence or absence of an M-spike).

I don't have anything groundbreaking to add here that you haven't heard, other than suggesting you stick to your dermatologist's advice.

Hopefully, once vividsailor7 is feeling better, they might weigh in with some insight from a gastroenterology perspective.

Best regards. 🙂
Maria Young7 Maria Young7 Newcomer
2 messages
joined Jun 2013
#687 ·
I’d love to get some thoughts on this—is this kind of differential count normal?
eosinophilic granulocytes - 3.9 (0-7)
basophilic granulocytes - 0.1 (0-1)
lymphocytes - 29.4 (20-46)
monocytes - 8.5 (2-12)
neutrophilic granulocytes - 4.7 (34-69)

Usually, whenever I have bloodwork done, the sum of all these components adds up to 100, so I'm wondering if this looks okay. Also, my white blood cell count is 8.2.
velvetmoose9 velvetmoose9 Active Member
163 messages
joined Apr 2020
#688 ·
nimblegull23 said:Carotid color Doppler:

Transcranial color Doppler ultrasound:
PSV ADV -20, AVS -20 cm/s

Conclusion: insufficient PSV values bilaterally.
Question regarding the cervical spine. Consult a physiatrist.

Can someone please weigh in on how dangerous this actually is?

I work at a computer all day, so obviously my neck is killing me—can a physiatrist actually help with these results?
thanks.


Look, if your physiatrist can walk you through the proper ergonomic setup—like how to position your monitor, how often you should be shifting your head position, what kind of quick stretches you need to do during your shift versus which ones you should tackle regularly during your downtime—then yeah, there’s definitely hope that things could improve quite a bit.
Of course, the catch is that you actually have to be disciplined and patient enough to stick to those changes.

As for the TCD, I can't really comment on that since I don't know the specifics of what symptoms you were dealing with.
Nicholas Myers Nicholas Myers Active Member
163 messages
joined Jan 2012
#689 ·
Maria Young7 said:I'd like some input on this CBC. Is it possible?
eosinophilic granulocytes - 3.9 (0-7)
basophilic granulocytes - 0.1 (0-1)
lymphocytes - 29.4 (20-46)
monocytes - 8.5 (2-12)
neutrophilic granulocytes - 4.7 (34-69)

Usually, when I get bloodwork done, these components all add up to 100. I'm wondering if this is right. My WBC count is 8.2.

Hello,

You have a sharp eye. There was likely a clerical error somewhere.

Pinpointing the exact mistake is difficult. It’s possible the percentage listed under "neutrophilic granulocytes" actually refers to unsegmented neutrophils, and the actual neutrophil percentage was skipped (though since the total WBC is normal, an elevated unsegmented count seems unlikely).

The other possibility is that they accidentally entered the absolute number instead of the percentage. If we calculate the percentage (100% - 3.9% - 0.1% - 29.4% - 8.5% = 58.1%), and apply that to a WBC of 8.2, the absolute neutrophil count would be 8.2 x 0.581 = 4.7642. This matches the 4.7 figure provided.

If the neutrophil percentage were truly only 4.7%, you would be facing severe neutropenia. Given that you're feeling well enough to post here, I doubt that is the case.

Regardless, you need clarification. The physician who ordered the labs should contact the lab and the supervising official to resolve this discrepancy.

Best regards. 🙂
Maria Young7 Maria Young7 Newcomer
2 messages
joined Jun 2013
#690 ·
Much appreciated for the response, best regards 🙂
ironseal78 ironseal78 Newcomer
1 message
joined Dec 2009
#691 ·
Maria Fisher46 said:Hi there,

If you're dealing with recurring keratitis—specifically when you see ulcerations, thinning around the edges of the cornea, or just general inflammation—you really need to look at the bigger picture. We're talking systemic autoimmune issues here. Rheumatoid arthritis is the big one, followed by SLE or maybe Sjögren’s syndrome. You also have to consider things like polyarteritis nodosa or Wegener granulomatosis. Plus, if you look at recent medical literature in the States, testing for Hepatitis C is becoming a standard recommendation. Then there's that frustrating thing called a Moore ulcer, where the cornea gets damaged and doctors honestly can't pinpoint the cause. It's a headache.

Since you mentioned pyoderma gangrenosum alongside those digestive issues—it really makes sense to look into inflammatory bowel disease (specifically ulcerative colitis). Usually, with IBD, people deal more with uveitis—that inflammation behind the cornea—rather than issues with the cornea itself.

Even if you ran all those tests Dr. Sentić suggested and they came back clear—which happens—you have to remember how unpredictable systemic autoimmune diseases can be. It’s frustrating, but sometimes the lab work just doesn't catch anything until it's too late, leaving patients stuck in this weird limbo waiting for a diagnosis. Honestly, I don't think you should have given up on getting a follow-up or a second opinion from Dr. Sentić just because the results looked normal at the time.

Looking at the results you posted—it’s clear your iron stores are tanking—your ferritin is low. That usually means you're losing iron somewhere, and when you factor in those digestive issues, it’s no wonder you were sent to see a gastroenterologist. Honestly, though—for younger women—low ferritin and the resulting anemia is almost always just a side effect of heavy periods.

The IgM levels are looking a bit high too—which can happen with autoimmune issues, sure, but there’s a whole laundry list of other things that cause it. Honestly, getting a protein electrophoresis would be the smartest move here to figure out if we're dealing with polyclonal or monoclonal IgM—basically, you just need to check if there's a spike in the results.

I don't have anything new or particularly brilliant to add to this discussion—honestly, you've probably heard it all already—other than just following whatever your dermatologist tells you to do.

I’m hoping that once vividsailor7 gets back on his feet, he might actually drop some knowledge from the gastroenterology side of things—it'd be nice to hear something useful for once.

Hey there. 🙂

Hey everyone—just checking in.

My keratitis is exactly like this! I remember one time—after my ophthalmologist told me to finally stop using steroid drops since I'd been on them forever—I ended up with a corneal ulcer. They treated it with that "hot ointment" in my eye, and thank God, it cleared up fine. Back then, there wasn't any scarring, but over time, some scarring started forming on the side of my cornea near my nose, along with thinning and those "cloudy patches." When you look at my eye now, the border isn't solid anymore; it’s broken up and white in two spots. It doesn't really mess with my vision yet, though I've been nearsighted for ages. One doctor at a private clinic actually told me I only have about ten years left with that eye. Ugh. 🙄 I've dealt with uveitis before—spent way too much time Googling symptoms and asking doctors for second opinions—but everyone keeps telling me that what I'm dealing with now isn't actually that.

I started seeing Dr. Sentić about two years ago—after I’d already gone through three or four different immunologists—once that ulcer issue cleared up. Honestly, though, I finally gave up on those appointments because I just couldn't stomach hearing about all those "terrifying" diseases you guys were listing. Back then, my eye was really my only problem, and she told me straight up that there wasn't enough evidence for a systemic diagnosis yet—just that I needed to stay on her radar. I get that these conditions are long games and it's a nightmare to tell them apart, so I'll definitely be heading back this fall—and I've already booked an appointment with my GI specialist, too.

Thanks a ton for the reply and all the effort you put into this 🙂
steelpuma89 steelpuma89 Newcomer
1 message
joined Jul 2013
#692 ·
Hi there,
I was wondering if someone might be able to help me make sense of these blood gas results:
pH 7.384 (7.35-7.45)
pCO2 4.9 (4.3-6.0) kPa
PO2 8.5L (10-12.8) kPa
Actual HCO3 21.4 mmol/L (18-23)
tCO2 22.5 mmol/L (22-29)
SBE -3.0 mmol/L (-4 to +2)
sO2 92.2 L % (94-98)

I had these tests done about a year ago during a pulmonary workup. I was referred because I struggle quite a bit with physical exertion and have dealt with frequent coughing fits for as long as I can remember... things were actually pretty rough back in elementary school, though by the time I hit college, it seemed to settle down a little. Since then, I’ve crossed the threshold into being an adult, which means I can't exactly head back to the pediatric wing at the children's hospital anymore. Now I'm left wondering if I really need to transition over to an adult hospital for follow-ups, especially since I don't feel many symptoms unless I'm exercising—which is why I tend to keep my workouts fairly light, just so I don't end up winded... oh, and maybe the occasional five-day coughing bout during the winter months? Also, I deal with some mucus drainage from my throat every single morning, but once I clear it out, it doesn't bother me much for the rest of the day.
As for other tests, my spirometry (FVC 87%, FEV1 80%, TI-8, MEF 73%), X-ray, and EKG all came back normal.
In the meantime, I did get some standard blood work done because my doctor requested it following a routine checkup—they heard "systolic murmur" and wanted to check my heart, though I'm still waiting on the cardiology appointment. Everything looked fine except for my potassium, which was just a tiny bit low at 3.6 mmol/L.

My main question is: should I actually schedule a follow-up with a pulmonologist? It’s been a year since my last visit, and since I've aged out of pediatric care, and my doctor wasn't entirely certain about a diagnosis yet (the report just noted "unspecified asthma")...

Thanks so much! 🙂
Sam Flores3 Sam Flores3 Newcomer
4 messages
joined Mar 2010
#693 ·
Hey everyone. Since my appointment with the doctor isn't until next month, I was hoping someone could make sense of these results for me. My physician ordered these tests because my periods have been all over the place lately—just super long and irregular cycles. I had my blood drawn on day 43 of my cycle, so since things aren't exactly predictable right now, I’m assuming those "reference ranges" are meant for the luteal phase. I've got a nagging suspicion it might be PCOS given some of the symptoms I'm dealing with—like breaking out in acne even though I'm already 25—but I won't know for sure until I get an ultrasound done. In the meantime, I'd really appreciate any insight you guys can offer. Thanks.

image
wiredtinker18 wiredtinker18 Newcomer
5 messages
joined Aug 2011
#694 ·
Hello,

My fasting glucose from a routine checkup came back at 6.17 mmol/L (normal range is 3.3–5.6).

Because of my family history, I was referred to the Mayo Clinic, where they repeated the fasting test; this time, the glucose level was 6.3 mmol/L.

At my doctor's request, I also underwent an OGTT. Here are the results (fasting; 60 min; 120 min):
Glucose (5.9 ; 7.7 ; 6.9)
Insulin (6.64 ; 71.44 ; 29.96).

Female, 40 years old, 5'10", 174 lbs.
I would appreciate some insight on these numbers—the insulin levels are particularly worrying to me. My endocrinologist insists everything is fine and suggests I simply focus on diet and exercise, given my genetic predisposition and recent weight gain (I’ve put on about 20 pounds in just six months).

A few other relevant lab values:
Total cholesterol - 4.25 mmol/L (ref. < 5.2)
Triglycerides - 0.98 mmol/L (ref. < 2)
HDL cholesterol - 1.63 mmol/L (ref. > 0.9)
LDL cholesterol - 2.18 mmol/L (ref. < 4)
AST - 15.40 U/L (ref. < 31)
ALT - 11.01 U/L (ref. < 31).

Also, there is one more thing bothering me: two months ago, I had an incision made for a perianal abscess. Now, about an inch away from the surgical site, a walnut-sized lump has appeared. It isn't painful to the touch. My surgeon claims it will eventually resolve on its own, though he can't say when, stating it depends on how my body reacts. It was such a frustrating answer—it felt like asking a stranger on the street for medical advice, but that's just how things go sometimes here in North Mexico... anyway, I am feeling quite lost and unsure of who to turn to. Here are the results:
WBC - 8.1 Gpt/L (ref. 4.4–11.3)
Granulocytes - 69.8% (ref. 55–80)
Lymphocytes - 19.5% (ref. 25–40)
Monocytes - 10.7% (ref. 2–12)
# Granulocytes - 5.7 Gpt/L (ref. 1.2–6.8)
# Lymphocytes - 1.6 Gpt/L (ref. 1.4–3.2)
# Monocytes - 0.9 Gpt/L (ref. 0.3–0.8)
ESR - 15 mm/h (ref. < 25).

Thank you.
Rebecca Phillips25 Rebecca Phillips25 Newcomer
4 messages
joined Jul 2013
#695 ·
Would anyone be willing to explain what it actually means when my Alkaline phosphatase levels come back "low" (26), given the reference range is 54 - 119?
My liver panel results are all within the normal range, along with my glucose, urea, creatinine, red blood cells, white blood cells, platelets, triglycerides, cholesterol, hematocrit, hemoglobin, iron, and so on.

Thanks!
Lawrence Alvarez2 Lawrence Alvarez2 Member
29 messages
joined Mar 2008
#696 ·
The CBC looks totally normal, but the CRP is sitting at 24 (normal range is 0-8)
Is it actually possible to have inflammation going on if the white blood cell count and everything else on the CBC is fine?
velvetmoose9 velvetmoose9 Active Member
163 messages
joined Apr 2020
#697 ·
Laura Barnes said:The kid's CBC looks totally normal, but their CRP is sitting at 24 (normal range is 0-8).
Is it actually possible to have some kind of inflammation going on even if the white cell count and everything else on the CBC looks fine?

Yeah, it is.
Lawrence Alvarez2 Lawrence Alvarez2 Member
29 messages
joined Mar 2008
#698 ·
velvetmoose9 said:Yeah.

I’ve been digging through stuff online and apparently even a standard viral thing can bump up your CRP levels. And then you’ve got cases where the white blood cell count spikes right along with the CRP during an infection. Honestly, I’m just totally lost here. 😕
velvetmoose9 velvetmoose9 Active Member
163 messages
joined Apr 2020
#699 ·
Laura Barnes said:I've been scrolling through some forums online and reading that even a regular viral thing can bump up your CRP levels. And apparently, if there's an actual infection going on, your white blood cell count might spike right along with the CRP too. Honestly, I'm totally lost here 😕

Generally speaking, you see elevated CRP when there's a bacterial infection involved—though obviously, bacteria aren't the only thing that can trigger a jump in those numbers. As for white blood cells, they don't always shoot up significantly right away; sometimes they actually lag behind the CRP spike... Biology isn't always as straightforward as 2+2=4 😁
Did you get a urinalysis done?
Clinically speaking, what kind of symptoms were you dealing with that led your doctor to order these tests in the first place?
Lawrence Alvarez2 Lawrence Alvarez2 Member
29 messages
joined Mar 2008
#700 ·
velvetmoose9 said:Generally speaking, CRP spikes when there's bacterial inflammation going on (though obviously, a bacterial infection isn't the *only* reason CRP climbs). Your white blood cell count doesn't always jump significantly, either—sometimes they actually lag behind the CRP rise... It’s not always a straightforward case of 2+2=4 😁
What about a urine test?
Clinically speaking, what symptoms actually drove the doctor to order these tests in the first place?

Well, my doctor diagnosed bronchitis just by doing a physical exam. I ended up paying out of pocket for the labs because she never sends anyone for blood work or anything else; she just jumps straight to prescribing antibiotics based on her assessment. One time, she finally sent him for blood tests after two different rounds of antibiotics didn't work, and that's when the results showed it was actually just a virus.

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