COPD :: Two Nodules Measuring 4mm In Each Lung


Jun 10, 2014

I went for a CAT scan for my heart and it was discovered that I have two nodules measuring 4mm in each lung. I haven't seen the doctor as yet. Has anyone experienced this and what was done for it? I am quite anxious.

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I had a Mri scan for back pain, result found 2 small nodules in lung. Seeing specialist in July, I get a little short of breath and a little wheezy at times nothing to alarm myself, but I have terrible fatigue also have red lumps on forehead chin and buttocks. Worried this could be sarcoidosis my father had this sadly died 26 years, I have read different views on this being hereditary, so worried seems ages till July I am female age 55 & a smoker, any thoughts ?

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COPD :: Noncalcified Nodule In The Middle Lobe Of My Right Lung

I am a 49 year old woman and I have a 8mm noncalcified nodule in the middle lobe of my right lung. For some reason, it does NOT show up on an X-ray but it was found on a CT. Shouldn't it show on an x-ray also?? The ER found it by accident...they thought I had a blood clot that had travelled to my lung...nope! It's a nodule. It was found 51 weeks ago and I did have another scan 2 months after it was found and there was no change in the size. But, since I don't have health insurance, I have been unable to have another CT scan as recommended (every 3 months). My husband makes too much money for us to qualify for any financial assistance but we can't afford a pulmonologist or scan. I have been a smoker for 30 years and I do get backaches and I can't do much without getting short of breath but that doesn't mean it's cancer. My main question is why is it not showing on an X-ray...I've had 2 since they found it on a CT scan so unless it mysteriously disappeared, I don't understand. I have been checked for histoplasmosis and other things like that and they were all negative. Can anyone tell me why it's not apparent on a chest x-ray???? Thanks!!

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Diagnosed With Endometriosis Of Lung

I have been diagnosed with Endometriosis in the lung. I was wondering if any one else out their had this condition? It's such a rare condition doctors don't know what to do...

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18 With 2 Thyroid Nodules And High Blood Pressure

So a couple of months ago I found out that I have 2 small thyroid nodules. Of course I freaked out but now calm and just waiting for the results of my 2nd thyroid ultrasound. I am also struggling with my blood pressure. For the past months I have been nervous all the time because of all the stuff that has been happening to me (different tests). My doctor keeps on saying that I have high blood pressure (which is weird cause I am younger than 18) because it would be 130/80 to 150/90 to 145/80 or around those readings. But when she does check it I am always nervous and freaking out and shaking. I am wondering if its cause of that. When I do check it at home, it sometimes is high or normal. Since my doctor and parents have been talking about high blood pressure and what it could do to your body I have been scared to take it being afraid it would be sky rocket high. Im wondering if it is my thyroid, fast heart rate (which my doctor thinks it's because of my nodules) my nervousness, my family history, or just me. I'm going to a cardiologist to check with my heart next month which is freaking me out.

*Now my doctor is prescribing me hypertension medication (Enalapril 5mg once a day) when im not even 18 yet! I am very young having to take BP medication?? My doctor thinks my hypertension is because of my thyroid or, nervousness.I feel so old. I feel like when I take this medication, my blood pressure will drop tremendously. Not I don't even know what to do now.

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Headaches :: Thyroid Grew Nodules And Became A Goiter

I suppose a little history would be fitting first...I've been hypothyroid since birth (born without thyroid function), and was placed on a regimen of Synthroid for years. From there, my thyroid grew nodules and became a goiter, and at the age of 23, had to be removed completely. Since then, I struggled on the Synthroid, and finally found a doctor who agreed to try me on Armour. At first, I seemed to do well on it. I've been on Armour for about 2 1/2 years now.

Over the past year, I've developed migraine- like headaches that completely incapacitate me. For the most part, these would come on a frequent basis but I could go about my daily routine without disruption...until about four months ago. The headaches became non-stop. There is no break in the pain (the doctors don't understand this concept- they keep calling them "episodes"). The intensity changes, but the pain is ALWAYS there. I've been treated for migraines, but the medication for it doesn't work, and the pain isn't quite the same as a migraine. It's very hard to describe...almost like a twisting sensation in my skull and across my forehead.

That's not all of it. The pain gets worse with exertion. If I try to go out and run a few simple errands or do some household chores, my body heat goes through the roof- along with a lovely fever and I'm done. I can't do anything else for the rest of the day because I'm in too much pain (from the headache AND body aches from the fever).

I'd love to say I'm making this all up. But would I really put myself through all the blood work, a lumbar puncture that went awry (yes, it was downright awful), and bounce from doctor to doctor? I finally found one who had a brain in his head that said "it could very well be your thyroid!"

The biggest problem I've had is that every doctor I've seen has said "your thyroid levels look fine!" But they've only tested my T4 and TSH...shouldn't they be testing my T3 as well? I know I'm no doctor but...

I know I should be under the care of an endocrinologist, but they are really hard to find around my part of town (at least one that's any good). I just want some other points of view here before I subject myself to more poking and prodding.

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I had all my lung drama in the 1980s, two collapses on each side, then followed by each a major lung op, one side using a blebectomy (I think it was called) which was a partial lobectomy that was then stapled back together. The other was a filler where they used some seal to fill the space between the lung and the pleura. So many years later, I survived without needing other operations but heres what happened to my lungs...!

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Does anyone on this board have any experience with successfully dissolving or at least reducing the nodules/cysts?

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