Respiratory Disorders :: Bilateral Atelectasis, Narrowing Aorta
Jan 2, 2015
I have been having abdominal and pelvic pain for months since my daughter was born in May. I went to the er at 2 different hospitals and both did a CT scan and 1 found bilateral lower lobe atelectasis and the other a narrowing of my aorta valve of the celiac. I asked my family physician about the atelectasis but he said it was air pockets but nothing to worry about. I had a collapsed lung 3 years ago so are these things I should be concerned about because he is not.
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My father got his xray result just now. An examination on his Chest PA. And the impressions were: Bilateral PTB, Concurrent Pneumonia, and Atheromatous Aorta. Can someone please explain to me what is Bilateral PTB? And Concurrent Pneumonia?
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I have had a terrible affliction for more than 3 months now and it is greatly affecting my life. I am 25 years old and in general have never had a
problem with my health or anything. I have lived in São Paulo, Brazil for 6 years which has very polluted air due to its large population and high altitude.
I am having difficulty breathing in general. It feels like I am not processing the air that I breathe. Here I am going to list all of the symptoms I am feeling:
-Exercise is walking at best. If I try to do anything more than this I become at risk for feeling irregular heart palpitations and become even more out of breath.
-There are moments when I feel a little better and worse throughout the day. It is completely random but I think it might also have to do with eating. The only time I feel ok is when I am sleeping and I just wake up. Usually I lie around for a bit because it's nice to forget about it. As soon as I get up the difficulty breathing starts. If I get up just to use the bathroom at night it takes a while to stabilize after I lie back down.
-I have a chest pain on my left side. is right in the left pectoralis major. This pain never goes away however it is constant so I have coped with it. The
pain is like the pain you have when you have gas. It is a sharp pain I cannot move the muscles on my left chest otherwise it will feel like I'm being stabbed.
-It is common for me to be sitting doing nothing and feel strange heart palpitations which cause me to have even more difficulty breathing
-When I feel the palpitations (which have been occurring less but the chest pain hasn't subsided) It seems that my heart is in my throat or that I am going to burp up my heart. When This happens I have to lie completely still and focus on not passing out. My limbs, stomach face all go numb and start tingling like when your leg falls asleep and it's waking up.I usually sleep on my right side because sleeping on my left side causes difficulty breathing.
-I can't stand in one place for very long otherwise I will have considerable difficulty breathing and start to slouch, however I can get by walking.
-Sitting up straight makes it harder to breath. Slouching has helped me to get by and breath more easily.
-Riding in any vehicle causes me to have considerable difficulty breathing. It feels like the bumps on the road cause me to not be able to breathe well.
-Anxiety does cause my symptoms to worsen and my breathing to become considerably harder but it is not the underlying cause. I cannot run away from the chest pain or difficulty breathing no matter how calm or relaxed I am.
I have done a few heart and lung exams:
*3 ECG/EKG- nothing
*3 chest X-rays- nothing
*1 chest tomography- nothing
*1 Echocardiogram- nothing
*1 24 hour holter- nothing( I wasn't even able to
sleep within the 24 hours at any moment because I had to hold my cat who had surgery and took the whole night to recover from the anesthesia. Worst night of my life both of us suffering and nothing I could do. I left my cat with my wife when she woke up and went straight to the lab to remove the holter device.)
*Spirometry- nothing
*Laryngoscopy- Septal deviation(I've always had)
Rhinitis, pharyngitis and laryngitis
-the only day in the past 4 months that I have felt normal is the night of and day after I did the spirometry and laryngoscopy exams. I took anesthesia
in both nostrils for the laryngoscopy and 2 sprays of an inhaler for the spirometry exam. I started doing some exercises on the following morning and all
the symptoms returned.
-I am beginning to have dizzy spells. I suddenly get overtaken by strong dizziness.
When I was between the ages of 10 and 16 I had taken all sorts of antipsychotic medicine such as Geodon, Abilify, Seroquel and others because I was considered overactive. I am do worry that this might have affected my anatomy at a growing phase in my life. I have suspected heart arrhythmia or asthma but the tests I listed above say otherwise.
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I had a Barium swallow done to see if the goiter I have is causing my swallowing issues. My ENT told me today during our follow up visit that the Dr. who did the x ray noted that I have "linear opacity of the right mid thorax and he suggested a get a chest PA and lateral xray. My ENT then sent me to get a xray. I will not know the results until Thursday of this week. What does this all mean. I have had a cough for 3 1/2 weeks, random sharp chest pain on the right side and wheezing when I lay down only. I have my lungs listened to 2 times and I hear "your lungs sound good"...
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I am a 55 year old woman who was healthy as a horse until earlier this year when I had to have my gallbladder removed. I have never had asthma, allergies, breathing issues or heart issues. Two and a half weeks after surgery I woke up one morning feeling I wasn't getting 100% oxygen into my lungs. I had an anxiety attack the next afternoon as a result (never ever had an anxiety attack in my life before) and ended up at ER. Tests performed including cat scan and nothing was found. Have seen a pulmonologist - have gone through the breathing tests when sitting as well as on the treadmill at various speeds - all is normal. Arterial blood work - normal, echocardiogram - normal, no holes in heart, no clogged arteries. When I lie down at night I still have a bit of shortness of breath but at same time the breathing is more relaxed and I can sleep. As soon as I get up in the morning again, the shortness of breath picks up again. The breathing level remains consistent, does not get worse on exertion. For a period of time I was getting the tightness in the rib area at times but that hasn't occurred in 5 days now. I found it odd that when I saw the specialist a couple of weeks ago he asked me if I had any idea as to what I thought was going on. Later he told me I didn't give him much to go on (because of my test results). I am going back to his office next week for follow up. I think he wants to explore the possibility of asthma to rule that out but I get the impression he doesn't feel I have asthma. It's a mystery. Has anyone had this issue and it then got resolved?
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I used to be an incredibly fit person... played football about 5 times a week, went swimming a lot and run cross country. However, one day after football I felt really weak and couldn't breathe properly and generally felt as though I was dying.
The feeling was gone by the next day though I was coughing up really thick, but loose, clear white phlegm.
From this day onwards I more often than not (though sometimes not) got the same feeling after exercising. The doctors said they would only diagnose me when I was in the state I was talking about but reluctance to get into that state meant they could not diagnose the condition. They gave me asthma pumps and such but I didn't feel as though this is what the problem was.
Anyway, to cut a long story short I basically gave up exercise and it has been 5 years since I've done anything intensive to bring on the condition.
I have not experienced feeling this way in 5 years so I'd imagine it is exercise induced.
I stumbled across some information this morning which matches my condition 100%... it is called Pulmonary Edema though there doesn't seem to be too much information about it online.
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Is there a medication to remove the scar on my right lung?
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I am 43 for several days I have been having serious pain the right side of my chest when I breathe on a scale of 1 to 10 it is definitely a good 9....when I lay on my back there is a crackling sound and lots of pain when I breathe..if I laugh or hiccup awful...coughing is excruciating...and I been having migraines only on the opposite side of my head(left side) don't know if they are connected but I never get migraines I've had about four in last two weeks
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MRI:-
Central and Right Paracentral disc Protrusion at C5-C6 level causing thecal sac , Cord indentation, bilateral neural foraminal narrowing (Right >Left) and mild spinal canal narrowing ...
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I am debating if I should go to the Emergency Room, as it's a Sunday. My story - 26 year old male, healthy. Since age 10, I have had an intermittent feeling of my breath being stuck in my upper abdomen (solar plexus area) and a little in my chest but not much. Sometimes when going for a deep breath, I feel pain in the chest, but very rare. It almost feels like there is a wall in between my stomach and my lungs that prevents air coming out. I know it's weird because you breath out of your lungs not your stomach. The only way it comes out is when I finally catch my breath, which means I need to wait for it to be able to escape and then I finally get the deep breath I need. Also yawning often allows the breath to occur. When this is happening, I can still breath but it's like only 10% of my lungs fill up with air, like someone is standing on the other 90% of my lungs, preventing them from filling up.
My BASELINE/ usual status is having the breath being stuck symptom maybe 10 times a day, usually while eating. This has become normal for me and I don't even think about it until people who I am eating with say, "what is wrong with you?"
When it is GOOD, it happens even less, maybe once a day and I will barely realize it happened.
When it is BAD, it happens often, maybe 20 times an hour.
The last week it has been EXTREME to the point where I will be struggling for a full breath once a minute. It is so bad that I have been feeling light headed (main reason for the alarm here). I have class on weekends and I was walking to the train for class, and my body was telling me to stay home (i am the type of person who doesn't make a big deal out of anything and never skips stuff).
Background- I sleep very well, usually 7-8 hours a night, am very healthy, 6 feet tall, 180 pounds, run 6 miles 3 times a week (it happens the same when I run but it doesn't prevent me from running), played sports my whole life, doctors always tell me my blood work and everything is off the charts good. The reasons I just listed, combined with my Mom (nurse) always telling me I am fine have made me stop seeking cures for this. I had every test under the sun done when I was 15 (EKG, Barium Swallow, Blood work, etc) and everything came back clear. I have a concave chest (my chest caves in) and the doctor told me that my chest bone is interfering with my breathing (eyes rolling). But now that I am feeling light headed, I think it's time to go to the emergency room. I am going to go to a heart center in my town (Brooklyn, NY). Also, I LOVE doing research about stuff and have been reading about this a lot and tons of people have similar symptoms which has comforted me. But now it's time for me to get tested again I think. Maybe this just talked me into going to the ER.
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My Son is now 21 yrs of age and has been battling with perthes since the age of 5yrs. He has bilateral perthes. the left leg was the first and this was treated with non weight bearing, callipers and restricted activity and is now near normal, at the age of 8 it appeared in his right hip which he had a surgery ( varus osteotomy) with further surgery to remove plate and pins. He still struggled with pain and had hinged abduction and leg discrepancy. He was then given a valgus osteotomy as a salvage operation and further surgery to remove plate and pins at the age of 14. He struggled on through school still in pain. He has now grown to 6 ft and this has produced more problems as his thigh muscles do not work probably due to the position of the femur that the valgus placed it in. The ball of the femur is mushroom shaped and the main pain is directed through the knee which gives way unpredictably causing him to fall. He has been told by a specialist that he is too young for a hip replacement and to grin and bear with pain management for as long as he can. He has been able to do office work part time, but even this is painful do to the sitting position.His left leg does give him trouble from time to time. Nobody actually follows perthes up into adulthood as once you reach 18yrs you are discharged from the children's hospital and left to the care of your GP. There should be a call back system for check ups even if it was to help doctors to understand the disease. I don't know if surgery benefitted my son or if treatment with callipers was better, all I know was I could not bear to put him back in them for another 3 years and did what I thought was right at the time. Has anybody around this age experiencing similar problems ?
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I'm 36-year old male and about 3-weeks ago I went to my doctor with typical flu-like symptoms. He informed me I had a Respiratory Tract Infection and prescribed some antibiotics and pain killers which I took over the course of the following week. The problem did not clear-up and, after developing a chesty cough and severe pain in one ear, I returned to the doctor who then told me the infection had most likely spread to my chest and most certainly into my ears - particularly my left one. He prescribed stronger antibiotics and pain killers and a nasal steroid spray, all of which again I took religiously over the following week once again.
Although my cough and general flu symptoms have pretty much cleared up, for the past week or so I have been left with almost complete loss of hearing in my left ear. It feels as if there's still a wee bit of pressure both in and around the ear itself with a sort of numbness when i touch the skin on my face and head around the ear. This extends in to my hairline, over my left cheek and a short distance down my neck below my ear. There's also a small amount of ringing from within the ear and it sounds as if I'm hearing things "internally" all the time. Hard to explain but extremely frustrating and my concern is that the infection has somehow managed to damage my hearing permanently.
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I have bilateral frozen shoulder - idiopathic. Several professionals have stated my left is "severely affected". Right is manageable and seems to be on recovery but full ROM is not there yet. Ortho is considering MUA with a scope to clip any scar tissue on the left. I'm wondering what is the true pain level of this surgery? How soon after were you to "functioning"? I have 3 kids (9, 6 and 3).
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My 24 year old son was diagnosed with TMJ Arthritis and the surgeon wants to do a bilateral TMJ joint replacement. That seems extreme to me. I would like to know if anyone has had a jaw joint replacement and if you have had jaw problems post surgery.
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i thought I would share info. First 2-3 weeks, barely sleep. Pains as opposed
to aches, lost 15 lbs and my taste for food. No appetite. And exhausted.
approaching 6 weeks Tuesday and not as tired, doing constant PT in office and home.. Slowly getting appetite back, sleep somewhat better. Pain has migrated to itching and aches. Let's not forget stiffness in AM or after idle.
I can walk it off a bit, but never really without that dull ache feeling. I have good ROM. Stretching helps. I am 71, but in great shape. Two knees is not for the faint heart or out of shape. Glad to answer any questions. The recovery is slow, but one can see it come, "ever so slowly". I am physically ahead, but one must let all the tissue and nerves recover..reading other experiences is a bit of a comfort. Not alone.
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I was diagnosed very late with this condition. An acute GP noticed the murmur and was not convinced that all was normal. Test after test later it was confirmed. Months later i had a stent fitted which is 4cm x 2cm, I was not warned about the amount of bruising or the pain in the legs, 4 months later i am still having pain in the groin and the che chest. The cardiologist does not know why I have this pain that travels from my chest to my back and left arm. MY left leg feels heavy and numb down to the foot which is freezing cold at times again. I have started feeling tired and fed up with the whole ordeal. Yes i know i needed this procedure but through choice i would never have had it - my active happy go lucky lifestyle now revolves around this. When i get ill My poor GP has to send me into the hospital as they are not well versed with this condition. Can anyone tell me when will I feel well and strong again. Do you get back to normal? The hospital and the doctors have been wonderful but they just do not have the answers. They think it could be damage due to the surgery but not life threatening so at least that is something to be cheerful about. I would love to hear from other people that have undergone similar treatment.
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7 years ago i woke with tremendous pain in my neck. Took 5 years and many doctors before first MRI. MRI showed bilateral cervical ribs. Tests were performed which suggested TOS. From 1 specialist to the next, I have now been told to basically go home and live in pain. They won't perform the surgery because they told me 60% of patients are worse off. Have to live in this horrible pain forever. Lost in the system
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are there any exercises i can do to strengthen muscles? breathing now getting shallower and very frightened. I try weights to no avail
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I had a bilateral tubal ligation almost seven years ago. I am late with my period, nausea, lower back hurts and I am always tired. Could I have an ectopic pregnancy or a regular pregnancy
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For years I have been suffering with a pulsating stomach and ibs. That's what the doctor said it was, being that the scan I had done showed up nothing so the doctor put it down irritable bowel syndrome.
In May this year I went for an endoscopy and colonoscopy. A couple of biopsies were taken.
The results were normal, apart from a hiatus hernia and anaemia, the anaemia they put down to the fact that some time ago I was taking anti-inflammatory tablets for arthritis. On a course of iron tablets for the past three months.
Last Thursday I went for my blood test result, and I mentioned about the pulsating in my stomach. She told me t lie down on the bed while she felt my stomach. She told me that it was the aorta pulsating.
My stomach drives me nuts especially in the evening when I am Sat down.I don't know if the pulsating is due to the ibs or the hernia or both.
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My younger sister aged 50 was diagnosed with TAA of 5.1 cm in January and operated in February due to her small frame. She is recovering well which is encouraging. I have been meaning to go and have a check myself but kept putting it off. I went to my GP 2 weeks ago and he immediately picked up a murmur. Echo followed by a CT scan confirmed I also have an aneurysm but mine is still at 4.27 and I am 55 years old. Clearly we have a genetic disposition but mine is growing more slowly (so far) . I am in shock and still cannot get my head round it. I am fit, practise yoga, follow mainly a vegetarian diet, don't smoke, hardly drink and do not have high blood pressure. I am now now in 'watchful waiting' and will have another CT scan in 6 months time. I have been advised to take Beta Blockers and was wondering how patients react to them. I have a professional job in sales and need to keep my energy up. I have off course been considering giving up work but sitting at home waiting for my aneurysm to grow will not help me. I would also like to know if aneurysms always grow and if I need to accept that mine will be bigger by the time I have my next CT?
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