I have been diagnosed with a 32 gram prostate. Just wondering can anyone tell me what cc stands for? I have read some comments where the guy will say he has a 98 cc prostate. whats the difference from grams to cc when giving the prostate size. tx
My understanding is the #'s are interchangeable. So I assume 1 cc of prostate tissue weighs 1 gram
Pretty much correct 1 cc stands for cubic centimeter, which for water (main component of tissue) mean 1 g. So, for our purposes 1cc=1g. 32 g is a normal prostate size. Your problems are most likely not related to BPH, but bladder.
How many cc in 1 grams? The answer is 1. We assume you are converting between cubic centimetre and gram [water].
The density of prostate tissue is close to the density of water which is 1 gm/cc. So some people talk in terms of volume (cubic centimeter or cc) and others talk in terms of mass which is grams (gm). They are interchangeable just in this special case. Note also that some people use milliliters (ml) for volume which is the same as cc since 1cc = 1 ml. Confusing enough?
@ Gene,
Please refrain from Diagnosing someone else’s Health issues.
I had a 38 gram prostrate and according to the 4 Urologists and one IR Doctors I spoke with, all agreed that a normal prostate size is on average between 14-28 grams. And that some prostates grow outward, while others grow inward. Mine grew inward and constricted my urethra to the point where I was trying to urinate about 16 - 18 times a day (24 hour period) and still had significant bladder/urine retention. CIC / Self Cath ing were a main stay and helped me tremendously (*recommend Everyone check into that blessing of an option).
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After trying for many months to get a PAE, I acquiesced and under went a Bi-polar TURP at Stanford University. *About $5,500.oo Out-Of-Pocket expenses; after PPO Insurance payments. The past couple of months since the TURP, I have regained much more control of my Life. My flow has improved by about 80-90% and I only get up once (sometimes not at all) at night. And I have not had to CIC / Self Cath since a day after the Foley cath was removed (and it was only in after the procedure from about 4 pm to 8 am the next morning).
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I would not try to diagnose anyone else’s medical condition. This Site is a Blessing and great place to start, and it has a lot of Good, Caring People here. It was an invaluable resource for me. And I am grateful to all those who post their experiences, so others can learn. Please watch out for “opinions” and realize that many people who have Successful Procedures do not post here. So don’t try to analyze the “Percentages” of each Procedure; it most likely will not be representative or an accurate sample. Do you own Research; and this Site is one of those Good Research Sources.
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Best of Luck to all who are suffering from BPH / LUTS and any associated conditions. I pray you each find Relief and Success in dealing with them.
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Chuck
ty for replying you gave me some relief with your comment!
Chuck,
I’m not trying to diagnose anybody. Prostate doesn’t grow inwards our outwards, it’s just growing with adenomatose tissue, and you are correct some have enormous prostate without much restriction of flow, some, some have obstruction with relatively small prostate. Your urologist is right: in most men 25 cc is the upper limit for normal size. Mine was 40 at 35 without any symptoms. 30 cc vs 25 cc is only 20% increase with results in only 6% increase in radius according to the laws of geometry. Common sense tell me that 6% increase can’t cause obstruction. Yours was 38 g, a bit more. Effects are possible. at 30 cc unlikely.
Definitely in your case PAE was obsolete.
Please refrain from Diagnosing someone else’s Health issues.
You have just exposed one of the main problems of this site: people with no medical training speculating on the cause of problems of some stranger. The other issue in my view is people coming to this site and asking strangers with no medical training to diagnose (or speculate) on the cause of their medical problems. In my view, if one has a medical issue, one should see a doctor first and then do some research, not the other way around. As the TV monitor I have seen in multiple doctors’ offices states “Google is not a doctor.”
BTW, your bi-polar TURP experience pretty much parallels mine. Minimal discomfort/inconvenience and major quality of life improvement. I must have better insurance because my OOP expense was less than $1000 but I didn’t go to Stanford for the procedure!
Chuck,
Who did your bi-Polar TURP at Stanford ? I live near there, it is an option for me. Did you have an enlarged median lobe ? Did the bi-Polar TURP cause Retrograde Ejaculation (RE), or any other side effects ? Do you have medicare ?
Thomas
You didn’t ask me but I’ll answer for myself anyway! I had an enlarged median lobe and I have retro (which I had before from the alpha-blocker I was on). No other side effects. I am on Medicare with a $1500 out-of-pocket max on my supplemental plan. I think bi-polar TURP is pretty standard these days and many doctors are either doing the entire procedure with a button electrode or (as my guy did), using a loop to start with (because it’s faster) then finishing up with the button to cauterize any bleeders and smooth the surface. I also left the hospital without a catheter after 17 hours of continuous bladder irrigation. Resumed all normal activity after 3 weeks.
Interesting tidbit. The hospital is only 5 minutes from my house so when I got the bill for $750 (they billed Medicare $22,000!) I drove over to pay with my credit card and get the points. The billing gal says that will be $675. I say I thought it was $750. She says we give a 10% discount if paid within 45 days. I said the bill didn’t mention that so if I had sent in a check for $750 that’s what I would have paid. She says that’s right.
why would PSA be obsolete in his case?
I didn’t say PSA, I wrote PAE (prostate artery embolzation) which is effective only for prostate s larger than 60-70 cc and works best for prostate volumes >100 cc. It can shrink the total volume by 30-35% if successful.
Lee,
this forum exists for patients with PC and BPH who are willing to exchange their experiences, opinions and advices. I don’t think anybody should refrain from expressing their opinions. In the end it will be you and your doctor who will perform the chosen procedure. A good advice from a fellow patient could be more valuable than an opinion of of a paid (heftily ) urologist, who can be biased in the world of fee for service medicine.
Strongly disagree that “doctor know better” Only the educated patient knows the best treatment in case of not ER service. My medical experience verified that many times. I was strongly advised and denied PAE by my insurance, PCP and Urologist. It turned out the lifesaver and changed my life entirely as in case of many peers with successful PAE.
Don’t discourage people from freely expressing their opinion and even advise.
God bless.
When discussing prostates my previous GP used to say " You know more about this than I do"
I don’t think anybody should refrain from expressing their opinions.
I don’t have a problem with opinions, per se. What I take issue with are opinions presented as facts and opinions that are at odds with established data. I see a lot of that here and I’m sure that there are folks here who may not be willing or able to distinguish between the two. Hence my occasional disclaimers. At almost 1 year post-TURP, I’m about ready to leave anyway. There is no longer any information here that is useful to me.
You hit the nail on the head. People need to realize what a forum like this is and isn’t. I use it as one of many sources to educate and inform myself about my condition and methods of improving it. I’ve gained a wealth of valid info here in addition to reading many relevant medical journal papers, studying the anatomy of the prostate, and watching narrated videos of actual procedures being performed. This is in addition to consulting with half a dozen uros and an IR (who BTW asked me if I was a physician…lol). While there is a risk of someone drawing an incorrect conclusion from reading someone else’s opinion here and taking it as fact, I think the alternate risk is more harmful on average – people not reading here because they’re afraid they’ll get incorrect info.
FYI, My uro told me based on DRE that my prostate was ~30 grams. I had a CT scan for a bleeding problem and was told by the radiologist that my prostate is ~125 grams and very odd shaped. Mine did grow outward. I’m on finasteride and daily Cialis and I’m not sure the present size on my prostate. That said, I occasionally measure my flow rate using a graduated beaker and watch with a second hand. My flow is ~20-25 ML/sec. Some days as much as 30ML/sec. I bought one those funnel type things and overflowed it. I can eat moderate amounts of spicy foods, drink caffeine coffee and have a diet of mostly red meat. I drink alcohol so I can’t comment on that. All I’m saying is size doesn’t matter as much as some think.
I’d pay attention to a persons personal experiences but too many quote rumour and third party fable.
Stay to repay others who need help/advice as you earlier did.