Guest Posted December 1, 2017 Share Posted December 1, 2017 Hi sorry I. M new to this. I was admitted to hospital on monday with suspected appendicitis but that was ruled out after an ultrasound showed a 4cm cyst in the head of my pancreas. This was confirmed with two contact CT scans. My blood were ok no cancer markers and my liver and kidney function is normal. I have been referred to a GI MDT team and they discussed my case yesterday. A nurse rang and told me they want to see me again to explore further and I will get an appointment in the post but probably won't be before xmas. Is this waiting usual? I have been driving myself crazy googling everythingI am 43 mother of four and work full time usually totally fit and well never really had a sick day beforeI have a two week sick note my pain is ok some days none some days bouts of pain but being managedMy question I suppose is what do people think will happen next and what is a normal waiting time Thank you Link to comment Share on other sites More sharing options...
WifeampMum Posted December 1, 2017 Share Posted December 1, 2017 Hi Robette, So sorry you’re going through all this!I’ve found the following timescales advice on the PCUK website herehttps://www.pancreaticcancer.org.uk/information-and-support/facts-about-pancreatic-cancer/how-is-pancreatic-cancer-diagnosed/tests-for-pancreatic-cancer/“You may have to wait a few days – or as long as two weeks – for some scans or tests. Sometimes people have to wait longer than this. If you’ve been given an urgent referral for a test because of suspected cancer, it should be done within two weeks. If you haven’t heard anything within two weeks, speak to your doctor. It may also help to speak to the consultant’s secretary.”Hope it helpsW&M xx Link to comment Share on other sites More sharing options...
Guest Posted December 1, 2017 Share Posted December 1, 2017 Thank you that is helpful hopefully I will have an appointment soon Link to comment Share on other sites More sharing options...
Justamo Posted December 2, 2017 Share Posted December 2, 2017 IMPORTANT - I strongly advise you NOT to click on the link in the above reply on this thread. (The Russian one, not the reply from Wife & Mum, obviously !)Mo Link to comment Share on other sites More sharing options...
Guest Posted December 3, 2017 Share Posted December 3, 2017 I thought it looks a little dodgy Link to comment Share on other sites More sharing options...
Veema Posted December 3, 2017 Share Posted December 3, 2017 I reported the post yesterday...looked dodgy although I don't speak Russian!Thing is, I'm now desperate to click on it!Hope you get an appointment soon Roberts.Vx Link to comment Share on other sites More sharing options...
PCUK Nurse Jeni Posted December 4, 2017 Share Posted December 4, 2017 Thank you for alerting us to these posts.They have now been deleted. Dainne & Jeni,Pancreatic Cancer Specialist NursesSupport TeamPancreatic Cancer UKemail: nurse@pancreaticcancer.org.uksupport line: 0808 801 0707 Link to comment Share on other sites More sharing options...
Justamo Posted December 4, 2017 Share Posted December 4, 2017 Just in case you are all wondering, the deleted posts - both Russian - each contained a link. The first post was all about car washing in monumental detail, and the second one concerned itself with a type of sun roof for VW cars. They were both rather boring but highly suspect. Hope you get some news soon Robette. Keep us posted.Love, Mo Link to comment Share on other sites More sharing options...
Guest Posted December 5, 2017 Share Posted December 5, 2017 Quick update-telephone call from specialist nurse today to let me know that they have booked my appointment for endiscopic ultrasound and will be within next two weeks Link to comment Share on other sites More sharing options...
Guest Posted December 19, 2017 Share Posted December 19, 2017 Hi My ct scan has diagnosed me with a 4cm branch duct IPMN in the head of the pancreas which i'm lead to believe is very good outcome. I had an EUS and biopsy last week to further confirm this but I am still waiting for results. I met with the consultants registrar last week before the EUS and he seemed keen to take a conservative watch and wait approach which is reassuring but everywhere I read suggests anything over 3cm is best to be offered surgery . My mind is in overdrive any advice for me for next consultant appointment would be greatly appreciated Link to comment Share on other sites More sharing options...
Dandygal76 Posted December 19, 2017 Share Posted December 19, 2017 That is good news and gives a lot of hope to other people prediagnosis. I have said on here before I have a bronchogenic cyst of around 4-5cm sitting nicely against my Aorta and nerve for my voice. They have wanted to take it out for an age but I just get a 6 monthly scan instead for changes and nothing has changed. There is a small chance it can get infected and bleed and a 1-2% chance it can turn cancerous. Well I have certainly questioned the latter as I think we all nearly have a 1-2 in 3 chance of cancer in our lifetimes anyway. The operation I would have is on par with a whipples and can have significant consequences on my life, as with the whipples. I know they are not the same thing but is really a cost /benefit /risk appetite for you personally. If it was me it would depend on what else they offer up - how often will they scan, would they do MRI and not CT so not to keep poisoning me, how many people have they left with a 4cm cyst and outcomes etc. The current medical thinking was to remove mine but when I looked at the stats and results I managed to get the consultant to admit it is a grey and largely untested area. Also, stay off anything except professional sites in your research or you will drive yourself mad. Link to comment Share on other sites More sharing options...
WifeampMum Posted December 19, 2017 Share Posted December 19, 2017 Hi RobetteIn the scheme of things, as you say, your diagnosis is very good. But if I were in your situation I'd also be concerned by the advice you've been offered...I've just done some Googling and found articles from eminent institutions that back up the "over 3 cms" cut-off. I also found a recent article:https://pancreasfoundation.org/wp-content/uploads/2017/02/CLINICAL-MANAGEMENT-OF-INTRADUCTAL-PAPILLARY-MUCINOUS-NEOPLASMS-OF-THE-PANCREAS.pdfthat says:"Patients with branch duct IPMNs who are symptomatic should be treated with resection not only to alleviate the symptoms, but also because of a higher likelihood of malignancy. It is important to emphasize that the decision to treat should be individualized and based on patient preferences and willingness or unwillingness to undergo follow-up studies, as well as on the availability of safe pancreatic resection."So the fact that you are symptomatic is also something to take into account.During the 2.5 years that hubby and I have been on Planet PC we've sought second opinions several times and never regretted it. This is what we would do in this situation. Also we would speak to the wonderful nurses on the PCUK Support Line.But I hope you can derive a lot of comfort from the fact that there's a good chance that your ipmn is benign, and that if it isn't, it's very treatable.W&M xx Link to comment Share on other sites More sharing options...
Guest Posted December 19, 2017 Share Posted December 19, 2017 Hi dandygal76 and wifeandmum Thankyou for your replies they are very helpful Link to comment Share on other sites More sharing options...
Didge Posted December 19, 2017 Share Posted December 19, 2017 This is good news. Wait for the biopsy results and if they concern you (and if your consultant’s advice still concerns you after he/she has reviewed the situation) then ask for a second opinion and make sure it is from one of the specialist hospitals. It could even be from a more senior consultant (e.g Head of Department) at the same hospital if you’re already at a specialist hospital. But I hope this means that you will have a better Christmas than you were expecting! Link to comment Share on other sites More sharing options...
PCUK Nurse Jeni Posted December 19, 2017 Share Posted December 19, 2017 Hi Robette,Do you know if your case has been discussed with the specialist Multi-Disciplinary team, at whatever specialist centre your local hospital feeds into? Or did you have the EUS at a specialist centre? Robette, if you wish to make contact with us, then we can speak to you in more detail about this, and steps forward. Please feel free to call or email - our contact details are in the signature below.Kind regards,Jeni. Pancreatic Cancer Specialist NurseSupport TeamPancreatic Cancer UKemail: nurse@pancreaticcancer.org.uksupport line: 0808 801 0707 Link to comment Share on other sites More sharing options...
Justamo Posted December 24, 2017 Share Posted December 24, 2017 PLEASE DON'T CLICK ON ANY LINKS IN THE PREVIOUS POST, something a bit odd about them. Link to comment Share on other sites More sharing options...
PCUK Nurse Jeni Posted January 18, 2018 Share Posted January 18, 2018 Hi All,Thank you for alerting us to the post - I have now deleted this.Kind regards,Jeni. Jeni JonesPancreatic Cancer Specialist NurseSupport TeamPancreatic Cancer UKemail: nurse@pancreaticcancer.org.uksupport line: 0808 801 0707 Link to comment Share on other sites More sharing options...
Guest Posted April 11, 2018 Share Posted April 11, 2018 Just thought I would update I am currently on watch and wait surveillance for 6 months with what the consultant is confident is a side branch Ipmn in the head of the pancreas but the consultant thought my symptoms maybe from gallbladder so I have had that removed on Monday so will hopeful you be feeling better soon and next follow up will be around june~July time Link to comment Share on other sites More sharing options...
sandraW Posted January 23, 2019 Share Posted January 23, 2019 Hi Robette, Thanks for letting us know how well you are doing, its always good to get some good news although I am not sure you would feel having your gallbladder removed was actually good news, but it could have been much worse news. Please let us know your results later on in the year, sending love sandrax xx Link to comment Share on other sites More sharing options...
littlesister Posted March 11, 2019 Share Posted March 11, 2019 Robette, can you tell me the symptoms. I have IPMNs in the uncinate area and have been having pain in right hand side of my abdomen. Recently had catscan and am awaiting results. Strange that these are the pains which first took me to dr. and which led to the diagnosis of IPMN. They have come back with some force. Also nauseous if I eat and if I don't eat! Link to comment Share on other sites More sharing options...
PCUK Nurse Dianne Posted May 6, 2019 Share Posted May 6, 2019 Hi 'Littlesister'Please feel free to touch base with us on the support line if you would like some support, i note you have some questions about IPMNs.We can give you some guidance if this may be helpful. Please feel free to touch base with us on the support line. Our phone lines are open from Monday to Friday 10am - 4pm and you may email us on nurse@pancreaticcancer.org.uk, and we would certainly reply to you next week.With kind regards,DiannePancreatic Cancer Specialist NursePancreatic Cancer UK.Support Line: 0808 801 0707Email: nurse@pancreaticcancer.org.uk Link to comment Share on other sites More sharing options...
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