About a year & a half ago, I began having discomfort, sometimes pain, in the right side of my abdomen. At
firstFirst progesterone mc10
First progesterone mc5
First-progesterone vgs 100
First-progesterone vgs 200
First-progesterone vgs 25
First-progesterone vgs 400
First-progesterone vgs 50
First-testosterone
First-testosterone mc it was all over the right side, upper & lower, wrapping around into my back & even down into my
hipHip joint replacement
Hip pain. Now it's usually just in the liver area, sometimes radiating around and down. I saw my OB-GYN, who felt my ovaries, said they were fine. I then had an abdominal ultrasound to rule out gall stones. (April 2005) The report said that the liver, pancreas, gallbladder were
normalNormal saline flush, but that there was "a 1.1 x 1.1 cm. echogenic nodule in the right
hepaticAmebic liver abscess
Hepatic hemangioma
Hepatic ischemia
Hepatic vein obstruction (budd-chiari)
Liver transplant
Percutaneous transhepatic cholangiogram
Transjugular intrahepatic portosystemic shunt (tips) lobe which may represent an incidental
hemangiomaBirthmarks - red
Hemangioma
Hemangioma - angiogram
Hemangioma - ct scan
Hemangioma excision
Hemangioma on the chin
Hemangioma on the face (nose)
Hepatic hemangioma". I had a follow-up ultrasound in July 2005. The impression was "A vague 1 cm echogenic lesion in the liver dome which is likely the same questioned
hemangiomaBirthmarks - red
Hemangioma
Hemangioma - angiogram
Hemangioma - ct scan
Hemangioma excision
Hemangioma on the chin
Hemangioma on the face (nose)
Hepatic hemangioma on prior study. It is otherwise unchanged in size. An additional 6-9 month follow-up ultrasound is suggested to ensure continued stability." The final ultrasound was done on Feb. 2006. The report said, "Just under the hemidiaphragm there is a 1.2 cm hyperechoic mass lesion consistent with benign hemangioma. The finding is of doubtful clinical significance.", then, "Benign appearing mass lesion in the superior liver consistent with incidental hemagioma." I also had a contrast CT scan in July 2005 of my pelvic area & abdomen, and that was normal, except for the hemangioma. They don't want to follow this anymore. My concern is this: I am still having pain in that area, sometimes all over the right side of my abdomen and into my back. I haven't had a colonoscopy, doctor didn't feel I need one, and yet I know that colon tumors don't show up on ultrasounds or CT scans. So, I'm worried that I could have a tumor in the "hepatic flexure" of my colon, and that the "hemangioma" may be a tumor. My doctor told me I have IBS, but I have none of the classic symptoms of IBS. I honestly think he's written me off as a hypochondriac, but this pain is very real and almost non-stop.
Also, my GGT liver enzyme is slightly elevated, but that could be because I take Dilantin.
Thanks for reading all of this!! I wanted you to have all the info I have.
My doctor did suggest that I not take birth control pills because they contain estrogen. Since alcohol raises estrogen levels, I am assuming it would be better to abstain from that as well. Is anyone taking any special dietary supplements? This is all so new to me.
From what I've read, I would not take medications which affect blood flow in an attempt to stem the pain - pain is caused either by bleeding into the tumour, or by blood clots. Therefore taking meds to increase blood flow could exacerbate pain if caused by bleeding. Likewise, typically blood flow within haemangioma is sluggish already and taking something to slow flow is liable to increase the risk of clot (thrombosis).
I think at this stage finding a method of controlling pain is the first port of call - obviously there is a problem with doctors not taking the pain seriously generally. But bear in mind there are risks with any of the definitive procedures such as radiofrequency ablation, embolism and surgery, and it may just be that until the lesion reaches a certain size the risks outweigh the benefits.
Having said this, if you have pain from haemangioma you should be under a gastroenterologist to monitor it rather than a general physician.
If pills are not enough ask about referral to a pain specialist for advice.
I'm relatively recently diagnosed only - but appears that palpation by the doctor, bumpy car journeys, etc set off my pain and I'll definitely be seeking more definitive solutions than pain control long term as I can't work when the pain is active - can't sleep properly, can't drive to work etc.