Dercum's Disease - From a patient

Main Category: Pain / Anesthetics
Article Date: 09 Jan 2004 - 0:00 PDT

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'Dercum's Disease - From a patient'

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by Dorrit Hvam, Denmark (a Dercum's patient) Dercum's Disease is a chronic, almost unknown disease, described for the first time by the American neurologist Francis X. Dercum (President Wilson's personal doctor) in 1888.

In spite of the fact that the disease has been known and described for more than 100 years very little research is going on - as solving the enigma of such a rare disease offers neither money nor prestige.

The disease is also known under the names of Lipomatosis Dolorosa, Adiposi(ta)s Dolorosa, Morbus Dercum and Dercum's Syndrome.

Dercum's Disease can emerge quickly or develop over a long period. As for now, the cause of the disease is not known. Among the guesses are an auto immune defence disease, a virus, or a genetic fault.

Some families seem to carry an inherited factor. The symptoms are lipomas or 'cushion'-like fatty swellings, chronic pain, described as burning or smarting. The pain can be found in all of the subcutaneous fat, but also in the skeleton and joints.

The pain can vary regarding strength and localization, but is almost always symmetrical.

In almost all cases the patients will become heavy overweight, about 50% above their normal weight.

Fatigue is a very important symptom which can arise very suddenly in connection with even slight physical strain and put a stop to any kind of activity. The disease makes it difficult for the patient to walk or stand up for long periods, and can in the long run develop into a real handicap.

The swellings or lumps, which can be very tender and sore, can develop all over the body, often starting with the knees, thighs, and arms. The tenderness and pain make it difficult to sit or lie in the same position for very long.

Apart from that, other symptoms can occur (e.g. Sjogren's syndrome and others, listed in the Fagher article on Maureen's website, see below).

In some cases temporary pain relief can be obtained by lidocaine IV. This treatment is not without a certain risk and does not help all patients.

Liposuction has been used as a treatment, but most commonly the swellings or lipomas turn up again after a while. Ordinary pain killers have little or no effect. Many patients will need morphine.

All kinds of exercise, physiotherapy etc. make the condition worse. Losing weight is almost impossible and does not ease the pain.

Most Dercum patients must give up their work and will need aids and appliances in their home as well as for getting around. Social life is affected in various degrees. Small thing that used to be easy will suddenly turn impossible to perform. Even wearing clothes or taking a shower might be very painful.

Some differences have been proven between the cells of Dercum patients and those of normal overweight people. Dercum-cells are bigger and have a higher production of heat and contain larger amounts of some fatty acids (for further information, please read Dr. Fagher's scientific work at Maureen's website
http://dercums_data.tripod.com/fat_heat.html).

The prognosis is not good, due to the fact that there is no treatment or cure available, and the disease may increase over time. It might even be lethal if attacking inner organs.

Please feel welcome to visit my homepage about Dercum's Disease at
www.algon.dk/dercum.

By using the link:

http://www.algon.dk/dercum/dercumeng3.php

from the English section you will find a list of the best web sites with information about Dercum's Disease.

Article adapted by Medical News Today from original press release.
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Visitor Opinions (latest shown first)

Dercums - No help available

posted by Ben on 5 Apr 2012 at 4:21 pm

I was diagnosed with dercums in my late twenties. I have visible lumps in both my thighs, my belly, lower back and arms. Skeletal pain in my wrists and hips. I have only had 1 lump removed, despite numerous requests over the past few years to have the ones in my forearms and lower back removed, my consultant has refused stating 'the NHS does not do cosmetic surgery'. I feel for anyone with this awful condition, most people think I'm just complaining for the sake of it, if only they knew what it felt like to have a lump put constant pressure on nerves. My weight is also a problem, I'm far from obese but find it a huge struggle to keep in shape. Overall-not a good condition to be diagnosed with.

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Have Heel pain

posted by Kevin on 1 Feb 2012 at 6:10 pm

Hi,

I also suffer from alot of heel and toe pain from dercums disease. My arms are getting tired now from lifting up the fork numerous times during eating and it causes a great deal of pain in my arms. My arms kinda feel like they are starting to get numbness in them causing pain and difficulty doing anything with them. God Bless You

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dercums

posted by donald on 9 Nov 2011 at 5:17 pm

i have had multiple surguries an the tumors keep coming back with no end in sight .My son has the same thing but not as bad .At this point i have had 300 tumors removed from my back arms an ribs now my legs are in bad shape .Is there any way to get relief from the pain .

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ouch - dercum's disease

posted by Deanna on 16 Sep 2011 at 9:17 pm

I started having pain in my feet 2 years ago thats how it all started. Then my health went in the crapper. -8 months later severe back pain . Got mri showed ok. Now I have a lump in the inner interior left elbow and some smaller ones in the belly. Then the crease of my knees are sore and swollen.Whats up ? In pain all the time. Cant live like this. Tired all the time . Drs think I am a hypocondriac. Please help me.

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Does Anybody Else Have These Symptoms?

posted by Pam on 7 Sep 2011 at 9:36 pm

I found this whole Dercums Disease by accident. The more I read, the more I am convinced this is what is wrong with me. Symptoms appearing over the last 15 years. Lipomas on arms, legs, trunk ( back). Lipomas are now tender to the touch. Gradually growing more and more. Dr. dismisses as fatty tumors. Fibromyalgia, diagnosed 8 years ago. IBS diagnosed 10 years ago. Terrible, terrible pains in the stomach during attacks. Osteoarthritis diagnosed 8 years ago. Pain in elbows, knees, back, some days, every joint in my body. Doc dismisses as fibro. Right foot started swelling and hurting like mad. Can't find anything wrong with it. Diagnosis: poor circulation! Now pain in stomach, incredible pain in feet and ankles, incredible pain in back. Pain in the feet got so bad, I couldn't wait to get out of the shower because it hurt so bad. Compression hose are helping, but aleviating all the pain. Back pain started low and now is low and moved up my back. Dr. dismisses as fibro. I am complaining of serious memory issues and have been for a long time. I get distracted very easily. I have had sleep disturbances for the last 15 years. Am on sleep medication. Thank God, face and hands are not affected yet other than I drop things all the time. It just appears to me that when you go to a different doc for each different ailment, they are not getting the entire picture. So I took a list of all my ailments recently to my Rheumatologist, he didn't even look at the list, although his PA did and she handed it back to me. He said he wasn't my PC. Took the list to my PC. He didnt look at it. Told PC everything going on. Treated me for fibromyalgia. Will someone please listen to me?? I have totally changed my routine. Everyday chores are now a huge deal to me. I can only get one thing done a day and now I have trouble doing that. Now that I am armed with some info on this disease I will be persistant until they convince me otherwise.

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Angio Lipomas

posted by Michelle G on 11 Aug 2011 at 8:43 pm

I had never heard of this disease until yesterday, and I wonder if it is what has been plaguing me my entire life.

I initially presented around age 5 with a "soft tissue" growing pain that doctors could not explain, and the lack of explanation as well as continued pain kept my parents searching for an answer. Two years later, when I was 7, they got a doctor to listen long enough and a CT scan was done at the time (pre MRI) and a small growth appeared on the results. Doctors feared it was cancer, but excised the tumor and explained to my parents that they had seen nothing like it. I was sent home because it wasn't cancer, told to be a kid and then things got bad again.

From ages 7 - 19 I dealt with constant pain in the quadrant where the original tumor had been excised, and the area slowly rounded and became more and more painful over the years. One morning when I was 19, I woke up and could literally not flex (bend) my leg. We called the doctor, a family friend, and the next thing I knew I was being scheduled for a CT scan which lead to a same day MRI (due to spotting a large tumor) and surgery within the week. The surgeon excised what was called an angio lipoma, which weighed roughly 2 lbs. I was told it had killed the majority of the muscle in my inner thigh, and that I would have structural pain for the rest of my life. I was told that the tumor would not come back again.

Five years later the pain was becoming intense again, and the old familiar sensation of barely being able to touch a portion of my leg was back. I went to the University of Minnesota (where the last round of surgery happened), they did a MRI again and said "tumors back but let's watch it." They said (again) that it was the same angiolipoma.

I just decided to live with the pain instead of waiting and going back to the doctor. My preference is to have the leg chopped off, because it has screwed up the structural integrity of my knee joint.

I do possess some of the other symptoms of dercums.

Does it sound like this could be the reason for my problem.

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dercums

posted by cathy on 2 Aug 2011 at 3:51 pm

the problems with the pain are bad i have the lipomas on my ribcage and are starting in other places. i also have fibromialga,i am so tired of all the pain. this is a terrible disease and feel for everyone that has these problems.

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does gastric banding helps people with dercums disease

posted by donna on 4 Oct 2010 at 9:29 am

does any one know if gastric banding helps people with dercums disease. kind regards donna

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also in The Netherlands,Dercum's hurts!

posted by Barbara Eliasar on 26 Sep 2010 at 8:08 am

Excuses for my bad English but this website and the article, was heaven and an eyeopener for me! Because now I am sure I have this disease. My dermatologist took an biopt because they still think I have Herpes Zoster. I hope to get the results next week. I'm in terrible pain an very ill for the last 4 weeks. Big red lups on my belly and it's spreading every day. One lump was 10 cm big! It's burning and the pain comes as an attack, especcialy in bed. If anybody have some information,I gain all the information I can get.
All the best to all the DD patients.
Barbara
Sneek - The Netherlands

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Dercums Info

posted by Elaine on 5 Aug 2010 at 6:10 pm

It has been 2 years since being diagnosed with this disease. I have type 3 when diagnosed which is non obese. I have become mildly obese but not sure it is all from this disease. I had many lipomas removed in innerthigh. I find each day is harder for me to work due to pain and stressand many other syptoms caused by Dercums. Thebody is a constant struggle to maintain and function with daily activities. but there are many cites esp... on facebook so join and meet others and gain more info! Elaine

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Heel pain

posted by sue on 29 Jul 2010 at 9:15 pm

I am just trying to find out what is going on with my body and the pain I'm having ... I did have a lot of pain in my heel and couldn't even walk at one point.. I bought a sneaker called "shape Ups" by sketcher and haven't had any pain in my heel while wearing the sneakers.... Hope this helps you

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everything hurts

posted by Linda Smith on 6 Jul 2010 at 4:37 pm

Just would like to know has anyone been suffering with pain in their heels? Trying to convince people I'm not just moaning, that I am really hurting badly at times really brings me down.

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Not Obese With Dercums

posted by Elaine on 2 Jul 2009 at 5:34 pm

Dercum's is mostly found in obese people but now they are finding out that it occurs in non obese patients. After diagnosing more patients they are finding that you do not have to be obese to have it. It states that in different descriptions in the disease also in national orginization of rare diseases NORD

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Differential Diagnosis for DD

posted by Margie Lavendt on 24 Jan 2006 at 7:48 am

I was ill for many years. I was positive I had DD. Recently I had a lot of lab work. I tested positive for 4 tick-borne diseases, including Lyme Disease. The symptoms are very similar to DD. I reccomend being evaluated by a Lyme Literate Medical Doctor! LD is treatable!

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Thanks

posted by Tammy Hartzler on 3 May 2005 at 12:31 am

I also have Dercum's Disease and would like to thank the writer of the article. Very good summary of Dercum's, in my opinion.

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The Dercum Difference

posted by Bernadette Peck on 25 Apr 2005 at 10:07 pm

My brother and I are both over 50 and have dercums disease and are not obese, Whats up with this?

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