Anyone else have Hematidrosis (bleeding)?
 

Here's a new one folks. I have suffered from this miserable condition for 8 years now. The other day I thought I was going to die from the intense crushing/burning we all get. I looked down at my arm and it was oozing blood out of the pores. Freaked me out bad. I rushed to the ER and they were just as freaked as I was. They were clueless. It took massive amounts of IV pain meds to get it under control. It was a real mess.

My pm doctor sent me to a dermatologist and he confirmed that it was "hematidrosis", a condition when pain and anxiety collide and cause the small capillaries around your sweat glands to burst, mix with the sweat and exit your body thus causing a bloody mess. It left severe bruising for days, weeks after.

Has anyone else had this happen? Now that I know what it is, I won't be so freaked out next time (if) it happens. Kinda scary. :confused:

Hi Jetjock1, WOW...never heard of that one. I have acquired some type of blood blisters that have opened and drained but that was usually following a form of repetative injury. Are you taking anything for anxiety? I have learned that treating my anxiety has actually decreased my pain, something you may need to address with your doctor. That must have been horrifying in itself. I hope your pain and anxiety are better under control. I also use meditation, reading, visualization techniques to control anxiety and pain. I do hope this is not another symptom of this little critter (RSD). Sorry for your pain and will pray this does not happen to you again in the future.

Jeanie

Bleeding from pores
 

This has happened to my daughter. From skin, tear ducts as well

Scary Indeed
 

Thanks Wilbyfree,

Yes, I'm taking anxiety meds. That is the reason for hematidrosis. It's just that it's a kind of anxiety on a whole different level than what we usually get. If everything goes right, I know when it's heading there and I take the meds fast, along with extra break through pain meds. Scares the living daylights out of me.

I do all the other stuff too; meditation, artistic outlets, biofeedback, etc. but nothing works as well as the combination of meds they have me use to knock it down.

I don't mean to alarm anyone else that is courageously fighting the good fight. It's extreeeeeeemly rare. 99.9% of us will never experience this phenomenon. At least that's what the docs say.

Jet

jetjock1 -

I've had a modified form it off and on the same spot since shortly after I was diagnosed with a positive response to a LSB. On the inside of my left ankle. Which is of note only because while I suffered a bilateral injury to my tendons and have RSD in both feet, there is no corresponding bruising on my right foot. Also the first time I showed it to a "pain specialist" he had no idea what to make of it!

That said, mine don't bleed through, all I have is the apparent "bruise." My understanding of the process may be a little different than yours, however. Based on what I have read, the walls of all blood vessels other than capillaries are filled with nerves (they are said to be "innervated") that are in general controlled by the sympathetic nervous system. In CRPS/RSD there are two principal dysfunctions of the vascular system, and while in theory they happen sequentially, I've got them at the same time in different parts of my body: neurogenic vasodilatation and neurogenic constriction. In the former, vascular tone is lost, initially resulting in the loss of mater from the vessel through "extravasation" (essentially, osmosis) - which is called edema - and then finally, as the wall of the vessel loses all tone, spaces appear that are large enough for the hemoglobin to escape, and we have a bruise or an outright hematidrosis if it makes it's way through the skin.

On the other hand, with neurogenic vasoconstriction, the flood flow is reduced or lost altogether. In my case that's most obviously manifest by my inability to be fitting with any iv larger than a 22 gauge: this is something that was first picked up in me about 20 months into the RSD, whereas while I also had the bruising from close to the start, it wasn't accompanied with dramatic edema for another six years. (Another example of no two cases of RSD being the same.)

Where the theories get tricky is in explaining the signaling mechanisms to the nerves. And for that I can only lay out what I understand to be the two leading contemporary schools of thought.

Anne Louis Oaklander, MD, PhD, sees this, and virtually every other aspect of CRPS as part and parcel of small-fiber neuropathy, which is doubtless going on, but there is some question as to whether the two are casually related or simply act as co-variants of a common underlying cause. See, e.g., Oaklander AL, Fields HL, Is reflex sympathetic dystrophy/complex regional pain syndrome type I a small-fiber neuropathy? Ann Neurol. 2009 Jun;65(6):629-38:

Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. aoaklander@partners.org

Abstract
Neurologist S. Weir Mitchell first described "causalgia" following wartime nerve injury, with its persistent distal limb burning pain, swelling, and abnormal skin color, temperature, and sweating. Similar post-traumatic symptoms were later identified in patients without overt nerve injuries after trauma. This was labeled reflex sympathetic dystrophy (RSD; now complex regional pain syndrome type I [CRPS-I]). The pathophysiology of symptoms is unknown and treatment options are limited. We propose that persistent RSD/CRPS-I is a post-traumatic neuralgia associated with distal degeneration of small-diameter peripheral axons. Small-fiber lesions are easily missed on examination and are undetected by standard electrophysiological testing. Most CRPS features-spreading pain and skin hypersensitivity, vasomotor instability, osteopenia, edema, and abnormal sweating-are explicable by small-fiber dysfunction. Small fibers sense pain and temperature but also regulate tissue function through neuroeffector actions. Indeed, small-fiber-predominant polyneuropathies cause CRPS-like abnormalities, and pathological studies of nerves from chronic CRPS-I patients confirm small-fiber-predominant pathology. Small distal nerve injuries in rodents reproduce many CRPS features, further supporting this hypothesis. CRPS symptoms likely reflect combined effects of axonal degeneration and plasticity, inappropriate firing and neurosecretion by residual axons, and denervation supersensitivity. The resulting tissue edema, hypoxia, and secondary central nervous system changes can exacerbate symptoms and perpetuate pathology. Restoring the interest of neurologists in RSD/CRPS should improve patient care and broaden our knowledge of small-fiber functions. [Emphasis added.]

PMID: 19557864 [PubMed - indexed for MEDLINE]

http://www.ncbi.nlm.nih.gov/pubmed/19557864

In principle contrast is the inflammation theme expounded upon by, among others, Frank Birklein and Martin Schmelz in Neuropeptides, Neurogenic Inflammation and Complex Regional Pain Syndrome (CRPS), Neurosci Letters. 2008; 437:199-202, FREE FULL TEXT at http://www.rsds.org/2/library/articl...in_Schmelz.pdf

Abstract
This review explains symptoms and nature of neuropeptide signaling and its importance for clinical symptoms of CRPS. Neurogenic inflammation regularly accompanies excitation of primary afferent nociceptors. It has two major components-plasma extravasation and vasodilatation.The most important mediators are the calcitonin gene-related peptide (CGRP) and substance P(SP). After peripheral trauma immune reaction (e.g. cytokines) and the attempts of the tissue to regenerate (e.g. growth factors) sensitize nociceptors and amplify neurogenic inflammation. This cascade of events has been demonstrated in rat models of CRPS. Clinical findings in these animals strongly resemble clinical findings in CRPS, and can be prevented byanticytokine and anti-neuropeptide treatment. In CRPS patients, there is meanwhile also plenty of evidence that neurogenic inflammation contributes to clinical presentation. Increased cytokine production was demonstrated, as well as facilitated neurogenic inflammation. Very recently even "non-inflammatory" signs of CRPS (hyperhidrosis, cold skin) have been linked to neuropeptide signaling. Surprisingly, there was even moderately increased neurogenic inflammation in unaffected body regions. This favors the possibilitythat CRPS patients share genetic similarities. The future search for genetic commonalities will help us to further unravel the "mystery" CRPS.

PMID: 18423863 [PubMed - indexed for MEDLINE]

http://www.ncbi.nlm.nih.gov/pubmed/18423863

And as set forth in the text:

. . . it has become clear that action potentials from activated nociceptors invade end branches of primary afferent neurons by retrograde conduction ("axon reflex") and release neuropeptides from their terminals [62]. The acute effects of primary afferent fiber induced neuropeptide release are vasodilation and protein extravasation, which has been therefore termed "neurogenic inflammation". Pivotal neuropeptides in the induction of neurogenic inflammation are calcitonin gene-related peptide (CGRP) for vasodilation and substance P (SP) for the induction of protein extravasation-at least in rodents [27]. As a result of previous studies, mechano-insensitive, but heat-and chemo-sensitive C-nociceptors have been found to be responsible for the neurogenic vasodilation in pig [38] and human skin [57] . . . . [at 199]

Notes
[27] P. Holzer, Neurogenic vasodilatation and plasma leakage in the skin, Gen. Pharmacal. 30 (1998) 5-11.
[38] B. Lynn, S. Schutterle, EK. Pierau, The vasodilator component of neurogenic inflammation is caused by a special subclass of heat-sensitive nociceptors in the skin of the pig, J. Physiol. (Lond.) 494 (1996) 587-593.
[57] M. Schmelz, K. Michael, e. Weidner, R. Schmidt, H,E, Torebjiirk, H.O. Handwerker, Which nerve fibers mediate the axon reflex flare in human skin? Neuroreport 11 (2000) 645-648.
[62] J. Szolcsanyi, Capsaicin-sensitive sensory nerve terminals with local and systemic efferent functions: facts and scopes of an unorthodox neuroregulatory mechanism, Prog. Brain Res. 113 (1996) 343-359

That said, this may all just be the tip of the iceberg. For a cogent and readable treatment of what appears to cover perhaps 80% of the science today, see, Maihofner C, Seifert F, Markovic K, Complex Regional Pain Syndromes: New Pathophysiological Concepts and Therapies, Eur J Neurol. E-pub 18 Feb 2010, FREE FULL TEXT at http://www.rsds.org/2/library/articl...eurol_2010.pdf

I hope this is useful.

Mike

:grouphug:my daughter was just diagnosed with hematidrosis, they have her taking buspar but it doesn't help much they just started her on steriods. What do you take and does it seem to help.

I am so sorry. I feel so awful for children and parents having this. I'm a Mom, with RSD. your friend, loretta:grouphug:

Hi Jet, I'm so sorry you have gone thru this. Must have been so scary.
Yes, I have heard of this condition. It is when a person is in extreme stress.
Biofeedback and meditation, visualization are wonderful tools to use. My Dr. a
Neurologist, Phychiatrist, and Pharmacologist says the anxiety meds are as important or more so as pain meds. They will bring the pain down.
Anxiety is a big part of this disorder. It has to do with the Limbic System in the Brain. Before I knew I had RSD, Had panic disorders for first time in life and couldn't figure what was going on.
That plane still looks a lot like the one my son in law flies.:) I hope for calmness and peace for you. Your friend, loretta

Hi flb, So sorry to hear about your daughter. You'll find a lot of caring compassionate people here, adults and children. Has she been diagnosed with another condition-RSD? We are here for you, support and in addition to a lot of educated friends. Take care, loretta:grouphug:

Thanks Mike, Appreciate so much your research and sharing with us. This is very interesting-will share with my Dr. who is very interested in more information.
He completed his two new clinics with double HBOT in each of them here in Scottsdale and Paradise Valley. A neuro called him and asked him to take a patient for the HBOT treatment. She was involved in a car accident. Two other cars collided on freeway and ran into fence-one of the metal poles became a missle and went thru her windshield and pierced her shoulder to the back of her seat. After 17 surgeries, her neuro asked my Dr. to treat her with HBOT for frozen shoulder-After 6 treatments she was waiving her arm to the TV crew people. ( I had 100 treatments of pt to get use of my shoulder)
Do you have an opinion of HBOT? I'm definetly going to try it. Thanks Mike, your friend, loretta

Thank you so muhch for this information. I have never heard of it. Now IF it happens to me I will know not to be as scared. I have had rsd for 8 yrs as well and so far have not had to deal with that. It is the first time I have ever heard of it and I am so sorry for everyone that is or has gone thru it. I am just glad that it was shared with us all so for the ones of us that have never experienced it or heard of it will know about it. Thank you so much to everyone for there input on this whole deal. it will help me not to be as frightened if it happens to me. Thanks to everyone and god bless everyone.

Sincerely,
Tracy

Hi, I'm trying to find other people with this condition to learn more about it, since my boyfriends little 12 year old sister has a severe case of this in Japan and we are trying to bring her here to the U.S to get treatment. If you read this message and can share some information I would really appreciate it!

First time I've ever heard of this. OMG, must be horrible to go through.

I hope you find the care you need. Can't they do anything in Japan? It's not exactly a 3rd world country, right? ;)