Itching: Does anyone have itching that is NOT on... - MPN Voice

MPN Voice

10,886 members15,201 posts

Itching

ERei profile image
ERei
25 Replies

Does anyone have itching that is NOT on the palms of their hands or soles of their feet? Lately I've had it on my chest & my neck. My hematologist says it is not from my PV because if it were from PV it would be on my hands & feet and also that my #s are not high enough right now.

Written by
ERei profile image
ERei
To view profiles and participate in discussions please or .
25 Replies
C2Cnext profile image
C2Cnext

I most commonly get itching on my arms and thighs and sometimes on my neck/décolletage. I think current thinking is that it related to mast cells and I am not sure why your hematologist thinks mast cells would only be in one bit of your body??

Cat1001954 profile image
Cat1001954

hi I get terrible I Ching on my legs and sometimes my arms but mainly legs

LittleLuna profile image
LittleLuna

i get hands, feet, legs, arms itch. My numbers are also low and per my MPN Specialist numbers do not determine the symptom burden levels we experience.

I would suggest your haematologist does some research on patient experiences of symptoms.

It can be so so annoying. Some people here will advice on good tips to help. I am not too bad so not had to resort to anti histamines or any other meds yet.

Water does tend to be an aggravater for a lot of people on here.

Hope u feel better and get some relief.

ERei profile image
ERei in reply toLittleLuna

Thank you. This is actually my 3rd hematologist! I also see an MPN specialist who is far away every 3 months.

john0084 profile image
john0084

The itch is a well documented symptom of pv, blurry vision is another, the only relief I've discovered after itching for years is beta-alaine a sports supplement, it's not perfect but a small teaspoon before showering helps.

ainslie profile image
ainslie

ive been a Olympic PV itcher for many years prior to Rux, I have never had it on hands or feet, counts didn’t make any difference , your Haem has room for improvement

S031251 profile image
S031251

I agree entirely with ainslie and littleluna.

I hope you find something to help although only Rux helped me and now I’m free or it

Anna

RazB profile image
RazB

hi, I have ET. I itch everywhere! I’m always aware that I’m like a child who finds it hard to sit still and forgets and itches constantly! X

Anouchka profile image
Anouchka

I have itching on insides of my heels or calves. I relate it to my PV but never thought of clarifying it with my haem cos the itching started before diagnosis and was told then it was related. Now it’s sporadic and my numbers are “stable”….

JP1952 profile image
JP1952

I also agree with Ainslie and little Luna.I itched all over my body except for palms of my hands, soles of my feet, and my scalp.

Only Rux stopped it completely but anti histamines and oil based soap/moisturizer helped a little.

Good luck. Itching is horrible.

Threelions profile image
Threelions

Calfs & thighs for me. So far no itching on feet or palms of hands.

Hopetohelp profile image
Hopetohelp

I get the itching after the bath. For many years it was front of neck and arms. It seemed to be where I caught the sun. Then it spread to my back but that thank goodness that has disappeared.

STK52 profile image
STK52

I get itch or skin tightness when my body gets rubbed or after shower. But not in my hands or feet!!!

DEGate profile image
DEGate

My wife suggested I try Solgar Stinging Nettle Leaf extract tablets which she uses for prickly heat and they have certainly helped my itching.

Showering is definitely an issue; I tried much cooler showers but that didn't help. I have been taking anti-histamine which seemed to help for a while but I've stopped recently and it doesn't seem to make any difference. I will look into Beta-alanine as suggested by John0084.

hunter5582 profile image
hunter5582

You have already heard from others that MPN-related itching and pruritis are not confined to hands and feet. While some people report a reduction in itching with cytoreduction, it is not related to the numbers of RBCs. RBCs have nothing to do with itching.

Suggest that you consult with a MPN Specialist for accurate information about MPNs. Here are two lists.

mpnforum.com/list-hem./

pvreporter.com/mpn-speciali...

NY45 profile image
NY45

I think I have found itching to be a side effect of my immunotherapy and some moisturizers with anti-itch ingredients have helped.

ERei profile image
ERei in reply toNY45

Which moisturizers have you tried?

Murdoch01 profile image
Murdoch01

Hi ERei the only thing that really helps me is an ice pack I don’t get in on my hands and feet, mostly on my arms and getting hot makes it worse. I hope you find something that helps you.

AndyKay profile image
AndyKay

Yes, the tops and bottoms of my feet itch; sometimes my ankles do to.

Itch profile image
Itch

Hi, as with others, I haven’t experienced itching on hands & feet, but had unbearable itching, burning stabbing in upper arms until prescribed Fexofenadine ( anti histamine) . I now take 120mg twice daily & now which has eased it completely. Good luck 🤞

Maurabawn profile image
Maurabawn

Hi! Hopefully you are reassured from the above replies that itching goes with the disease! One of my symptoms before being diagnosed with ET, MPL driver, was intense itching on the top of my head and the base of my spine! Thankfully, Hydroxycarbamide has reduced this significantly. Hope you find relief soon.

K-itty profile image
K-itty

Before I was diagnosed with ET in 2015 and eventually with PV, my neck would constantly itch. It continues to do. I always thought it was from the PV, however my hematocrit #s have been low, so I suspect it's the ETand elevated platelets. I recently started on Jakafi, and both inflammation and itching have subsided.

finlay2106 profile image
finlay2106

Just come across your post. As per the others I've never had itching on palms or soles. Mostly back and forearms and sometimes front of thighs and it comes and goes. My haematologist confirmed it's mast cells de-granulating that causes it but said they don't know why it actually happens. Yes it's made worse with showering or rubbing and I try to have a cold or tepid shower (on gentle setting) which still can cause itching but it wears off pretty quickly. I never use moisturiser as skin is not dry and don't see the point. If really bad especially at night then I take paracetamol and cetirizine hydrochloride (anti-histamine) which calms things down. I have PV, take hydroxycarbamide 1gm daily and 75mg aspirin. Blood count variations don't appear to have any impact on where and when I itch.

I think your haematologist needs to do some research/education!

MAP44 profile image
MAP44

hi ERei,

Not true! I have PV and I am itchy mostly on my arms and legs and occasionally on the trunk but never on my hands and feet.

Pte82 profile image
Pte82

Hey ERei, vitamin C is an antihistamine. My wife found relief from itching when on Hydroxy by using a liposomal whole vitamine C complex supplement. Ascorbic acid is only a part of the whole vitamin C complex and liposomal delivery offers several advantages one being it lasts longer. Check it all out and consult with your health care professional before using any supplement.

Not what you're looking for?

You may also like...

Itching

Hello Everyone, I am 42 and diagnosed with PV 5 years ago. So far I am just taking aspirin and...
DN515 profile image

Itching during the night

Hi everyone, I have PV and have recently been experiencing extremely itchy skin during the night....
Spam1979 profile image

Hydroxyurea & itching

Hi ... can anyone please please tell me if hydroxyurea got rid of PV itching ??????? OH my Lord.....

PV and burning Feet

Hello everyone, am new here and joined this forum to keep abreast with the latest MPN news as my...
Rheanick profile image

Itching & MPNs

From our friends at MyMPNTeam. A nice and quick piece on itching with MPNs. Yes, it occurs...
hunter5582 profile image

Moderation team

Debinha profile image
DebinhaAdministrator
Mazcd profile image
MazcdPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.