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Eosinophilic esophagitis

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A dx of EE isn't dependant on having eos in the blood. It is usually

dx by biopsy. DS was worked up for EE, but was already on the

elimination diet at time of endoscopy. There is an EGID board

& lots of parents there will tell you that their child is dx w/EE,

but it wasn't found in the bloodwork. Tx can consist of elimination

diet, elemental diet, & /or inhaled steroids. It is believed to be

either allergy based or immune based. I know of another child who

was worked up for achalasia & it was found he has EE. Here are some

very good links about EE:

http://www.apfed.org

eosinophilgastro/

http://www.cincinnatichildrens.org/svc/alpha/e/eosinophilic/

in OH, mom to: Grant 2 yo w/reflux, dysphagia w/aspiration &

on thickened liquids, in OT & PT, hypotonia, feeding therapy,

intolerant to lots with immunologic responses, nodules found in

duodenum indicate possible food allergy, possible oral allergy

syndrome, on prevacid, E028 only but not drinking enough, losing

weight due to swallowing difficulty, possible achalasia

Aleah 5 yo w/reflux, cyclic vomiting (Now not sure if accurate dx

since eliminating dairy), delayed gastric emptying, MPI, chronic

sinusitis, hypotonia, in OT, on prevacid & rhinocort

> Hi all,

> The words eosinophilic esophagitis caught my eye, as my 16 yr old

> boy is currently awaiting results of a blood test for it. He was

> diagnosed with Achalasia a year ago and had the Heller's Lap/no

wrap

> surgery, but the GI is still not happy with the esophagus as shown

> on the barium swallow and manometry; the endoscopy showed

> eosinophils-and esophagitis, but the scope passed through easily

> enough. His only 'bad' symptom at present is the chest

> pain,controlled with cold drinks and not affecting his everyday

life

> as long as he remembers to carry a drink around. He is on a trial

of

> domperidone(motility), and proton pump inhibitors for the chest

> pain, to rule out acid reflux. (doesn't seem to be working).

> There has been talk of another Hellers-open this time, and I would

> like to avoid that for as long as possible, or maybe dilatation-

> although the GI seemed to think the results would be affected

> because of the Hellers a year ago.

> We are waiting for the follow-up to decide what to do next.

> Sally mother of Stefan

> London

> England

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This group is great! It's so nice to hear of people who even know

what EE is! Most people I discuss any of my husband's case with have

no idea what I'm talking about. Is EE found mostly in children? My

husband had blood tests and biopsies of esophagus sites to check for

EE at Univ. of Mich. The doctor said that he could go back and biopsy

more sites, but the original biopsies didn't show EE. Instead, he went

on to do the barium swallow, manometry, and 24 hr ph probe (which

ruled out reflux). I wonder if Cleveland Clinic will revisit this

issue when we are there. I didn't realize that a person could have

both achalasia and EE.

Sally, good luck with making a decision for your son's treatment!

I hope he can get relief from the easiest method possible. I don't

blame you for wanting to delay more surgery as long as possible!

, it sounds like you have a lot on your plate these days! I'm

so sorry your little ones have so many problems! I hope all the

treatments and therapies help them. Wouldn't it be nice if they just

outgrew all of these things? Thank you both for your input!

> Hi all,

> The words eosinophilic esophagitis caught my eye, as my 16 yr old

> boy is currently awaiting results of a blood test for it. He was

> diagnosed with Achalasia a year ago and had the Heller's Lap/no wrap

> surgery, but the GI is still not happy with the esophagus as shown

> on the barium swallow and manometry; the endoscopy showed

> eosinophils-and esophagitis, but the scope passed through easily

> enough. His only 'bad' symptom at present is the chest

> pain,controlled with cold drinks and not affecting his everyday life

> as long as he remembers to carry a drink around. He is on a trial of

> domperidone(motility), and proton pump inhibitors for the chest

> pain, to rule out acid reflux. (doesn't seem to be working).

> There has been talk of another Hellers-open this time, and I would

> like to avoid that for as long as possible, or maybe dilatation-

> although the GI seemed to think the results would be affected

> because of the Hellers a year ago.

> We are waiting for the follow-up to decide what to do next.

> Sally mother of Stefan

> London

> England

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Hi Jenn, and thanks for the interesting information and Links. I think

I caused a misunderstanding in my post: I meant that Stefan had a blood

test to check for allergies, not to check for EE. Although he was

diagnosed with A, he didn't have the endoscopy (with biopsies &

discovery of eosinophils) until a year later, then had the PPI trial,

(ongoing for two more weeks) & blood test for allergies. He had Asthma

badly as a toddler, and gets the chest pain and swallowing problems

still. We wait with bated breath for the results...........

Sally and Stefan

London

UK

> A dx of EE isn't dependant on having eos in the blood. It is usually

>

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  • 5 years later...

Its called mold colonization.. give it some intraconzole nasal spray for a yr

and see what happens

From: osisposis <jeaninem660@...>

Subject: [] Eosinophilic esophagitis

Date: Wednesday, October 6, 2010, 5:24 PM

Eosinophilic esophagitis: the newest esophageal inflammatory disease

http://www.nature.com/nrgastro/journal/v6/n5/full/nrgastro.2009.45.html

IgE and non-IgE-mediated food allergy: treatment in 2007.: Non-IgE-Mediated Food

Allergies

http://www.medscape.com/viewarticle/559690_3

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