Joka muuten on sellaisen vaivan joskus kokenut, tietää mitä on inhottava kutina siinä kohtaa kehoa, josa on eniten hermoääteitä, kämmenissä ja jalanpohjissa.
nimittäin- itselläni oli nuoruudessa tuollainen vaihe, kun sitä ihottumaa oli vuosi vuodelta aikamoinen kirjonsa, vaihteleva , ja kuten sanottu , olihan sitä naftalan pastaa.
Ei ollut käsitystä mistään dieetin merkityksestä iholle.
kun sittemmin tuli anergiaa huonomman kunnon ja ehkä röntgentyönkin jälkeen varsinainen lyhyt pustuloosivaihe ohittui - välillä oli sormien ja varpaiden ihovälit vetiset , punoitavat ja kutiavat. Sen vaiheen ohittumisen jälkeen tuli suolisto-oireita eniten, jasitten lopulta 30 vuoden iässä oli pääoire.
Jossain vaiheessa huomasin että varsinkin kaura aiheutti ihon kutinan. Nuorena söin usein kaurapuroa aamulla aivan 18 vuotiaaksi asti, jolloin muutin kotoa opiskelemaan ja lopetin kauran jokapäiväisen käytön. Kauraleivät olivat helppoja paistaa ( kaurahiutaleta, sokerissa ja voita taikinaksi, rautaisessa lättypannussa uuniin) Niitä teimme silloin tällöin iltaisin. ne olivat herkullisia.
Nyt ajattelin katsoa yhteyttä Pustulosis palmoplantaris , kaura.(oat).
Löytyy erikoisia asioita, missä kauralla on jokin ominaisuus jota voi ihoon hyödyntää, mutta ei varmastikaan olisi minun hoitoaineitani.jos vanha allergisuus kauralle on vielä solumuistissa olemassa.
....
(1) Saattaa olla, että kaura jotenkin assosioituu ihoon enemmän kuin muut viljat. Mitähän asia koskee?
Mikä molekyylikaurassa on niin ihovetoinen?
Näyttää olevan kaurassa paljon hyviä antioksidatiivisiä ja antikutinaaineita jotka varmasti suurimmalle osalle ihmiskuntaa sopivat:
Saattaa olla enttä entinen kauralaari , joka meidän isonkeittiön vehnälaarin vieressä sijaitsi, saattoi sisältää vehnäpölyn tuomia immunologisia hitusia gliadiinia ja gliadiini taas antigeeninä massiivisen kauran sisällä saattoi antaa iho-oireita suolioireiden sijasta.
Aventanthramideshttps://www.sciencedirect.com/topics/agricultural-and-biological-sciences/avenanthramides
- J Drugs Dermatol. 2010 Sep;9(9):1116-20.
Mechanism of action and clinical benefits of colloidal oatmeal for dermatologic practice.Cerio R1, Dohil M, Jeanine D, Magina S, Mahé E, Stratigos AJ. Abstract
Colloidal
oatmeal has a long history of beneficial use in dermatology. It is a
natural product that has an excellent safety record and has demonstrated
efficacy for the treatment of atopic dermatitis, psoriasis,
drug-induced rash and other conditions. In recent years, in vitro and
in vivo studies have begun to elucidate the multiple mechanisms of
action of naturally derived colloidal oatmeal. Evidence now describes
its molecular mechanisms of anti-inflammatory and antihistaminic
activity. The avenanthramides, a recently described component of whole oat
grain, are responsible for many of these effects. Studies have
demonstrated that avenanthramides can inhibit the activity of nuclear
factor kappaB and the release of proinflammatory cytokines and
histamine, well known key mechanisms in the pathophysiology of
inflammatory dermatoses. Topical formulations of natural colloidal
oatmeal should be considered an important component of therapy for
atopic dermatitis and other conditions and may allow for reduced use of
corticosteroids and calcineurin inhibitors.
- PMID:
- 20865844
- [Indexed for MEDLINE]
(3) Miten kauran todella hyvät edut voidaan saada esiin ja välttää haitat? Edulliset osat otetaan käyttöön ja mahdollinen haittaava proteiiniosa ( kauran aveniinit ja gluteliinit) jätetään pois, koska niille joku allergisoituu kuitenkin.
J Eur Acad Dermatol Venereol. 2018 Apr;32 Suppl 1:1-15. doi: 10.1111/jdv.14846.
Effects of a protein-free oat plantlet extract on microinflammation and skin barrier function in atopic dermatitis patients.
Atopic dermatitis (AD) is a common, highly pruritic, chronic inflammatory skin
disease. Dysfunction of the epidermal barrier is witnessed by an
increased transepidermal water loss in lesional and non-lesional AD skin. The inflammation in lesional AD skin is well characterized. Non-lesional skin
of AD patients shows histological signs of a subclinical inflammation
and a pro-inflammatory cytokine milieu. This microinflammation is
present even in seemingly healed skin and must be taken into account regarding treatment of AD. Emollients provide a safe and effective method of skin barrier improvement, because they provide the skin
with a source of exogenous lipids, thus improving its barrier function.
The use of emollients is recommended for all AD patients irrespective
of overall disease severity. Patients with moderate to severe AD should
combine the emollients with a proactive therapy regimen of topical
calcineurin inhibitors or topical corticosteroids. Skin
areas affected by active eczema in flare should receive daily
anti-inflammatory therapy first before introducing emollients, to induce
rapid relief of skin
lesions and pruritus. The microinflammation persisting in seemingly
healed AD lesions should be addressed by a proactive treatment approach,
consisting of minimal anti-inflammatory therapy and liberal, daily use
of emollients. An emollient containing an extract of Rhealba oat
plantlet has shown anti-inflammatory and barrier repairing properties,
and was clinically tested in studies targeting the microinflammation in
AD. All emollients based on Rhealba oat plantlet extract are free of oat protein, as the Rhealba extract is derived from the aerial parts of the oat plantlet and is unrelated to oatmeal proteins. The Rhealba oat
plantlet extract is produced in a specific process, allowing the
extraction of high levels of active principles such as flavonoids and
saponins, whilst being virtually free of oat proteins to minimize the risk for allergic reactions.
© 2018 European Academy of Dermatology and Venereology.
- PMID:
- 29533490
- DOI:
- 10.1111/jdv.14846
https://www.ncbi.nlm.nih.gov/pubmed/28764899AbstractOBJECTIVE:
To further characterize clinical characteristics, etiologic factors, associated disorders, and treatment of palmoplantar pustulosis (PPP). PATIENTS AND METHODS:
We conducted a retrospective review of patients with PPP at Mayo Clinic between January 1, 1996, and December 31, 2013. RESULTS:
Of 215 patients with PPP identified, 179 (83%) were female, and the mean age at onset was 45.3 years. Most patients (n=165, 77%) were current or former smokers. At diagnosis, 15 patients (7%) had an anxiety diagnosis and 9 (4%) had an infection. Nineteen cases (9%) were drug induced. Comorbid conditions included thyroid disease in 18 patients (8%), gluten sensitivity in 3 (1%), and type 2 diabetes mellitus in 21 (10%). In all, 194 patients (90%) received topical corticosteroids, 55 (26%) received phototherapy, and 54 (25%) received systemic agents. CONCLUSION:
More than three-fourths of the patients in this study had a history of smoking, which is considered a triggering or aggravating factor for PPP. Regarding comorbid conditions, gluten sensitivity and thyroid disease were found less frequently than previously reported in the literature. Treatment regimens and responses in this cohort varied considerably.
We conducted a retrospective review of patients with PPP at Mayo Clinic between January 1, 1996, and December 31, 2013. RESULTS:
Of 215 patients with PPP identified, 179 (83%) were female, and the mean age at onset was 45.3 years. Most patients (n=165, 77%) were current or former smokers. At diagnosis, 15 patients (7%) had an anxiety diagnosis and 9 (4%) had an infection. Nineteen cases (9%) were drug induced. Comorbid conditions included thyroid disease in 18 patients (8%), gluten sensitivity in 3 (1%), and type 2 diabetes mellitus in 21 (10%). In all, 194 patients (90%) received topical corticosteroids, 55 (26%) received phototherapy, and 54 (25%) received systemic agents. CONCLUSION:
More than three-fourths of the patients in this study had a history of smoking, which is considered a triggering or aggravating factor for PPP. Regarding comorbid conditions, gluten sensitivity and thyroid disease were found less frequently than previously reported in the literature. Treatment regimens and responses in this cohort varied considerably.
Copyright © 2017 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc. All rights reserved.
- PMID:
- 28764899
- DOI:
- 10.1016/j.mayocp.2017.05.029