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<title>Keratoderma</title>

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<h1 id="firstHeading" class="firstHeading mw-first-heading"><span class="mw-page-title-main">Keratoderma</span></h1>

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<th colspan="2" style="background:#99CCFF; color:#202122; text-align:center; font-size:115%; border:2px solid #99CCFF;">Klassifikation nach <a href="ICD-10" title="ICD-10">ICD-10</a>

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<td style="min-width:8ex;">L85.1

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<td>Erworbene Keratosis palmoplantaris [Erworbenes Keratoma palmoplantare]

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<td>L86

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<td>Keratom bei anderenorts klassifizierten Krankheiten inkl.: Keratosis follicularis, Xeroderma

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<td>Q82.8

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<td>Hereditäre Palmoplantarkeratose

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<td><span style="display:none;">Vorlage:Infobox ICD/Wartung</span>

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<td colspan="2" style="border-top:0.2ex solid #CCCCCC; padding:.4ex 1ex .4ex 0; text-align:center; vertical-align:top;"><a rel="nofollow" class="external text" href="https://klassifikationen.bfarm.de/icd-10-who/kode-suche/htmlamtl2019/index.htm">ICD-10 online (WHO-Version 2019)</a>

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<p>Der Begriff <b>Keratoderma</b> bezeichnet eine die Haut betreffende Verhornungsstörung (<a href="Hyperkeratose" title="Hyperkeratose">Hyperkeratose</a>).<sup id="cite_ref-Derma-net_1-0" class="reference"><a href="#cite_note-Derma-net-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>

</p><p>Hierunter fallen eine Vielzahl von Erkrankungen, die wie folgt eingeteilt werden können:<sup id="cite_ref-Derma-net_1-1" class="reference"><a href="#cite_note-Derma-net-1"><span class="cite-bracket">[</span>1<span class="cite-bracket">]</span></a></sup>

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<div class="mw-heading mw-heading2"><h2 id="Angeborene_Formen">Angeborene Formen</h2></div>

<div class="mw-heading mw-heading3"><h3 id="Hereditäre_Palmoplantarkeratosen"><span id="Heredit.C3.A4re_Palmoplantarkeratosen"></span><a href="Heredit%C3%A4re_Palmoplantarkeratose" title="Hereditäre Palmoplantarkeratose">Hereditäre Palmoplantarkeratosen</a></h3></div>

<ul><li>Diffuse palmoplantare Hyperkeratosen</li>

<li>Fokale palmoplantare Hyperkeratosen</li>

<li><a href="Punktierte_Palmoplantarkeratose" title="Punktierte Palmoplantarkeratose">Punktierte Palmoplantarkeratosen</a></li>

<li><a href="Ektodermale_Dysplasie" title="Ektodermale Dysplasie">Ektodermale Dysplasien</a> mit palmoplantaren Hyperkeratosen

<ul><li><a href="Papillon-Lef%C3%A8vre-Syndrom" title="Papillon-Lefèvre-Syndrom">Papillon-Lefèvre-Syndrom</a><sup id="cite_ref-Leiber_2-0" class="reference"><a href="#cite_note-Leiber-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup></li>

<li><a href="Naegeli-Syndrom" title="Naegeli-Syndrom">Naegeli-Syndrom</a></li>

<li><a href="Pachyonychia_congenita" title="Pachyonychia congenita">Pachyonychia congenita</a></li>

<li>Fokales palmoplantares und orales Mukosa-Hyperkeratose-Syndrom<sup id="cite_ref-3" class="reference"><a href="#cite_note-3"><span class="cite-bracket">[</span>3<span class="cite-bracket">]</span></a></sup></li>

<li><a href="Clouston-Syndrom" title="Clouston-Syndrom">Clouston-Syndrom</a></li>

<li><a href="Sch%C3%B6pf-Schulz-Passarge-Syndrom" title="Schöpf-Schulz-Passarge-Syndrom">Schöpf-Schulz-Passarge-Syndrom</a></li></ul></li></ul>

<ul><li>Syndrome mit ektodermalen Dysplasien und palmoplantaren Hyperkeratosen

<ul><li><a href="Naxos-Krankheit" title="Naxos-Krankheit">Naxos-Krankheit</a></li>

<li><a href="Wollhaare-Palmoplantarkeratose-dilatative_Kardiomyopathie-Syndrom" class="mw-redirect" title="Wollhaare-Palmoplantarkeratose-dilatative Kardiomyopathie-Syndrom">Wollhaare-Palmoplantarkeratose-dilatative Kardiomyopathie-Syndrom</a> (Synonyme: Carvajal Syndrom; Carvajal Variante des Naxos Syndroms; <a href="Englische_Sprache" title="Englische Sprache">englisch</a> Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome)<sup id="cite_ref-4" class="reference"><a href="#cite_note-4"><span class="cite-bracket">[</span>4<span class="cite-bracket">]</span></a></sup></li></ul></li></ul>

<ul><li>Unklassifizierte Formen

<ul><li>Nichtepidermolytische Palmoplantarkeratose (Synonyme: Diffuses palmoplantares Keratoderm Typ Norrbotten; NEPPK; Palmoplantarkeratose, diffuse, autosomal-dominante, Typ Norrbotten; PALMOPLANTAR KERATODERMA, BOTHNIAN TYPE; PPKB)<sup id="cite_ref-5" class="reference"><a href="#cite_note-5"><span class="cite-bracket">[</span>5<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-6" class="reference"><a href="#cite_note-6"><span class="cite-bracket">[</span>6<span class="cite-bracket">]</span></a></sup>

<ul><li><a href="Kindler-Syndrom" title="Kindler-Syndrom">Kindler-Syndrom</a></li>

<li><a href="Dermatopathia_pigmentosa_reticularis" title="Dermatopathia pigmentosa reticularis">Dermatopathia pigmentosa reticularis</a></li></ul></li></ul></li></ul>

<div class="mw-heading mw-heading3"><h3 id="Erythrokeratodermien"><a href="Erythrokeratodermie" title="Erythrokeratodermie">Erythrokeratodermien</a></h3></div>

<div class="mw-heading mw-heading4"><h4 id="Follikuläre_Hyperkeratosen"><span id="Follikul.C3.A4re_Hyperkeratosen"></span>Follikuläre Hyperkeratosen</h4></div>

<ul><li>Keratosis follicularis (Synonyme: Keratosis pilaris)<sup id="cite_ref-7" class="reference"><a href="#cite_note-7"><span class="cite-bracket">[</span>7<span class="cite-bracket">]</span></a></sup>

<ul><li>Ulerythema ophryogenes (Synonyme: Keratosis pilaris atrophicans faciei (KPAF), Folliculitis rubra)<sup id="cite_ref-8" class="reference"><a href="#cite_note-8"><span class="cite-bracket">[</span>8<span class="cite-bracket">]</span></a></sup></li></ul></li>

<li>Keratosis pilaris (Synonyme: Keratosis pilaris rubra atrophicans; Keratosis pilaris atrophicans)

<ul><li>Keratosis follicularis spinulosa decalvans<sup id="cite_ref-9" class="reference"><a href="#cite_note-9"><span class="cite-bracket">[</span>9<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-10" class="reference"><a href="#cite_note-10"><span class="cite-bracket">[</span>10<span class="cite-bracket">]</span></a></sup></li>

<li>Atrophoderma vermiculatum (Synonyme: Ulerythema acneiforme; Folliculitis ulerythematosa reticulata; <a href="Englische_Sprache" title="Englische Sprache">englisch</a> honeycomb atrophy)<sup id="cite_ref-11" class="reference"><a href="#cite_note-11"><span class="cite-bracket">[</span>11<span class="cite-bracket">]</span></a></sup><sup id="cite_ref-12" class="reference"><a href="#cite_note-12"><span class="cite-bracket">[</span>12<span class="cite-bracket">]</span></a></sup></li></ul></li></ul>

<div class="mw-heading mw-heading4"><h4 id="Dyskeratotisch-akantholytische_Keratosen">Dyskeratotisch-akantholytische Keratosen</h4></div>

<ul><li><a href="Morbus_Darier" title="Morbus Darier">Morbus Darier</a></li>

<li><a href="Acrokeratosis_verruciformis" title="Acrokeratosis verruciformis">Acrokeratosis verruciformis</a> Hopf</li>

<li>Pemphigus, benigner chronischer familiärer (Synonyme: Morbus Hailey-Hailey; Chronischer benigner familiärer Pemphigus) OMIM 169600<sup id="cite_ref-13" class="reference"><a href="#cite_note-13"><span class="cite-bracket">[</span>13<span class="cite-bracket">]</span></a></sup></li></ul>

<div class="mw-heading mw-heading3"><h3 id="Porokeratosen"><a href="Porokeratose" title="Porokeratose">Porokeratosen</a></h3></div>

<div class="mw-heading mw-heading4"><h4 id="Syndrome_mit_Keratoderma">Syndrome mit Keratoderma</h4></div>

<ul><li>Palmoplantarkeratose – spastische Lähmung (Synonyme: Palmoplantare Hyperkeratose-spastische Paralyse-Syndrom; Powell-Venencie-Gordon-Syndrom)<sup id="cite_ref-14" class="reference"><a href="#cite_note-14"><span class="cite-bracket">[</span>14<span class="cite-bracket">]</span></a></sup></li>

<li>Stern-Lubinsky-Durrie-Syndrom (Synonyme: Korneo-dermato-ossäres-Syndrom; <a href="Englische_Sprache" title="Englische Sprache">englisch</a> Corneodermatosseous syndrome)<sup id="cite_ref-15" class="reference"><a href="#cite_note-15"><span class="cite-bracket">[</span>15<span class="cite-bracket">]</span></a></sup></li>

<li><a href="Kardio-fazio-kutanes_Syndrom" title="Kardio-fazio-kutanes Syndrom">Kardio-fazio-kutanes Syndrom</a></li>

<li><a href="Bureau-Barri%C3%A8re-Thomas-Syndrom" title="Bureau-Barrière-Thomas-Syndrom">Bureau-Barrière-Thomas-Syndrom</a></li>

<li><a href="Hanhart-Syndrom" title="Hanhart-Syndrom">Hanhart-Syndrom</a></li>

<li>Helikotrichie-Keratose-Syndrom (Synonym: Keratodermia palmo-plantaris varians mit Helikotrichie)<sup id="cite_ref-Leiber_2-1" class="reference"><a href="#cite_note-Leiber-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup></li>

<li><a href="Gorlin-Goltz-Syndrom" title="Gorlin-Goltz-Syndrom">Gorlin-Syndrom</a></li>

<li><a href="CEDNIK-Syndrom" title="CEDNIK-Syndrom">CEDNIK-Syndrom</a></li>

<li><a href="Cole-Krankheit" title="Cole-Krankheit">Cole-Krankheit</a></li>

<li><a href="Epidermolysis_bullosa_simplex" title="Epidermolysis bullosa simplex">Epidermolysis bullosa simplex</a> durch Plakophilin-Mangel</li>

<li><a href="Epidermolysis_bullosa_simplex" title="Epidermolysis bullosa simplex">Epidermolysis bullosa simplex</a> Typ Dowling-Meara</li>

<li><a href="Pityriasis_rubra_pilaris" title="Pityriasis rubra pilaris">Pityriasis rubra pilaris</a></li>

<li>Incontinentia pigmenti (<a href="Bloch-Sulzberger-Syndrom" title="Bloch-Sulzberger-Syndrom">Bloch-Sulzberger-Syndrom</a>)</li>

<li><a href="Sj%C3%B6gren-Larsson-Syndrom" title="Sjögren-Larsson-Syndrom">Sjögren-Larsson-Syndrom</a></li></ul>

<div class="mw-heading mw-heading2"><h2 id="Erworbene_Formen">Erworbene Formen</h2></div>

<ul><li>AIDS-assoziiertes Keratoderma</li>

<li>Arsen-bedingte Keratose</li>

<li><a href="Hornschwiele" title="Hornschwiele">Hornschwielen</a></li>

<li>Keratodermia climacterica Haxthausen (Synonym: Haxthausen Hyperkeratosis)<sup id="cite_ref-Leiber_2-2" class="reference"><a href="#cite_note-Leiber-2"><span class="cite-bracket">[</span>2<span class="cite-bracket">]</span></a></sup></li>

<li><a href="H%C3%BChnerauge" title="Hühnerauge">Hühnerauge</a></li>

<li><a href="Dermatitis" title="Dermatitis">Dermatitis</a></li>

<li><a href="Humane_Papillomaviren" class="mw-redirect" title="Humane Papillomaviren">Humane Papillomaviren</a></li>

<li>Keratoderma blenorrhagicum</li>

<li><a href="Lichen_ruber_planus" title="Lichen ruber planus">Lichen ruber planus</a></li>

<li><a href="Kr%C3%A4tze" title="Krätze">Krätze</a></li>

<li>Paraneoplastisches Keratoderma</li>

<li><a href="Psoriasis" class="mw-redirect" title="Psoriasis">Psoriasis</a> (Schuppenflechte)</li>

<li><a href="Reaktive_Arthritis" title="Reaktive Arthritis">Reaktive Arthritis</a> (Reiter-Syndrom)</li>

<li><a href="Syphilis" title="Syphilis">Syphilis</a></li>

<li><a href="Fu%C3%9Fpilz" title="Fußpilz">Fußpilz</a></li>

<li><a href="S%C3%A9zary-Syndrom" title="Sézary-Syndrom">Sézary-Syndrom</a></li>

<li>Tuberculosis verrucosa cutis</li>

<li>Medikamenten-induziertes Keratoderma<sup id="cite_ref-Bolognia_16-0" class="reference"><a href="#cite_note-Bolognia-16"><span class="cite-bracket">[</span>16<span class="cite-bracket">]</span></a></sup></li></ul>

<div class="mw-heading mw-heading2"><h2 id="Siehe_auch">Siehe auch</h2></div>

<ul><li><a href="Ichthyose" title="Ichthyose">Ichthyosen</a></li></ul>

<div class="mw-heading mw-heading2"><h2 id="Literatur">Literatur</h2></div>

<ul><li>Freedberg et al. (2003): <i>Fitzpatrick's Dermatology in General Medicine.</i> (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.</li></ul>

<div class="mw-heading mw-heading2"><h2 id="Einzelnachweise">Einzelnachweise</h2></div>

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<li id="cite_note-Leiber-2"><span class="mw-cite-backlink">↑ <sup><a href="#cite_ref-Leiber_2-0">a</a></sup> <sup><a href="#cite_ref-Leiber_2-1">b</a></sup> <sup><a href="#cite_ref-Leiber_2-2">c</a></sup></span> <span class="reference-text">Bernfried Leiber (Begründer): <cite style="font-style:italic">Die klinischen Syndrome. Syndrome, Sequenzen und Symptomenkomplexe</cite>. Hrsg.: G. Burg, J. Kunze, D. Pongratz, P. G. Scheurlen, A. Schinzel, J. Spranger. 7., völlig neu bearb. Auflage. <span style="white-space:nowrap">Band<span style="display:inline-block;width:.2em"> </span>2</span>: <i>Symptome</i>. Urban & Schwarzenberg, München u. a. 1990, ISBN 3-541-01727-9.<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:Keratoderma&rft.au=Bernfried+Leiber+%28Begr%C3%BCnder%29&rft.btitle=Die+klinischen+Syndrome.+Syndrome%2C+Sequenzen+und+Symptomenkomplexe&rft.date=1990&rft.edition=7.%2C+v%C3%B6llig+neu+bearb.&rft.genre=book&rft.isbn=3541017279&rft.place=M%C3%BCnchen+u.+a.&rft.pub=Urban+%26+Schwarzenberg&rft.volume=Band+2%3A+Symptome" style="display:none"> </span></span>

</li>

<li id="cite_note-3"><span class="mw-cite-backlink"><a href="#cite_ref-3">↑</a></span> <span class="reference-text">G. Bethke, G. Kolde, G. Bethke, P. A. Reichart: <i>[Focal palmoplantar and oral mucosa hyperkeratosis syndrome].</i> In: <i>Mund-, Kiefer- und Gesichtschirurgie : MKG.</i> Bd. 5, Nr. 3, Mai 2001, S. 202–205, <a href="https://doi.org/10.1007/s100060100306" class="extiw external" title="doi:10.1007/s100060100306">doi:10.1007/s100060100306</a>, <a class="external mw-magiclink-pmid" rel="nofollow" href="https://www.ncbi.nlm.nih.gov/pubmed/11432338?dopt=Abstract">PMID 11432338</a>.</span>

</li>

<li id="cite_note-4"><span class="mw-cite-backlink"><a href="#cite_ref-4">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://www.orpha.net/de/disease/detail/65282"><i>Carvajal-Syndrom.</i></a> In: <i><a href="Orphanet" title="Orphanet">Orphanet</a></i> (Datenbank für seltene Krankheiten)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-5"><span class="mw-cite-backlink"><a href="#cite_ref-5">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://www.orpha.net/de/disease/detail/2337"><i>Diffuse Palmoplantarkeratose vom Bottnischen Typ.</i></a> In: <i><a href="Orphanet" title="Orphanet">Orphanet</a></i> (Datenbank für seltene Krankheiten)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-6"><span class="mw-cite-backlink"><a href="#cite_ref-6">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://omim.org/entry/600231"><i>PPKB.</i></a> In: <i><span lang="en"><a href="Online_Mendelian_Inheritance_in_Man" title="Online Mendelian Inheritance in Man">Online Mendelian Inheritance in Man</a></span>.</i> (englisch)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-7"><span class="mw-cite-backlink"><a href="#cite_ref-7">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://omim.org/entry/604093"><i>Keratosis pilaris.</i></a> In: <i><span lang="en"><a href="Online_Mendelian_Inheritance_in_Man" title="Online Mendelian Inheritance in Man">Online Mendelian Inheritance in Man</a></span>.</i> (englisch)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-8"><span class="mw-cite-backlink"><a href="#cite_ref-8">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://www.orpha.net/de/disease/detail/3406"><i>Ulerythema ophryogenes.</i></a> In: <i><a href="Orphanet" title="Orphanet">Orphanet</a></i> (Datenbank für seltene Krankheiten)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-9"><span class="mw-cite-backlink"><a href="#cite_ref-9">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://omim.org/entry/308800"><i>KFSDX.</i></a> In: <i><span lang="en"><a href="Online_Mendelian_Inheritance_in_Man" title="Online Mendelian Inheritance in Man">Online Mendelian Inheritance in Man</a></span>.</i> (englisch)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-10"><span class="mw-cite-backlink"><a href="#cite_ref-10">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://www.orpha.net/de/disease/detail/2340"><i>Keratosis follicularis spinulosa decalvans.</i></a> In: <i><a href="Orphanet" title="Orphanet">Orphanet</a></i> (Datenbank für seltene Krankheiten)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-11"><span class="mw-cite-backlink"><a href="#cite_ref-11">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://www.orpha.net/de/disease/detail/79100"><i>Atrophodermia vermiculata.</i></a> In: <i><a href="Orphanet" title="Orphanet">Orphanet</a></i> (Datenbank für seltene Krankheiten)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-12"><span class="mw-cite-backlink"><a href="#cite_ref-12">↑</a></span> <span class="reference-text"><a rel="nofollow" class="external text" href="https://omim.org/entry/209700"><i> ATROPHODERMA VERMICULATA.</i></a> In: <i><span lang="en"><a href="Online_Mendelian_Inheritance_in_Man" title="Online Mendelian Inheritance in Man">Online Mendelian Inheritance in Man</a></span>.</i> (englisch)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-13"><span class="mw-cite-backlink"><a href="#cite_ref-13">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://www.orpha.net/de/disease/detail/2841"><i>Hailey-Hailey-Krankheit.</i></a> In: <i><a href="Orphanet" title="Orphanet">Orphanet</a></i> (Datenbank für seltene Krankheiten)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-14"><span class="mw-cite-backlink"><a href="#cite_ref-14">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://www.orpha.net/de/disease/detail/2201"><i>Palmoplantarkeratose-spastische Paralyse-Syndrom.</i></a> In: <i><a href="Orphanet" title="Orphanet">Orphanet</a></i> (Datenbank für seltene Krankheiten)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-15"><span class="mw-cite-backlink"><a href="#cite_ref-15">↑</a></span> <span class="reference-text">Eintrag zu <a rel="nofollow" class="external text" href="https://www.orpha.net/de/disease/detail/3194"><i>Korneo-dermato-ossäres-Syndrom.</i></a> In: <i><a href="Orphanet" title="Orphanet">Orphanet</a></i> (Datenbank für seltene Krankheiten)<span class="editoronly" style="display:none;"></span></span>

</li>

<li id="cite_note-Bolognia-16"><span class="mw-cite-backlink"><a href="#cite_ref-Bolognia_16-0">↑</a></span> <span class="reference-text"><span class="book">Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L.: <cite class="lang" lang="en" dir="auto" style="font-style:italic">Dermatology: 2-Volume Set</cite>. Mosby, St. Louis 2007, ISBN 1-4160-2999-0, <span style="white-space:nowrap">S.<span style="display:inline-block;width:.2em"> </span>778</span> (englisch).<span class="Z3988" title="ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Abook&rfr_id=info:sid/de.wikipedia.org:Keratoderma&rft.au=Rapini%2C+Ronald+P.%3B+Bolognia%2C+Jean+L.%3B+Jorizzo%2C+...&rft.btitle=Dermatology%3A+2-Volume+Set&rft.date=2007&rft.genre=book&rft.isbn=1416029990&rft.pages=778&rft.place=St.+Louis&rft.pub=Mosby" style="display:none"> </span></span></span>

</li>

</ol>

<div class="mw-heading mw-heading2"><h2 id="Weblinks">Weblinks</h2></div>

<ul><li><a rel="nofollow" class="external text" href="https://emedicine.medscape.com/article/1108406-overview#a1">Medscape</a></li></ul>

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Dieser Artikel behandelt ein Gesundheitsthema. Er dient weder der Selbstdiagnose noch wird dadurch eine Diagnose durch einen Arzt ersetzt. Bitte hierzu den Hinweis zu Gesundheitsthemen beachten!</div>

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