A case of Papillon–Lefevre syndrome associated with xanthogranulomatous pyelonephritis and hepatitis
Identifieur interne : 004F33 ( Istex/Curation ); précédent : 004F32; suivant : 004F34A case of Papillon–Lefevre syndrome associated with xanthogranulomatous pyelonephritis and hepatitis
Auteurs : A. Tülin Mansur ; Fatih Göktay ; Nüket Dem Rok [Turquie]Source :
- The Journal of Dermatology [ 0385-2407 ] ; 2006-01.
English descriptors
- KwdEn :
- Abdominal ultrasonography, Abscess, Actinomycosis, Cathepsin, Clin periodontol, Compensatory hypertrophy, Costal margin, Erythrocyte sedimentation rate, Extensor surfaces, Focal areas, Gallbladder, Hepatic, Hepatic pseudotumor, Histopathological, Histopathological examination, Immune, Kala azar, Leucocyte functions, Leukocyte, Leukocyte functions, Macrophage, Macroscopic features, Monocyte, Mononuclear cells, Ndings, Neutrophil, Pediatr, Pediatr surg, Permanent teeth, Plaque, Primary sclerosing cholangitis, Proteinase, Pseudotumor, Psoriasiform plaques, Pyelonephritis, Pyogenic, Pyogenic liver abscess, Rare association, Recent years, Research hospital, Right kidney, Scaly plaques, Syndrome, Weight loss, Xanthogranulomatous, Xanthogranulomatous hepatitis, Xanthogranulomatous pyelonephritis.
- Teeft :
- Abdominal ultrasonography, Abscess, Actinomycosis, Cathepsin, Clin periodontol, Compensatory hypertrophy, Costal margin, Erythrocyte sedimentation rate, Extensor surfaces, Focal areas, Gallbladder, Hepatic, Hepatic pseudotumor, Histopathological, Histopathological examination, Immune, Kala azar, Leucocyte functions, Leukocyte, Leukocyte functions, Macrophage, Macroscopic features, Monocyte, Mononuclear cells, Ndings, Neutrophil, Pediatr, Pediatr surg, Permanent teeth, Plaque, Primary sclerosing cholangitis, Proteinase, Pseudotumor, Psoriasiform plaques, Pyelonephritis, Pyogenic, Pyogenic liver abscess, Rare association, Recent years, Research hospital, Right kidney, Scaly plaques, Syndrome, Weight loss, Xanthogranulomatous, Xanthogranulomatous hepatitis, Xanthogranulomatous pyelonephritis.
Abstract
Papillon–Lefevre syndrome (PLS) is an autosomally recessive palmoplantar keratoderma accompanied by psoriasiform plaques on the extensor surfaces of extremities and leading to premature loss of deciduous and permanent teeth by progressive periodontitis. Patients with PLS may exhibit mental retardation, intracranial ectopic calcifications, nail dystrophies and a tendency to various infectious disorders, in addition to skin and oral findings. Herein, we report a 26‐year‐old man with PLS, who had experienced xanthogranulomatous pyelonephritis and hepatitis during childhood and adolescence. To the best of our knowledge, this is the first report of PLS associated with xanthogranulomatous inflammation.
Url:
DOI: 10.1111/j.1346-8138.2006.00012.x
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A. Tülin Mansur<affiliation><mods:affiliation>Department of Dermatology, Haydarpaşa Numune Training and Research Hospital</mods:affiliation><wicri:noCountry code="subField">Hospital</wicri:noCountry></affiliation><affiliation><mods:affiliation>Department of Dermatology, Haydarpaşa Numune Training and Research Hospital</mods:affiliation><wicri:noCountry code="subField">Hospital</wicri:noCountry></affiliation>Le document en format XML
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Tülin Mansur</name><affiliation><mods:affiliation>Department of Dermatology, Haydarpaşa Numune Training and Research Hospital</mods:affiliation><wicri:noCountry code="subField">Hospital</wicri:noCountry></affiliation></author><author><name sortKey="Goktay, Fatih" sort="Goktay, Fatih" uniqKey="Goktay F" first="Fatih" last="Göktay">Fatih Göktay</name><affiliation><mods:affiliation>Department of Dermatology, Haydarpaşa Numune Training and Research Hospital</mods:affiliation><wicri:noCountry code="subField">Hospital</wicri:noCountry></affiliation></author><author><name sortKey="Dem Rok, Nuket" sort="Dem Rok, Nuket" uniqKey="Dem Rok N" first="Nüket" last="Dem Rok">Nüket Dem Rok</name><affiliation wicri:level="1"><mods:affiliation>Department of Radiology, Metin Sabanu Baltalimani Bone Diseases Training and Research Hospital, Istanbul, Turkey</mods:affiliation><country xml:lang="fr">Turquie</country><wicri:regionArea>Department of Radiology, Metin Sabanu Baltalimani Bone Diseases Training and Research Hospital, Istanbul</wicri:regionArea></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">The Journal of Dermatology</title><title level="j" type="alt">JOURNAL OF DERMATOLOGY</title><idno type="ISSN">0385-2407</idno><idno type="eISSN">1346-8138</idno><imprint><biblScope unit="vol">33</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="59">59</biblScope><biblScope unit="page" to="63">63</biblScope><biblScope unit="page-count">5</biblScope><publisher>Blackwell Publishing Asia</publisher><pubPlace>Melbourne, Australia</pubPlace><date type="published" when="2006-01">2006-01</date></imprint><idno type="ISSN">0385-2407</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0385-2407</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Abdominal ultrasonography</term><term>Abscess</term><term>Actinomycosis</term><term>Cathepsin</term><term>Clin periodontol</term><term>Compensatory hypertrophy</term><term>Costal margin</term><term>Erythrocyte sedimentation rate</term><term>Extensor surfaces</term><term>Focal areas</term><term>Gallbladder</term><term>Hepatic</term><term>Hepatic pseudotumor</term><term>Histopathological</term><term>Histopathological examination</term><term>Immune</term><term>Kala azar</term><term>Leucocyte functions</term><term>Leukocyte</term><term>Leukocyte functions</term><term>Macrophage</term><term>Macroscopic features</term><term>Monocyte</term><term>Mononuclear cells</term><term>Ndings</term><term>Neutrophil</term><term>Pediatr</term><term>Pediatr surg</term><term>Permanent teeth</term><term>Plaque</term><term>Primary sclerosing cholangitis</term><term>Proteinase</term><term>Pseudotumor</term><term>Psoriasiform plaques</term><term>Pyelonephritis</term><term>Pyogenic</term><term>Pyogenic liver abscess</term><term>Rare association</term><term>Recent years</term><term>Research hospital</term><term>Right kidney</term><term>Scaly plaques</term><term>Syndrome</term><term>Weight loss</term><term>Xanthogranulomatous</term><term>Xanthogranulomatous hepatitis</term><term>Xanthogranulomatous pyelonephritis</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Abdominal ultrasonography</term><term>Abscess</term><term>Actinomycosis</term><term>Cathepsin</term><term>Clin periodontol</term><term>Compensatory hypertrophy</term><term>Costal margin</term><term>Erythrocyte sedimentation rate</term><term>Extensor surfaces</term><term>Focal areas</term><term>Gallbladder</term><term>Hepatic</term><term>Hepatic pseudotumor</term><term>Histopathological</term><term>Histopathological examination</term><term>Immune</term><term>Kala azar</term><term>Leucocyte functions</term><term>Leukocyte</term><term>Leukocyte functions</term><term>Macrophage</term><term>Macroscopic features</term><term>Monocyte</term><term>Mononuclear cells</term><term>Ndings</term><term>Neutrophil</term><term>Pediatr</term><term>Pediatr surg</term><term>Permanent teeth</term><term>Plaque</term><term>Primary sclerosing cholangitis</term><term>Proteinase</term><term>Pseudotumor</term><term>Psoriasiform plaques</term><term>Pyelonephritis</term><term>Pyogenic</term><term>Pyogenic liver abscess</term><term>Rare association</term><term>Recent years</term><term>Research hospital</term><term>Right kidney</term><term>Scaly plaques</term><term>Syndrome</term><term>Weight loss</term><term>Xanthogranulomatous</term><term>Xanthogranulomatous hepatitis</term><term>Xanthogranulomatous pyelonephritis</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Papillon–Lefevre syndrome (PLS) is an autosomally recessive palmoplantar keratoderma accompanied by psoriasiform plaques on the extensor surfaces of extremities and leading to premature loss of deciduous and permanent teeth by progressive periodontitis. Patients with PLS may exhibit mental retardation, intracranial ectopic calcifications, nail dystrophies and a tendency to various infectious disorders, in addition to skin and oral findings. Herein, we report a 26‐year‐old man with PLS, who had experienced xanthogranulomatous pyelonephritis and hepatitis during childhood and adolescence. To the best of our knowledge, this is the first report of PLS associated with xanthogranulomatous inflammation.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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