Multicentric Reticulohistiocytosis in a 14‐Year‐Old Girl
Identifieur interne : 002203 ( Main/Exploration ); précédent : 002202; suivant : 002204Multicentric Reticulohistiocytosis in a 14‐Year‐Old Girl
Auteurs : J. David Outland ; Stephen J. Keiran ; Kenneth N. Schikler [États-Unis] ; Jeffrey P. CallenSource :
- Pediatric Dermatology [ 0736-8046 ] ; 2002-11.
English descriptors
- Teeft :
- Active disease, Amphophilic cytoplasm, Arthritis, Arthritis rheum, Autoimmune diseases, Case report, Dermatol, Distal interphalangeal joints, Erythematous papules, Fourth decade, Interphalangeal, Joint symptoms, Lateral aspects, Lesion, Methotrexate, Multicentric, Multicentric reticulohistiocytosis, Multinucleated giant cells, Ngers, Nodule, Numerous reports, Papule, Papulonodular skin lesions, Pediatric dermatology, Psoriatic arthritis, Reticulohistiocytosis, Sjogren syndrome, Skin lesions, Skin nodules, Systemic complications, Unknown etiology, Vesicular nuclei, Weight loss.
Abstract
Abstract: Multicentric reticulohistiocytosis is a rare multisystem disorder in which an infiltration of histiocytic cells causes papulonodular skin lesions and potentially a destructive polyarthritis. The active disease typically resolves spontaneously after 5–8 years, but the articular destruction can lead to permanent joint deformities. We present a case of multicentric reticulohistiocytosis in a 14‐year‐old girl. The number of papules on her hands decreased in number and her arthritic symptoms improved after 4 months of oral naproxen. Thirty months later her joint symptoms remained inactive and only six very small papules remained on her hands. Small flexor deformities were present in the distal interphalangeal joints of both index fingers. This case is an example of how multicentric reticulohistiocytosis can be a relatively stable and self‐limited disease but still cause permanent joint deformities.
Url:
DOI: 10.1046/j.1525-1470.2002.00226.x
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001346
- to stream Istex, to step Curation: 001346
- to stream Istex, to step Checkpoint: 001030
- to stream Main, to step Merge: 002225
- to stream Main, to step Curation: 002203
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Multicentric Reticulohistiocytosis in a 14‐Year‐Old Girl</title><author><name sortKey="Outland, J David" sort="Outland, J David" uniqKey="Outland J" first="J. David" last="Outland">J. David Outland</name></author><author><name sortKey="Keiran, Stephen J" sort="Keiran, Stephen J" uniqKey="Keiran S" first="Stephen J." last="Keiran">Stephen J. Keiran</name></author><author><name sortKey="Schikler, Kenneth N" sort="Schikler, Kenneth N" uniqKey="Schikler K" first="Kenneth N." last="Schikler">Kenneth N. Schikler</name></author><author><name sortKey="Callen, Jeffrey P" sort="Callen, Jeffrey P" uniqKey="Callen J" first="Jeffrey P." last="Callen">Jeffrey P. Callen</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:50DF8B1DA652EA82AC533A8E7F5B463C1F8981DD</idno><date when="2002" year="2002">2002</date><idno type="doi">10.1046/j.1525-1470.2002.00226.x</idno><idno type="url">https://api.istex.fr/ark:/67375/WNG-5H1X04TS-R/fulltext.pdf</idno><idno type="wicri:Area/Istex/Corpus">001346</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001346</idno><idno type="wicri:Area/Istex/Curation">001346</idno><idno type="wicri:Area/Istex/Checkpoint">001030</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">001030</idno><idno type="wicri:doubleKey">0736-8046:2002:Outland J:multicentric:reticulohistiocytosis:in</idno><idno type="wicri:Area/Main/Merge">002225</idno><idno type="wicri:Area/Main/Curation">002203</idno><idno type="wicri:Area/Main/Exploration">002203</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main">Multicentric Reticulohistiocytosis in a 14‐Year‐Old Girl</title><author><name sortKey="Outland, J David" sort="Outland, J David" uniqKey="Outland J" first="J. David" last="Outland">J. David Outland</name><affiliation><wicri:noCountry code="subField">and</wicri:noCountry></affiliation></author><author><name sortKey="Keiran, Stephen J" sort="Keiran, Stephen J" uniqKey="Keiran S" first="Stephen J." last="Keiran">Stephen J. Keiran</name><affiliation><wicri:noCountry code="subField">and</wicri:noCountry></affiliation></author><author><name sortKey="Schikler, Kenneth N" sort="Schikler, Kenneth N" uniqKey="Schikler K" first="Kenneth N." last="Schikler">Kenneth N. Schikler</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><placeName><region type="state">Kentucky</region></placeName><wicri:cityArea>Department of Pediatrics, Division of Rheumatology, University of Louisville, Louisville</wicri:cityArea></affiliation></author><author><name sortKey="Callen, Jeffrey P" sort="Callen, Jeffrey P" uniqKey="Callen J" first="Jeffrey P." last="Callen">Jeffrey P. Callen</name><affiliation><wicri:noCountry code="subField">and</wicri:noCountry></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Pediatric Dermatology</title><title level="j" type="alt">PEDIATRIC DERMATOLOGY</title><idno type="ISSN">0736-8046</idno><idno type="eISSN">1525-1470</idno><imprint><biblScope unit="vol">19</biblScope><biblScope unit="issue">6</biblScope><biblScope unit="page" from="527">527</biblScope><biblScope unit="page" to="531">531</biblScope><biblScope unit="page-count">5</biblScope><publisher>Blackwell Science Inc</publisher><pubPlace>Malden, US</pubPlace><date type="published" when="2002-11">2002-11</date></imprint><idno type="ISSN">0736-8046</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0736-8046</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Active disease</term><term>Amphophilic cytoplasm</term><term>Arthritis</term><term>Arthritis rheum</term><term>Autoimmune diseases</term><term>Case report</term><term>Dermatol</term><term>Distal interphalangeal joints</term><term>Erythematous papules</term><term>Fourth decade</term><term>Interphalangeal</term><term>Joint symptoms</term><term>Lateral aspects</term><term>Lesion</term><term>Methotrexate</term><term>Multicentric</term><term>Multicentric reticulohistiocytosis</term><term>Multinucleated giant cells</term><term>Ngers</term><term>Nodule</term><term>Numerous reports</term><term>Papule</term><term>Papulonodular skin lesions</term><term>Pediatric dermatology</term><term>Psoriatic arthritis</term><term>Reticulohistiocytosis</term><term>Sjogren syndrome</term><term>Skin lesions</term><term>Skin nodules</term><term>Systemic complications</term><term>Unknown etiology</term><term>Vesicular nuclei</term><term>Weight loss</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: Multicentric reticulohistiocytosis is a rare multisystem disorder in which an infiltration of histiocytic cells causes papulonodular skin lesions and potentially a destructive polyarthritis. The active disease typically resolves spontaneously after 5–8 years, but the articular destruction can lead to permanent joint deformities. We present a case of multicentric reticulohistiocytosis in a 14‐year‐old girl. The number of papules on her hands decreased in number and her arthritic symptoms improved after 4 months of oral naproxen. Thirty months later her joint symptoms remained inactive and only six very small papules remained on her hands. Small flexor deformities were present in the distal interphalangeal joints of both index fingers. This case is an example of how multicentric reticulohistiocytosis can be a relatively stable and self‐limited disease but still cause permanent joint deformities.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>Kentucky</li></region></list><tree><noCountry><name sortKey="Callen, Jeffrey P" sort="Callen, Jeffrey P" uniqKey="Callen J" first="Jeffrey P." last="Callen">Jeffrey P. Callen</name><name sortKey="Keiran, Stephen J" sort="Keiran, Stephen J" uniqKey="Keiran S" first="Stephen J." last="Keiran">Stephen J. Keiran</name><name sortKey="Outland, J David" sort="Outland, J David" uniqKey="Outland J" first="J. David" last="Outland">J. David Outland</name></noCountry><country name="États-Unis"><region name="Kentucky"><name sortKey="Schikler, Kenneth N" sort="Schikler, Kenneth N" uniqKey="Schikler K" first="Kenneth N." last="Schikler">Kenneth N. Schikler</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002203 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002203 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Sante
|area= ChloroquineV1
|flux= Main
|étape= Exploration
|type= RBID
|clé= ISTEX:50DF8B1DA652EA82AC533A8E7F5B463C1F8981DD
|texte= Multicentric Reticulohistiocytosis in a 14‐Year‐Old Girl
}}
| This area was generated with Dilib version V0.6.33. |  |