Interstitial mycosis fungoides initially diagnosed as interstitial granulomatous drug reaction
Identifieur interne : 001D11 ( Main/Exploration ); précédent : 001D10; suivant : 001D12Interstitial mycosis fungoides initially diagnosed as interstitial granulomatous drug reaction
Auteurs : Karyn Fuller [Australie]Source :
- Australasian Journal of Dermatology [ 0004-8380 ] ; 2006-11.
English descriptors
- Teeft :
- Adelaide, Annual conference, Atypical, Australasian, Biopsy, Carcinoma, Carcinosarcoma, Case series, Cutaneous, Dermatology, Differential diagnosis, Electron microscopy, Extraskeletal osteosarcomas, Fungoides, Genetic results, George hospital, Granulomatous, Histological, Histological features, Histopathological features, Igdr, Interstitial granulomatous drug reaction, Leishmaniasis, Likelihood ratio, Major types, Malignant, Medial, Medial ankle, Metastatic osteosarcoma, Mycosis, Mycosis fungoides, Nodule, Osteosarcoma, Panniculitis, Rare variant, Recurrent tumour, Royal adelaide hospital, Squamous cell carcinoma, Tumour.
Abstract
A 74 year old woman presented with a 1‐month history of symmetrical erythematous annular plaques involving her groin and medial thigh 3 to 4 years post commencing simvastatin. Initial histology was consistent with the diagnosis of interstitial granulomatous drug reaction (IGDR), however 11 months post cessation of Simvastatin the plaques were expanding in size. Repeat biopsy demonstrated features of interstitial mycosis fungoides (IMF). IMF is a rare variant of mycosis fungoides. It has been reported to resemble granuloma annulare, inflammatory morphoea and IGDR with an interstitial lymphocytic infiltrate. IGDR presents most commonly with a history of asymptomatic, erythematous to violaceous plaques in an annular pattern, mainly involving the intertriginous areas, medial thighs and inner aspects of the arms. There is a temporal association between the initiation of drug therapy and lesional onset and resolution after cessation of the drug. It has clinical and histological features that overlap with IMF. This case of a rare variant of mycosis fungoides initially diagnosed as interstitial granulomatous drug reaction is presented to highlight the importance of recognising this differential diagnosis when presumed IGDR fails to resolve.
Url:
DOI: 10.1111/j.1440-0960.2006.00311_1.x
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001B85
- to stream Istex, to step Curation: 001B85
- to stream Istex, to step Checkpoint: 000B79
- to stream Main, to step Merge: 001D23
- to stream Main, to step Curation: 001D11
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Interstitial mycosis fungoides initially diagnosed as interstitial granulomatous drug reaction</title><author><name sortKey="Fuller, Karyn" sort="Fuller, Karyn" uniqKey="Fuller K" first="Karyn" last="Fuller">Karyn Fuller</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:DC749F4B7FEBAAE08931D686FF27EAE5DC446F4A</idno><date when="2006" year="2006">2006</date><idno type="doi">10.1111/j.1440-0960.2006.00311_1.x</idno><idno type="url">https://api.istex.fr/ark:/67375/WNG-85C6X8V5-K/fulltext.pdf</idno><idno type="wicri:Area/Istex/Corpus">001B85</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001B85</idno><idno type="wicri:Area/Istex/Curation">001B85</idno><idno type="wicri:Area/Istex/Checkpoint">000B79</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">000B79</idno><idno type="wicri:doubleKey">0004-8380:2006:Fuller K:interstitial:mycosis:fungoides</idno><idno type="wicri:Area/Main/Merge">001D23</idno><idno type="wicri:Area/Main/Curation">001D11</idno><idno type="wicri:Area/Main/Exploration">001D11</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main">Interstitial mycosis fungoides initially diagnosed as interstitial granulomatous drug reaction</title><author><name sortKey="Fuller, Karyn" sort="Fuller, Karyn" uniqKey="Fuller K" first="Karyn" last="Fuller">Karyn Fuller</name><affiliation wicri:level="1"><country xml:lang="fr">Australie</country><wicri:regionArea>Department of Dermatology, Royal Adelaide Hospital, Adelaide, South Australia</wicri:regionArea><wicri:noRegion>South Australia</wicri:noRegion></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Australasian Journal of Dermatology</title><title level="j" type="alt">AUSTRALASIAN JOURNAL DERMATOLOGY</title><idno type="ISSN">0004-8380</idno><idno type="eISSN">1440-0960</idno><imprint><biblScope unit="vol">47</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="A57">A57</biblScope><biblScope unit="page" to="A57">A57</biblScope><biblScope unit="page-count">1</biblScope><publisher>Blackwell Publishing Asia</publisher><pubPlace>Melbourne, Australia</pubPlace><date type="published" when="2006-11">2006-11</date></imprint><idno type="ISSN">0004-8380</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0004-8380</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Adelaide</term><term>Annual conference</term><term>Atypical</term><term>Australasian</term><term>Biopsy</term><term>Carcinoma</term><term>Carcinosarcoma</term><term>Case series</term><term>Cutaneous</term><term>Dermatology</term><term>Differential diagnosis</term><term>Electron microscopy</term><term>Extraskeletal osteosarcomas</term><term>Fungoides</term><term>Genetic results</term><term>George hospital</term><term>Granulomatous</term><term>Histological</term><term>Histological features</term><term>Histopathological features</term><term>Igdr</term><term>Interstitial granulomatous drug reaction</term><term>Leishmaniasis</term><term>Likelihood ratio</term><term>Major types</term><term>Malignant</term><term>Medial</term><term>Medial ankle</term><term>Metastatic osteosarcoma</term><term>Mycosis</term><term>Mycosis fungoides</term><term>Nodule</term><term>Osteosarcoma</term><term>Panniculitis</term><term>Rare variant</term><term>Recurrent tumour</term><term>Royal adelaide hospital</term><term>Squamous cell carcinoma</term><term>Tumour</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A 74 year old woman presented with a 1‐month history of symmetrical erythematous annular plaques involving her groin and medial thigh 3 to 4 years post commencing simvastatin. Initial histology was consistent with the diagnosis of interstitial granulomatous drug reaction (IGDR), however 11 months post cessation of Simvastatin the plaques were expanding in size. Repeat biopsy demonstrated features of interstitial mycosis fungoides (IMF). IMF is a rare variant of mycosis fungoides. It has been reported to resemble granuloma annulare, inflammatory morphoea and IGDR with an interstitial lymphocytic infiltrate. IGDR presents most commonly with a history of asymptomatic, erythematous to violaceous plaques in an annular pattern, mainly involving the intertriginous areas, medial thighs and inner aspects of the arms. There is a temporal association between the initiation of drug therapy and lesional onset and resolution after cessation of the drug. It has clinical and histological features that overlap with IMF. This case of a rare variant of mycosis fungoides initially diagnosed as interstitial granulomatous drug reaction is presented to highlight the importance of recognising this differential diagnosis when presumed IGDR fails to resolve.</div></front></TEI><affiliations><list><country><li>Australie</li></country></list><tree><country name="Australie"><noRegion><name sortKey="Fuller, Karyn" sort="Fuller, Karyn" uniqKey="Fuller K" first="Karyn" last="Fuller">Karyn Fuller</name></noRegion></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 001D11 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001D11 | 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:DC749F4B7FEBAAE08931D686FF27EAE5DC446F4A
|texte= Interstitial mycosis fungoides initially diagnosed as interstitial granulomatous drug reaction
}}
| This area was generated with Dilib version V0.6.33. |  |