Zobrazeno 1 - 10
of 49
pro vyhledávání: '"L, Tisseau"'
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 144:284-289
Resume Introduction Le syndrome de Wells, ou cellulite a eosinophiles, est une dermatose inflammatoire rare de pathogenie inconnue, caracterisee par un aspect clinique de dermo-hypodermite prurigineuse le plus souvent localisee aux extremites avec, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3c857f813e6eec8c7328627746a6b60
https://doi.org/10.1016/j.annder.2016.09.676
https://doi.org/10.1016/j.annder.2016.09.676
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 145:152-154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c728090ef6f9ed119a0c1ac839533cb
https://doi.org/10.1016/j.annder.2017.10.005
https://doi.org/10.1016/j.annder.2017.10.005
Publikováno v:
Annales de dermatologie et de venereologie. 145(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98dd6df53064f51447f87064ecc74ce6
https://pubmed.ncbi.nlm.nih.gov/29128240
https://pubmed.ncbi.nlm.nih.gov/29128240
Publikováno v:
Annales de dermatologie et de venereologie. 144(4)
Wells syndrome, or eosinophilic cellulitis, is an uncommon inflammatory dermatosis of unknown etiology that is characterized by clinical features of pruritic cellulitis-like plaques on the extremities and a histological picture of eosinophilic infilt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a1140b1feff1b16119afdd661c1cafb6
https://pubmed.ncbi.nlm.nih.gov/27839729
https://pubmed.ncbi.nlm.nih.gov/27839729
Publikováno v:
Revue de médecine périnatale. 1:89-91
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cffdc0da697da72f1bbb2a4f191a2673
https://doi.org/10.1007/s12611-009-0017-4
https://doi.org/10.1007/s12611-009-0017-4
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 142:285-286
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ceee1c42a8cb30d46fc4d470fd32d2d7
https://doi.org/10.1016/j.annder.2015.01.016
https://doi.org/10.1016/j.annder.2015.01.016
Autor:
Pierre Wolkenstein, V. Claude, Olivier Chosidow, L. Tisseau, A.-M. Rouxel-Coat, L. Rethers, Y. Pasquier, F. Cotton, J. Kapfer, D. Bouhraoua, L.-H. Thai, S. Oro, Nicolas Ortonne, Bertrand Godeau, D. Petrot, V. Papillon, M.-L. Tucker-Kleitz, R. Helenon
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 141:S348-S349
Introduction La maladie de Kikuchi-Fujimoto (KFD) se caracterise par des adenopathies douloureuses, avec ou sans atteinte cutanee, et comporte un infiltrat lympho-histiocytaire et des debris nucleaires sans reaction granulocytaire. Elle s’associe d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6653993bd5e983283014bacd3a52caa9
https://doi.org/10.1016/j.annder.2014.09.281
https://doi.org/10.1016/j.annder.2014.09.281
Publikováno v:
Dermatology (Basel, Switzerland). 217(4)
We report the case of a man who presented cutaneous aseptic abscesses, a rare form of neutrophilic disease, associated with Yersinia enterocolitica infection and who was later diagnosed as having Crohn's disease (CD). Genetic analysis showed that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b98ccfeb572b3729be9d141b529bfc83
https://pubmed.ncbi.nlm.nih.gov/18799880
https://pubmed.ncbi.nlm.nih.gov/18799880
Publikováno v:
Revue des maladies respiratoires. 20(4)
Necrotising sarcoid granulomatosis is a rare clinical entity, characterised by the development of nodular pulmonary opacities, the diagnosis if which is based on the identification of characteristic pathological lesions.A 44-years-old male smoker pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bbe361d407a30eb07f8d548062c5d902
https://pubmed.ncbi.nlm.nih.gov/14528164
https://pubmed.ncbi.nlm.nih.gov/14528164
Publikováno v:
Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie. 10(4)
Malakoplakia is a granulomatous inflammatory disorder occurring rarely in the prostate. We report our experience with three patients aged from 54 to 75 years old. Clinical presentations were unspecific. All patients presented with a past history of u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::847bcc52d2b8cd4ba713c9ad7e20f391
https://pubmed.ncbi.nlm.nih.gov/11064905
https://pubmed.ncbi.nlm.nih.gov/11064905