نتایج جستجو برای: disseminated granuloma faciale

تعداد نتایج: 34348  

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1999
U Querfeld W Groth E F Eder B Hoppe S Sollberg

Journal: :BMC Dermatology 2002
Alexander Kreuter Thilo Gambichler Peter Altmeyer Norbert H Brockmeyer

BACKGROUND Granuloma annulare is a granulomatous disease of unknown etiology. Various therapies have been tried in disseminated granuloma annulare (DGA), including corticosteroids, several variants of psoralen plus ultraviolet-A radiation, ultraviolet- A1 radiation, systemic retinoids, and dapsone, with variable success. We report a patient with recalcitrant DGA who was treated with fumaric aci...

2017
Izabella Dolka Anna Gruk-Jurka Piotr Jurka Beata Dolka Joanna Bonecka

BACKGROUND Hyaline ring granuloma (HRG) is an uncommon histopathologic finding of unsolved etiopathogenesis. According to the exogenous theory, HRG develops due to implantation of foreign material, most probably indigestible plant fragments. HRG is a comparatively rare condition in humans, mostly involving the oral cavity with very rare extraoral locations. CASE PRESENTATION An 1-year-old mix...

Journal: :BMJ case reports 2014
Tiago Mestre Ana Maria Rodrigues Jorge Cardoso

To cite: Mestre T, Rodrigues AM, Cardoso J. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2014-205883 DESCRIPTION Granuloma annulare is a granulomatous skin disease of unknown aetiology. It is more common in women and has a disseminated form in 10–15% of patients. A small portion of these patients have an associated disease such as diabetes mellitus, viral infe...

Journal: :Clinical advances in hematology & oncology : H&O 2013
Muhammad Rizwan Khawaja Thomas M Ulbright Shadia Jalal

Langerhans cell histiocytosis (LCH), also designated as histiocytosis-X or eosinophilic granuloma, is an uncommon dendritic cell disorder characterized by the infiltration of abnormally proliferating Langerhans cells into 1 or more organs.1 The clinical presentation of LCH varies depending on the site(s) of involvement and aggressiveness of disease. In children, it may present as LettererSiwe d...

Journal: :Acta dermato-venereologica 2015
Stéphanie Mallet Charlotte Rebelle Isabelle Ligi Didier Scavarda Corinne Bouvier Philippe Petit Sylvie Fraitag Michel Wassef Caroline Gaudy-Marqueste Sylvie Hesse Marie-Aleth Richard Jean-Jacques Grob Nicolas André

A full-term female newborn, with no significant past medical history, was referred to our department for treatment of an acute respiratory distress syndrome of neurological origin at day 8 of life. At birth, she presented with 3 small angiomatous papules and 4 subcutaneous nodules suggestive of neonatal haemangiomatosis (NH) (Fig. 1). A brain MRI revealed a highly vascularised brain stem tumour...

Journal: :Annales françaises d'Oto-rhino-laryngologie et de Pathologie Cervico-faciale 2021

Annales Francaises d'Oto-Rhino-Laryngologie et de pathologie cervico-faciale - Vol. 138 N° 5 p. 417-418

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