نتایج جستجو برای: frosted branch angiitis

تعداد نتایج: 80625  

Journal: :QJM: An International Journal of Medicine 2005

Journal: :Journal of cutaneous pathology 2007
Vincenzo Mustacchio D Cabibi M I Minervini E Barresi S Amato

We present a case of late granulomatous reactions from silicone that first appeared in a site different from that of the injection causing an incorrect diagnosis of liposarcoma in the beginning. The histological picture was a cystic-macrophagic granuloma in both the injection site (upper lip) and the migrating site (paranasal regions). We think that the foreign body has undergone an antigravity...

Journal: :Neuro-degenerative diseases 2014
S Bogner C Bernreuther J Matschke A Barrera-Ocampo D Sepulveda-Falla F Leypoldt T Magnus F Haag M Bergmann W Brück S Vogelgesang M Glatzel

BACKGROUND Primary angiitis of the central nervous system (PACNS) is a rare but serious condition. A fraction of patients suffering from PACNS concurrently exhibit pronounced cerebral amyloid angiopathy (CAA) which is characterized by deposits of amyloid-β (Aβ) in and around the walls of small and medium-sized arteries of the brain. PACNS with CAA has been identified as a distinct disease entit...

Journal: :Archives of ophthalmology 2004
Bennie H Jeng Jay M Stewart Stephen D McLeod David G Hwang

1. Takanashi T, Uchida S, Arita M, Okada M, Kashii S. Orbital inflammatory pseudotumor and ischaemic vasculitis in Churg-Strauss syndrome: report of two cases and review of the literature. Ophthalmology. 2001;108:1129-1133. 2. Masi AT, Hunder GG, Lie JT, et al. The American College of Rheumatology 1990 criteria for the classification of Churg-Strauss syndrome (allergic granulomatosis and angiit...

2013
Kamel El-Reshaid John Patrick Madda

We report our clinical experience with rituximab in the treatment of 2 patients with idiopathic cutaneous angiitis who relapsed after treatment with high-dose corticosteroids and cyclophosphamide. A 39-year-old woman and a 51-year-old man presented with ulcerating maculopapular rash in both lower limbs which relapsed 6 months after treatment with a combination of high-dose corticosteroids and c...

Journal: :Pediatric Rheumatology Online Journal 2008
Reem Abdwani Kristin Houghton Simon Dobson Maureen O' Sullivan Peter Malleson

We report a case of Wegener's Granulomatosis (WG) associated with blastomycosis. This appears to be the first case report of WG co-existing with a tissue proven blastomycosis infection. The temporal correlation of the two conditions suggests that blastomycosis infection (and therefore possibly other fungal infections), may trigger the systemic granulomatous vasculitis in a predisposed individua...

2012
Ishita Patel Mediola Ismajli Alan Steuer

Sarcoidosis is a multisystem granulomatous disease of unknown aetiology. Granulomatous inflammation involving the spleen is common and associated with splenomegaly. However, massive splenomegaly is a rare occurrence. Infrequently massive splenomegaly can result in splenic infarction. Massive splenic infarction in sarcoidosis has, to our knowledge, not been previously reported. We present a case...

2013
Maraya de Jesus Semblano Bittencourt Mario Fernando Ribeiro de Miranda Amanda Magno de Parijós Letícia Brito Mesquita Diana Mendes da Fonseca Diego Augusto Aiezza Jambo

Tattooing has been associated with a variety of complications including inflammatory and granulomatous reactions, transmission of infections, and neoplasms. We report a case of a 24-year-old male who presented with a 2-month history of an erythematous nodule involving a newly made tattoo on the right leg. An excisional biopsy was performed and the histopathological evaluation was consistent wit...

Journal: :JOURNAL OF THE ILLUMINATING ENGINEERING INSTITUTE OF JAPAN 1924

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