Results 71 to 80 of about 85,574 (254)
Immune checkpoint inhibitors are a promising new therapeutic strategy in oncology that aims to eliminate cancer cells by enhancing patients' immune response against tumor antigens.
Christina Salamaliki +2 more
doaj +1 more source
Acquired pure megakaryocytic aplasia successfully treated with cyclosporine [PDF]
Acquired pure megakaryocytic aplasia is a rare hematological disorder characterized by thrombocytopenia with absent or markedly reduced megakaryocytes in the bone marrow.
Aisha Al Khinji +8 more
core +2 more sources
The Videofluorographic Swallowing Study in Rheumatologic Diseases: A Comprehensive Review [PDF]
Autoimmune connective tissue diseases are a heterogeneous group of pathologies that affect about 10% of world population with chronic evolution in 20%-80%.
Costanzo, M. +13 more
core +3 more sources
Severe eosinophilic syndrome associated with the use of probiotic supplements: a new entity? [PDF]
Severe eosinophilic syndromes related to the administration or use of unsuspected immunogenic substances have been described previously. Many of these diseases presented initially as clusters or isolated cases.
Article Id +4 more
core +2 more sources
Eosinophilic Fasciitis Responds Well to Steroids and Methotrexate
Eosinophilic fasciitis (EF) is a rare systemic inflammatory disease with an unknown etiology. Making a diagnosis in such a case is always a challenge as it is a rare disease and mimics scleroderma and scleroderma-like syndrome but should be kept in mind ...
Asmaa Sabr Mahdi1*, +4 more
doaj +1 more source
Eosinophilic Fasciitis: Clinical Signs Leading to Diagnosis
Eosinophilic fasciitis is a rare disease characterized by peripheral eosinophilia and inflammatory infiltrate on muscular fascia and subcutaneous tissue. Patients present with edema and stiffening of limbs, progressing rapidly to fibrosis.
Túlio Marcos Coimbra +6 more
doaj +1 more source
Eosinophilic fasciitis after parasite infection
Eosinophilic fasciitis is a systemic inflammatory disease characterized by symmetrical swelling and skin induration of the distal portions of the arms and/or legs, evolving into a scleroderma-like appearance, accompanied by peripheral blood eosinophilia.
Marta Oliveira +2 more
doaj +1 more source
Eosinophilic fasciitis (EF), also known as Shulman syndrome, is a rare scleroderma-like disorder that is characterized by an acute onset of induration, swelling, erythema, and tenderness of the skin and deep fascia, often affecting all four limbs.
Jiwon Kim, L. Lee
semanticscholar +1 more source
Verruciform Xanthoma Within the Cyst Lining of Hidradenitis Suppurativa
ABSTRACT Verruciform xanthoma (VX) is a rare lesion most often seen in the oral mucosa or anogenital region, most commonly characterized histologically by verrucous epithelial hyperplasia and foamy histiocytes in the papillary dermis. While VX has been reported in association with inflammatory dermatoses such as lichen planus and lichen sclerosus, its ...
Deaquan Nichols +4 more
wiley +1 more source
A “groovy” diagnosis: Eosinophilic fasciitis
Clinical examination can be the key to pursuing a diagnosis, even in rare diseases. The “groove sign” is a typical finding in eosinophilic fasciitis and can be elicited by elevation of the arm to allow for venous return with visible “grooving” of the ...
Peter Korsten
doaj +1 more source

