2. Antic M, Lautenschlager S, Itin PH. Eosinophilic fasciitis 30 years after what do we really know? Report of 11 patients and review of the literature. Dermatology. 2006;213: 93--101. 3. Serrano-Grau P, Mascaró-Galy JM, Iranzo P. Desarrollo de fascitis eosinofílica tras la ingesta de simvastatina. Actas Dermosifiliogr. 2008;99:420--1. 4. Fonseca E. Manifestaciones cutáneas del síndrome tóxico ...

Diffuse eosinophilic fasciitis (Shulman disease) is a rare sclerodermiform syndrome that, in most cases, resolves spontaneously or after corticosteroid therapy. It has been associated with hematologic disorders, such as aplastic anemia. The clinical features and long-term outcomes of patients with eosinophilic fasciitis and associated aplastic anemia have been poorly described. We report the ca...

BACKGROUND Chronic eosinophilic pneumonia is a rare idiopathic interstitial lung disease. The nearly pathognomonic radiographic finding is the peripheral distribution of alveolar opacities. Pleural effusions are rarely seen. We report a case of chronic eosinophilic pneumonia with transudative eosinophilic pleural effusion. CASE PRESENTATION A 57-year-old Hispanic woman, a nonsmoker with a his...

CONCLUSION Our results demonstrate for the first time a potentially enhanced basal secretion of monocyte chemoattractant protein-1 (MCP-1) and interleukin (IL)-17A-stimulated secretion of IL-6 from nasal polyp fibroblasts, enhanced basal secretion of IL-6 from eosinophilic nasal polyp fibroblasts, and a remarkable up-regulation of IL-9 and granulocyte colony-stimulating factor (G-CSF) from nasa...

Eosinophilic pustular folliculitis is a rare dermatosis. Recently, in addition to oral indomethacin, other treatments have been applied for eosinophilic pustular folliculitis. The aim of this study was to assess the effectiveness of various therapies encompassing conventional to newly applied drugs for eosinophilic pustular folliculitis. Twenty patients with eosinophilic pustular folliculitis s...

BACKGROUND Chronic rhinosinusitis with nasal polyps is characterized by local inflammation and is categorized into two subtypes in Japan: eosinophilic chronic rhinosinusitis, and non-eosinophilic chronic rhinosinusitis. The objective of this study was to investigate the expression of key transcription factors for Treg and Th1/Th2/Th17 cells, in relation to the mRNA expression of representative ...

Eosinophilic polymyositis (EPM) is part of a rare disorder, eosinophilic myopathies (EM), which is a form of polymyositis characterized by the presence of eosinophils in muscle biopsy sections and occasionally blood eosinophilia. Herein, we are presenting an interesting case of eosinophilic polymyositis presenting with muscle pain with no other organ systems involved.

Although the key features of eosinophilic esophagitis have been increasingly described over recent years, this entity is still often not considered and consequently diagnosis is often either not made or delayed. Typical endoscopic findings may be present. The diagnosis of eosinophilic esophagitis, however, relies on the histological assessment of mucosal biopsies. This case report highlights a ...

Löffler's endocarditis is a recognised complication of diseases associated with eosinophilia. Eosinophilic heart disease is usually chronic, but there is a rare acute variety. Three patients with an unusual form of eosinophilic heart disease characterised by acute necrotising eosinophilic myocarditis after a possible initial viral infection and underlying allergic diathesis are reported. In con...

Eosinophils are involved in the initiation and propagation of diverse inflammatory responses, including antigen presentation and the release of proinflammatory cytokines, chemokines, lipid mediators and cytotoxic granules (1-4) (Fig. 1). Tissue damage and dysfunction resulting from secretion of these pleiotropic mediators is a common pathogenic component in several diseases, including atopic as...