Penile Pyoderma Gangrenosum: A Rare Presentation and Review of Management Strategies: Case Report. [PDF]
Clin Case RepABSTRACT Penile pyoderma gangrenosum is a rare but important differential diagnosis for ulcerative lesions of the genital region. Early recognition and systemic treatment, especially with corticosteroids, are crucial for effective management and avoiding the penile mutilating effect of the disease. Clinicians should consider PPG in cases of unexplained
Ngereja SJ +11 more
europepmc +2 more sources
Myelodysplastic Syndrome With Complex Chromosomal Karyotype Abnormalities Complicated by Multiple Intestinal Perforations: A Case Report and Literature Review. [PDF]
Case Rep Gastrointest MedBackground Myelodysplastic syndromes (MDSs) are clonal hematopoietic disorders often associated with cytogenetic abnormalities, among which trisomy 8 is one of the most common abnormalities. Trisomy 8 is linked to autoimmune manifestations, including Behçet‐like disease, especially with gastrointestinal involvement.
Niu ZY +5 more
europepmc +2 more sources
Clinical Manifestations and Diagnosis of Behçet’s Syndrome
European Medical Journal Rheumatology, 2021 Behçet’s syndrome (BS) is a systemic vasculitis with a wide range of clinical presentations and disease courses. It may involve the mucosa, skin, joints, vessels, eyes, and nervous and gastrointestinal systems.
Sara Beça, Gerard Espinosa
doaj
Mucocutaneous Manifestations of Behçet's Disease
Frontiers in Medicine, 2021 Behçet's disease (BD) is a chronic, relapsing, systemic inflammatory disease with clinical features showing mucocutaneous lesions involving the ocular, articular, and further miscellaneous organs.
Koichiro Nakamura +3 more
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Initial Presentation of HIV Infection With Two Successive Acute Arterial Thromboses: A Case Report. [PDF]
, 2014 IntroductionOne of the complications of HIV infection is greater risk of thromboembolic events. A variety of mechanisms has been found to be responsible for prothrombotic tendency in patients with HIV infection.Case presentationA 27-year-old heterosexual
Moslemi, Sam +2 more
core +1 more source
Frontiers in Immunology, 2021 ObjectivesWhen treating Behçet’s disease (BD), anti-tumor necrosis factor (TNF)-α agents have become a second-line therapy when conventional immunosuppressive drugs have failed.
Marta Arbrile +6 more
doaj +1 more source
Blastomycosis-Like PyodermaA Rare Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2016 Blastomycosis-like pyoderma is a rare, cutaneous bacterial infection of skin, seen in malnourished individuals, in a poor state of health and manifests as vegetating skin lesions.
Amrita A. Hongal, Somashekar Gejje
doaj +1 more source
In situ thrombosis in pulmonary arterial aneurysms due to Behçet’s disease and efficacy of ımmunosuppressive therapy [PDF]
, 2012 BehçetDisease (BD) is a systemic vasculitis characterized by recurrent oral and genital ulcers and uveitis, arthritis, and involvement of the gastrointestinal tract, central nervous system and blood vessels.
Asiye Yavuz +5 more
core +1 more source
Update on the Diagnosis of Behçet’s Disease
Diagnostics, 2022 Behçet’s disease (BD) is a systemic inflammatory disease with unknown etiology. It is characterized by recurrent mucocutaneous lesions and major organ disease such as ocular, neurologic, vascular, and gastrointestinal manifestations.
Fatma Alibaz-Oner, Haner Direskeneli
doaj +1 more source
A national cohort study on pediatric Behçet's disease: Cross-sectional data from an Italian registry [PDF]
, 2018 21noBACKGROUND: Behçet's disease is a rare multi-systemic inflammatory disease with unknown etiology which involves principally oral and genital mucosa, skin and eyes.
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