Results 81 to 90 of about 1,238,132 (184)
RARE CASE OF ESOPHAGUS LESION IN PATTENT WITH BEHCET’S DISEASE
, 2001 33-year-old patient with Behcet's disease developed severe lesion of gastro-intestmal tract involving esophagus. Behcet’s disease diagnosis was verified by recurrent aphtous stomatitis, genital ulcers and erythema nodosum.
Z. S. AIkeberova +3 more
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, 2013 FAPA syndrome (periodic fever, aphthous stomatititis, pharyngitis and adenitis) is a relatively new entity described in pediatric patients. In adults, reports of FAPA are limited to rare case reports. The differential diagnosis of FAPA in adults includes
Burke Cunha, Sigridh Muñoz-Gómez
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Vision-Threatening Behcet’s Disease: Severity of Ocular Involvement Predictors
, 2018 Purpose. To examine and spot systemic findings commonly associated with a serious form of ocular Behcet’s disease. This could potentially help ophthalmologists categorize their patients based on future risk and plan treatment accordingly.
Mohammed A. Hussein +2 more
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Delirium as presenting symptom of neuro-Behcet’s disease
, 2016 Objectives: Behcet’s disease is a multisystemic disorder. Most of its clinical manifestations are due to thrombosis or vasculitis. There is a predominance of mucocutaneous and ocular lesions; neurological manifestations are minority.
Rana Alnasser Alsukhni +3 more
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Chronic recurrent aphthous stomatitis as a symptom of Behcet’s disease
The article describes a clinical case of Behcet’s disease, manifested by recurrent aphthae in the oral cavity and genital ulcers. The disease occurred in childhood in the form of chronic recurrent aphthous stomatitis.
N.V. Rupasova +2 more
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Respirology Case ReportsBehcet's disease is a chronic, multisystem variable vessel vasculitis characterised by recurrent oral and genital ulcers, ocular inflammation and a wide range of systemic manifestations.
Rinoosha Rachel +4 more
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BEHCET’S DISEASE: REPORT OF A CASE AND REVIEW OF THE LITERATURE
, 2006 Behcet’s disease (BD) is an autoimmune disease of unknown aetiology with multisystem involvement presenting with relapsing orogenital ulcers and uveitis, involvement of central nervous system, joints, lungs, gastrointestinal tract and major blood vessels
J Macierewicz, S Wallis, B M Shrestha
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Behçet’s Disease and Neuro-Behçet’s Syndrome
European Medical Journal Neurology, 2018 Behçet’s disease is an idiopathic chronic relapsing multisystem vascular-inflammatory disease of unknown origin, which usually presents with orogenital ulceration and uveitis and is identified as the triple-symptom complex.
Ugur Uygunoglu +2 more
doaj
Breast manifestations of autoimmune diseases are rare but may present as localized disease or as part of a systemic disease. The most common clinical presentations of autoimmune mastitis are palpable masses and mastalgia, but patients can also be ...
Suk Jin Park +2 more
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A Case of Ileal Mucormycosis in a Patient with Gastrointestinal Behcet’s Disease [PDF]
, 2008 Zygomycosis (mucormycosis) is a rare fungal infectious disease, usually found in association with an immunocompromised state. Gastrointestinal mucormycosis is extremely rare and fatal, thus it is important to detect and manage this disease at an early ...
박재준 +9 more
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