Behçet hastalığı olarak bilinen Behçet Sendromu, tekrarlayan oral aftlar ile beraber genital aft, oküler hastalık,gastrointestinal tutulum, nörolojik tutulum, vasküler hastalık veya artrit gibi sistemik belirtilerden herhangi biri ile karakterizedir. Sarkoidoz dünyada genelinde görülen tuttuğu organlarda non -kazeife granülomlar ile karakterize olan etyoloji net olarak bilinmeyen granülomatöz bir hastalıktır. BS ve sarkoidozun klinik seyrinde üveit, poliartrit, menenjit, kardiyovasküler hastalık, göğüs radyografilerinde anormallik izlendiğinden her iki hastalık birbirleri ile karıştırılabilir.
YOK
YOK
Behçet syndrome(BS), also known as Behçet disease (BD), is characterized by recurrent oral aphthae and any of several systemic manifestations including genital aphthae, ocular disease, skin lesions, gastrointestinal involvement, neurologic disease, vascular disease or arthritis. Sarcoidosis is a multisystem granulomatous disorder of unknown etiology that affects individuals worldwide and is characterized pathologically by the presence of noncaseating granulomas in involved organs. BD may be confused with sarcoidosis because they are both multisystem inflammatory disorders presenting with uveitis, polyarthritis, meningitis, cardiovascular disease, erythema nodosum, and other cutaneous lesions, and abnormal chest radiographs.
YOK
Primary Language | English |
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Subjects | Clinical Sciences |
Journal Section | Letter to the Editor |
Authors | |
Project Number | YOK |
Publication Date | December 28, 2022 |
Acceptance Date | November 2, 2022 |
Published in Issue | Year 2022 Volume: 47 Issue: 4 |