Behcets disease is DEFINED as an auto-inflammatory systemic vasculitis of unknown etiology. It is characterized by mucocutaneous manifestations, including recurrent oral and genital ulcerations, ocular manifestations, especially chronic relapsing uveitis, and systemic vasculitis involving arteries and veins of all sizes. Behcets disease usually affects young adults 20 to 40 years of age and is also seen in children less frequently.Both genders are equally affected by the disease although slight male preponderance is seen in japan[7] .we would like report a rare case series on Behcets aka silk road disease presenting in a 16 year old female complicated with SMA vascular insufficiency

Introduction: Jaundice is one of the most dreaded medical disorders in pregnancy. Infective causes of jaundice are often confused with pregnancy specific liver disorders (P-sLD) like HELLP syndrome and acute fatty liver of pregnancy. Delivery may be needed in some situations irrespective of the etiology.Case Report: We report a case of preeclampsia (PE) complicated by HELLP syndrome which mimicked thrombotic microangiopathy (TMA) in the postpartum period coexistent with atypical scrub typhus. The diagnostic dilemma at presentation, the challenges surrounding its management, and the recovery following antibiotic treatment with doxycycline are described with a review of the literature.