Shitiz Sriwastava

Parry-Romberg Syndrome (PRS) is a rare neurocutaneous disorder characterized by gradual facial hemiatrophy. We present a case study of a 64-year-old woman with late-onset PRS and linear scleroderma. The patient exhibited atypical PRS symptoms including leg numbness, hyper-reflexia, trigeminal neuralgia, and severe headaches. Diagnostic evaluations revealed chronic left-sided cerebral infarction, microhemorrhages, and nerve involvement.

Section 1 A 47-year-old man with a history of isolated, severe, recurrent episcleritis of the left eye, on adalimumab and methotrexate for the past 2 years, presented with acute vertigo. Two days later, in addition to ongoing vertigo, he developed a mild headache behind his right eye, which intensified over 5 days and worsened with Valsalva maneuver and when lying down. He denied nausea, vomiting, light or sound sensitivity, or a history of headaches.