Abstract We report a case of an unusually located site acute localized exanthematous pustulosis in the right lower limb patient treated with beta‐lactams which resolved upon cessation. This highlights need for vigilance as well index suspicion atypical presentations.

BACKGROUND Recurrent Kawasaki disease is rare. CASE CHARACTERISTICS An eight-month old infant had classic Kawasaki disease with transient coronary artery dilatation. OBSERVATIONS Recurrence of incomplete Kawasaki disease after two years of initial diagnosis. OUTCOME The index episode of Kawasaki disease was resistant to single infusion of immunoglobulin, while repeat episode responded wit...

objectives our objectives were to determine if: 1) imaging pattern at recurrence is associated with delayed diagnosis, and 2) appearance at recurrence can be predicted based on appearance at presentation. conclusion imaging appearance at baseline does not reliably predict imaging appearance at recurrence. therefore, a high index of suspicion for the infiltrative pattern is required in assessmen...

PURPOSE Plasma cell meningitis is an uncommon neurologic complication of multiple myeloma with a very poor prognosis (median overall survival of 3 months). CASE REPORT We describe a previously heavy treated 54-year-old caucasian female with Bence Jones multiple myeloma who developed, shortly after a good partial response to a third line therapy, a plasma cell meningitis. Intrathecal chemother...

A six-month-old Caucasian boy presents with a three-day history of fever. The parents report that he had red eyes without pus two days previously. On examination, otitis media is noted as well as a nonexudative pharyngitis. Amoxicillin is prescribed. They return on the sixth day of illness and report that the child is still febrile, not responding to antipyretics and has a rash. The rash appear...

Diagnosis of central diabetes inspidus (CDI)requires a high index clinical suspicion especially in patients with traumatic brain injury or following neurosurgery. We would like to report rare case necrotising infundibulohypophysitis(NIH) young male CDI and discuss the radiological findings differential diagnosis.