This rare disease is also known as necrotizing histiocytic lymphadenitis or Kikiuch Fujimoto disease. Most commonly presented as non-specific tender posterior cervical lymph adenitis. It has been linked to infectiouse as well as autoimmune etiology. The expansion occurs pericortically in LN, with apoptotic CD123+ plamacytoid monocytes (same as SLE). It has been treated with steroids, immunoglobulins as well as antibiotics.
No comments:
Post a Comment