Abstract
In this study, we reported a patient who presents with multicentric
reticulohistiocytosis (MRH)-like clinical feature, but the histology is
not compatible with it. Like our patient, a couple of patients described
previously also had the dilemma that they could not be classified
appropriately into any current histiocytosis entity. Considering the
clinical and pathological features together, all these patients had a
similar clinical profile: xanthomatous rash, erosive arthritis and
histopathological findings showing xanthomized histiocytes. Therefore,
we propose a new disease entity - xanthomatous erosive arthritis (XEA),
to accommodate these patients that cannot be classified appropriately
into the current system.