Introduction Rosai-Dorfman disease (RDD) is a rare histiocytic proliferative disorder of unknown etiology. Usually it presents with massive painless cervical lymph node enlargement. Histologically, it ...

Department of Ophthalmology, Cullen Eye Institute, Baylor College of Medicine, Houston, Texas, USA Correspondence to: Dr R L Font Ophthalmic Pathology Laboratory, Cullen Eye Institute, Baylor College ...

Histiocytoses represent a group of diverse rare disorders characterized by the abnormal accumulation of cells derived from the mononuclear phagocyte system in various tissues and organs. The ...

The mother of a three-month-old baby girl diagnosed with a rare blood disorder is urging people to sign the stem cell register in a bid to save her daughter's life. Doctors initially suspected ...

Nine patients had a syndrome characterized by the presence of a sea-blue histiocyte and splenomegaly. Lipid analysis of liver from the most recent patient revealed accumulations of specific ...

Les symptômes d’une histiocytose varient selon l’organe atteint. © jarun011, Adobe Stock Maladie rare, l'histiocytose est liée à une accumulation anormale de ...

Langerhans cell histiocytosis comprises a heterogeneous range of clinical manifestations secondary to clonal proliferation of histiocytes, characterized by the accumulation of these cells in various ...

Histiocytic disorders in children are marked by the abnormal proliferation of cells from the mononuclear phagocyte system, which includes dendritic cells, monocytes, and macrophages. These cells, ...

Thanks to new treatments, more people survive histiocytic neoplasms, but their survival comes with challenges, according to findings published in Blood. “Advances in targeted therapeutics for ...

Hemophagocytic lymphohistiocytosis (HLH) is a rare disease that usually occurs in infants and young children. It may also occur in adults. Children usually inherit the disease. In adults, many ...