1. Rosai J, Dorfman RF. Sinus histiocytosis with massive lymphadenopathy: a newly recognized benign clinicopathological entity. Arch Pathol. 1969;87 (1):63-70. 2. Foucar E, Rosai J, Dorfman R. Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): review of the entity. Semin Diagn Pathol. 1990;7(1):19-73. 3. Eisen RN, Buckley PJ, Rosai J. Immunophenotypic characterization of ...

Intestinal lymphangiectasia may occur as a primary congenital disorder or a secondary disorder. Secondary lymphangiectasia could be associated with diseases such as abdominal carcinoma, retroperitoneal fibrosis or chronic pancreatitis. This is the first reported case of intestinal lymphangiectasia associated with recurrent histiocytosis X. This case report illustrates the need for more prospect...

detection of trace metals in the cell-free BAL fluid, showing high concentrations of tungsten (W), tantalum (Ta) and cobalt (Co) in hard metal lung disease [163]. The quantification of asbestos bodies is best done by filtration of 5-15 ml fresh BAL fluid, cells included, onto millipore filters, and counting the number of asbestos bodies [179]. Uncoated asbestos fibres can only be counted by ele...

We report our experience with seven cases of eosinophilic granuloma in which unusual and/or confusing features were encountered. These features include: histologic confusion with desquamative interstitial pneumonitis, diffuse histiocytic lymphoma, eosinophilic pneumonia; cysts filled with air and/or fluid; radiographic onset in the eighth decade of life; intratracheal mass; and focal parenchyma...

A one-month-old female baby had been noted to have multiple vesicles and pustules over the head, face, trunk and four extremities since she was one-week-old. Under the impression of disseminated herpes virus infection, intravenous acyclovir was given after admission. Serum herpes simplex virus and varicella zoster virus enzyme-linked immunosorbent assay test and virus culture were all fruitless...

The fourteenth annual meeting of the Society for Pediatric Dennatology was held in Quebec City, Quebec, Canada and hosted by Drs. Beraice Krafchik, Lionel Boxall, and the dennatology staff of L'Hotel-Dieu de Quebec, particularly Drs. Raymond Lessard and Richard Cloutier. The fifth annual Sidney Hurwitz Lecture was presented by Professor Ruggero Caputo of the University of Milan. He discussed th...

Histiocytosis is a term applied to a group of rare disorders of the reticuloendothelial system. Eosinophilic granuloma, the most benign and localized of the three Langerhans cell histiocytosis entities, may be solitary or multiple. Eosinophilic granuloma can affect almost any bone, but commonly involves the mandible when the jaws are affected. Conventional treatment of LCH is with surgery, radi...

Langerhans' cell histiocytosis summarizes a spectrum of diseases on the basis of histogenetic criteria. These are characterized by an accumulation of cells with Langerhans' cell phenotype in one or multiple organs. Up to 50% of patients with either single or multi-organ manifestation of Langerhans' cell histiocytosis initially present with cutaneous symptoms. Nevertheless, cutaneous Langerhans'...