Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Blaise E. Favara"'
Publikováno v:
Cancer. 36:2132-2137
Publikováno v:
Pediatric and Developmental Pathology. 5:130-140
Macrophage activation and secondary hemophagocytic syndrome are rarely reported in association with Langerhans cell histiocytosis (LCH). The authors reviewed their pathology files for cases of LCH in which evidence of macrophage activation coexisted
Autor:
Alfred C. Feller, Jon Pritchard, Lawrence M. Weiss, R. Maarten Egeler, Blaise E. Favara, Göran Elinder, Peter Bucsky, Jan-Inge Henter, Shinsaku Imashuku, Mary V. Gresik, Elaine S. Jaffe, Macro Pauli, Maurizio Aricò, Ron Jaffe, Helmut Gadner, Christian Nezelof, Gritta Janka-Schaub, Stephan Ladisch
Publikováno v:
Medical and Pediatric Oncology, 157-166. Wiley-Liss Inc.
ISSUE=29;STARTPAGE=157;ENDPAGE=166;ISSN=0098-1532;TITLE=Medical and Pediatric Oncology
Karolinska Institutet
ISSUE=29;STARTPAGE=157;ENDPAGE=166;ISSN=0098-1532;TITLE=Medical and Pediatric Oncology
Karolinska Institutet
Pathologists and pediatric hematologist/ oncologists of the World Health Organization's Committee on Histiocytic/Reticulum Cell Proliferations and the Reclassification Working Group of the Histiocyte Society present a classification of the histiocyti
Autor:
Ann Steele, Blaise E. Favara
Publikováno v:
Pediatric Pathology & Laboratory Medicine. 17:769-787
The morphology of Langerhans cell histiocytosis (LCH) involving lymph nodes was analyzed in 43 biopsies from 39 patients and findings were correlated with clinical data. Five histological motifs were recognized: sinusoidal, limited sinusoidal, epithe
Autor:
Blaise E. Favara
Publikováno v:
Pediatric Pathology & Laboratory Medicine. 16:413-433
Liver biopsies were studied in 47 cases representing various histiocytosis syndromes. These included 32 cases of hemophagocytic syndrome, 11 cases of Langerhans cell histiocysis (LCH), and 4 cases of other histiocytic disorders. All cases of hemophag
Publikováno v:
Orbit. 15:41-45
The clinical and pathological findings in a five month-old black male infant with an orbital lesion are reported. By light microscopy, immunohistochemistry, and electron microscopy the tumor was diagnosed as juvenile xanthogranuloma. Touton giant cel
Publikováno v:
Pediatric Pathology & Laboratory Medicine. 15:169-174
(1995). Case 3 Atypical Juvenile Xanthogranuloma. Pediatric Pathology & Laboratory Medicine: Vol. 15, No. 1, pp. 169-174.
Publikováno v:
American Journal of Hematology. 47:16-20
Langerhans cell histiocytosis (LCH) is an enigmatic histiocytic proliferative disorder of unknown etiology that affects children primarily. We have investigated the possibility that viruses are etiological or that they have a "triggering effect" in L
Autor:
Heinz-Jochen Radzun, Gritta Janka-Schaub, Christian Nezelof, Alfred C. Feller, Blaise E. Favara, Peter Bucsky, Brigitte Schlegelberger
Publikováno v:
Medical and Pediatric Oncology. 22:200-203
A workshop of the Histiocyte Society was recently held, in order to discuss the problems and confusion of malignant histiocytosis (MH) and large cell anaplastic (Ki-1) lymphoma (LCAL). The aims of this workshop were to clarify the terminology for mal
Publikováno v:
Pediatric Pathology. 11:131-142
A case of fatal congenital hepatoblastoma is described in which the autopsy provided the first evidence of Beckwith-Wiedemann syndrome. Aneuploid quantitative DNA patterns were found by image analysis of the tumor and the cytomegalic adrenal gland.