Clinicopathologic features of histiocytic lesions following ALL, with a review of the literature

Pediatric and Developmental Pathology

Volumn 13, Issue 3, 2010, Pages 225-237

  Castro, Eumenia C C ^a   Blazquez, Cristina ^b   Boyd, Jaime ^c   Correa, Hernán ^d   De Chadarevian, J P ^e   Felgar, Raymond E ^f   Graf, Nicole ^g   Levy, Norman ^h   Lowe, Eric J ⁱ   Manning Jr , John T ^j   Proytcheva, Maria A ^k   Senger, Christof ^l   Shayan, Katayoon ^m   Sterba, Jaroslav ⁿ   Werner, Alice ⁱ   Surti, Urvashi ^o   Jaffe, Ronald ^a  

^a CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

^b HOSPITAL DE JEREZ   (Spain)

^c Pediatra Hematólogo Oncólogo   (Panama)

^d MONROE CARELL JR CHILDREN S HOSPITAL AT VANDERBILT   (United States)

^e ST CHRISTOPHER'S HOSPITAL FOR CHILDREN   (United States)

^f PRESBYTERIAN UNIVERSITY HOSPITAL   (United States)

^g CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^h DARTMOUTH HITCHCOCK MEDICAL CENTER   (United States)

ⁱ CHILDREN S HOSPITAL OF THE KING S DAUGHTERS   (United States)

^j Division of Pathology and Laboratory Medicine   (United States)

^k CHILDREN'S MEMORIAL HOSPITAL   (United States)

^l BC CHILDREN S HOSPITAL   (Canada)

^m RADY CHILDREN'S HOSPITAL   (United States)

ⁿ UNIVERSITY HOSPITAL BRNO   (Czech Republic)

^o UNIVERSITY OF PITTSBURGH   (United States)

more..

Author keywords

Acute lymphoblastic leukemia; Atypical histiocytosis; Histiocytes

Indexed keywords

ANTINEOPLASTIC AGENT; CD14 ANTIGEN; CD163 ANTIGEN; CD68 ANTIGEN; F13A PROTEIN; FASCIN; IMMUNOGLOBULIN HEAVY CHAIN; LANGERIN; PROTEIN; PROTEIN S 100; T LYMPHOCYTE RECEPTOR GAMMA CHAIN; T6 ANTIGEN; UNCLASSIFIED DRUG;

ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ADULT; AGED; ALLOGENEIC STEM CELL TRANSPLANTATION; ARTICLE; CANCER CHEMOTHERAPY; CANCER GRADING; CANCER MORTALITY; CANCER RECURRENCE; CANCER SURGERY; CHILD; CLINICAL ARTICLE; CYTOLOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE IDENTIFICATION; GENE REARRANGEMENT; HISTIOCYTE; HISTIOCYTIC SARCOMA; HISTIOCYTOSIS X; HISTOLOGY; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; JUVENILE XANTHOGRANULOMA; LANGERHANS CELL SARCOMA; LEUKEMIA REMISSION; MALE; MULTIMODALITY CANCER THERAPY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGNOSIS; RETICULOHISTIOCYTOSIS; ROSAI DORFMAN DISEASE; SCHOOL CHILD; T LYMPHOCYTE RECEPTOR GENE; TURNOVER TIME; CLINICAL TRIAL; GENETICS; HISTIOCYTOSIS; IMMUNOLOGY; MORTALITY; MULTICENTER STUDY; MULTIPLE CANCER; PATHOLOGY; REVIEW; SURVIVAL RATE; TREATMENT OUTCOME;

ADOLESCENT; AGED; CHILD; CHILD, PRESCHOOL; COMBINED MODALITY THERAPY; FEMALE; GENE REARRANGEMENT, B-LYMPHOCYTE; GENE REARRANGEMENT, BETA-CHAIN T-CELL ANTIGEN RECEPTOR; HISTIOCYTES; HISTIOCYTOSIS; HUMANS; IMMUNOGLOBULIN HEAVY CHAINS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; NEOPLASMS, MULTIPLE PRIMARY; PRECURSOR CELL LYMPHOBLASTIC LEUKEMIA-LYMPHOMA; PROGNOSIS; SURVIVAL RATE; TREATMENT OUTCOME;

EID: 77956214943     PISSN: 10935266     EISSN: 16155742     Source Type: Journal    
DOI: 10.2350/09-03-0622-OA.1     Document Type: Article

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