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An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T-cell acute lymphoblastic leukemia.

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An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T-cell acute lymphoblastic leukemia. / Perez-Becker, Ruy; Szczepanowski, Monika; Leuschner, Ivo; Janka-Schaub, Gritta; Gokel, Michael; Imschweiler, Thomas; Völpel, Sigrid; Niehues, Tim; Klapper, Wolfram.

in: PEDIATR BLOOD CANCER, Jahrgang 56, Nr. 5, 5, 2011, S. 859-862.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung

Harvard

Perez-Becker, R, Szczepanowski, M, Leuschner, I, Janka-Schaub, G, Gokel, M, Imschweiler, T, Völpel, S, Niehues, T & Klapper, W 2011, 'An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T-cell acute lymphoblastic leukemia.', PEDIATR BLOOD CANCER, Jg. 56, Nr. 5, 5, S. 859-862. <http://www.ncbi.nlm.nih.gov/pubmed/20848640?dopt=Citation>

APA

Perez-Becker, R., Szczepanowski, M., Leuschner, I., Janka-Schaub, G., Gokel, M., Imschweiler, T., Völpel, S., Niehues, T., & Klapper, W. (2011). An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T-cell acute lymphoblastic leukemia. PEDIATR BLOOD CANCER, 56(5), 859-862. [5]. http://www.ncbi.nlm.nih.gov/pubmed/20848640?dopt=Citation

Vancouver

Perez-Becker R, Szczepanowski M, Leuschner I, Janka-Schaub G, Gokel M, Imschweiler T et al. An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T-cell acute lymphoblastic leukemia. PEDIATR BLOOD CANCER. 2011;56(5):859-862. 5.

Bibtex

@article{1ec1b46c7fba4d288bfec2c9d5332819,
title = "An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T-cell acute lymphoblastic leukemia.",
abstract = "Juvenile xanthogranuloma (JXG) is a disorder of disputed origin thought to be related to the dermal/interstitial macrophage. A 5-year-old female presented with an aggressive systemic JXG that developed 5 months after the diagnosis of T-cell acute lymphoblastic leukemia (T-ALL). Examination of the T-cell receptor gamma (TCR- ) rearrangement in T-ALL blasts, JXG infiltrated lymph node biopsies and micro-dissected JXG histiocytes revealed an identical bi-allelic TCR- rearrangement in all samples, thus providing evidence for a clonal relationship between T-ALL and JXG in this case.",
author = "Ruy Perez-Becker and Monika Szczepanowski and Ivo Leuschner and Gritta Janka-Schaub and Michael Gokel and Thomas Imschweiler and Sigrid V{\"o}lpel and Tim Niehues and Wolfram Klapper",
year = "2011",
language = "Deutsch",
volume = "56",
pages = "859--862",
journal = "PEDIATR BLOOD CANCER",
issn = "1545-5009",
publisher = "Wiley-Liss Inc.",
number = "5",

}

RIS

TY - JOUR

T1 - An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T-cell acute lymphoblastic leukemia.

AU - Perez-Becker, Ruy

AU - Szczepanowski, Monika

AU - Leuschner, Ivo

AU - Janka-Schaub, Gritta

AU - Gokel, Michael

AU - Imschweiler, Thomas

AU - Völpel, Sigrid

AU - Niehues, Tim

AU - Klapper, Wolfram

PY - 2011

Y1 - 2011

N2 - Juvenile xanthogranuloma (JXG) is a disorder of disputed origin thought to be related to the dermal/interstitial macrophage. A 5-year-old female presented with an aggressive systemic JXG that developed 5 months after the diagnosis of T-cell acute lymphoblastic leukemia (T-ALL). Examination of the T-cell receptor gamma (TCR- ) rearrangement in T-ALL blasts, JXG infiltrated lymph node biopsies and micro-dissected JXG histiocytes revealed an identical bi-allelic TCR- rearrangement in all samples, thus providing evidence for a clonal relationship between T-ALL and JXG in this case.

AB - Juvenile xanthogranuloma (JXG) is a disorder of disputed origin thought to be related to the dermal/interstitial macrophage. A 5-year-old female presented with an aggressive systemic JXG that developed 5 months after the diagnosis of T-cell acute lymphoblastic leukemia (T-ALL). Examination of the T-cell receptor gamma (TCR- ) rearrangement in T-ALL blasts, JXG infiltrated lymph node biopsies and micro-dissected JXG histiocytes revealed an identical bi-allelic TCR- rearrangement in all samples, thus providing evidence for a clonal relationship between T-ALL and JXG in this case.

M3 - SCORING: Zeitschriftenaufsatz

VL - 56

SP - 859

EP - 862

JO - PEDIATR BLOOD CANCER

JF - PEDIATR BLOOD CANCER

SN - 1545-5009

IS - 5

M1 - 5

ER -