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Article Dans Une Revue Pediatric Dermatology Année : 2011

Plexiform fibrohistiocytic tumor with molecular and cytogenetic analysis.

Résumé

A child with plexiform fibrohistiocytic tumor is presented, in whom a superficial biopsy was misdiagnosed as an inflammatory granuloma. Cytogenetic analysis revealed a 46,X,del(X)(q13)[3]/46,XX[23] karyotype. However, fluorescence in situ hybridization (FISH) and array-comparative genomic hybridization (CGH) analysis failed to detect any numerical or quantitative genomic anomaly. Because of lack of specific chromosomal hallmarks, a molecular diagnosis of plexiform fibrohistiocytic tumor with the currently available tools is not reliable.

Dates et versions

hal-00592168 , version 1 (11-05-2011)

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Stéphanie Leclerc-Mercier, Florence Pedeutour, Thibault Fabas, Christophe Glorion, Nicole Brousse, et al.. Plexiform fibrohistiocytic tumor with molecular and cytogenetic analysis.. Pediatric Dermatology, 2011, 28 (1), pp.26-9. ⟨10.1111/j.1525-1470.2010.01370.x⟩. ⟨hal-00592168⟩
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