par Dargent, Jean-Louis ;Devalck, Christine ;De Mey, Albert ;Vandeweyer, Eric ;Lespagnard, Laurence ;Heimann, Pierre
Référence Pediatric and developmental pathology, 9, 6, page (468-473)
Publication Publié, 2006
Référence Pediatric and developmental pathology, 9, 6, page (468-473)
Publication Publié, 2006
Article révisé par les pairs
Résumé : | Marginal zone B-cell lymphoma (MZBCL) of mucosa-associated lymphoid tissue type is a peculiar variant of B-cell neoplasm showing distinct clinical and pathologic features. Its occurrence in children or adolescents is extremely uncommon. We describe the case of an 11-year-old boy who developed such a lymphomatous process involving primarily the skin. The tumor was characterized by a maturing plasma cell population that included immunoblasts, heavy-chain but not light-chain restriction suggestive of monoclonality, and a prevalent, focally granulomatous component of histiocytes. As an additional interesting feature, a trisomy 3 was demonstrated by fluorescence in situ hybridization analysis. The clinical, morphological, phenotypic, and genetic characteristics seen in our patient do not differ significantly from those described in primary cutaneous MZBCL occurring in adults. |