International audienceAdult's mastocytosis is usually associated with persistent systemic involvement and c-kit 816 mutation, while pediatrics disease is mostly limited to the skin and often resolves spontaneously. We prospectively included 142 adult patients with histologically proven mastocytosis. We compared phenotypic and genotypic features of adults patients whose disease started during childhood (Group 1, n = 28) with those of patients whose disease started at adult's age (Group 2, n = 114). Genotypic analysis was performed on skin biopsy by sequencing of c-kit exons 17 and 8 to 13. According to WHO classification, the percentage of systemic disease was similar (75 vs. 73%) in 2 groups. C-kit 816 mutation was found in 42% and 77% of p...
Mastocytosis presents as a focal or generalized increase of mast cells, particularly in the skin, bu...
Adult-onset urticaria pigmentosa/mastocytosis in the skin almost always persists throughout life. Th...
The term mastocytosis encompasses a heterogeneous group of clonal diseases characterized by prolifer...
International audienceAdult's mastocytosis is usually associated with persistent systemic involvemen...
Background Mastocytosis is a heterogeneous group of clinical disorders characterized by the abnormal...
Mastocytosis is a rare disease characterized by a primary pathological increase in mast cells in dif...
Adult mastocytosis is an incurable clonal disease associated with c-KIT mutations, mostly in exon 17...
International audienceBackground: Mastocytosis is a neoplastic condition characterized by the accumu...
Pediatric mastocytosis presents with heterogeneous cutaneous lesions and symptoms that are caused by...
Adult mastocytosis is usually persistent and caused by c-KIT codon 816–activating mutations. Pediatr...
Mastocytosis is a rare clonal disorder characterized by excessive proliferation and accumulation of ...
Mastocytosis is a rare clonal disorder, characterized by excessive proliferation and accumulation of...
Pediatric mastocytosis is a heterogeneous disease characterized by accumulation of mast cells in the...
Mastocytosis presents as a focal or generalized increase of mast cells, particularly in the skin, bu...
Adult-onset urticaria pigmentosa/mastocytosis in the skin almost always persists throughout life. Th...
The term mastocytosis encompasses a heterogeneous group of clonal diseases characterized by prolifer...
International audienceAdult's mastocytosis is usually associated with persistent systemic involvemen...
Background Mastocytosis is a heterogeneous group of clinical disorders characterized by the abnormal...
Mastocytosis is a rare disease characterized by a primary pathological increase in mast cells in dif...
Adult mastocytosis is an incurable clonal disease associated with c-KIT mutations, mostly in exon 17...
International audienceBackground: Mastocytosis is a neoplastic condition characterized by the accumu...
Pediatric mastocytosis presents with heterogeneous cutaneous lesions and symptoms that are caused by...
Adult mastocytosis is usually persistent and caused by c-KIT codon 816–activating mutations. Pediatr...
Mastocytosis is a rare clonal disorder characterized by excessive proliferation and accumulation of ...
Mastocytosis is a rare clonal disorder, characterized by excessive proliferation and accumulation of...
Pediatric mastocytosis is a heterogeneous disease characterized by accumulation of mast cells in the...
Mastocytosis presents as a focal or generalized increase of mast cells, particularly in the skin, bu...
Adult-onset urticaria pigmentosa/mastocytosis in the skin almost always persists throughout life. Th...
The term mastocytosis encompasses a heterogeneous group of clonal diseases characterized by prolifer...