Mastocitosi cutanee: il mastocitoma in età pediatrica

Background: Mastocytosis is a rare disease involving mast cells (MC) and their CD34+ progenitors. According to the WHO consensus classification, cutaneous mastocytosis (CM) is considered a benign disease confined to the skin, preferentially seen in young children with a marked tendency to regress sp...

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Main Author: Tabanelli, Michela <1974>
Other Authors: Patrizi, Annalisa
Format: Doctoral Thesis
Language:it
Published: Alma Mater Studiorum - Università di Bologna 2011
Subjects:
Online Access:http://amsdottorato.unibo.it/3396/
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spelling ndltd-unibo.it-oai-amsdottorato.cib.unibo.it-33962014-03-24T16:29:08Z Mastocitosi cutanee: il mastocitoma in età pediatrica Tabanelli, Michela <1974> MED/35 Malattie cutanee e veneree Background: Mastocytosis is a rare disease involving mast cells (MC) and their CD34+ progenitors. According to the WHO consensus classification, cutaneous mastocytosis (CM) is considered a benign disease confined to the skin, preferentially seen in young children with a marked tendency to regress spontaneously. Aim of our study was the long-term assessment of the outcome of solitary (SM) and multiple (MM) mastocytomas in a pediatric population. Materials and methods: From January 1996 to December 2010, 241 pediatric patients with a diagnosis of CM were followed-up at the outpatient division of pediatric dermatology of the University of Bologna. We focused our retrospective evaluation on patients affected by SM or MM. We collected, through the analysis of medical records and with a telephone questionnaire for patients and their families, information on clinical aspects of the disease evolution and on the efficacy of topical steroid therapy. Results: Over the 241 considered patients we recorded: SM or MM in 176 (73%) pts., urticaria pigmentosa in 53 (22%) pts., telangiectasia macularis eruptiva perstans in 9 (4%) pts., diffuse CM in 2 (0,9%) pts. and polymorph CM in 1 (0,4%) pt. On 176 children affected by SM or MM (97 M vs. 79 F), 130 (74%) patients were followed-up with a mean of 56,3 (r. 4-142) months. A satisfactory outcome was recorded in 99 (76%) cases of whom 52 (53%) treated with topic steroids. Mean time to complete regression was 16.4 m. on treated patients vs. 34.7 m. on non treated patients (p=0,001). Conclusions: From our study emerged that resolution of the disease is independent from therapy, but the time to regression and to complete recovery of the coetaneous lesions is faster and favored by the application of topic steroid with an improvement of the quality of life for children and their families. Alma Mater Studiorum - Università di Bologna Patrizi, Annalisa 2011-04-07 Doctoral Thesis PeerReviewed application/pdf it http://amsdottorato.unibo.it/3396/ info:eu-repo/semantics/openAccess
collection NDLTD
language it
format Doctoral Thesis
sources NDLTD
topic MED/35 Malattie cutanee e veneree
spellingShingle MED/35 Malattie cutanee e veneree
Tabanelli, Michela <1974>
Mastocitosi cutanee: il mastocitoma in età pediatrica
description Background: Mastocytosis is a rare disease involving mast cells (MC) and their CD34+ progenitors. According to the WHO consensus classification, cutaneous mastocytosis (CM) is considered a benign disease confined to the skin, preferentially seen in young children with a marked tendency to regress spontaneously. Aim of our study was the long-term assessment of the outcome of solitary (SM) and multiple (MM) mastocytomas in a pediatric population. Materials and methods: From January 1996 to December 2010, 241 pediatric patients with a diagnosis of CM were followed-up at the outpatient division of pediatric dermatology of the University of Bologna. We focused our retrospective evaluation on patients affected by SM or MM. We collected, through the analysis of medical records and with a telephone questionnaire for patients and their families, information on clinical aspects of the disease evolution and on the efficacy of topical steroid therapy. Results: Over the 241 considered patients we recorded: SM or MM in 176 (73%) pts., urticaria pigmentosa in 53 (22%) pts., telangiectasia macularis eruptiva perstans in 9 (4%) pts., diffuse CM in 2 (0,9%) pts. and polymorph CM in 1 (0,4%) pt. On 176 children affected by SM or MM (97 M vs. 79 F), 130 (74%) patients were followed-up with a mean of 56,3 (r. 4-142) months. A satisfactory outcome was recorded in 99 (76%) cases of whom 52 (53%) treated with topic steroids. Mean time to complete regression was 16.4 m. on treated patients vs. 34.7 m. on non treated patients (p=0,001). Conclusions: From our study emerged that resolution of the disease is independent from therapy, but the time to regression and to complete recovery of the coetaneous lesions is faster and favored by the application of topic steroid with an improvement of the quality of life for children and their families.
author2 Patrizi, Annalisa
author_facet Patrizi, Annalisa
Tabanelli, Michela <1974>
author Tabanelli, Michela <1974>
author_sort Tabanelli, Michela <1974>
title Mastocitosi cutanee: il mastocitoma in età pediatrica
title_short Mastocitosi cutanee: il mastocitoma in età pediatrica
title_full Mastocitosi cutanee: il mastocitoma in età pediatrica
title_fullStr Mastocitosi cutanee: il mastocitoma in età pediatrica
title_full_unstemmed Mastocitosi cutanee: il mastocitoma in età pediatrica
title_sort mastocitosi cutanee: il mastocitoma in età pediatrica
publisher Alma Mater Studiorum - Università di Bologna
publishDate 2011
url http://amsdottorato.unibo.it/3396/
work_keys_str_mv AT tabanellimichela1974 mastocitosicutaneeilmastocitomainetapediatrica
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