Management of Symptomatic Mesenchymal Hamartoma of the Chest Wall: Surgical Resection Only in Symptomatic Cases

Autor: Virgone, C, Dall'Igna, P, Alaggio, Rita, Burnelli, R, Zanon, GIOVANNI FRANCO, Cecchetto, Giovanni, Virgone, Calogero
Rok vydání: 2013
Předmět:
Zdroj: Klinische Pädiatrie. 225:420-422
ISSN: 1439-3824
0300-8630
DOI: 10.1055/s-0033-1354355
Popis: Mesenchymal hamartoma of the chest wall (MHCW) is a rare neonatal benign tumor with an estimated incidence of 1 in 3 000 among primary bone tumors, and 1 in one million in the general population. Traditionally, the treatment of choice was an "en bloc" resection, but surgery limited to symptomatic cases, is now suggested by most authors due to the numerous cases of spontaneous regressions. We report 2 patients of symptomatic MHCW, characterized by progressive respiratory distress, who underwent surgical treatment with prompt resolution of symptoms. Surgeons and neonatologists should be aware of this rare condition and its possible fatal or nearly-fatal complications.
Databáze: OpenAIRE