{Reference Type}: Case Reports
{Title}: [Recurrent benign multicystic peritoneal mesothelioma: Approach to this rare condition].
{Author}: García-Mayor Fernández RL;Fernández-González M;López-Rodríguez A;Martínez-Almeida Fernández R;
{Journal}: Cir Cir
{Volume}: 84
{Issue}: 6
{Year}: Nov 2016 0
{Factor}: 0.416
{DOI}: 10.1016/j.circir.2015.08.013
{Abstract}: BACKGROUND: Benign multicystic mesothelioma is a rare benign tumour derived from the peritoneal mesothelium. The aim of this paper is to present a case of this rare tumour and review the clinical features, diagnosis and treatment of this disease.
METHODS: The case is presented of a 22-year-old female diagnosed with multicystic mesothelioma after an urgent resection of intra-abdominal tumour in the context of acute abdominal pain. In the subsequent follow-up, the patient had a recurrence of the lesion, and at 2 years was treated by further resection.
CONCLUSIONS: Benign multicystic mesothelioma is a benign tumour of unknown origin, and with a non-specific clinical manifestation. The most effective treatment is surgical, although there is a high tendency to local recurrence.