Il megacolon nella distrofia miotonica: case report e review della letteratura


COD: 2000_06_729-734 Categorie: ,

A. Torretta, D. Mascagni, K.P. Zeri, M. Falcone, R. Mancini, S. Arcieri, Lu. Giacomelli, N. Peparini, M.T. Papetti, L. Cerutti, A. Filippini

Ann. Ital. Chir., LXXI, 6, 2000

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Myotonic dystrophy (MD) is an autosomal dominant inherit disease, slowly progressive, involving multiple organ systems. Disorders at any level of the gastrointestinal tract are relatively common and manifest as disturbances in motility, such as impaired esophageal transport, delayed gastric emptying, and megacolon. A 51 years-old man was admitted to our surgical department with obstructive symptoms. Diagnostic evaluation showed megacolon and the typical clinical features of the MD, such as weakness, myotonia, frontal baldness and testicular atrophy. Risk of perforation and dehydratation led to emergency total colectomy with ileorectal stapled anastomosis. The patient didn’t suffer for complicance related to surgical treatment but, after 1 month in intensive care, died of pneumonia and myocardial infarct. The overall frequency of perioperative complications in patients with MD ranges from 8.2 to 42.9%.