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Two Cases of Spontaneous Isolated Dissection of Superior Mesenteric Artery in One Night: Report of a (Noninvasive) Double Challenge

Case series Patients: Male, 54-year-old • Male, 45-year-old Final Diagnosis: Spontaneous isolated dissection of superior mesenteric artery Symptoms: Abdominal pain • fever Medication: — Clinical Procedure: — Specialty: Radiology OBJECTIVE: Management of emergency care BACKGROUND: Spontaneous isolate...

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Detalles Bibliográficos
Autores principales: Evola, Giuseppe, Reina, Giuseppe Angelo, Cavallaro, Dario, Foti, Pietro Valerio, Musumeci, Andrea Giovanni, Palmucci, Stefano, Basile, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053640/
https://www.ncbi.nlm.nih.gov/pubmed/33848284
http://dx.doi.org/10.12659/AJCR.929538
Descripción
Sumario:Case series Patients: Male, 54-year-old • Male, 45-year-old Final Diagnosis: Spontaneous isolated dissection of superior mesenteric artery Symptoms: Abdominal pain • fever Medication: — Clinical Procedure: — Specialty: Radiology OBJECTIVE: Management of emergency care BACKGROUND: Spontaneous isolated dissection of the superior mesenteric artery (SID-SMA) is a rare but potentially fatal condition. Although many cases of SID-SMA have been reported in the literature in recent years because of the increased use of contrast-enhanced computed tomography (CT) scanning, optimal management has not yet been firmly established. CASE REPORTS: We report 2 cases of SID-SMA that were managed with stenting and angioplasty via transfemoral access. In case 1 a 54-year-old man presented with diffuse abdominal pain without Blumberg sign. Laboratory data were unremarkable. Abdominal CT scanning revealed SID-SMA and initial bowel ischemia. The angiogram revealed a dissected true lumen of SMA with a narrowing of the ileo-colic artery managed, respectively, with self-expandable stent placement and angioplasty. In case 2, a 45-year-old man presented with severe abdominal cramping and pain of 3 days’ duration. Physical examination revealed abdominal tenderness with positive Blumberg sign. Laboratory tests showed leukocytosis and increased lactate dehydrogenase. Abdominal CT scan revealed SID-SMA and initial bowel ischemia. After an SMA angiogram, 2 self-expandable stents were placed and an angioplasty was performed. Although a postprocedural angiogram showed good patency of the SMA in both patients, the first patient had a recurrence of abdominal pain after 5 days with a new narrowing tract of the SMA and more inferiorly a dissection with aneurysm of a false lumen, detected on CT scan, treated respectively with stenting and coils. CT follow-up showed successful morphological results in both patients. CONCLUSIONS: In our experience, endovascular treatment of SID-SMA is safe and effective, including in cases of recurrence and postprocedural evolution.