Objective: The aim of this article is to describe the clinical, pathophysiology and diagnostic imaging aspects of median arcuate ligament syndrome (MALS) by presenting clinical cases and literature review. Development: The median arcuate ligament syndrome corresponds to a clinical syndrome secondary to the extrinsic compression of the celiac trunk by fibrous bands of the median arcuate ligament. In recent decades, some authors have questioned its true meaning and existence given the reported cases of asymptomatic patients who presented extrinsic compression of the celiac trunk by MAL. However, the presence of intestinal angina symptoms and certain specific imaging findings leads to consider its differential diagnosis and directs toward the corresponding study. The diagnosis is made by using Doppler ultrasound, Multislice Computed Tomography (CT) Angiography and Magnetic Resonance Angiography (MRA), the Angiography-fluoroscopy being left out of the first-line study. In recent years use of MRA has increased due to the absence of ionizing radiation and the high efficiency in the diagnosis. Within its complications include acute mesenteric angina and pancreaticoduodenal artery aneurysms secondary to the extensive formation of adjacent collateral circulation. Surgical treatment has been the most effective, having a very low recurrence.

RESUMENLos trastornos del olfato son frecuentes, aunque la anosmia e hiposmia son síntomas poco referidos, suelen afectar de forma importante la calidad de vida de los pacientes. Las causas de anosmia pueden ser adquiridas o congénitas, y la prevalencia de anosmia congénita aislada en la población general se estima en 1:10.000. En estos casos, la anosmia es el único síntoma referido por el paciente. Se presenta el caso de un paciente de sexo masculino de 23 años, sin antecedentes mórbidos de importancia, diagnosticado con anosmia congénita aislada. La historia y evaluación clínica, evaluación neuroendocrinológica, y el uso de la resonancia magnética de cerebro permitió establecer el diagnóstico final. ABSTRACTDisorders of olfaction are common, however, anosmia and hyposmia are not frequently self-reported, and these symptoms can lead to a significant impairment in quality of life. Causes of anosmia can be acquired or congenital, and the prevalence of isolated congenital anosmia is estimated to be 1:10000 in the general population. In these cases, anosmia is the only symptom referred by the patient. We hereby present the case of a 23-year-old male patient, with no prior medical history, diagnosed with isolated congenital anosmia. The findings from the medical history and physical examination, neuroendocrine evaluation, and the use of magnetic resonance imaging of the brain helped reach a final diagnosis.