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1.
Abdom Radiol (NY) ; 49(5): 1747-1761, 2024 05.
Artigo em Inglês | MEDLINE | ID: mdl-38683215

RESUMO

Vascular compression syndromes are a diverse group of pathologies that can manifest asymptomatically and incidentally in otherwise healthy individuals or symptomatically with a spectrum of presentations. Due to their relative rarity, these syndromes are often poorly understood and overlooked. Early identification of these syndromes can have a significant impact on subsequent clinical management. This pictorial review provides a concise summary of seven vascular compression syndromes within the abdomen and pelvis including median arcuate ligament (MAL) syndrome, superior mesenteric artery (SMA) syndrome, nutcracker syndrome (NCS), May-Thurner syndrome (MTS), ureteropelvic junction obstruction (UPJO), vascular compression of the ureter, and portal biliopathy. The demographics, pathophysiology, predisposing factors, and expected treatment for each compression syndrome are reviewed. Salient imaging features of each entity are illustrated through imaging examples using multiple modalities including ultrasound, fluoroscopy, CT, and MRI.


Assuntos
Síndrome do Quebra-Nozes , Humanos , Síndrome do Quebra-Nozes/diagnóstico por imagem , Síndrome do Ligamento Arqueado Mediano/diagnóstico por imagem , Diagnóstico por Imagem/métodos , Abdome/diagnóstico por imagem , Abdome/irrigação sanguínea , Diagnóstico Diferencial , Doenças Vasculares/diagnóstico por imagem , Pelve/diagnóstico por imagem , Pelve/irrigação sanguínea , Síndrome de May-Thurner/diagnóstico por imagem , Síndrome de May-Thurner/complicações , Síndrome da Artéria Mesentérica Superior/diagnóstico por imagem
2.
Urol Case Rep ; 54: 102728, 2024 May.
Artigo em Inglês | MEDLINE | ID: mdl-38601085

RESUMO

Retrocaval ureter is a rare congenital anomaly with few reported cases worldwide. In this case report, we describe a clinical presentation that demonstrates the stereotypical imaging features of a retrocaval ureter on ultrasound, computed tomography and nuclear imaging studies in a 38-year-old male patient who fits the classic reported patient demographics.

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