Intimomedial mucoid degeneration, a rare vascular disorder characterized by mucinous deposition in the intima and media layers, causes aneurysmal degeneration of the vessel wall in young patients. Because of the potential for involvement of multiple vessels, these patients may require full body imaging and long-term follow-up. We describe three patients with intimomedial mucoid degeneration and variable clinical presentations. One patient presented emergently with a spontaneously ruptured nonaneurysmal subclavian artery; one patient presented with a known posterior tibial artery aneurysm and new onset of focal pain and paresthesias over the aneurysm; and one patient presented with a self-discovered dorsalis pedis artery aneurysm.
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http://dx.doi.org/10.1016/j.jvscit.2019.04.005 | DOI Listing |
Ann Med Surg (Lond)
March 2024
Faculty of Medicine, Damascus University, Damascus, (The) Syrian Arab Republic.
Introduction And Importance: Intimomedial mucoid degeneration is a rare vascular disorder first depicted in 1977. It involves mucin deposition in arterial layers. This will cause elastic tissue degeneration and aneurysm formation.
View Article and Find Full Text PDFVasc Med
October 2023
Unit of Vascular Surgery, Azienda Ospedaliera Santa Maria, Terni, Italy.
J Vasc Surg Cases Innov Tech
December 2019
Vascular and Endovascular Surgery Division, Stony Brook Medicine, Stony Brook, NY.
Intimomedial mucoid degeneration, a rare vascular disorder characterized by mucinous deposition in the intima and media layers, causes aneurysmal degeneration of the vessel wall in young patients. Because of the potential for involvement of multiple vessels, these patients may require full body imaging and long-term follow-up. We describe three patients with intimomedial mucoid degeneration and variable clinical presentations.
View Article and Find Full Text PDFForensic Sci Med Pathol
December 2019
University Center of Legal Medicine, Rue Michel-Servet 1, 1205, Geneva, Switzerland.
The body of a 43-year-old African woman with a history of aortic aneurysm and hypertension was forensically investigated after her sudden death. The cause of death was related to a cardiac tamponade due to a ruptured aneurysm of the ascending aorta. Post-mortem gross examination showed an abnormal whitish discoloration of the intima with fibrous thickening of the aortic wall.
View Article and Find Full Text PDFNon-immune hydrops fetalis (NIHF) has a high mortality rate [1]. Many etiologies of NIHF have been identified, including cardiovascular abnormalities, severe anemia, and genetic defects. In patients with cardiovascular etiology, structural malformations lead to fluid accumulation resulting in increased intravascular hydrostatic pressure.
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