A Case of Segmental Mediolytic Arteriopathy Involving Both Intracranial and Intraabdominal Arteries
References (18)
- et al.
Intraabdominal hemorrhage as a result of segmental mediolytic ateritis of an omental artery: case report
J Vasc Surg
(1990) - et al.
Spontaneous intraabdominal haemorrhage caused by segmental mediolytic arteritis in a patient with systemic lupus erythematosus—an underestimated entity of autoimmune origin?
Eur J Vasc Surg
(1994) - et al.
Ruptured inferior mesenteric artery aneurysm due to segmental mediolytic arteritis
Cardiovasc Surg
(1996) Systemic, cerebral, and pulmonary segmental mediolytic arteriopathy: villainous masqueraders of vasculitis
Cardiovasc Pathol
(1996)- et al.
Segmental mediolytic arteries: a case report with review of the literature
Pathol Res Pract
(1998) - et al.
Segmental mediolytic arteritis involving hepatic arteries
Arch Pathol Lab Med
(1992) - et al.
A pathological study of intracranial posterior circulation dissecting aneurysms with subarachnoid hemorrhage: report of three autopsied cases and review of the literature
Neurosurgery
(1993) - et al.
Acase of dissection of intracranial cerebral arteries with segmental mediolytic “arteritis”
Clin Neuropathol
(1994) - et al.
Segmental mediolytic arteritis: clinicopathologic study and three-dimensional analysis
Acta Pathol Jpn
(1992)
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Intracranial dissections: A pictorial review of pathophysiology, imaging features, and natural history
2021, Journal of NeuroradiologyCitation Excerpt :Several suspected risk factors have been identified through small case series. Patients with underlying connective tissue disorders, including Ehlers-Danlos syndrome type IV, Marfan syndrome, Loeys-Dietz syndrome, fibromuscular dysplasia, cystic medial necrosis, segmental arterial mediolysis, and Moyamoya disease, have been described [21–30]. Studies have shown that patients with extracranial dissection have subclinical connective tissue abnormalities on skin and artery biopsies, but no such relationship has been identified in patients with IAD [31,32].
A Ruptured Blood Blister–Like Aneurysm Associated With Intraperitoneal Hemorrhage Due to Segmental Arterial Mediolysis: A Case Report And Literature Review
2020, World NeurosurgeryCitation Excerpt :The concomitant manifestation of SAM with SAH is very rare and only 13 cases have been reported including the present case, as far as we are aware (Table 1).9-20 Of 13 cases with SAH, 1 case had a simultaneous presentation of a massive retroperitoneal hemorrhage and SAH, 2 cases had incidental and asymptomatic SAM-related intraperitoneal aneurysms that were detected on the treatment of SAH, and interestingly the remaining 10 cases manifested symptomatic SAM-related abdominal hemorrhage from zero to 16 days after SAH onset.9-20 However, SAM-related abdominal hemorrhage after SAH has never been described as a complication during the treatment of a ruptured BBA of the ICA like our case.
Epidemiology, pathophysiology, diagnosis, and management of intracranial artery dissection
2015, The Lancet NeurologyCitation Excerpt :Only isolated instances of intracranial artery dissection and fibromuscular dysplasia have been reported,76,77 and patients with fibromuscular dysplasia were excluded from many reported series of patients with intracranial artery dissection. Overlap between intracranial artery dissection and segmental arterial mediolysis (a rare arterial disease that presents with life-threatening haemorrhages through ruptured aneurysms in the abdominal cavity), the retroperitoneum, and more seldom the base of the brain, is unclear.78,79 Clinical presentation of intracranial artery dissections is not specific.
Segmental arterial mediolysis: A systematic review of 85 cases
2014, Annals of Vascular SurgeryPutamen hemorrhage occurred simultaneously with Stanford type A acute aortic dissection: A case report
2013, American Journal of Emergency Medicine