Background. Intramural hematoma of the thoracic aorta (IMH) is a diagn
osis of exclusion and represents spontaneous, localized hemorrhage int
o the wall of the thoracic aorta in the absence of bona fide aortic di
ssection, intimal tear, or penetrating atherosclerotic ulcer. This pro
cess may arise from primary vasa vasorum hemorrhage within the aortic
media or rupture of an atherosclerotic plaque. The clinical presentati
on of patients with IMH mimics that of acute aortic dissection; moreov
er, considerable diagnostic confusion exists despite the use of many d
ifferent imaging modalities. The optimal mode of management of patient
s with IMH (medical versus medical plus surgical) remains problematic
because of the paucity of information available. Methods and Results.
Thirteen patients with IMH were managed at two medical centers between
1983 and 1992. Patients with IMH caused by giant penetrating atherosc
lerotic ulcers were specifically excluded. There were 8 women and 5 me
n (mean age, 70 years [range, 54 to 82 years]). The admitting clinical
diagnosis was acute aortic dissection, and all patients had a history
of hypertension. There was no evidence of aortic dissection or intima
l disruption as assessed by computed tomographic (CT) scan (n=11), aor
tography (n=10), magnetic resonance imaging (MRI) scan (n=9), transeso
phageal echocardiography (TEE) (n=6), or intravascular ultrasound (n=1
). The diagnosis of IMH was established by exclusion. The descending t
horacic aorta was involved in 10 cases and the ascending/arch in 3. Co
nservative medical management was attempted initially. All 3 patients
with IMH involving the ascending aorta ultimately required operative i
ntervention, and 2 individuals died; 2 of 10 patients with descending
aortic involvement eventually underwent surgery. Average hospital stay
was 11 days; the mean follow-up interval for discharged patients was
29 months. Conclusions. IMH is a distinct pathological entity, should
not be confused with aortic dissection, and probably will be identifie
d more frequently in the future. All patients with IMH should be monit
ored carefully and treated with aggressive antihypertensive therapy. F
requent serial assessment is necessary using TEE or MRI/CT scans. Base
d on this small experience, patients with ascending/arch IMH, ongoing
pain, or IMH expansion should probably undergo early graft replacement
. Patients with IMH involving the descending thoracic aorta who have n
o evidence of progression and become pain free can probably be treated
conservatively but require antihypertensive therapy and serial aortic
imaging surveillance indefinitely.