Autopsy findings of 10 patients with Takayasu arteritis (TA) are presented.
These patients include six females and four males with a mean age of 22.61
+/-10.2 years. Hypertension was the commonest mode of presentation. On auto
psy, the vascular lesions in the aorta comprised of stenosis (eight), dilat
ation (six), aneurysm (two) and dissection of aorta involving its arch, tho
racic and abdominal aorta (one). Abdominal aorta was the commonest site of
involvement (nine patients) and renal artery was involved in six patients.
Histologically, the three types of lesions were identified - active, fibrot
ic and combination of active and fibrotic lesions. Active inflammatory lesi
ons in the arterial circuit were present despite a clinically chronic (sile
nt) phase of the disease. Cardiac involvement included left ventricular hyp
ertrophy (nine), right ventricular hypertrophy (four), biventricular hypert
rophy (three), myocarditis (two) (rheumatic and Takayasu's myocarditis - on
e patient each) and involvement of coronary artery (one). The pulmonary art
ery was involved in two patients. Kidneys showed changes of malignant hyper
tension and benign nephrosclerosis in one patient each. Associated tubercul
osis was present in four patients. The causes of mortality were congestive
heart failure (four), chronic renal failure (two), intracranial bleed, aneu
rysmal rupture and pulmonary thromboembolism in one patient each. Thus, the
major causes of morbidity and mortality in Indian patients with TA is due
to severe uncontrolled hypertension and its effect on heart, kidney and bra
in. The disease appears to have a persistent activity for a prolonged perio
d even when it appears to be clinically silent. (C) 1998 Elsevier Science I
reland Ltd. All rights reserved.