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J Clin Pathol 60:94-97 doi:10.1136/jcp.2005.035360
  • Case report

Non-atherosclerotic coronary pathology causing sudden death

  1. Fabio De Giorgio1,
  2. Antonio Abbate2,
  3. Giuseppe Vetrugno3,
  4. Arnaldo Capelli4,
  5. Vincenzo Arena4
  1. 1Institute of Legal Medicine, Catholic University of the Sacred Heart, School of Medicine, Rome, Italy
  2. 2Department of Internal Medicine, Virginia Commonwealth University, Richmond, Virginia, USA
  3. 3Medical Directorate, Catholic University of the Sacred Heart, School of Medicine, Rome, Italy
  4. 4Institute of Pathological Anatomy, Catholic University of the Sacred Heart, School of Medicine, Rome, Italy
  1. Correspondence to:
    Dr F De Giorgio
    Institute of Legal Medicine, Catholic University of the Sacred Heart, School of Medicine, Largo Francesco Vito 1, 00168 Rome, Italy; fdegiorgio{at}tiscalinet.it
  • Accepted 6 February 2006

Abstract

Coronary atherosclerosis is responsible for >50% of all cases of sudden death and for 90% of sudden coronary death. Four cases encountered in routine autopsy evaluation at our institute in 2004 in which non-atherosclerotic coronary pathology was responsible for sudden cardiac death are reported. The cases of a 31-year-old man with epicardial coronary arteritis, a 57-year-old man with intramyocardial vasculitis, a 45-year-old woman with spontaneous coronary dissection and a 50-year-old man with vascular fibrosis are described. Searching for non-atherosclerotic coronary disease is relevant for both the clinician and the pathologist to prevent coronary causes of sudden death going unrecognised.

Non-atherosclerotic coronary artery disease is a condition often unrecognised in the living and in the dead. In a survey of 278 cases of sudden death in Italy, 28 cases were due to non-atherosclerotic coronary artery disease.1 Similar rates have been reported elsewhere.2 In living patients with acute myocardial ischaemia, non-atherosclerotic coronary disease is occasionally recognised but only when the lesions are seen in coronary angiography as congenital abnormalities or lesions causing coronary lumen stenoses or aneurysms.1,3–5

We report four cases encountered in routine autopsy evaluation at our institute in 2004 in which non-atherosclerotic coronary disease was responsible for sudden cardiac death. Box 1 lists the most common causes of sudden cardiac death.

Box 1: Most common causes of sudden cardiac death

  • Coronary disease

Atherothrombosis

Dissection

Congenital anomalies

Arteritis/vasculitis

Aneurysms

Intimal humps

Trauma

Myocardial bridging

  • Myocardial pathology

Myocardial scarring (ischaemic)

Dilated cardiomyopathy (any aetiology)

Hypertrophic cardiomyopathy

Right ventricular dysplasia

Myocarditis

Aortic stenosis

Congenital heart disease

  • Functional diseases

Long QT syndrome (congenital or acquired)

Catecholaminergic polymorphic ventricular tachycardia

Pre-excitation syndromes (ie, Wolf–Parkinson–White)

Brugada syndrome

Complete heart block (sinoatrial or atrioventricular block)

  • Pathology of the great vessels

Aortic dissection

Pulmonary embolism

Pulmonary artery dissection

  • Miscellaneous

Mixoma

Cardiac metastases

Pericardial effusion/tamponade

Case 1: epicardial coronary arteritis

A 31-year-old man brought to hospital by the emergency medical services (EMS) was pronounced dead on arrival. Death had occurred suddenly, with no anticipatory symptoms of chest pain or discomfort. Medical history was non-contributory.

The gross pathological examination was mostly unremarkable, except for a mildly discoloured region of the anterolateral myocardium. Histological examination showed signs of recent ischaemic damage. Examination of the left descending anterior artery showed no evidence of intraluminal thrombus or lumen stenosis. Serial sections of the artery were taken for histological examination. Light microscopical examination after standard haematoxylin–eosin staining showed the presence of a circumferential transmural inflammatory cell infiltrate extending from the adventitia to the intima and composed predominantly of CD8+ T lymphocytes (fig 1). The remaining coronary arteries and the other (non-coronary) arteries were disease free.

Figure 1

 (A) Epicardial coronary arteries with circumferential transmural periadventitial inflammatory cell infiltrate, composed mainly of CD8+ T lymphocytes (B). (C, D) Intramyocardial vasculitis, showing the lymphocytic infiltrate in the small intramyocardial vessel wall. (D) Immunohistochemical detection showing CD4+ T lymphocytes. (E, F) Intimal “humps” with variable degrees of luminal stenosis of the intramyocardial arterioles of the ventricular septum.

In face of the early ischaemic changes—variable waviness of fibres—but no evident necrosis, the cause of death was deemed arrhythmic death secondary to myocardial ischaemia caused by non-atherosclerotic non-thrombotic coronary disease.

Case 2: intramyocardial vasculitis

A 57-year-old man was found in cardiac arrest by the EMS and pronounced dead at the scene. Death had occurred unexpectedly. Medical history was unremarkable. Findings of the gross pathological examination were unremarkable. The left and right ventricles had a normal appearance at gross examination. The coronary arteries were free of disease along their epicardial course. Serial coronary artery and myocardial sections were studied. The light microscopical examination after standard haematoxylin–eosin staining showed the presence of a diffuse cell infiltrate in the wall of the small intramyocardial vessels. Inflammatory cells were CD4+ and CD8+ T lymphocytes. The epicardial coronary arteries were spared, as were the other (non-coronary) arteries. The cause of death was considered arrhythmic death secondary to myocardial ischaemia caused by non-atherosclerotic non-thrombotic coronary disease. Figure 1 shows the lymphocytic infiltrate in the small intramyocardial vessel wall.

Case 3: spontaneous coronary dissection

A 45-year-old woman was admitted to hospital with severe hepatic failure. A few days after admission, cardiac arrest occurred. At autopsy, coronary dissection of the left main coronary artery extending to the left anterior descending and circumflex arteries was noted. Histological examination showed a multistage process, as granulation tissue consistent with subacute changes was present in the left main coronary artery, whereas acute haemorrhage was present in the left anterior descending and circumflex arteries. The coronary lumen was almost completely occluded (fig 2). Ischaemia-induced lethal arrhythmia was considered to be the cause of death.

Figure 2

 Spontaneous coronary dissection. (A) Coronary dissection in the left main coronary artery extending to the left anterior descending and circumflex arteries. (B, C) Acute haemorrhage in the left anterior descending (C) and circumflex arteries (B). Panel B highlights the coronary lumen almost completely lost by “ab extrinseco” compression by the false lumen. (C) Concentric haematoma between the media and the adventitia.

Case 4: intramyocardial vascular humps

A 50-year-old man was found unresponsive by the EMS and brought to hospital. The patient was pronounced dead on arrival. The toxic screen was negative for commonly used drugs of misuse. Gross examination of the heart and coronary arteries was unremarkable. The only finding was the presence of a prominent medial and fibrointimal thickening of the intramyocardial vasculature at histological examination. There was a range of arterial changes, including eccentric intimal obstructive humps that were periodic acid-Schiff positive and Congo Red negative. The myocardium showed “patchy” fibrosis adjacent to the small vessels (fig 1). Cardiac arrhythmia was considered the cause of death.

DISCUSSION

In the four cases presented here, non-atherosclerotic coronary artery disease was identified as the cause of sudden death of otherwise healthy adults.

Coronary vasculitis is usually a feature of coronary involvement in the setting of more widespread vasculitis such as Takayasu’s type and panarteritis nodosa.6 Most classifications of systemic vasculitis are based on the size of the blood vessels involved, the anatomical site, histology and clinical manifestations.7 As only medium and small-sized coronary arteries were affected and no other organs had signs of inflammation, we were able to exclude most forms of vasculitis. Not meeting the criteria for polyarteritis nodosa, Kawasaki disease or microscopic polyangiitis, atypical isolated coronary vasculitis was diagnosed. Similarly, isolated involvement of intramyocardial vasculature, as found in case 2, is atypical.8

In the third case, spontaneous coronary dissection was observed. Spontaneous coronary artery dissection remains a rare but important cause of acute coronary syndromes and sudden cardiac death. The true incidence is probably underestimated as most of cases are diagnosed after death. It occurs in three major groups: in young women in the peripartum period, in patients with atherosclerotic disease and in an idiopathic group. There are several associated conditions, but the pathogenesis remains unclear.9,10

In the fourth case, the intramyocardial small arterioles showed prominent medial and fibrointimal thickening, so-called intimal humps, with variable degrees of luminal stenosis of the intramyocardial arterioles of the ventricular septum. In the presence or even in the absence of myocardial damage, the abnormally small vessels may result in poor blood flow, inadequate perfusion, arrhythmias and sudden death. Intramyocardial small vessel abnormalities are not commonly recognised. Small vessel disease has been reported as an isolated cardiac anomaly in individuals with sudden death and may also be associated with other cardiac conditions.11

In conclusion, in all cases, the probable mechanism of sudden death was ventricular arrhythmia due to myocardial ischaemia secondary to non-atherosclerotic coronary disease.

In all cases, other causes of sudden cardiac death (involvement or infiltration of the conduction system, coronary anomalies, myocarditis, aortic or pulmonary artery dissection and other) were excluded by a thorough pathological examination. Clinicians and forensic pathologists, in particular, should be aware of the possibility of non-atherosclerotic coronary disease causing myocardial ischaemia and death. Non-atherosclerotic causes of myocardial ischaemia, although rare, should be considered when assessing the pretest likelihood of coronary disease. Moreover, in sudden unexplained deaths, signs of non-atherosclerotic coronary disease should be sought.

Acknowledgments

We thank Mr Egidio Stigliano, Mr Benito Peri and Mr Giuliano Pacchiarotti for their technical support.

Footnotes

  • Competing interests: None declared.

REFERENCES