2004 Summer Meeting - Amsterdam - The Pathological Society of ...
2004 Summer Meeting - Amsterdam - The Pathological Society of ...
2004 Summer Meeting - Amsterdam - The Pathological Society of ...
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97<br />
Cardiomyopathy and Intravascular Involvement <strong>of</strong> Gut in<br />
Systemic Senile Amyloidosis<br />
S Haider 1 , M Lesna 1 , PJ Gallagher 2<br />
1 Royal Bournemouth Hospital, Bournemouth, United Kingdom, 2<br />
Southampton University Hospital, Southampton, United Kingdom<br />
In 1956 Symmers reported that the gastrointestinal tract was involved in 70% <strong>of</strong><br />
cases <strong>of</strong> primary amyloidosis. Since that time it has been infrequently<br />
mentioned in the literature.<br />
Cardiac amyloidosis is rare and presents as a restrictive cardiomyopathy or low<br />
output cardiac failure. Despite the advances in cardiac imaging techniques,<br />
tissue diagnosis usually requires an endomyocardial biopsy.<br />
We have analysed the data from 9 cases <strong>of</strong> systemic amyloidosis collected over<br />
a period <strong>of</strong> 10 years; 6/9 had an autopsy, 3/9 were diagnosed histochemically in<br />
biopsy samples. <strong>The</strong> age <strong>of</strong> the patients varied from 74 to 97 years, all but one<br />
were males.<br />
Our study has shown a frequent association <strong>of</strong> cardiac amyloidosis with<br />
intravascular amyloid in the sub mucosal arterioles and venules <strong>of</strong> the gut,<br />
particularly <strong>of</strong> stomach. In the heart the amyloid was deposited in the basement<br />
membrane <strong>of</strong> the myocardial cells and media <strong>of</strong> the arterioles. <strong>The</strong>re were<br />
similar intravascular deposits in the medium sized blood vessels <strong>of</strong> lungs and<br />
kidneys but the glomeruli were spared.<br />
We propose that in certain cases <strong>of</strong> restrictive cardiomyopathy, endomyocardial<br />
biopsy could be replaced by less demanding gastric biopsy if amyloidosis is<br />
considered to be a cause.<br />
98<br />
An Investigation Into <strong>The</strong> Relationship Between Sudden<br />
Unexpected Cardiac Death And Lung Weight<br />
E Beeson , R. E Owers , P. J Gallagher , M Walker<br />
Pathology Department, Southampton University Hospitals Trust,<br />
Southampton, United Kingdom<br />
Sudden unexpected cardiac death (SUCD) is an important cause <strong>of</strong> mortality in<br />
developed countries with a frequency <strong>of</strong> 10.5-13 per 100,000 populations per<br />
annum in the UK. At post mortem pulmonary oedema is found in many, though<br />
not all, cases <strong>of</strong> SUCD. In this study we have investigated the relationship<br />
between pulmonary oedema and demographic, clinical and pathological<br />
findings. Our particular objective was to relate pulmonary oedema to the degree<br />
<strong>of</strong> certainty <strong>of</strong> cardiac death.<br />
Data was taken from observed autopsies and past autopsy records <strong>of</strong> 990<br />
Southampton cases over a 38 month period. Each cardiac death was classified<br />
into one <strong>of</strong> five categories. For example definite cardiac deaths (certainty grade<br />
1) had fresh myocardial infarction or recent coronary thrombosis whilst sudden<br />
arrhythmic death syndrome cases (SADS, grade 5) had no cardiac<br />
abnormalities). Up to 14 other variables were recorded and compared with lung<br />
weight using Minitab.<br />
<strong>The</strong>re was no relationship between lung weight and the degree <strong>of</strong> certainty <strong>of</strong><br />
cardiac death. In particular there was no evidence that lung weight was higher<br />
in patients with definite evidence <strong>of</strong> infarction or thrombosis. Lung weights<br />
were higher in males. Heart weights were higher in patients with a history <strong>of</strong><br />
previous infarction or hypertension and in patients taking diuretics, ACE<br />
inhibitors, aspirin and statins but this did not apply to beta blockers or calcium<br />
channel blocking agents.<br />
This study has not added significantly to our understanding <strong>of</strong> cardiogenic<br />
pulmonary oedema at post mortem. We believe that we have studied adequate<br />
numbers <strong>of</strong> cases and that our data base is sound. <strong>The</strong> cause <strong>of</strong> post mortem<br />
pulmonary oedema is largely unexplained.<br />
99<br />
ATRIAL MORPHOLOGY DOES NOT PREDICT THE<br />
ONSET OF POSTOPERATIVE ATRIAL FIBRILLATION<br />
RJ Flavin , B Foley , J Cosgrave , D.S. O'Briain , E Fitzpatrick ,<br />
K Bennett , E McGovern , M Tolan , V Young , P Crean , M Walsh<br />
St.James's Hospital and Trinity College Medical School, Dublin, Ireland<br />
Atrial fibrillation remains the commonest complication <strong>of</strong> cardiac surgery.<br />
Prophylactic therapies have been studied but their utility has been limited by the<br />
inability to accurately identify patients who will develop this complication.<br />
Recent studies have suggested that atrial myolysis or lip<strong>of</strong>uscin pigmentation<br />
predict atrial fibrillation.<br />
To determine whether there is an association between pre-operative atrial<br />
morphology and subsequent post coronary artery bypass surgery (CABG) atrial<br />
fibrillation, samples <strong>of</strong> right atrial appendage were obtained from 94 patients<br />
undergoing CABG. Tissue was formalin fixed and paraffin embedded. Four µm<br />
sections were cut and stained with H&E. Sections were examined for the<br />
following parameters: fibrosis, myolysis, inflammation, nuclear size, pericardial<br />
exudates, lip<strong>of</strong>uscin pigment, arteriolar hypertrophy, contraction banding,<br />
mesothelial hyperplasia and atrial diverticulae. Results were graded into absent,<br />
mild, moderate or severe. Slides were reviewed by two independent observers<br />
who were blinded to the clinical outcomes. Univariate and multivariate analysis<br />
were carried out.<br />
39% <strong>of</strong> the patients developed atrial fibrillation. No correlation was found<br />
between the 10 features assessed including myolysis and lip<strong>of</strong>uscin<br />
pigmentation and the development <strong>of</strong> atrial fibrillation.<br />
In conclusion, conventional microscopy provides no evidence <strong>of</strong> a<br />
morphological basis in the right atrial appendage for post-operative atrial<br />
fibrillation.<br />
100<br />
Sudden Maternal Death Due To Cardiovascular Causes<br />
GC Behrendt 1 , AG Nicholson 1 , SB Lucas 2 , MN Sheppard 1<br />
1 Royal Brompton Hospital, London, United Kingdom, 2 St Thomas<br />
Hospital, London, United Kingdom<br />
Introduction: Between 89-126 cases <strong>of</strong> maternal deaths occur each<br />
year in the UK and there has been criticism <strong>of</strong> autopsy reports in these deaths 1 .<br />
Obvious causes linked to pregnancy are common but the hemodynamic changes<br />
associated with pregnancy may worsen pre-existing cardiovascular disorders,<br />
which may or may not be established before autopsy. Pathologists need to be<br />
aware <strong>of</strong> these.<br />
Material We examined cardiovascular causes <strong>of</strong> maternal deaths in our files<br />
referred to our hospital between 1995 and 2003. 14 cases were identified and<br />
slides and reports reviewed. Additional clinical information was requested<br />
where necessary.<br />
Results: <strong>The</strong> following causes <strong>of</strong> death were found: Eisenmengers syndrome<br />
due to (operated) congenital heart disease (4), thrombotic microangiopathies<br />
(3), idiopathic myocardial fibrosis (1), peripartum cardiomyopathy (1), sudden<br />
adult death (1), floppy mitral valve (1), pulmonary arterio-venous malformation<br />
(1), coronary artery dissection (1) and chronic recurrent thromboembolic<br />
disease (1).<br />
Discussion: A variety <strong>of</strong> common and rare cardiovascular disorders<br />
can cause death in pregnancy or post-partum. Detailed examination <strong>of</strong> heart and<br />
lungs including histology is necessary as some cases show subtle pathologic<br />
changes.<br />
Reference List<br />
1. Why Mothers Die? 1997-1999 Confidential Enquiry into Maternal Deaths in<br />
the United Kingdom. Royal College <strong>of</strong> Obstetricians and Gynaecologists Press<br />
London 2001. p27-45.<br />
51