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[Sudden cardiac death in acromegaly. Anatomopathological observation of a case].

Involvement of the cardiovascular system in patients affected by acromegaly is an important factor in morbidity and mortality. The diagnosis in these subjects is acromegalic cardiomyopathy with cardiac decompensation, arrhythmias and sudden death. The pathologic substrate has rarely been described. The present study reports the findings in a case of sudden death in a 54-year-old man, affected by acromegaly. Subsequent diagnostic investigation revealed the characteristic aspects of acromegalic cardiomyopathy in the common myocardium and the presence of hyperacute myocardial infarct of the antero-septal wall of the left ventricle. Examination of conduction tissue revealed slight fibrolipomatosis and dispersion of the atrio-ventricular node (AVN), which extended to the His bundle and bifurcation. The right branch was prematurely intramural with sclerosis and lipomatosis. This location in atrio-ventricular conduction system has seldom been reported in the literature and if so, with different lesions from those found in the case we investigated. The results of microscopic examination convalidate the hypothesis of electrical instability in the heart, as confirmed by the subject's history of ventricular extrasystoles, left branch block and attacks of angina after effort. Death was correlated to hyperacute myocardial infarction of the anteroseptal wall of the left ventricle, in a subject with history of angina, affected by acromegalic cardiomegaly and electric instability. In this case, sudden death could also be considered arrhythmogenic in relation to the additional workload by persistent hormonal stimulation.

Acromegaly↗

[Florid glandular cystitis: study of 3 cases and review of the literature].

The authors report three cases of florid, recurrent cystitis glandularis in white men, inducing dilatation of the upper urinary tract due to invasion of the ureteric meatus. Treatment consisted of cystectomy, with preservation of the prostatic capsule, allowing preservation of continence and sexual potency. Cystitis glandularis is a rare, generally asymptomatic, benign metaplasia; it is favoured by chronic irritation and is sometimes associated with pelvic lipomatosis. Its transformation into adenocarcinoma is exceptional and occurs in the case of persistence of the predisposing factor. However, annual surveillance by cystoscopy with bladder biopsies is necessary. The florid form is much rarer and more disabling and usually requires wide resection of the lesions.

Adult↗

[Secret information provided by lumbosacral myelography].

The authors emphasize the misleading images of lumbar myelography encountered in common vertebral diseases: disk disease, posterior interapophyseal joint diseases, degenerative and narrow spinal canal, in which dynamic views in the upright position represent the most original contribution of lumbosacral myelography as compared to new techniques. The authors also describe the postoperative appearances observed on lumbosacral myelography and some rarer diseases which must not be missed, such as epidural arachnoid cysts and epidural lipomatosis.

Angiography↗