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Biomedical subjects

J Salazar Mena

Publications and source records attributed to J Salazar Mena.

16 recordsLinked to original sources

[Pericardial defect with atrial herniation].

Pericardial defects are rare in childhood and outcome is usually benign. Patients can be asymptomatic, but they may experience vague chest pain, angina, myocardial ischemia, emboli, and arrhythmia and some cases of sudden death have even been described in the literature. We report the case of a 3-month-old girl who, in the context of an episode of fever, underwent chest X-ray examination, which showed a left heart border anomaly. This finding strongly suggested a congenital partial pericardial defect, which was subsequently confirmed by other techniques. The interest of this case lies in the ability of the pediatrician to establish a presumptive diagnosis by examining the chest X-ray. We conclude by stressing the need for a high degree suspicion for congenital heart anomalies because of the life-threatening nature of some partial pericardial defects, which can lead to left-ventricular herniation.

Cardiomyopathies↗

[Clinical presentation, diagnosis and treatment of four cases of cor triatriatum].

We report four cases of cor triatriatum. In two of them the fibromuscular membrane was obstructive and associated with an atrial septal defect between the left atrial accessory chamber and the right atrium; in those cases the clinical findings were due to the pulmonary hypervascularity. The third case was associated to a small patent foramen ovale, and the clinical findings were due to the obstruction to flow through the membrane in the left atrium, producing venocapilar pulmonary hypertension. In these three cases surgical treatment was carried out through a right atriotomy. In all of them a good corelationship was found between the echocardiographic and the surgical findings. The follow-up has been good, all previous symptoms disappearing, remaining symptom free. The fourth case is an asymptomatic 5-year-old girl, with a non-obstructive membrane and without any associated anomalies.

Child, Preschool↗

[Diverticulum of the right ventricle with biventricular myocardiopathy].

We report a 18-days-old newborn boy with right ventricular diverticulum associated with biventricular cardiomyopathy, diagnosed by two-dimensional and Doppler echocardiography and angiography. Heart transplant was carried out at the age of four months, dying the next day. The histologic study showed endocardial fibroelastosis.

Cardiomyopathies↗

[Neonatal cardiac insufficiency caused by a cerebral arteriovenous fistula. Review of the authors' cases].

UNLABELLED: Four cases of newborn infants presenting congestive heart failure in the first two weeks of life with the clinical suspicion of cerebral arteriovenous fistula which was subsequently confirmed by cerebral echography or TAC and, after death, by necropsy, are described. Only one patient survived, the one treated surgically. CONCLUSION: It is necessary to carry out urgent diagnosis with an early surgical operation, the only possibility of survival for these children.

Arteriovenous Fistula↗

[Myxoma of the right atrium].

A case of right atrial myxoma is reported in a 6-year-old boy. This type of cardiac tumour is infrequent at this age and its localisation on the right atrium is extremely rare. The clinical diagnosis may be evoked in the presence of a changing cardiac murmur; two-dimensional cardiac ultrasonography is currently the best method for non-invasive assessment. Good surgical results are linked to an early resection, with careful manipulation of the tumour and large removal of the implantation base.

Child↗

[Spontaneous pneumopericardium in a 9-year-old child].

The authors report the first case of spontaneous pneumopericardium of unknown cause, in their hospital, affecting an adolescent who had not had any previous asthmatic process. The differential diagnosis, evolution and treatment are commented.

Child↗

[Acute rheumatic carditis. Follow-up (author's transl)].

Thirteen cases with a first attack of acute theumatic carditis are presented, analyzing the clinical picture and long-term follow-up. Although the clinical acute attack was quite benign, incidence and importance of residual heart disease has not changed.

Acute Disease↗