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Biomedical subjects

F Plenat

Publications and source records attributed to F Plenat.

At least 55 records · Page 3Linked to original sources

[Biopsy of the rectal mucosa in pediatric surgery. Technic--diagnostic value. Apropos of 193 biopsies].

193 series of punch biopsy of the rectal mucosa for the diagnosis of Hirschsprung's disease using the histochemical method are reported. These biopsies concern 176 children from 4 days to twelve years old. The authors insist on the simplicity of the method which requires few equipment: nasal speculum and biopsy forceps. The pieces are carried fresh to the laboratory and treated immediately. The method uses the medium described by Karnovsky and Roots but enzymatic inhibitor of the non selective esterase activity is not used. This shortens the time of the manipulation to about 1 h 30 and limits its cost and toxicity. Three histologists have studied the slides without knowing the clinical facts. Of 36 children suffering from a Hirschsprung's disease all presented a mucosal AChE increased activity, 28 times at once, 8 times after further biopsies. In four patients there was an inadequate biopsy at the beginning of the experience, the other four were very young (less than 1 month). The biopsy was negative at the beginning but it became positive when the patients were about aged 3 months. In the 138 children not suffering of a Hirschsprung's disease, 2 had a AChE increased activity, One is a children suffering from a severe ganglionic displasia obvious on the surgical piece, the other is a colonic mucosal neuromatosis. So, the authors confirm the reliability of the simplified method which required an unsophisticated equipment and whose technique is faster looking for mucosal AChE increased activity and not for the ganglionic cells of the sub-mucosa.(ABSTRACT TRUNCATED AT 250 WORDS)

Acetylcholinesterase↗

[Nasal glioma (author's transl)].

Rare tumors are sometimes encountered in maxillofacial surgical practice and the operative approach, external, intranasal, or endocranial, may be difficult to choose. Preliminary angiography and particularly computer tomography can be of invaluable assistance in making the decision, especially in cases of nasofrontal glioma with heterotopic localization of glial tissue but without brain connections.

Female↗

[Cranio-encephalic scanography of the premature infant. Morphogenetic aspects. Radio-anatomical comparisons].

Fifty infants born before 38 weeks of amenorrhea have been studied by computerized tomography. The authors dwell on three points: the malleability of the cranial vault, the normal appearance of the germinal layer before 32 weeks, and the persisting hypodensity of the frontal region. The evolution of the morphology of the subarachoïdian cisterns, of the ventricular system and of the parenchyma are related between 28 weeks and term.

Brain↗

Giant lobar emphysema--neonatal diagnosis.

Giant emphysema of a lung lobe has distinctive features. Classically there is overdistension of the affected lung lobe, with one lobe only being involved, and, 50% of cases occur in the newborn infant [1, 4, 8]. The authors describe a particularly severe example with marked mediastinal shift and initially the hemithorax on the side of the lesion was opaque. Angiography was carried out and followed by resection when the infant was 4 months old.

Angiocardiography↗

[Brachial plexus birth injuries. An experimental study (author's transl)].

The authors present an experimental study of obstetrical Brachial plexus Palsy. They study traction injury to 16 Brachial pleux. The first lesions were always disruption of the upper roots C5 and C6. After that, the Lower Plexus (C7 - C8 - T1) was disrupted. The two upper roots are usually interrupted and surgical graft seen to be possible. On the Lower Plexus, avulsions are found and intercostal nerves transfer must be performed.

Birth Injuries↗

[Tracheo-bronchial malformation associated with an aberrant left pulmonary artery].

A new case of pulmonary artery sling in a three months old boy is reported. After the sudden death of the patient, a precise anatomic study of the malformation was realized. With a complete cartilaginous ring usual in this malformation, there is a right upper lobe bronchus arising from the trachea above the anomalous vessel. The other anomalies of the tracheobronchial tree are discussed.

Bronchi↗

[Neonatal aortic valvular stenosis. Apropos of 8 cases].

Congenital aortic stenosis presenting in the neonate must be distinguished from the commoner hypoplastic left heart-syndrome, which is beyond surgical correction. It is certainly a serious problem, but early diagnosis and supporting angiography to rule out the presence of an associated left ventricular malformation and to check the volume of the left ventricular cavity should lead to a decision to operate. Out a 4 neonates from this series who were presented for surgery, the 2 survivors had good long-term results.

Aortic Valve Stenosis↗

[Hydranencephaly. Major cerebral lesions with normal neonatal neurologic behavior].

Case report of an 8 days old girl who had a discrete increase in head circumference associated with moderate EEG abnormalities. Familial and obstetrical histories were negative. Skull transillumination, contrast ventriculography and carotid arteriography led to the diagnosis of hydranencephaly. The cerebral lobes whose blood supply is dependent from the internal carotids were missing and were replaced by cavities. The normal neonatal neurological behaviour which did not change till death at 3 months, is a stiking phenomenon.

Anencephaly↗

[Ebstein's malformation in newborn infants. Apropos of 8 cases].

In relation with 8 cases, the features of Ebstein's malformation were studied in the neonatal form. In spite of its rarity, it should be recognized because of its peculiar prognosis, as it is liable to be permanently improved by medical treatment, after a difficult adaptation period. Besides, it is essential to distinguish it from other neonatal heart diseases which ressemble to it, but require an urgent surgical treatment.

Humans↗

Experimental emphysema following one intravenous infusion of trypsin.

This study was undertaken to investigate the effects of a deficit in protease inhibitor (AT) induced by intravenously administered trypsin on the development of elastase-induced emphysema. Rats receiving a perfusion of trypsin (4.5 mg/kg body wt) intravenously (TIV rats) or one instillation of elastase (92 IU/subject) into the trachea (ELAS rats) were compared with rats receiving both trypsin and elastase (TIVELAS rats). Compared with 8 sham-injected rats, the serum AT activity of 14 TIV rats decreased slightly (5.5%) 150 min after the beginning of the perfusion. In six other TIV rats sacrificed early after the perfusion, a granulocyte sequestration with edema and vascular thrombi demonstrated early lung injury. Anatomical studies of lung and determination of the mean linear intercept (MLI) were carried out 56 days after the administration of the enzymes. Emphysema was confirmed by a significant (P less than .001) MLI increase (about 150 microns) in 22/24 TIV, 20/21 ELAS, and 21/21 TIVELAS rats in comparison with 40 control rats (78 microns). These similar results of the treated rats show that trypsin did not worsen elastase-induced emphysema and also indicate that trypsin given intravenously alone induces emphysema as does elastase when introduced into the airways. The AT activity decrease consequent to proteolysis by trypsin and pulmonary leucostasis may contribute to this trypsin-triggered emphysema.

Animals↗

Role of iron in lymphoma-induction by ATP.

Iron complexed by ATP induces lymphomas in mouse organs other than the specific targets of the lympho-adenitis provoked by sodium ATP: lymph nodes, spleen and liver. The reduction of life spans and the production of substantial volumes of ascites, that are lacking in the case of sodium ATP, are an index of the degree of malignancy of the induced lymphomas. On the basis of the known characteristics of iron-ATP complex of cellular calcium homeostasis alteration, the mechanism of these phenomena is discussed.

Adenosine Triphosphate↗