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Biomedical subjects

J Palacios

Publications and source records attributed to J Palacios.

At least 91 records · Page 5Linked to original sources
PubMed1991

Cystic adenomatoid tumor of the uterus.

We describe a case of cystic adenomatoid tumor of the uterus in a 38-year-old woman. The tumor was a subserosal cystic mass with a maximum diameter of 8 cm and located at the posterior wall of the right cornual region. Histologically, the tumor was composed of multiple cavities lined by flattened cells, lying among thin septa of connective tissue. The neoplasm showed small solid areas with a more typical histologic pattern of adenomatoid tumor. Immunohistochemical techniques showed the cells to be positive for keratins. They showed desmosomes, abundant intracytoplasmic filaments, and microvilli on ultrastructural study. The histologic, immunohistochemical, and ultrastructural characteristics of the present case closely resemble those of benign cystic mesothelioma and strongly support the mesothelial origin of the adenomatoid tumor of the uterus.

Adenoma↗
PubMed1990

New acrofacial dysostosis syndrome in 3 sibs.

We performed clinical and autopsy studies on 3 sibs with an acrofacial dysostosis (AFD) syndrome. All 3 died neonatally from respiratory complications derived from their severe mandibular hypoplasia. They presented a malformation syndrome characterized by mandibulofacial dysostosis, predominantly preaxial limb deficiencies, rare postaxial limb anomalies, shoulder/pelvis girdle hypoplasia, and cardiac and CNS malformations. This syndromal form of AFD could represent a distinct entity with autosomal-recessive inheritance. Its delineation from other AFD syndromes is discussed.

Diagnosis, Differential↗
PubMed1990

Severe postaxial acrofacial dysostosis: an anatomic and angiographic study.

We describe a severe case of postaxial acrofacial dysostosis syndrome [POADS] or Genée-Wiedemann syndrome in a stillborn female. The report includes an arteriographic and anatomic study of the limbs. Previously unreported findings such as hypoplasia of the femora, ossification defect of the ischium and pubis, bilobed tongue, and lung hypoplasia were noted. This case documents further variability in the POADS or Genée-Wiedemann syndrome.

Angiography↗
PubMed1990

Extrinsic fetal akinesia and skeletal development: a study in oligohydramnios sequence.

Long-bone morphometry and cephalometry were performed in 13 newborns with oligohydramnios sequence (OS) in order to establish whether or not skeletal changes existed in extrinsic fetal akinesia similar to those observed in the fetal akinesia deformative sequence (FADS) (i.e., hypoplastic long bones and micrognathia). Oligohydramnios sequence was caused by bilateral renal agenesis in five cases and obstructive uropathy in eight cases. Twenty-one stillborns and newborns who had died from conditions other than renal anomalies or congenital malformations were used as controls. Normal longitudinal and periosteal long-bone growth and absence of micrognathia were found in OS patients. Skeletal differences between FADS and OS may be explained not only by timing, duration, and degree of reduced motility but also, and more importantly, by the normal muscular stress in OS patients.

Amniotic Fluid↗
PubMed1990

Changes in breast muscle composition in the young chick.

Nitrogen, protein and nucleic acids concentrations in the breast muscle (pectoralis thoracica), composition of sarcoplasmic and myofibrillar protein, and serum level of 3-methylhistidine were determined in female Warren chicks at 2, 3, 4 and 6 wk of age. Sarcoplasmic nitrogen and protein concentrations showed opposite changes to those presented by myofibrillar concentrations, with a maximum value at 3 and 4 wk of age and decreasing at 6 wk of age. Ribonucleic acid concentration decreased and protein/ribonucleic acid ratio increased from 2 to 6 wk of age. Differences were observed in the electrophoretical banding pattern of myofibrillar protein at 3 wk of age. Serum level of 3-methylhistidine increased from 2 to 4 wk of age (from .71 to 3.25 nmol/g), and no change was observed at 6 wk of age (3.46 nmol/g).

Age Factors↗
PubMed1989

Changes in the concentration and composition of biliary and serum bile acids in the young domestic fowl.

1. Concentrations of biliary and serum bile acids, their molecular compositions and serum cholesterol concentrations were determined in chicks at 2, 3, 4 and 6 weeks of age. 2. The concentration of biliary bile acid was maximal at 3 to 4 weeks, decreasing by 6 weeks of age. 3. The serum concentration of bile acid was maximal at three weeks of age. 4. Serum total cholesterol increased from two weeks and was maximal at 6 weeks of age. 5. Chenodeoxycholic acid was the predominant biliary unconjugated bile acid. 6. Tauro-chenodeoxycholic acid and tauro-cholic acid were the dominant molecular species of biliary and serum conjugated bile acid.

Age Factors↗
PubMed1988

Effects of immobilization on fetal bone development. A morphometric study in newborns with congenital neuromuscular diseases with intrauterine onset.

The effects of immobilization on fetal bone development were studied through post-mortem radiographs in 11 newborns with congenital neuromuscular diseases (CNMD) of intrauterine onset. Quantitative parameters were determined in the following bones: tibia, femur, humerus, radius, 3rd lumbar vertebra, and 5th rib. Thirty stillborns or newborns of similar gestational age and deceased from causes other than neuromuscular or related diseases were used as controls. No significant differences in bone lengths were observed between both groups. However, external diameters, cortex thicknesses, and cortical areas values were significantly lower in newborns with CNMD than in the control group. In newborns with CNMD, the medullary diameter of long bones showed good correlation with gestational age. However, this diameter was greater than that expected according to the reduced external diameter. These results suggest that intrauterine immobilization induces a decrease in mechanical usage of bone, mainly influencing bone modeling and probably bone remodeling. No changes were observed in longitudinal bone growth. Bones showed osteopenia and mechanical defects and were prone to fractures. In summary, reduced immobilization in utero produces bone osteoporosis of the fetus.

Bone Development↗
PubMed1988

Malignant rhabdoid tumor of the tongue. A case report with immunohistochemical and ultrastructural findings.

An extrarenal malignant rhabdoid tumor of the tongue in a 10-day-old boy is described. The tumor produced severe respiratory distress and had an aggressive clinical course. The patient died 17 days after the initial diagnosis. The tumor was mostly composed of poorly differentiated, round, polygonal or elongated cells. Ultrastructural examination showed intracytoplasmic filamentous inclusions in many of the cells. The cytoplasm was diffusely positive to anti-vimentin antibodies with focal, scarce positivity to anti-keratin antibodies. To the best of our knowledge, this is the first reported case of malignant rhabdoid tumor of the oral cavity.

Cell Nucleus↗
PubMed1988

Changes in the long bones due to fetal immobility caused by neuromuscular disease. A radiographic and histological study.

The long bones in eleven newborn infants who had neuromuscular disease were studied and were found to be thin, hypomineralized, and elongated. In most of the bones, there were multiple diaphyseal or metaphyseal fractures, or both. By light microscopy, the outstanding findings were fractures through the growth plate and diaphysis and thinning of the cortices. The etiology of the fractures and the insufficient substance of the bone is the reduction in the intrauterine motion of the fetus, which leads to fragility of the bones and contractures of the joints. The severity of the alterations may have been related to the time of the onset of the abnormalities and to the duration and degree of the intrauterine akinesia.

Abnormalities, Multiple↗
PubMed1987

Neuroepithelial cyst in the optic nerve. Case report.

A 34-year-old woman presented with progressive loss of vision in her left eye of 2 months' evolution. Computerized tomography showed a hypodense lesion in the suprasellar region. At surgery a cystic lesion was found inside the optic nerve. Histological study proved it to be a neuroepithelial cyst. The pathogenesis of a neuroepithelial cyst in such an exceptional site is discussed.

Adult↗
PubMed1986

Fragmented electrograms and continuous electrical activity in atrial flutter.

Multiple endocardial bipolar electrograms were recorded in 13 patients with atrial flutter (AF) to locate areas of fragmented electrical activity. Stable fragmentation patterns were found in each case, covering between 36% and 100% of the flutter cycle. Double or triple spike patterns were common. The direction of atrial activation was approximately defined in 11 patients, and in all of them at least part of the areas showing fragmentation was included in the circuit. In 1 patient an area of continuous electrical activity was found. AF circuits appeared to be included in the right atrium in 12 patients and in the left atrium in 1 patient. During atrial stimulation changes in fragmented electrograms coincided with changes in AF pattern before its interruption, while restoration of stable AF after stimulation was accompanied by reappearance of previous stable fragmented electrograms. In 6 patients electrograms were recorded after sinus rhythm was reestablished, and all showed marked decreases or disappearance of fragmentation. It is concluded that fragmented electrograms are often found in AF and may be related to abnormal local conduction in relation to the reentrant activation circuits.

Adult↗