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1.
Anatomy & Cell Biology ; : 274-278, 2014.
Artigo em Inglês | WPRIM | ID: wpr-62478

RESUMO

We report on an extremely rare case of multiple absences of the branches of abdominal aorta with congenital absence of the portal vein, unilateral adrenal agenesis and persistent ductus arteriosus in an adult female cadaver. Specifically, instead of celiac trunk, superior and inferior mesenteric arteries, solely a single arterial trunk aroused from the anterior aspect of abdominal aorta, inferior phrenic and ovarian arteries were absent in both sides. Left kidneys drained by two veins. There were not superior, splenic and mesenteric veins, while left renal vein received an additional vein, which run downward and drained primarily all parts of digestive tract and its associated glands (portal vein did not exist). Right adrenal gland was absent. To the best of our knowledge, it is the only reported case with such widespread anomalies. We think the importance of this case is beyond the surgical consideration and needs more profound developmental studies.


Assuntos
Adulto , Feminino , Humanos , Glândulas Suprarrenais , Aorta Abdominal , Artérias , Cadáver , Canal Arterial , Trato Gastrointestinal , Rim , Artéria Mesentérica Inferior , Veias Mesentéricas , Veia Porta , Veias Renais , Veias
2.
IJRM-Iranian Journal of Reproductive Medicine. 2012; 10 (2): 121-126
em Inglês | IMEMR | ID: emr-124487

RESUMO

Nitric oxide [NO] is a molecule that incorporates in many physiological processes of female reproductive system. Recent studies suggested the possible role of endothelial isoform of nitric oxide synthase [eNOS] enzyme in female infertility. The aim of this study is to evaluate the expression of endothelial nitric oxide synthase in endometrial tissue of women with unexplained infertility. In this case-control study a total of 18 endometrial tissues obtained from 10 women with unexplained infertility and 8 normal and fertile women by endometrial biopsy, 6 to 10 days after LH surge. Specimens were fixed in 4% paraformaldhyde fixative and frozen sectioned for semi-quantitative immunohistochemical evaluation using monoclonal anti-human eNOS antibody. Hematoxilin and Eosin was used for Histological dating. Localization of endothelial nitric oxide synthase was seen in glandular and luminal epithelium, vascular endothelium and stroma in both fertile women and women with unexplained infertility. Although there were differences in immunoreactivity of glandular epithelium [p=0.44], vascular endothelium [p=0.60] and stroma [p=0.63] but only over-expression of eNOS in luminal epithelium [p=0.045] of women with unexplained infertility compared to fertile women was statistically significant [p<0.05]. This study suggests that changes in luminal expression of eNOS may influence receptivity of endometrium


Assuntos
Humanos , Feminino , Imuno-Histoquímica , Endométrio , Infertilidade , Infertilidade Feminina , Estudos de Casos e Controles
3.
IJRM-Iranian Journal of Reproductive Medicine. 2011; 9 (4): 277-280
em Inglês | IMEMR | ID: emr-113500

RESUMO

Non obstructive azoospermia [NOA] is one of the causes of male infertility in which spermatogenesis process is disturbed. Recent studies suggested the possible role of endothelial nitric oxide synthase [eNOS] in spermatogenesis process. The aim of the present study is to evaluate the expression of eNOS in human testicular tissue in men with NOA and men with normal spermatogenesis by using immunocytochemistry. In this case-control study, testicular biopsies were obtained from 10 men with NOA and 7 men with normospermia who were attended to infertility center for diagnosis or infertility treatment. Immunohistochemistry was used to localize the isoform of eNOS in these tissues and the intensity of staining was semi quantitively assessed. In addition, the histopathological evaluation was examined in both groups. The isoform of eNOS enzyme activity was detected in the cytoplasm of sertoli and leydig cells in both groups. There was, however, a considerable variability in the intensity of staining between two groups. The expression of eNOS in Leydig cells in control group was significantly [p<0.05] higher than those in the NOA group. In contrast, expression of eNOS in Sertoli cells in NOA was more than those in the control group. eNO Simmune staining was absent in the normal germ cells but was intense in the abnormal germ cells with piknotic neucleous. The most histopathological finding were hypospermatogenesis [27.2%], Sertoli cell only syndrome [18.1%] and tubular fibrotic [13.6%]. These results suggested that increase level of eNOS may play an important role in the apoptosis process in the abnormal germ cells and disturbance of spermatogenesis process

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