Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 18 de 18
Filter
Add more filters










Publication year range
1.
Am J Med Genet A ; 143A(6): 553-7, 2007 Mar 15.
Article in English | MEDLINE | ID: mdl-17318852

ABSTRACT

The aim of this article is evaluate the sonograhic findings in fetuses with trisomy 18 at different gestational ages. The cases were recruited from pregnant women, who underwent to prenatal diagnosis in the period from October 1995 to September 2006. Seventy-one fetuses with trisomy 18 were diagnosed. On review of the sonograms the majority of these cases had ultrasound anomalies (sensitivity of 91.5%). The most frequent anomalies were abnormalities of extremities (40.8%) and fetal growth restriction (35.2%). More frequently (54.9%) two or more anomalies were present. Nearly all fetuses with trisomy 18 had sonographic abnormalities. Likely improved high-resolution equipment and attention to details by skilled operators led to the detection of most anomalies to trisomy 18. Knowledge of types of specific ultrasound findings can improve prenatal diagnosis in order to provide invasive procedures only when indicated, and to avoid amniocentesis when ultrasound signs are not observed in women at high risk from positive biochemical testing.


Subject(s)
Chromosomes, Human, Pair 18/genetics , Fetal Diseases/diagnostic imaging , Trisomy/diagnosis , Ultrasonography, Prenatal , Abnormalities, Multiple/diagnostic imaging , Abnormalities, Multiple/genetics , Adult , Female , Fetal Diseases/genetics , Gestational Age , Humans , Maternal Age , Pregnancy , Review Literature as Topic
2.
Fetal Diagn Ther ; 19(5): 440-7, 2004.
Article in English | MEDLINE | ID: mdl-15305101

ABSTRACT

OBJECTIVE: To evaluate sonographic appearance, natural history, and neonatal outcome of fetal venous anomalies. METHODS: We performed an observational study, including all fetuses affected by abnormalities of the venous system diagnosed by ultrasound during the prenatal period. RESULTS: 26 fetuses were identified. Other malformations were present in 5 cases (19.2%), 1 fetus had trisomy 21, and 1 fetus had intrauterine growth retardation (IUGR). Twenty-five pregnancies ended in liveborn infants, and there was 1 case of unexplained intrauterine death in the fetus with IUGR affected by varix of the umbilical vein. CONCLUSIONS: Fetal venous anomalies are very rare and may be associated with fetal malformations or IUGR. Conservative management appears to be an adequate medical practice in the absence of other fetal problems, but in the presence of a varix of the umbilical vein, serial follow-up scans are needed to exclude the onset of hydrops or thrombosis of the varix.


Subject(s)
Veins/abnormalities , Abnormalities, Multiple/diagnostic imaging , Female , Fetus/abnormalities , Fetus/blood supply , Humans , Infant, Newborn , Male , Pregnancy , Retrospective Studies , Ultrasonography, Prenatal , Umbilical Veins/abnormalities , Umbilical Veins/diagnostic imaging , Veins/diagnostic imaging
3.
Ann Ital Chir ; 74(3): 319-26, 2003.
Article in English | MEDLINE | ID: mdl-14677289

ABSTRACT

BACKGROUND AND AIMS: Improved medical therapy and bowel sparing and sphincter saving techniques have changed surgery for UC and CD. Collaboration between gastroenterologists and surgeons is necessary to uniform the indications for surgical treatment reducing emergency operations. GISMII multicentric study aimed to show indications, timing and impact of surgery, through retrospective analysis of cases observed between 1992 to 1996. METHODS: Data were obtained by 16 departments of General Surgery. RESULTS: 102 UC and 376 CD patients were analyzed. In UC patients surgery was performed for failure of medical therapy in 54%, complications in 28.4%, cancer or dysplasia in 10% of cases, 83.3% elective procedures. 30.4% ileo-anal pouch, 30.4% total procto-colectomies with definitive ileostomies, 32.4% total colectomies with ileo-rectal anastomosis, 6.8% segmental resections, were performed. In CD patients surgery was performed in 21% for medical therapy failure, in 79% for complications. 53.4% of patients were submitted to 1 operation, 84% elective procedures. Reoperations were performed in 46.6% of patients, 70.3% elective procedures. In the first operation bowel resection was performed in 79.1%, stricturoplasty in 14.3%; in the subsequent operations bowel resection 62.8%, stricturoplasty 21.7%, increasing number of temporary or definitive ileo-stomies. CONCLUSIONS: Collaboration between gastroenterologists and surgeons is necessary to obtain optimal results, reducing the incidence of emergency surgery, and complications. The short period observed between diagnosis and operation (21.4 months) is due to the increasing tendency of gastroenterologists to anticipate a surgical procedure when young patients with a chronic disease need a prolonged medical therapy.


Subject(s)
Inflammatory Bowel Diseases/surgery , Adolescent , Adult , Anastomosis, Surgical/statistics & numerical data , Colectomy/statistics & numerical data , Colonic Pouches/statistics & numerical data , Female , Hospitals, General/statistics & numerical data , Humans , Ileostomy/statistics & numerical data , Intestinal Neoplasms/surgery , Italy/epidemiology , Male , Middle Aged , Patient Care Team , Postoperative Complications/epidemiology , Reoperation/statistics & numerical data , Retrospective Studies , Surgery Department, Hospital/statistics & numerical data
4.
J Clin Gastroenterol ; 21(1): 27-9, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7560829

ABSTRACT

We evaluate the periodicity in relapses of ulcerative colitis and Crohn's disease in this multicenter prospective study. In 275 relapses among 184 patients with inflammatory bowel disease, a statistically significant biphasic annual periodicity, with peaks in the spring and autumn, was documented only for ulcerative colitis relapses (p = 0.006). This finding may be important in understanding relapse risk factors and in terms of prevention.


Subject(s)
Colitis, Ulcerative/epidemiology , Crohn Disease/epidemiology , Periodicity , Female , Humans , Male , Prospective Studies , Recurrence
5.
Hepatogastroenterology ; 42(2): 100-2, 1995 Apr.
Article in English | MEDLINE | ID: mdl-7672754

ABSTRACT

Although Hirschsprung's disease is diagnosed most commonly during infancy and childhood, some cases are seen in adults, when clinical features are usually similar to those described in younger patients. We report a case whose unusual clinical presentation led to an initial diagnosis and subsequent treatment of colonic Crohn's disease. The correct diagnosis was made only after motility measurements suggested the possibility of adult Hirschsprung's disease and prompted the histological examination of the myoenteric plexus, which led to the establishment of the correct diagnosis.


Subject(s)
Crohn Disease/diagnosis , Hirschsprung Disease/diagnosis , Adult , Diagnostic Errors , Hirschsprung Disease/physiopathology , Hirschsprung Disease/therapy , Humans , Male
6.
Rev Esp Enferm Dig ; 86(3): 694-8, 1994 Sep.
Article in Spanish | MEDLINE | ID: mdl-7986606

ABSTRACT

Two cases of pancreatic F-cell malignant tumors, producing only pancreatic polypeptide (PP) with clinical, biochemical and immunohistochemical features are described. No PP-associated endocrine symptoms were present. In both tumors, definitive diagnosis was immunohistochemical, and surgical treatment was carried out. Clinical evolution in the two patients was different: one of them died within the postoperative period with upper gastrointestinal bleeding by multiple duodenal ulcers, whereas the other--with lymph node metastasis at intraoperative diagnosis--is alive six years after treatment. F-cell tumors can be classified among the group of silent endocrine tumors of the pancreas. The reason for their discrepancy in the clinical behavior is unknown.


Subject(s)
Carcinoma, Islet Cell/pathology , Pancreatic Neoplasms/pathology , Aged , Carcinoma, Islet Cell/metabolism , Carcinoma, Islet Cell/surgery , Fatal Outcome , Female , Humans , Immunohistochemistry , Islets of Langerhans/metabolism , Islets of Langerhans/pathology , Lymph Node Excision , Lymphatic Metastasis , Pancreatectomy , Pancreatic Neoplasms/metabolism , Pancreatic Neoplasms/surgery , Pancreatic Polypeptide/metabolism , Splenectomy
7.
J Clin Gastroenterol ; 18(2): 99-104, 1994 Mar.
Article in English | MEDLINE | ID: mdl-8189031

ABSTRACT

We reviewed the medical records of 79 patients with primary gastrointestinal lymphoma (GI-NHL), defined according to the criteria of Dawson et al. (without involvement of liver, spleen, peripheral or mediastinal lymph nodes, or bone marrow), observed and treated in our institution between 1973-90. The most common disease site was the stomach (70 patients), followed by the small bowel (five patients) and the large bowel (four patients). The stage was IE in 36 cases and IIE in 43. Radical surgery or surgical debulking was the main therapeutic approach (67 patients); 12 patients received only chemotherapy, eight of whom had tumors considered unresectable at laparotomy. After surgery, most of the patients received chemotherapy; radiotherapy (RT) was given to only four patients. Surgically calculated overall survival (OS) rates at 5 years for the patients treated with surgery plus chemotherapy were 64% (radical surgery) and 46% (surgical debulking with microscopic lymphoma residue). For the 12 patients treated with chemotherapy alone, OS at 5 years was 0%. Our findings, in accordance with most published data, suggest that surgery, together with stage and tumor size, remains an important prognostic factor of survival in primary GI-NHL, especially when it is radical. In patients with negative prognostic factors (bulky disease, high-grade histologic type, microscopic residue, and stage II), postoperative chemotherapy and RT decrease the risk of distant failure and local recurrence.


Subject(s)
Gastrointestinal Neoplasms/pathology , Lymphoma, Non-Hodgkin/pathology , Adult , Aged , Aged, 80 and over , Female , Gastrointestinal Neoplasms/mortality , Gastrointestinal Neoplasms/therapy , Humans , Lymphoma, Non-Hodgkin/mortality , Lymphoma, Non-Hodgkin/therapy , Male , Middle Aged , Neoplasm Staging , Retrospective Studies , Survival Analysis
8.
Pathologica ; 82(1082): 687-93, 1990.
Article in Italian | MEDLINE | ID: mdl-2094839

ABSTRACT

Morphology of pancreas (either esocrine, either endocrine) was studied in 29 cases of surgically treated chronic pancreatitis (27 cases of chronic calcifying pancreatitis and 2 cases of chronic obstructive pancreatitis). Parenchymal sclerosis in chronic calcifying pancreatitis (CCP) which represents the goal of our study was graded as mild (10 cases), moderate (10) and severe (7). Immunoperoxidase staining (PAP method) for insulin, glucagon, somatostatin, pancreatic polipeptide (PP), vasoactive intestinal polipeptide (VIP) and gastrin, was used to investigate endocrine pancreas. Acinar sclerosis and endocrine damage were closely related. Progression of sclerosis into islet appears to follow vascular pedicles producing a fragmentation into small cell groups as final result. In all cases of moderate or severe sclerosis, A/B cell ratio was increased due to the reduction of insulin positive cells. "Adenoma-like complexes", i.e., apparent concentration of islets, resulting from the loss of the acinar component, were observed in 7 cases with moderate or severe sclerosis. Nesidioblastosis was a prominent feature in all cases but one, with a positivity for insulin in 11 cases, for glucagon in 13, for somatostatin in 6 and for PP in 17. No positivity for gastrin was observed, while VIP was detected in a few ganglia. An increased amount of PP cells in islet and budding from the ducts was noticed and their presence outside the pancreatic head was demonstrable in 4 out of the 7 distal pancreatectomy specimens. Our data confirm the secondary involvement of the endocrine pancreas in the sclerotic acinar process.


Subject(s)
Calcinosis/pathology , Pancreatitis/pathology , Adult , Aged , Chronic Disease , Constriction, Pathologic , Humans , Middle Aged , Pancreatic Ducts
12.
Radiol Med ; 68(6): 449-54, 1982 Jun.
Article in Italian | MEDLINE | ID: mdl-7111793

ABSTRACT

The purpose of this study was to establish the value of xeroradiographic patterns and their applicability in the automatic diagnosis of breast diseases. Such an evaluation is based on the comparison with the histologic examination, irrespective of the overall diagnostic judgement previously formulated. From an analysis of the material examined it was possible to ascertain the distribution frequency, the sensitivity, the specificity, the discriminating capacity, and finally the weight of each radiologic sign considered. There are xeroradiographic signs that are apparent almost exclusively in the malignant pathology and therefore can be considered as positive indices of the malignancy of the alteration. The specificity of the radiologic signs considered is very high, whereas the same cannot be said for the sensitivity. Moreover, a linear discriminating analysis made it possible to identify those semiologic elements which, with a minor probability of error, would attribute the pathologic process to the class verified histologically, for malignant neoplasms as well as benign tumors and dysplastic processes.


Subject(s)
Mammography , Xeromammography , Breast Diseases/diagnostic imaging , Breast Neoplasms/diagnostic imaging , Humans
13.
Tumori ; 67(5): 447-53, 1981 Oct 31.
Article in English | MEDLINE | ID: mdl-7324175

ABSTRACT

The analytical study of the case material has allowed a precise evaluation of the distribution by age groups of the different pathologic processes of the breast, of the localization and dimensions of malignant tumors, as well as the diagnostic accuracy for those cases histologically ascertained and those with a follow-up. The diagnostic accuracy and the consequent reliability of the xeroradiographic method for the diagnosis of breast cancer is distinctly superior to that reported in the literature for traditional mammography, whereas for the differential diagnosis between circumscribed dysplastic manifestations and benign tumors xeromammography is not sufficiently reliable. The authors critically discuss the results and in particular the problem of false positives, which also include diagnostic errors that cannot be avoided in that they directly derive from the pathologic morphology of the disease process (plasma cell mastitis and sclerosing adenosis). As regards the problem of false negatives, they can be reduced within certain limits by resorting to other instrumental investigations. However, there are cases (1% of the malignant neoplasias histologically ascertained) that present a completely negative xeroradiographic finding. There are the limits of the radiologic investigation which cannot in any way be surmounted.


Subject(s)
Breast Neoplasms/diagnostic imaging , Mammography , Xeromammography , Adolescent , Adult , Aged , Breast Neoplasms/pathology , False Negative Reactions , False Positive Reactions , Female , Humans , Middle Aged
17.
Pathol Eur ; 10(3): 193-5, 1975.
Article in English | MEDLINE | ID: mdl-1187196

ABSTRACT

The effects of cycloheximide (CHM) and chloramphenicol (CAP) on rat serum proteins and on their electrophoretic patterns have been investigated. It has been shown that total serum protein is decreased by both treatments. CHM causes a fall in transferrin and alpha2(3-8) globulin content, while CAP reduces only alpha2(3-8) globulins. Different microscopic features of hepatic steatosis are described with both drugs. The results are briefly discussed.


Subject(s)
Blood Proteins , Chloramphenicol/pharmacology , Cycloheximide/pharmacology , Animals , Blood Protein Electrophoresis , Female , Rats
SELECTION OF CITATIONS
SEARCH DETAIL
...