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1.
Radiol Med ; 115(1): 105-14, 2010 Feb.
Article in English, Italian | MEDLINE | ID: mdl-20017007

ABSTRACT

PURPOSE: The aim of this study was to assess the radiation dose of dose-reduced unenhanced abdominal multidetector computed tomography (MDCT) scan protocols for suspected renal colic in patients within normal weight range and overweight-obese patients and to record the cumulative dose of repeated examinations. MATERIALS AND METHODS: Over a 2-year period, we performed 1,026 unenhanced CT examinations for urolithiasis; among these, 675 were performed on 636 patients referred from the emergency department. Patients were divided into two groups on the basis of body mass index (BMI): normal weight (BMI <25 kg/m(2) group 1); overweight and obese (BMI >25 kg/m(2) group 2). For patients in group 1 and group 2, the protocols of our 64-row scanner prescribe tube current settings at 70 mAs and 150 mAs, respectively. The dose-length product (DLP) estimated by using the manufacturer's software was converted into effective dose (ED). RESULTS: Mean DLP and ED were 177 and 345 mGy/cm and 2.4 and 4.8 mSv for group 1 and group 2, respectively. A subset of 25 patients (3.7%) underwent two or more examinations, with estimated ED ranging from 4.8 to 19.2 mSv. CONCLUSIONS: Although radiation dose is nearly double in overweight-obese patients undergoing MDCT, it remains lower than that delivered by a standard-dose protocol. Patients with flank pain, who are often young, are at increased risk for serial CT examinations. Use of a low-dose protocol is mandatory in both normal-weight and obese patients to minimise radiation exposure.


Subject(s)
Body Size , Obesity/diagnostic imaging , Radiation Dosage , Radiographic Image Interpretation, Computer-Assisted , Renal Colic/diagnostic imaging , Tomography, X-Ray Computed , Urolithiasis/diagnostic imaging , Adult , Aged , Aged, 80 and over , Body Mass Index , Body Size/radiation effects , Body Weight , Contrast Media , Female , Humans , Male , Middle Aged , Overweight/diagnostic imaging , Reproducibility of Results , Retrospective Studies , Sensitivity and Specificity
2.
Clin Microbiol Infect ; 9(7): 632-9, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12925103

ABSTRACT

OBJECTIVE: To determine specificity, sensitivity and predictive values of a rapid immunochromatographic assay (ICT tuberculosis) for the diagnosis of tuberculosis (TB) in an Italian clinical setting, and to identify tentative new guidance for the interpretation of test results. METHODS: The ICT tuberculosis test is an immunochromatographic test based on the detection of IgG antibodies directed against five highly purified antigens secreted by Mycobacterium tuberculosis during active growth. Sera from 60 patients with active pulmonary (48 sputum smear-positive and six sputum smear-negative cases) and extrapulmonary (six cases) TB were obtained. Personal, anamnestic and clinical data were investigated and recorded for each patient. The control groups comprised 156 subjects: 40 healthy individuals, half of them Mycobacterium bovis BCG-vaccinated, and 116 patients with mycobacterial diseases other than TB (five cases), with nonmycobacterial lung diseases (30 cases), with nonmycobacterial nonlung diseases (30 cases), with nonmycobacterial diseases and rheumatoid factors positivity (30 cases), and with asymptomatic HIV infection (21 cases). For 21 individuals the test was simultaneously performed with both serum and whole blood sample. Each positive result of the ICT test was reported with regard to the number (1-4), position (A, B, C, D) and color intensity (+ to ++++) of the evidenced lines in order to assess the quality of the antibody response. RESULTS: The overall sensitivity and specificity were 56.7% and 90.4%, respectively. The sensitivity for pulmonary TB patients was 61.1% (66.7% for smear-positive and 16.7% for smear-negative cases) and 16.7% for extrapulmonary TB patients. The difference between ICT results in pulmonary TB patients and control subjects was statistically significant (P < 0.0001). The analysis of the positive ICT tests revealed that samples with strong color intensity (>/=++) and specific antibodies bound to antigens immobilized on line D were significantly more frequent in TB patients than in controls (P = 0.001 and P= 0.027, respectively). ICT test results with the presence of at least three visible lines were more often observed in the TB patients than in controls, although not reaching statistical significance (P = 0.052). No difference was observed between the results of the ICT test performed both on serum and whole blood sample. CONCLUSIONS: The ICT tuberculosis test was confirmed to be rapid and easy to perform without requiring special equipment, both on serum and whole blood sample. Our data, in accordance with those obtained in a previous study conducted in extra-European countries, confirmed higher sensitivities for the smear-positive TB patients than for the smear-negative TB patients, and for pulmonary TB patients than for the extrapulmonary TB patients. Data obtained on the quality of antibody response in the ICT positive samples, might be used to improve the performance of the test.


Subject(s)
Chromatography/methods , Immunochemistry/methods , Immunoglobulin G/analysis , Tuberculosis/diagnosis , Tuberculosis/immunology , Adolescent , Adult , Aged , Aged, 80 and over , Bayes Theorem , Female , Humans , Immunoglobulin G/blood , Male , Middle Aged
3.
Psychiatr Serv ; 52(5): 679-81, 2001 May.
Article in English | MEDLINE | ID: mdl-11331806

ABSTRACT

For a study designed to examine the accuracy of information about HIV transmission, risk behavior, and preventive measures among individuals with psychiatric disorders in Italy, 214 psychiatric patients-114 outpatients and 100 inpatients-and 88 nonpsychiatric patients completed the AIDS Risk Behavior Knowledge Test. Levels of knowledge were lower among psychiatric patients than among control subjects. Patients with chronic illness and a diagnosis of schizophrenia were found to have less knowledge than other patients about HIV transmission. These findings confirm the need for HIV-related educational and behavior-modification programs for patients with chronic and severe mental illness in the community in Italy.


Subject(s)
HIV Infections/prevention & control , HIV Infections/transmission , Health Knowledge, Attitudes, Practice , Mental Disorders/psychology , Adolescent , Adult , Community Mental Health Centers , HIV Infections/psychology , Humans , Italy , Middle Aged , Needs Assessment , Psychiatric Department, Hospital , Risk Factors , Schizophrenia , Surveys and Questionnaires
4.
Cancer Genet Cytogenet ; 124(1): 16-9, 2001 Jan 01.
Article in English | MEDLINE | ID: mdl-11165317

ABSTRACT

The karyotype of a new tumorigenic Kaposi sarcoma (KS)-derived cell line, as defined by cytogenetic and fluorescence in situ hybridization (FISH) analysis is 49,XY,i(1)(q10),i(7)(p10),+i(7) (q10),+der(8)t(8;13)(p11;q11),-13,+del(14)(q22),+der(17)t(1;17)(p13;p13). Our aim was to point out some characteristics and recurrent chromosome changes probably playing a relevant role in the malignant progression of KS, by a comparison of the cytogenetic results obtained in the present study with data from the literature. The interpretation of the cytogenetic results is that KS development occurs by multiple steps: an initial reactive polyclonal cell proliferation is associated with chromosome instability; the cells in a later stage acquire clonal chromosome changes. If many chromosome changes are present, particularly 8q and 1q trisomy, 3p14-->pter deletion, 1p13, 13p14.3, 7q22, 8p11, 13q11, and 19q13 band rearrangements, KS acquires a neoplastic aggressive state.


Subject(s)
Chromosome Aberrations/genetics , Sarcoma, Kaposi/genetics , Tumor Cells, Cultured , Humans , Iatrogenic Disease , In Situ Hybridization, Fluorescence , Karyotyping , Ploidies
5.
Ann Genet ; 43(1): 45-50, 2000.
Article in English | MEDLINE | ID: mdl-10818221

ABSTRACT

A new case of a de novo trisomy 10cen-->10pter is described. The karyotype was exactly defined by high resolution banding and FISH analysis; the chromosome aberration was of maternal meiotic origin as demonstrated by RFLP analysis. Clinical data are reported and correlated with other trisomy 10p cases from the literature. A critical review of the literature was made to define the phenotype of trisomy 10p syndrome.


Subject(s)
Chromosomes, Human, Pair 10 , Polymorphism, Restriction Fragment Length , Trisomy , Adolescent , Chromosome Mapping , Female , Genomic Imprinting , Humans , In Situ Hybridization, Fluorescence , Karyotyping , Lymphocyte Activation , Lymphocytes/pathology , Male
6.
Cancer Genet Cytogenet ; 118(2): 136-43, 2000 Apr 15.
Article in English | MEDLINE | ID: mdl-10748294

ABSTRACT

Cytogenetic analysis performed on 73 sporadic basal cell carcinomas (BCCs) and three squamous cell carcinomas (SCCs) showed different findings in direct preparations (24 hours) and in short-term cell cultures. Except for loss of the Y chromosome, not one of the other clonal (+6, +16, add(2)(q37), del(3)(q13), add(1)(p31), and near triploidy) or sporadic changes found in direct preparations was found in cell cultures and vice versa. Clonal trisomy 6 found in two BCC direct preparations and demonstrated by interphase fluorescence in situ hybridization in 8 other cases seems to be a nonrandom change in basal cell carcinoma. Immunohistochemistry showed that the cell type investigated was different in the two methods of analysis used: epithelial in direct preparations and fibroblastic in cell cultures. Thus, the results obtained in direct preparations indicate the BCC or SCC epithelial karyotype, whereas the aberrations found in cell cultures indicate the presence of chromosome instability in the fibroblastic stroma. The apparent lack of correspondence between direct and indirect preparations and the presence of clonal chromosome changes in both epithelial and stromal cells suggest tumor cell heterogeneity of BCC. The fibroblastic stroma seems to be implicated in the neoplastic process. This is not evident in SCC, in which clonal changes are present only in direct preparations. The chromosomal distribution of the breakpoints involved in structural changes in direct and cell culture preparations is random; together with those reported in the literature, the breakpoints found in BCC cultures show, however, a cluster to 1p36, 3q13, 9q22, 14p11, 15p11, and Xp11 bands. We did not find any significant correlations between BCC cytogenetic results and the clinical data (site, age, sex, recurrence). The incidence of cases of BCC (38%) and of SCC (100%) showing clonal chromosome changes agree with their benign and malignant nature, respectively. Finally, a significantly high incidence of constitutional inv(9) and dup(9)(q11q21) was found in the group of patients with BCC.


Subject(s)
Carcinoma, Basal Cell/genetics , Carcinoma, Squamous Cell/genetics , Cell Culture Techniques/methods , Chromosome Aberrations , Head and Neck Neoplasms/genetics , In Situ Hybridization, Fluorescence , Abdominal Neoplasms/genetics , Adult , Aged , Aged, 80 and over , Female , Fibroblasts/ultrastructure , Humans , In Situ Hybridization , Male , Middle Aged , Thoracic Neoplasms/genetics
7.
Radiol Med ; 100(6): 429-35, 2000 Dec.
Article in Italian | MEDLINE | ID: mdl-11307503

ABSTRACT

PURPOSE: To present an "algorithm" for detection and diagnosis of skeletal metastases, which may be applied differently in symptomatic and asymptomatic cancer patients. MATERIAL AND METHODS: February to March 1999 we randomly selected and retrospectively reviewed the clinical charts of 100 cancer patients (70 women and 30 men; mean age: 63 years, range: 55-87). All the patients had been staged according to TNM criteria and had undergone conventional radiography and bone scan; when findings were equivocal, CT and MRI had been performed too. RESULTS: The primary lesions responsible for bone metastases were sited in the: breast (51 cases), colon (30 cases: 17 men and 13 women), lung (7 cases: 6 men and 1 woman), stomach (4 cases: 2 men and 2 women), skin (4 cases: 3 men and 1 woman), kidney (2 men), pleura (1 woman), and finally liver (1 men). The most frequent radiographic pattern was the lytic type (52%), followed by osteosclerotic, mixed, lytic vs. mixed and osteosclerotic vs lytic patterns. The patients were divided into two groups: group A patients were asymptomatic and group B patients had local symptoms and/or pain. DISCUSSION: Skeletal metastases are the most common malignant bone tumors: the spine and the pelvis are the most frequent sites of metastasis, because of the presence of high amounts of red (hematopoietic active) bone marrow. Pain is the main symptom, even though many bone metastases are asymptomatic. Pathological fractures are the most severe consequences. With the algorithm for detection and diagnosis of skeletal metastases two different diagnostic courses are available for asymptomatic and symptomatic patients. Bone scintigraphy remains the technique of choice in asymptomatic patients in whom skeletal metastases are suspected. However this technique, though very sensitive, is poorly specific, and thus a negative bone scan finding is double-checked with another physical examination: if the findings remain negative, the diagnostic workup is over. On the contrary, in patients with a positive bone scan or with local symptoms and pain, radiography and CT are used for screening of metastatic lesions: results may be negative (for low sensitivity of conventional radiology) or questionable (in which case bone biopsy is necessary), or else symptoms may be due to different causes than metastatic lesions (i.e., osteoarthritis). Before bone biopsy is made, MRI must be performed, because it is the only technique that allows to distinguish between bone marrow components. The limitation of MRI is the poor specificity of its findings, which may provide misleading findings.


Subject(s)
Algorithms , Bone Neoplasms/diagnosis , Bone Neoplasms/secondary , Aged , Aged, 80 and over , Bone Neoplasms/diagnostic imaging , Diagnosis, Differential , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Radionuclide Imaging , Retrospective Studies , Spinal Neoplasms/diagnosis , Spinal Neoplasms/diagnostic imaging , Spinal Neoplasms/secondary , Tomography, X-Ray Computed
8.
Psychother Psychosom ; 68(1): 31-8, 1999.
Article in English | MEDLINE | ID: mdl-9873240

ABSTRACT

BACKGROUND: Over the last years the way in which patients with chronic physical illness respond to their illness (illness behavior) has been explored by several studies. This study sought to examine characteristics of illness behavior and to investigate the association between illness behavior and psychosocial and clinical variables among asymptomatic HIV-infected subjects. METHODS: Seventy-three asymptomatic HIV+ outpatients completed self-report questionnaires to evaluate illness behavior (Illness Behavior Questionnaire), psychological stress symptoms (Brief Symptom Inventory), personality variables (External Locus of Control and Courtauld Emotional Control Scales) and social support (Social Provision Scale). RESULTS: Psychological morbidity ('caseness' = 34%) was associated with a pattern of illness behavior characterized by conviction of disease progression, irritability, dysphoria, psychological perception of illness and low denial. Individual capacity to express emotions, adequate levels of social support and low levels of depression, as well as clinical variables (high number of CD4+ cells, recent notification of HIV infection and nonintravenous drug use category) influenced a more adaptive illness behavior. Psychological stress and low CD4+ cell count were the main predictors of the affective dimension of illness behavior. CONCLUSIONS: Psychosocial variables resulted to influence the tendency to interpret illness in a nonadaptive way in asymptomatic HIV-infected subjects. Such variables merit to be routinely examined within the doctor-patient relationship in AIDS clinics.


Subject(s)
HIV Seropositivity/psychology , Sick Role , Stress, Psychological/etiology , Adaptation, Psychological , Adolescent , Adult , Attitude to Health , Female , Homosexuality , Humans , Male , Middle Aged , Personality , Physician-Patient Relations , Psychological Tests , Regression Analysis , Stress, Psychological/diagnosis
9.
Psychosomatics ; 39(4): 350-9, 1998.
Article in English | MEDLINE | ID: mdl-9691704

ABSTRACT

The study examined the relationship between coping and psychosocial variables (psychological stress symptoms, locus of control, emotional repression, and social support) among 108 human immunodeficiency virus (HIV)-infected patients. The authors administered several tests, including one that measures fighting spirit and degree of hopelessness, to assess each patient's individual coping style. The patients who were adjusting well to their HIV-positive status tended to have a higher level of fighting spirit and lower degree of hopelessness than those patients who were not adjusting well to their HIV-positive status. A coping style based on incapacity to face and confront HIV infection was associated with symptoms of psychological stress, repression of anger, external locus of control, and low social support in the latter group. These patients showed symptoms indicating maladjustment to HIV infection (43% of the sample) and differed from the "noncases" (the well-adjusted patients) in that the former group reported inadequate coping responses (lower fighting spirit and higher hopelessness, fatalistic attitude, and anxious preoccupation) and poorer social support, and had a greater tendency to repress anger and express sadness. The data support the hypothesis that coping with HIV infection is a complex phenomenon involving multiple and interacting variables. Interventions aimed at improving the coping style for many HIV patients are needed.


Subject(s)
Adaptation, Psychological , HIV Infections/psychology , Sick Role , Social Support , Adolescent , Adult , Defense Mechanisms , Female , Humans , Internal-External Control , Male , Middle Aged , Motivation , Personality Inventory , Social Adjustment
10.
Respir Med ; 92(4): 683-90, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9659537

ABSTRACT

The aim of the present multicentre, open, randomized, parallel group study was to evaluate the efficacy and safety of salmeterol versus theophylline in asthmatic patients. A total of 112 patients were randomized: 56 received inhaled salmeterol (50 micrograms twice daily) and 50 oral dose titrated theophylline twice daily. The study lasted 12 months. The efficacy of both drugs was evaluated for the first 3 months of the study and the safety for a further 9 months. Spirometric measurements were carried out for the total duration of the study. Salmeterol showed a greater and more significant efficacy than theophylline in reducing both day- and night-time symptoms (P < 0.001) and in reducing additional salbutamol requirement (P < 0.001). The subjective assessment of efficacy by physicians and patients was in favour of salmeterol from the first month of treatment (P < 0.001). Both drugs improved the quality of life as measured by the specific questionnaire 'Living with Asthma' with no significant differences. The total number of adverse events was slightly higher in the theophylline group compared with salmeterol (18 vs 9; P n.s.). Both salmeterol and theophylline increased morning and evening PEFR with no significant difference. FEV1 and FVC increased in both groups of patients; the difference between the effects of the two treatment was not statistically significant at 12 months. Our study suggests that salmeterol has higher efficacy and safety than theophylline in long-term treatment of asthmatic patients.


Subject(s)
Adrenergic beta-Agonists/administration & dosage , Albuterol/analogs & derivatives , Asthma/drug therapy , Bronchodilator Agents/administration & dosage , Theophylline/administration & dosage , Administration, Inhalation , Adrenergic beta-Agonists/therapeutic use , Albuterol/administration & dosage , Albuterol/therapeutic use , Asthma/physiopathology , Bronchodilator Agents/therapeutic use , Delayed-Action Preparations , Female , Forced Expiratory Volume , Humans , Lung/physiopathology , Male , Middle Aged , Peak Expiratory Flow Rate , Salmeterol Xinafoate , Theophylline/therapeutic use
11.
Am J Clin Oncol ; 21(1): 67-71, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9499262

ABSTRACT

The aim of this study was to identify a chemotherapy combination that would be active and well tolerated for palliative treatment of advanced non-small-cell lung cancer (NSCLC). From February 1992 to December 1994, a total of 77 patients affected by stage-IIIB and stage-IV NSCLC were treated with carboplatin 350 mg/m2 on day 1 and vinorelbine 25 mg/m2 on days 1 and 8 of each cycle, with cycles repeated every 28 days. All patients were evaluable for response and toxicity. A total of 24 patients showed a partial response (31% response rate; 95% CI = 21-41%). The median duration of overall survival was 41 weeks (95% CI = 31-51), and the median time to disease progression was 34 weeks (95% CI = 25-43). The treatment was well tolerated: no grade-4 toxicity was observed. The carboplatin-vinorelbine combination deserves to considered as a valid alternative to regimens that include cisplatin for palliative treatment of advanced NSCLC.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Non-Small-Cell Lung/drug therapy , Lung Neoplasms/drug therapy , Adult , Aged , Carboplatin/administration & dosage , Female , Humans , Male , Middle Aged , Survival Analysis , Vinblastine/administration & dosage , Vinblastine/analogs & derivatives , Vinorelbine
12.
Cancer Genet Cytogenet ; 99(1): 73-6, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9352799

ABSTRACT

The results of cytogenetic and FISH analysis performed in 26 cases of Dupuytren contracture are reported. Clonal or sporadic chromosome changes were found in 18 cases (69%). Clonal changes consisted of: +2, +16, -10, -Y, add(1)(p23), del(2)(q21), t(3;16)(p21;q24), add (3)(p24), del(18)(q21), t(Y;14)(p12;q24), +mar. The results differ from those obtained in normal palmar fascia used as control, in which -Y and +Y were the only clonal changes found in 2 of 11 analyzed cases (18%). No clonal trisomy 8 was found. FISH analysis performed in 11 cases (centromeric probe specific for chromosome 8) failed to show the presence of a cell population with +8. Clonal and sporadic structural changes were different from case to case and no clustering breakpoint was observed. The significance of the chromosome instability leading to clonal and sporadic chromosome changes not specific to Dupuytren contracture are discussed.


Subject(s)
Chromosomes, Human, Pair 8 , Dupuytren Contracture/genetics , Trisomy , Aged , Aged, 80 and over , Centromere/genetics , Humans , Interphase/genetics , Karyotyping , Male , Middle Aged , Y Chromosome
13.
Rev Saude Publica ; 31(1): 71-7, 1997 Feb.
Article in Portuguese | MEDLINE | ID: mdl-9430928

ABSTRACT

INTRODUCTION: The data presented are part of a World Health Organization (WHO) multicenter study of self-medication in Latin America. Brazilian sites included: Belo Horizonte, Fortaleza, the city of S. Paulo and outlying locations. The objective was to characterize self-medication practices by analyzing drugs sought by consumers in pharmacies without a physician's prescription. MATERIAL AND METHOD: Drugs were classified according to the Anatomic Therapeutic Classification codes, and analyzed with respect to 1) intrinsic value; 2) recognition as an essential drug (by either WHO or Brazil); 3) number of active ingredients; and 4) requirement for prescription. RESULTS: Five thousand, three hundred and thirty-two (5,332) different drugs, with 785 distinct active ingredients were sought. Of these, 49.5% were fixed dose combinations, 53.0% were of little intrinsic value, 44.1% required a physician's prescription, 71.0% were not essential drugs, and 40.0% of requests were based on prior prescriptions from the physician. The drugs most requested were analgesics (17.3%), nasal descongestants (7.0%), antirheumatic anti-inflammatory drugs (5.6%), and systemic anti-infective drugs (5.6%). CONCLUSIONS: Self-medication in Brazil reflects the needs and habits of the population. It is strongly influenced by physician's-prescribing habits and by the inadequate selectivity of the Brazilian pharmaceutical market.


Subject(s)
Self Medication/statistics & numerical data , Adult , Brazil , Female , Humans , Male , Nonprescription Drugs , Pharmacies , Surveys and Questionnaires
14.
Rev. bras. anal. clin ; 28(1): 34-36, 1996. tab
Article in Portuguese | LILACS | ID: lil-535148

ABSTRACT

Os autores descrevem a epidemiologia das infecções causadas por Klebsiella sp num hospital universitário. Algumas características da biologia, patogenia e perfil de sensibilidade são também comentadas.


Subject(s)
Humans , Bacterial Infections , Cross Infection , Klebsiella , Klebsiella Infections , Prevalence
15.
Hum Reprod ; 10(12): 3136-8, 1995 Dec.
Article in English | MEDLINE | ID: mdl-8822430

ABSTRACT

Torsion of the adnexa has traditionally been treated by adnexectomy because of the fear of emboli departing from thrombosed ovarian veins. Several recent reports have described successful conservative management with unwinding of the twisted adnexa. As the trend toward conservative management progresses, the incidence of recurrent adnexal torsion may increase. We present a case of a 33 year old gravida 3, para 2 Caucasian female who presented at 7 weeks gestation complaining of symptoms similar to those experienced during an episode of right ovarian torsion treated by laparoscopic unwinding 6 years earlier. Colour Doppler sonography revealed absent flow in the right adnexa. The twisted right adnexa containing the presumed corpus luteum of pregnancy was laparoscopically unwound. Using an extracorporeal suturing technique, a laparoscopic oophoropexy was performed to prevent any further rotatory movement. This appears to be the first reported case of laparoscopic oophoropexy for a recurrent ovarian torsion; we encourage the use of this simple, minimally invasive procedure in cases of recurrent adnexal torsion.


Subject(s)
Adnexal Diseases/complications , Adnexal Diseases/surgery , Laparoscopy/methods , Ovary/surgery , Pregnancy Complications/surgery , Adult , Female , Humans , Pregnancy , Recurrence , Suture Techniques , Torsion Abnormality
16.
J Pediatr (Rio J) ; 71(6): 341-3, 1995.
Article in Portuguese | MEDLINE | ID: mdl-14688985

ABSTRACT

We report a case of peritonitis caused by Trichosporon beigelii in a 2-year-old child during treatment by continuous ambulatory peritoneal dialysis (CAPD). Diagnosis was established by direct examination and culture of dialysis effluent. Infections caused by Trichosporon beigelii in children are commented.

17.
Cancer Genet Cytogenet ; 83(1): 28-31, 1995 Aug.
Article in English | MEDLINE | ID: mdl-7656200

ABSTRACT

Cytogenetic analysis was performed on 23 samples from non-neoplastic ureters. Clonal chromosome abnormalities were found in eight. They were: loss of Y chromosome, as a single abnormality (five cases) or associated with trisomy 10 and 20 (one case) or with trisomy 2 (one case); and duplication of Y chromosome (one case). Different numerical and structural sporadic abnormalities were found in nine cases. Immunohistochemical analysis and direct observation using the inverted microscope showed that the cells were mainly of the fibroblastic type. FISH analysis with chromosome 7 alpha-satellite probes failed to detect the presence of trisomy 7 in three epithelial cases tested.


Subject(s)
Ureter/chemistry , Ureter/pathology , Urologic Neoplasms/genetics , Adult , Aged , Chromosome Aberrations , Chromosomes, Human, Pair 7 , Clone Cells , Female , Humans , Immunoenzyme Techniques , In Situ Hybridization, Fluorescence , Karyotyping , Male , Middle Aged , Ureter/ultrastructure , Urologic Neoplasms/ultrastructure
18.
Ann Genet ; 38(3): 145-50, 1995.
Article in English | MEDLINE | ID: mdl-8540685

ABSTRACT

The authors have analyzed cytogenetically 28 cultured lymphocytes from females with Diffuse Scleroderma and 28 female controls between 30 and 70 years of age. Recurrent chromosome abnormalities were +8, +X, -X, and the PCD(X) phenomenon. Triplo X cells were significatively more frequent in patients than in controls. The incidence of +X and PCD(X) was significatively higher in the patients between 30 and 50 years of age, while the frequency of -X cells was higher in controls than in patients. None of these chromosome changes was correlated with the presence of anticentromere antibodies (ACA) in the patients' serum. Random structural chromosome abnormalities were also observed in the patients, but no break point clustering was observed. The incidence of chromosome breaks was significatively higher in patients than in controls. These data suggest a general tendency of females with Scleroderma to develop X polisomies and +X and the PCD(X) phenomenon may be considered Scleroderma related in younger patients.


Subject(s)
Chromosome Aberrations/genetics , Lymphocytes/physiology , Scleroderma, Systemic/genetics , Adult , Aged , Case-Control Studies , Female , Humans , Middle Aged , Sex Chromosome Aberrations/genetics , X Chromosome
19.
Rev Soc Bras Med Trop ; 27(3): 171-4, 1994.
Article in Portuguese | MEDLINE | ID: mdl-7972947

ABSTRACT

The protean manifestations of progressive disseminated histoplasmosis in AIDS patients (PDH/AIDS) specially the cutaneous lesions, may confuse the clinician or the pathologist. A case of PDH/AIDS diagnosed by direct and histologic examination and cultures of subcutaneous nodule aspirate and skin biopsy is reported. The requirement of special histologic and cultures procedures is emphasized. Clinical manifestations of the disease are discussed.


Subject(s)
AIDS-Related Opportunistic Infections/complications , Dermatomycoses/complications , Histoplasmosis/complications , Adult , Humans , Male
20.
Cancer Genet Cytogenet ; 74(1): 25-9, 1994 May.
Article in English | MEDLINE | ID: mdl-8194043

ABSTRACT

Metaphases from a cultured cerebral germ cell tumor (CGCT) in a boy with a 46,XY constitutional karyotype had 47 chromosomes with an additional X chromosome and a translocation (1;21)(q11;p11). CGCT appear to be nonrandomly associated with Klinefelter syndrome, and a supernumerary X chromosome and trisomy of the 1q21-->1qter region may be clonal abnormalities in these tumors. The predisposition of Klinefelter patients to develop CGCT may be due to the pathogenetic relevance of the extra X chromosome both as an acquired and a constitutional abnormality.


Subject(s)
Brain Neoplasms/genetics , Chromosome Aberrations , Teratoma/genetics , X Chromosome , Adolescent , Adult , Child , Child, Preschool , Humans , In Vitro Techniques , Karyotyping , Klinefelter Syndrome/genetics , Male , Tumor Cells, Cultured
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