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1.
IDCases ; 20: e00769, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32420028

RESUMO

Although the relationship between paracoccidioidomycosis (PCM) and solid tumors has been described more than 80 years ago, reports of PCM and gastric cancer are rare. PCM can present before or concomitantly with the diagnosis of cancer, and its clinical presentation may rise the suspicion of malignancies or be part of reactivation by immunosuppression. We present the case of a 52-year-old Peruvian man with a signet-ring cell (SRC) gastric adenocarcinoma who after 6 chemotherapy sessions with FLOT (docetaxel, oxaliplatin, leucovorin, 5-fluorouracil) presented rapidly growing lung nodules. The lung biopsy showed yeasts compatible with Paracoccidioides sp., so he received initial treatment with itraconazole and after gastrectomy maintenance therapy with trimethoprim/sulfamethoxazole accompanied by tomographic resolution of lesions.

2.
IDCases ; 20: e00788, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32426232

RESUMO

In all health care settings, particularly those in developing countries, healthcare workers have a high risk for exposure to tuberculosis. Tuberculosis can involve any organ, including the skin. Cutaneous tuberculosis is uncommon and may be secondary to an exogenous inoculation. We report the case of a surgical resident at a tertiary care hospital in Lima, Peru who developed cutaneous inoculation tuberculosis after sustaining a needlestick injury while performing a diagnostic cervical lymph node aspiration from a patient with HIV infection and tuberculous cervical lymphadenopathy.

3.
IDCases ; 19: e00695, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32021799

RESUMO

We report the first case of Myroides phaeus isolated from blood, causing bacteremia in an immunocompromised patient using the automated MicroScan Walk Away 96 system, followed by bacterial identification by amplification-sequencing of the 16S rDNA. The sequences obtained were compared with the reference sequence of the BLAST ® platform - National Library of Medicine, USA, and the isolation was identified as Myroides phaeus strain with 99.67 % identity in Blast report. In the literature we did not find previous reported cases of infections by this bacterium, however its pathogenic role is still controversial; therefore, this isolation alerts us to carry out an exhaustive surveillance of other possible acquisition routes.

4.
J Clin Endocrinol Metab ; 41(5): 833-40, 1975 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-1184720

RESUMO

Gonadal function was studied in three post-pubertal siblings (two male and one female) and one unrelated male patient with myotonic dystrophy. The diagnosis was confirmed in all cases by electromyography and muscle biopsy. Basal levels of plasma immunoreactive LH, FSH, testosterone, and estradiol were measured. Hypothalamic, pituitary, and gonadal reserve and responsiveness were evaluated by clomiphene, LHRH, and HCG tests. Histologic examination of gonadal biopsies was also performed. The results showed that gonadal failure present in the four patients had different characteristics. In the same family, hypothalamic amenorrhea was observed in the female patient, and hypothalamic eunuchoidism and hypergonadotropic hypogonadism with marked tubular and leydig cells failure in the male patients. The non-related male patient had hypergonadotropic hypogonadism with tubular failure but with a compensatory leydig-cell hyperplasia. These data are interpreted as demonstrating different expressivity of the hypogonadism associated with the same inherited muscle disease.


Assuntos
Hipogonadismo/fisiopatologia , Hipotálamo/fisiopatologia , Distrofia Miotônica/fisiopatologia , Hipófise/fisiopatologia , Testículo/fisiopatologia , Adulto , Clomifeno/farmacologia , Estradiol/sangue , Feminino , Hormônio Foliculoestimulante/sangue , Genes Dominantes , Humanos , Hipogonadismo/sangue , Hipogonadismo/genética , Hormônio Luteinizante/sangue , Masculino , Distrofia Miotônica/sangue , Distrofia Miotônica/genética , Linhagem , Progesterona/farmacologia , Testículo/patologia , Testosterona/sangue
5.
J Clin Endocrinol Metab ; 41(5): 946-52, 1975 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-1184725

RESUMO

A 16-yr-old 46 XY individual with a familial incomplete male pseudohermaphroditism closely resembling the syndrome described by Gilbert-Dreyfus et al. was studied. The patient's habitus was masculine despite the presence of a small phallus, pseudo-vaginal perineal hypospadias, bifid scrotum, gynecomastia, and diminished virilization. Blood samples obtained at 20-min intervals were submitted to hormone analysis. Episodic fluctuations of plasma gonadotropins with mean values of LH above the normal male range and FSH within normal limits were observed. Moderately elevated plasma testosterone and increased plasma estradiol also showed episodic oscillations. The administration of LH-releasing hormone resulted in a significative increase of plasma LH and FSH. Testicular biopsy revealed the presence of seminiferous tubules with few spermatogonia and no spermatocytes, and normal sertoli and interstitial cells. Gonadal stimulation with hCG for 4 consecutive days induced a significative increase of plasma testosterone and estradiol. The daily administration of 50 mg of testosterone propionate for 3 days neither depressed the circulating levels of gonadotropins nor modified the pulsatile pattern of gonadotropins release. Administration of testosterone and 5alpha-dihydrotestosterone propionate failed to diminish plasma LH and FSH levels. Testosterone administration for 10 weeks also failed to induce virilization. These results are similar to those observed in patients with testicular feminization syndrome, and the underlying abnormality involves a partial defect of the mechanism of action of testosterone rather than decreased androgen biosynthesis. According to a recently proposed classification this individual corresponds to the type 1 incomplete male pseudohermaphroditism.


Assuntos
Transtornos do Desenvolvimento Sexual/genética , Testosterona/farmacologia , Adolescente , Transtornos do Desenvolvimento Sexual/embriologia , Transtornos do Desenvolvimento Sexual/metabolismo , Humanos , Hipospadia/genética , Masculino , Síndrome , Testículo/embriologia , Testículo/patologia , Testosterona/biossíntese
6.
Obstet Gynecol ; 98(3): 463-5, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11530130

RESUMO

OBJECTIVE: To compare hCG levels, obtained by biologic and immunologic means, in women with normal pregnancies and women with preeclampsia. METHODS: Peripheral blood samples from women in the third trimester with preeclampsia (n = 30) or normal pregnancies (n = 30) were assayed for immunoactive and bioactive hCG (mouse Leydig cell testosterone production assay). RESULTS: Serum bioactive hCG levels tended to be lower than normal, and immunoactive hCG levels tended to be higher in women with preeclampsia, but the differences were not statistically significant. However, the ratio of bioactive to immunoactive hCG was significantly lower than normal for preeclamptic women (0.70 +/- 0.28 vs. 1.15 +/- 0.35 for normotensive pregnant women [mean +/- standard deviation], P <.001). CONCLUSION: The ratio of bioactive to immunoreactive serum hCG is lower among preeclamptic than among normotensive pregnant women.


Assuntos
Gonadotropina Coriônica/sangue , Pré-Eclâmpsia/sangue , Bioensaio , Feminino , Glicosilação , Humanos , Imunoensaio , Gravidez , Terceiro Trimestre da Gravidez
8.
J Bacteriol ; 178(9): 2533-8, 1996 May.
Artigo em Inglês | MEDLINE | ID: mdl-8626319

RESUMO

In Salmonella typhimurium, thiamine is a required nutrient that is synthesized de novo. Labeling studies have demonstrated probable precursors for both the 4-amino-5-hydroxymethyl-2-methylpyrimidine pyrophosphate moiety and the 4-methyl-5-(beta-hydroxyethyl) thiazole monophosphate moiety. The isolation of thiamine auxotrophs with mutations in at least five different genetic loci is reported. The majority (22 of 25) of the mutants required only the thiazole moiety of thiamine to satisfy their growth requirement. Most (14 of 25) of the mutants were affected in the thi cluster at min 90 on the S. typhimurium genetic map. Data provided herein indicate that this cluster encodes an operon whose transcription is regulated by thiamine and suggest that thiamine pyrophosphate, or a molecule derived form it, is the effector molecule. Mutants with altered regulation of this operon were isolated, and we propose that they are defective in thiamine phosphate kinase, the product of the thiL gene.


Assuntos
Regulação Bacteriana da Expressão Gênica/efeitos dos fármacos , Salmonella typhimurium/genética , Tiamina Pirofosfato/farmacologia , Tiamina/biossíntese , Sequência de Aminoácidos , Sequência de Bases , Genes Bacterianos/genética , Modelos Químicos , Dados de Sequência Molecular , Mutagênese Insercional , Óperon/genética , Salmonella typhimurium/metabolismo , Tiamina/farmacologia , Tiamina Monofosfato/farmacologia , Transcrição Gênica/efeitos dos fármacos
9.
Eur J Pediatr ; 145(1-2): 70-2, 1986 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-3089799

RESUMO

To evaluate whether the hypothyroxinaemia, previously noted in hyperbilirubinaemic newborns immediately after exchange transfusion for Rh or AB0 incompatibility, was due to impairment in the secretion of thyroid stimulating hormone (TSH) by the pituitary, we studied the thyroid hormone response to thyrotropin releasing hormone (TRH) and compared this response to that seen in a control population of healthy neonates. All infants studied responded with a brisk TSH increase; 30 min after TRH injection the mean TSH concentration of the hyperbilirubinaemic patients was 37 microU/ml, ten times their basal level, which was not different from the value noted in the control population. No significant change in total thyroxine (T4), 3,5,3' triiodothyronine (T3), free thyroxine (FT4) or 3,3',5' triiodothyronine (rT3), (FT4) or (rT3) was noted after TRH administration in either group of neonates. In addition the effect of exchange transfusion on the thyroid axis of hyperbilirubinaemic newborns was evaluated. Before the exchange transfusion TSH, T4, rT3, T3 and FT4 levels were higher in the hyperbilirubinaemic newborns than in donor blood; immediately post-exchange transfusion TSH and T4 concentrations of the hyperbilirubinaemic neonates decreased significantly and remained significantly below pre-exchange values 30 h later. Newborns undergoing an exchange transfusion respond appropriately to TRH stimulation and seem to have an intact pituitary-thyroidal axis.


Assuntos
Transfusão Total , Icterícia Neonatal/fisiopatologia , Hormônios Tireóideos/sangue , Hormônio Liberador de Tireotropina , Tireotropina/sangue , Humanos , Recém-Nascido , Icterícia Neonatal/sangue , Icterícia Neonatal/terapia , Adeno-Hipófise/fisiopatologia , Glândula Tireoide/fisiopatologia , Tiroxina/sangue , Fatores de Tempo , Tri-Iodotironina/sangue , Tri-Iodotironina Reversa/sangue
10.
Biol Reprod ; 48(6): 1395-403, 1993 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-8318592

RESUMO

A primary cell culture system was developed to study the epidermal growth factor (EGF) receptor in the fetal bovine mesonephros and its urogenital derivatives. Radioreceptor assays demonstrated EGF binding as early as Day 37 in mesonephric cells and in cells derived from the fetal reproductive ducts, gonads, and metanephros--all mesonephric derivatives. Immunocytochemical studies revealed that EGF receptors were localized in the ductal and tubular epithelium of these urogenital organs. EGF induced DNA synthesis and tyrosine phosphorylation in the bovine mesonephric cells, suggesting that EGF receptors detected in these cells were functional. In addition, transforming growth factor alpha, the putative fetal ligand for the EGF receptor, was found to specifically compete for EGF binding to the receptor, as well as to induce DNA synthesis in a manner similar to that of EGF. Estrogen did not regulate EGF receptors or specifically bind to bovine mesonephric cells. The development of estrogen receptors in the bovine species occurs markedly later than that of the EGF receptor, in contrast to the mouse, where both receptors are observed at very early stages of reproductive tract development.


Assuntos
Receptores ErbB/metabolismo , Mesonefro/metabolismo , Sistema Urogenital/embriologia , Animais , Bovinos , Fator de Crescimento Epidérmico/metabolismo , Feminino , Imuno-Histoquímica , Masculino , Mesonefro/química , Proteínas Tirosina Quinases/metabolismo , Ensaio Radioligante , Distribuição Tecidual , Sistema Urogenital/metabolismo
12.
Rev. obstet. ginecol. Venezuela ; 43(3): 139-44, 1983.
Artigo em Espanhol | LILACS | ID: lil-19783

RESUMO

En este trabajo se hace una actualizacion del hirsutismo y se propone de acuerdo a las modalidades fisiopatologicas expuestas un tratamiento racional y orientado a solventar este problema. A pesar de ello, en muchos casos estas variedades de tratamiento son desalentadoras por no poder lograr los resultados deseados


Assuntos
Humanos , Feminino , Espironolactona , Corticosteroides , Anticoncepcionais Orais , Hirsutismo , Síndrome do Ovário Policístico
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