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1.
J Dtsch Dermatol Ges ; 1(10): 785-9, 2003 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16281814

RESUMO

BACKGROUND: A standard therapy for advanced cutaneous T-cell lymphomas has not yet been defined. Bexarotene is a new retinoid x receptor-specific retinoid that has been approved for systemic second-line therapy for cutaneous T-cell lymphomas in the USA and Europe. In order to evaluate the efficacy of bexarotene in cutaneous T-cell lymphomas, a pilot trial was initiated. PATIENTS AND METHODS: In a pilot project 10 patients with advanced cutaneous T-cell lymphomas, who had received a variety of previous treatments, were treated with bexarotene at the departments of dermatology in Münster, Minden and Charité Berlin, Germany. The patients received bexarotene at a dose of 300 mg/m2 body surface daily. According to the percentage of tumour reduction and affected body surface, the response rates were divided in complete and partial remission, stable disease and progressive disease. Laboratory parameters i.e. cholesterol, triglycerides transaminases, T3, T4, and TSH were screened regularly. RESULTS: In 2 patients a short partial remission was achieved; however, after a few weeks progression followed. In 4 patients a lasting stabilisation was obtained. The other 4 patients showed a progressive disease during therapy. 6 patients developed hypertriglyceridemia with levels up to 2000 mg/dl; therapy had to be suspended in 3 patients because of these adverse drug events. CONCLUSION: Weighing benefits and risks, bexarotene can at present not be recommended as standard therapy in the treatment of patients with progressive cutaneous lymphomas.


Assuntos
Anticarcinógenos/uso terapêutico , Linfoma Cutâneo de Células T/tratamento farmacológico , Neoplasias Cutâneas/tratamento farmacológico , Tetra-Hidronaftalenos/uso terapêutico , Adulto , Idoso , Aminoquinolinas/uso terapêutico , Anticarcinógenos/administração & dosagem , Anticarcinógenos/efeitos adversos , Antineoplásicos , Protocolos de Quimioterapia Combinada Antineoplásica , Bexaroteno , Terapia Combinada , Ciclofosfamida , Progressão da Doença , Doxorrubicina , Feminino , Humanos , Imiquimode , Imunossupressores/uso terapêutico , Interferons/uso terapêutico , Linfoma Cutâneo de Células T/patologia , Linfoma Cutâneo de Células T/radioterapia , Masculino , Pessoa de Meia-Idade , Estadiamento de Neoplasias , Terapia PUVA , Projetos Piloto , Prednisona , Indução de Remissão , Pele/patologia , Neoplasias Cutâneas/patologia , Neoplasias Cutâneas/radioterapia , Tacrolimo/uso terapêutico , Tetra-Hidronaftalenos/administração & dosagem , Tetra-Hidronaftalenos/efeitos adversos , Fatores de Tempo , Resultado do Tratamento , Vincristina
2.
Hautarzt ; 53(11): 744-8, 2002 Nov.
Artigo em Alemão | MEDLINE | ID: mdl-12402138

RESUMO

Immunosuppressive and immune-modulating substances such as corticosteroids, chloroquin, hydroxychloroquin, azathioprin, methotrexate, and others are standards in therapy of cutaneous lupus erythematosus. However, alternative substances are necessary when standard therapy regimens fail or are associated with side effects. Describing the course of disease in five female patients, we demonstrate alternative treatment of subacute cutaneous lupus erythematosus with thalidomide, showing good symptom response and possible side effects. By careful patient selection, we observed no polyneuropathy as it is most commonly described. In two cases, maculopapulous exanthema induced by medication was seen. The teratogeny of the substance must be taken into account in prescription. In selected cases, thalidomide can be a highly effective therapeutic option in the treatment of subacute cutaneous lupus erythematosus.


Assuntos
Lúpus Eritematoso Cutâneo/tratamento farmacológico , Talidomida/uso terapêutico , Adulto , Toxidermias/etiologia , Quimioterapia Combinada , Feminino , Humanos , Imunossupressores/efeitos adversos , Imunossupressores/uso terapêutico , Testes Intradérmicos , Pessoa de Meia-Idade , Testes do Emplastro , Prednisolona/administração & dosagem , Prednisolona/efeitos adversos , Talidomida/efeitos adversos
3.
Ultraschall Med ; 20(3): 104-9, 1999 Jun.
Artigo em Alemão | MEDLINE | ID: mdl-10444780

RESUMO

PURPOSE: Eleven dermatology clinics from all over Germany took part in our multicenter prospective study with the aim of evaluating 20 MHz sonography in the preoperative diagnosis of malignant melanomas and other pigmented skin tumours. It was to be assessed how effective sonographic measurement of thickness would compare to histology and the clinical palpation of tumour thickness and also the significance of differential diagnosis in sonography of malignant melanomas. METHOD: The prospective multicenter study proceed as follows. To the end of August 1997 264 patients with a primary malignant melanoma and 417 patients with benign skin tumours were examined via 20 MHz sonography. Two different examiners estimated the clinical thickness of the tumour by palpation. The tumour was then excised and examined for postoperative correlation with the histology sections. RESULTS: The final results showed good correlation between the histological and sonographic estimation of tumour thickness (r = 0.97). Estimation of tumour thickness by palpation showed no correlation with the histology (r = 0.59). Most of the benign (44%) and malignant tumours (38.7%) were spindle shaped. There was no significant difference between the benign and malignant tumour groups in relation to the sonographic presented shapes or echo signs. No different diagnosis could be made. CONCLUSION: The technique of high frequency sonography in relation to preoperative diagnosis of malignant melanomas has high priority. In contrast to clinical estimation of tumour thickness, sonography provided a good correlation to histology. The effectiveness of sonography with regard to the valence of the skin tumours is limited and there is no possibility of differentiating between malignant and benign tumours from the morphological face value. Hence, there is a demand for developing a 150 MHz apparatus which will be able to supply evidence regarding the valence of skin tumours.


Assuntos
Melanoma/diagnóstico por imagem , Nevo Pigmentado/diagnóstico por imagem , Neoplasias Cutâneas/diagnóstico por imagem , Ultrassonografia/métodos , Testes Diagnósticos de Rotina , Alemanha , Humanos , Melanoma/patologia , Estadiamento de Neoplasias , Nevo Pigmentado/patologia , Variações Dependentes do Observador , Palpação , Estudos Prospectivos , Análise de Regressão , Neoplasias Cutâneas/patologia
4.
Hautarzt ; 47(2): 106-8, 1996 Feb.
Artigo em Alemão | MEDLINE | ID: mdl-8868453

RESUMO

In spite of its high incidence, not much is known about the etiology of chronic urticaria. We performed gastroscopic evaluation of 10 patients in whom no cause for chronic urticaria had been found. In 8 of these 10 patients, Helicobacter pylori was identified in the gastric mucosa. The chronic urticarial lesions disappeared within a few days after starting therapy with amoxicillin and omeprazol.


Assuntos
Gastrite/complicações , Infecções por Helicobacter/complicações , Helicobacter pylori , Urticária/etiologia , Adulto , Amoxicilina/uso terapêutico , Doença Crônica , Quimioterapia Combinada , Feminino , Gastrite/diagnóstico , Gastrite/tratamento farmacológico , Infecções por Helicobacter/diagnóstico , Infecções por Helicobacter/tratamento farmacológico , Helicobacter pylori/efeitos dos fármacos , Humanos , Masculino , Pessoa de Meia-Idade , Omeprazol/uso terapêutico , Antro Pilórico , Urticária/tratamento farmacológico
5.
Hautarzt ; 47(1): 24-8, 1996 Jan.
Artigo em Alemão | MEDLINE | ID: mdl-8835000

RESUMO

Sézary syndrome is the leukemic and erythrodemic form of cutaneous T-cell lymphoma (CTCL). Since 1987 extracorporeal photochemotherapy (ECP) has been available for treatment of erythrodermic CTCL in the USA. Through a group of case reports, we want to emphasize ECP as the treatment of choice for erythrodermic CTCL.


Assuntos
Fotoquimioterapia , Síndrome de Sézary/tratamento farmacológico , Biópsia , Feminino , Seguimentos , Humanos , Masculino , Síndrome de Sézary/diagnóstico , Síndrome de Sézary/patologia , Pele/patologia , Resultado do Tratamento
6.
Clin Endocrinol (Oxf) ; 40(3): 341-9, 1994 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-7514512

RESUMO

OBJECTIVE: The potential use of testosterone preparations for substitution therapy for ageing men and for male contraception, in addition to the well established substitution therapy of male hypogonadism, make increased testosterone use likely. However, little clinical information is available on the effect of testosterone therapy on the prostate in hypogonadal men. DESIGN AND MEASUREMENTS: In a controlled cross-sectional study, prostate volume measured by transrectal ultrasonography, serum levels of prostate-specific antigen (PSA) and sex hormones, and uroflow parameters were determined. PATIENTS: Three groups of age-matched men were enrolled in the study: 47 newly diagnosed hypogonadal men before testosterone treatment, 78 hypogonadal men with at least 6 months of effective testosterone therapy and 75 normal men. RESULTS: Regression analysis revealed a significant positive correlation of prostate volume with age in normal men and testosterone-treated hypogonadal men, whereas no significant correlation was detected in untreated hypogonadal men. Prostate volume was significantly lower in untreated hypogonadal men (12.2 (11.0-13.5) ml) (mean (95% confidence limits)) compared to both other groups. However, no significant difference in prostate volume was detected between testosterone-treated hypogonadal men (21.3 (19.9-22.8) ml) and normal men (22.9 (21.4-24.4) ml). Similar results were obtained for PSA with comparable values in the testosterone-treated hypogonadal men (0.98 (0.88-1.10) micrograms/l) and normal men (1.02(0.91-1.14) micrograms/l), and significantly lower concentrations in the untreated hypogonadal men (0.64 (0.55-0.73) micrograms/l). No differences in uroflow parameters were detected between the three study groups. CONCLUSIONS: Effective testosterone treatment of hypogonadal men results in prostate volume and prostate-specific antigen levels comparable to age-matched normal men. Therefore, testosterone-induced prostate growth should not preclude hypogonadal men from testosterone substitution therapy.


Assuntos
Hipogonadismo/tratamento farmacológico , Próstata/efeitos dos fármacos , Testosterona/farmacologia , Adulto , Fatores Etários , Envelhecimento/sangue , Antropometria , Estudos Transversais , Humanos , Hipogonadismo/sangue , Masculino , Próstata/patologia , Antígeno Prostático Específico/sangue , Valores de Referência , Testosterona/administração & dosagem , Testosterona/sangue , Testosterona/uso terapêutico
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