RESUMEN
This consensus document analyzed the management and emotional journey of patients with GPP (generalized pustular psoriasis), and the desirable course of the disease while detecting critical points and translating them into needs and recommendations. This project was conducted in 3 phases with participation from an advisory committee (n=8), an expert panel (n=15) and patients with GPP (n=6). The patients' disease progression was heterogeneous due to disease variations, different health care models implemented and available resources, and the lack of diagnostic and treatment guidelines. A total of 45 different recommendations have been made to optimize management and address the emotional component of these patients. Five of them stand out for their impact and viability. Therefore, a roadmap of priorities has been made generally available to improve the management of patients with GPP.
RESUMEN
This consensus document analyzed the management and emotional journey of patients with GPP (generalized pustular psoriasis), and the desirable course of the disease while detecting critical points and translating them into needs and recommendations. This project was conducted in 3 phases with participation from an advisory committee (n=8), an expert panel (n=15) and patients with GPP (n=6). The patients' disease progression was heterogeneous due to disease variations, different health care models implemented and available resources, and the lack of diagnostic and treatment guidelines. A total of 45 different recommendations have been made to optimize management and address the emotional component of these patients. Five of them stand out for their impact and viability. Therefore, a roadmap of priorities has been made generally available to improve the management of patients with GPP.
RESUMEN
BACKGROUND: Prediction of the response to a biological treatment in psoriasis patients would allow efficient treatment allocation. OBJECTIVE: To identify polymorphisms associated with secukinumab response in psoriasis patients in a daily practice setting. METHODS: We studied 180 SNPs in patients with moderate-to-severe plaque psoriasis recruited from 15 Spanish hospitals. Treatment effectiveness was evaluated by absolute PASI ≤3 and ≤1 at 6 and 12 months. Individuals were genotyped using a custom Taqman array. Multiple logistic regression models were generated. Sensitivity, specificity and area under the curve (AUC) were analysed. RESULTS: A total of 173 patients were studied at 6 months, (67% achieved absolute PASI ≤ 3 and 65% PASI ≤ 1) and 162 at 12 months (75% achieved absolute PASI ≤ 3 and 64% PASI ≤ 1). Multivariable analysis showed the association of different sets of SNPs with the response to secukinumab. The model of absolute PASI≤3 at 6 months showed best values of sensitivity and specificity. Four SNPs were associated with the capability of achieving absolute PASI ≤ 3 at 6 months. rs1801274 (FCGR2A), rs2431697 (miR-146a) and rs10484554 (HLCw6) were identified as risk factors for failure to achieve absolute PASI≤3, while rs1051738 (PDE4A) was protective. AUC including these genotypes, weight of patients and history of biological therapy was 0.88 (95% CI 0.83-0.94), with a sensitivity of 48.6% and specificity of 95.7% to discriminate between both phenotypes. CONCLUSION: We have identified a series of polymorphisms associated with the response to secukinumab capable of predicting the potential response/non-response to this drug in patients with plaque psoriasis.
Asunto(s)
Anticuerpos Monoclonales Humanizados , Polimorfismo de Nucleótido Simple , Psoriasis , Humanos , Psoriasis/tratamiento farmacológico , Psoriasis/genética , Femenino , Masculino , Anticuerpos Monoclonales Humanizados/uso terapéutico , Persona de Mediana Edad , Adulto , Fármacos Dermatológicos/uso terapéutico , MicroARNs/genética , Índice de Severidad de la Enfermedad , Resultado del TratamientoRESUMEN
En el presente artículo, en base a una revisión de la literatura y su experiencia personal, un equipo multidisciplinar de 14 profesionales sanitarios (incluyendo dermatólogos, reumatólogos, neurólogos, gastroenterólogos, farmacéuticos y enfermeras) ha elaborado una serie de recomendaciones generales y específicas (basadas en la fisiopatología) para el manejo de los efectos adversos secundarios a apremilast que con mayor frecuencia conducen a la suspensión del tratamiento (diarrea, náuseas y cefalea). Se aportan algoritmos sencillos de manejo que incluyen aspectos clínicos de evaluación y sugerencias de tratamiento farmacológico. Los efectos adversos de apremilast pueden ser abordados desde un punto de vista multidisciplinar y la optimización en su manejo pretende proporcionar un beneficio clínico a los pacientes que los sufren
We present a series of general and specific recommendations based on pathophysiologic considerations for managing the most common adverse effects of apremilast that lead to treatment discontinuation: diarrhea, nausea, and headache. The recommendations are based on a review of the literature and the experience of a multidisciplinary team of 14 experts including dermatologists, rheumatologists, neurologists, gastroenterologists, pharmacists, and nurses. We propose a series of simple algorithms that include clinical actions and suggestions for pharmacologic treatment. The adverse effects of apremilast can be managed from a multidisciplinary approach. The purpose of optimizing management is to bring clinical benefits to patients
Asunto(s)
Humanos , Guías de Práctica Clínica como Asunto , Talidomida/análogos & derivados , Inhibidores de Fosfodiesterasa 4/efectos adversos , Cefalea/terapia , Diarrea/terapia , Náusea/terapia , Manejo de la Enfermedad , Cefalea/inducido químicamente , Diarrea/inducido químicamente , Náusea/inducido químicamente , Algoritmos , Grupo de Atención al PacienteRESUMEN
We present a series of general and specific recommendations based on pathophysiologic considerations for managing the most common adverse effects of apremilast that lead to treatment discontinuation: diarrhea, nausea, and headache. The recommendations are based on a review of the literature and the experience of a multidisciplinary team of 14 experts including dermatologists, rheumatologists, neurologists, gastroenterologists, pharmacists, and nurses. We propose a series of simple algorithms that include clinical actions and suggestions for pharmacologic treatment. The adverse effects of apremilast can be managed from a multidisciplinary approach. The purpose of optimizing management is to bring clinical benefits to patients.
Asunto(s)
Diarrea/inducido químicamente , Cefalea/inducido químicamente , Náusea/inducido químicamente , Inhibidores de Fosfodiesterasa 4/efectos adversos , Talidomida/análogos & derivados , Terapia Combinada , Diarrea/dietoterapia , Diarrea/tratamiento farmacológico , Diarrea/fisiopatología , Manejo de la Enfermedad , Cefalea/tratamiento farmacológico , Cefalea/fisiopatología , Cefalea/prevención & control , Humanos , Náusea/dietoterapia , Náusea/tratamiento farmacológico , Náusea/fisiopatología , Grupo de Atención al Paciente , Inhibidores de Fosfodiesterasa 4/uso terapéutico , Guías de Práctica Clínica como Asunto , Psoriasis/tratamiento farmacológico , Talidomida/efectos adversos , Talidomida/uso terapéuticoAsunto(s)
Betacoronavirus/patogenicidad , Infecciones por Coronavirus/complicaciones , Livedo Reticularis/diagnóstico , Neumonía Viral/complicaciones , Trombosis/diagnóstico , Biopsia , COVID-19 , Infecciones por Coronavirus/inmunología , Infecciones por Coronavirus/virología , Pie , Humanos , Livedo Reticularis/etiología , Livedo Reticularis/patología , Masculino , Persona de Mediana Edad , Pandemias , Neumonía Viral/inmunología , Neumonía Viral/virología , SARS-CoV-2 , Piel/patología , Trombosis/etiología , Trombosis/patologíaRESUMEN
INTRODUCCIÓN Y OBJETIVOS: La utilización clínica habitual de los fármacos biológicos en el tratamiento de la psoriasis es en segunda línea, es decir, tras el uso previo de un fármaco clásico. Sin embargo, en casos particulares -particularidades del paciente o criterio médico- se realiza la indicación en primera línea. No existen estudios sobre las características demográficas, clínicas y de seguridad de los pacientes que reciben fármaco biológico en primera línea. Como objetivo primario se pretende determinar dichas características de acuerdo con la iniciación de la terapia biológica en primera o segunda línea. MATERIAL Y MÉTODO: Se realizó un estudio descriptivo, multicéntrico, de 181 pacientes que iniciaron tratamiento biológico como primer fármaco sistémico para control de su psoriasis moderada-grave, y que forman parte del Registro Español de Acontecimientos Adversos Asociados con Medicamentos Biológicos en Dermatología, entre enero de 2008 y noviembre de 2016. RESULTADOS: Los pacientes de ambos grupos son muy similares, si bien se evidencia que el grupo que recibe el biológico en primera línea presenta una edad más avanzada, sin que se justifique por gravedad de la enfermedad (PASI) ni por el tiempo de evolución de esta desde el diagnóstico. En este grupo de pacientes es más frecuente la presencia de hipertensión, diabetes y hepatopatía. No hemos encontrado diferencias en motivos de suspensión ni seguridad entre ambos grupos. CONCLUSIONES: No se han encontrado diferencias relevantes entre los 2 grupos, lo cual refuerza la seguridad de los fármacos biológicos en este contexto
INTRODUCTION AND OBJECTIVES: Biologic drugs are usually prescribed as second-line treatment for psoriasis, that is, after the patient has first been treated with a conventional psoriasis drug. There are, however, cases where, depending on the characteristics of the patient or the judgement of the physician, biologics may be chosen as first-line therapy. No studies to date have analyzed the demographics or clinical characteristics of patients in this setting or the safety profile of the agents used. The main aim of this study was to characterize these aspects of first-line biologic therapy and compare them to those observed for patients receiving biologics as second-line therapy. MATERIAL AND METHOD: We conducted an observational study of 181 patients treated in various centers with a systemic biologic drug as first-line treatment for moderate to severe psoriasis between January 2008 and November 2016. All the patients were registered in the Spanish Registry of Adverse Events Associated with Biologic Drugs in Dermatology. RESULTS: The characteristics of the first- and second-line groups were very similar, although the patients receiving a biologic as first-line treatment for their psoriasis were older. No differences were observed for disease severity (assessed using the PASI) or time to diagnosis. Hypertension, diabetes, and liver disease were all more common in the first-line group. There were no differences between the groups in terms of reasons for drug withdrawal or occurrence of adverse effects. CONCLUSIONS: No major differences were found between patients with psoriasis receiving biologic drugs as first- or second-line therapy, a finding that provides further evidence of the safety of biologic therapy in patients with psoriasis
Asunto(s)
Humanos , Masculino , Femenino , Adulto , Persona de Mediana Edad , Anciano , Productos Biológicos/uso terapéutico , Inmunosupresores/uso terapéutico , Psoriasis/tratamiento farmacológico , Sistema de Registros , Anticuerpos Monoclonales/uso terapéutico , Distribución por Edad , Anticuerpos Monoclonales/efectos adversos , Productos Biológicos/efectos adversos , Comorbilidad , Sustitución de Medicamentos , Utilización de Medicamentos , Inmunosupresores/efectos adversos , Psoriasis/epidemiología , España/epidemiología , Factor de Necrosis Tumoral alfa/antagonistas & inhibidoresRESUMEN
INTRODUCTION AND OBJECTIVES: Biologic drugs are usually prescribed as second-line treatment for psoriasis, that is, after the patient has first been treated with a conventional psoriasis drug. There are, however, cases where, depending on the characteristics of the patient or the judgement of the physician, biologics may be chosen as first-line therapy. No studies to date have analyzed the demographics or clinical characteristics of patients in this setting or the safety profile of the agents used. The main aim of this study was to characterize these aspects of first-line biologic therapy and compare them to those observed for patients receiving biologics as second-line therapy. MATERIAL AND METHOD: We conducted an observational study of 181 patients treated in various centers with a systemic biologic drug as first-line treatment for moderate to severe psoriasis between January 2008 and November 2016. All the patients were registered in the Spanish Registry of Adverse Events Associated with Biologic Drugs in Dermatology. RESULTS: The characteristics of the first- and second-line groups were very similar, although the patients receiving a biologic as first-line treatment for their psoriasis were older. No differences were observed for disease severity (assessed using the PASI) or time to diagnosis. Hypertension, diabetes, and liver disease were all more common in the first-line group. There were no differences between the groups in terms of reasons for drug withdrawal or occurrence of adverse effects. CONCLUSIONS: No major differences were found between patients with psoriasis receiving biologic drugs as first- or second-line therapy, a finding that provides further evidence of the safety of biologic therapy in patients with psoriasis.
Asunto(s)
Productos Biológicos/uso terapéutico , Inmunosupresores/uso terapéutico , Psoriasis/tratamiento farmacológico , Sistema de Registros , Adulto , Distribución por Edad , Anciano , Anticuerpos Monoclonales/efectos adversos , Anticuerpos Monoclonales/uso terapéutico , Productos Biológicos/efectos adversos , Comorbilidad , Sustitución de Medicamentos , Utilización de Medicamentos , Femenino , Humanos , Inmunosupresores/efectos adversos , Masculino , Persona de Mediana Edad , Psoriasis/epidemiología , España/epidemiología , Factor de Necrosis Tumoral alfa/antagonistas & inhibidoresRESUMEN
El término de psoriasis en localizaciones de difícil tratamiento se emplea para hacer referencia a la psoriasis localizada en el cuero cabelludo, las uñas, las palmas y las plantas y que requiere un manejo diferenciado. A menudo los pacientes presentan un importante impacto físico y emocional, unido a la dificultad para controlar adecuadamente sus lesiones con tratamientos tópicos, debido a una insuficiente penetración de los principios activos y la escasa cosmeticidad de los vehículos empleados. Esta circunstancia justifica que la psoriasis en estas localizaciones pueda ser considerada grave, a pesar de su extensión limitada. La experiencia con terapias biológicas en estas localizaciones es escasa, en general en el contexto de ensayos clínicos de formas extensas de psoriasis moderada y grave, junto con series limitadas o casos aislados. En el presente artículo se presenta la calidad de la evidencia científica para los 4 agentes biológicos disponibles en España (infliximab, etanercept, adalimumab y ustekinumab) siendo de nivel i en el caso de la psoriasis ungueal (nivel de recomendación A) y algo inferior en la psoriasis del cuero cabelludo y palmoplantar
Psoriatic lesions affecting the scalp, nails, palms, and the soles of the feet are described as difficult-to-treat psoriasis and require specific management. Involvement of these sites often has a significant physical and emotional impact on the patient and the lesions are difficult to control with topical treatments owing to inadequate penetration of active ingredients and the poor cosmetic characteristics of the vehicles used. Consequently, when difficult-to-treat sites are involved, psoriasis can be considered severe even though the lesions are not extensive. Scant information is available about the use of biologic therapy in this setting, and published data generally comes from clinical trials of patients who also had moderate to severe extensive lesions or from small case series and isolated case reports. In this article we review the quality of the scientific evidence for the 4 biologic agents currently available in Spain (infliximab, etanercept, adalimumab, and ustekinumab) and report level i evidence for the use of biologics to treat nail psoriasis (level of recommendation A) and a somewhat lower level of evidence in the case of scalp involvement and palmoplantar psoriasis
Asunto(s)
Humanos , Psoriasis/tratamiento farmacológico , Terapia Biológica/métodos , Pautas de la Práctica en Medicina , Medicina Basada en la Evidencia/tendencias , Enfermedades de la Uña/tratamiento farmacológico , Dermatosis del Cuero Cabelludo/tratamiento farmacológicoRESUMEN
Psoriatic lesions affecting the scalp, nails, palms, and the soles of the feet are described as difficult-to-treat psoriasis and require specific management. Involvement of these sites often has a significant physical and emotional impact on the patient and the lesions are difficult to control with topical treatments owing to inadequate penetration of active ingredients and the poor cosmetic characteristics of the vehicles used. Consequently, when difficult-to-treat sites are involved, psoriasis can be considered severe even though the lesions are not extensive. Scant information is available about the use of biologic therapy in this setting, and published data generally comes from clinical trials of patients who also had moderate to severe extensive lesions or from small case series and isolated case reports. In this article we review the quality of the scientific evidence for the 4 biologic agents currently available in Spain (infliximab, etanercept, adalimumab, and ustekinumab) and report level i evidence for the use of biologics to treat nail psoriasis (level of recommendation A) and a somewhat lower level of evidence in the case of scalp involvement and palmoplantar psoriasis.
Asunto(s)
Factores Biológicos/uso terapéutico , Dermatosis del Pie/tratamiento farmacológico , Dermatosis de la Mano/tratamiento farmacológico , Enfermedades de la Uña/tratamiento farmacológico , Psoriasis/tratamiento farmacológico , Dermatosis del Cuero Cabelludo/tratamiento farmacológico , Terapia Biológica , Medicina Basada en la Evidencia , HumanosRESUMEN
Introducción y objetivos: La dermatitis atópica (DA) puede afectar tanto a niños como a adultos. Su principal síntoma es el prurito, afectando la calidad de vida relacionada con la salud (CVRS) de los pacientes. El presente manuscrito pretende evaluar el impacto de la DA en la vida de los pacientes, tanto pediátricos como adultos. Pacientes y métodos: Estudio epidemiológico, prospectivo, multicéntrico, en consultas de Dermatología. Se seleccionaron pacientes pediátricos (2-17 años) y adultos (≥18 años) con DA de más de un año de evolución, sin otra patología inflamatoria crónica dermatológica. Se recogieron variables sociodemográficas, clínicas de la DA y centradas en el paciente (cuestionarios Itch Severity Scale [ISS] y Children's Dermatology Life Quality Index [cDLQI] o Dermatology Life Quality Index [DLQI]). Resultados: Se incluyeron 151 pacientes pediátricos y 172 pacientes adultos. Los pediátricos tenían una edad media (DE) de 9,4 (4,5) años y el 51,7% eran niños; los adultos tenían una edad media (DE) de 32,3 (13,4) años y el 58,7% eran mujeres. Entre los pediátricos la puntuación del ISS aumenta con la gravedad (p<0,05); el 79% presentaban dificultad para conciliar el sueño. En adultos la frecuencia e intensidad del prurito fue superior, presentando más diferencias según la gravedad (p<0,05); el 87,1% presentaba dificultades para conciliar el sueño. En ambas poblaciones se observaron diferencias en la puntuación global y por dimensiones del DLQI/cDLQI según la gravedad de la enfermedad. Conclusiones: La DA afecta la CVRS de los pacientes, tanto pediátricos como adultos, correlacionándose con la presencia e intensidad del prurito (AU)
Background and objectives: Atopic dermatitis (AD) affects both children and adults. The main symptom of this disease is pruritus, which impacts health-related quality of life (HRQOL). The aim of this study was to evaluate the impact of AD on the lives of children and adults with this disease. Patients and methods: This was a multicenter prospective epidemiological study of children (2-17 years) and adults (≥18 years) with AD selected from dermatology offices in Spain. The patients had all had AD for at least a year and had no other chronic inflammatory skin diseases. In addition to sociodemographic information, the data collected included the clinical features of AD and the results of patient-centered questionnaires: the Itch Severity Scale (ISS), the Dermatology Life Quality Index (DLQI), and the childrens version of this questionnaire (cDLQI). Results: We studied 151 children and 172 adults. The mean (SD) age of the children was 9.4 (4.5) years and 51.7% were boys. In the case of adults, the mean age was 32.3 (13.4) years and 58.7% were women. Among the children, the ISS score increased with disease severity and in the adults, both the frequency and intensity of pruritus increased with disease severity (P <0 .05 in both cases); 79%of the children and 87.1% of the adults reported difficulty sleeping. In both populations, overall and subscale DLQI and cDLQI scores varied according to disease severity. Conclusions: AD affects HRQOL in both children and adults and its impact is correlated with the presence and intensity of pruritus (AU)
Asunto(s)
Humanos , Masculino , Femenino , Niño , Adulto , Dermatitis Atópica/epidemiología , Índice de Severidad de la Enfermedad , Prurito/epidemiología , Calidad de VidaRESUMEN
BACKGROUND AND OBJECTIVES: Atopic dermatitis (AD) affects both children and adults. The main symptom of this disease is pruritus, which impacts health-related quality of life (HRQOL). The aim of this study was to evaluate the impact of AD on the lives of children and adults with this disease. PATIENTS AND METHODS: This was a multicenter prospective epidemiological study of children (2-17 years) and adults (≥ 18 years) with AD selected from dermatology offices in Spain. The patients had all had AD for at least a year and had no other chronic inflammatory skin diseases. In addition to sociodemographic information, the data collected included the clinical features of AD and the results of patient-centered questionnaires: the Itch Severity Scale (ISS), the Dermatology Life Quality Index (DLQI), and the children's version of this questionnaire (cDLQI). RESULTS: We studied 151 children and 172 adults. The mean (SD) age of the children was 9.4 (4.5) years and 51.7% were boys. In the case of adults, the mean age was 32.3 (13.4) years and 58.7% were women. Among the children, the ISS score increased with disease severity and in the adults, both the frequency and intensity of pruritus increased with disease severity (P<.05 in both cases); 79% of the children and 87.1% of the adults reported difficulty sleeping. In both populations, overall and subscale DLQI and cDLQI scores varied according to disease severity. CONCLUSIONS: AD affects HRQOL in both children and adults and its impact is correlated with the presence and intensity of pruritus.
Asunto(s)
Dermatitis Atópica , Calidad de Vida , Adolescente , Adulto , Niño , Preescolar , Dermatitis Atópica/complicaciones , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Prurito/etiología , Índice de Severidad de la Enfermedad , España , Encuestas y Cuestionarios , Adulto JovenAsunto(s)
Aminoquinolinas/administración & dosificación , Antineoplásicos/administración & dosificación , Carcinoma Basocelular/tratamiento farmacológico , Neoplasias Inducidas por Radiación/tratamiento farmacológico , Neoplasias Cutáneas/tratamiento farmacológico , Administración Tópica , Anciano , Femenino , Humanos , Imiquimod , Resultado del TratamientoRESUMEN
No disponible
No disponible
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Humanos , Publicaciones Periódicas como Asunto/historia , Dermatología/historia , 50088 , Aniversarios y Eventos EspecialesRESUMEN
There is great interindividual variability in the response to drugs, both in effectiveness and toxicity. Different patients respond differently to the same medication as a consequence of genetic and non-genetic factors. Pharmacogenetics represents the study of the individual pharmacological response based on the genotype. Its objective is to optimize treatment in an individual basis, thereby creating an individualized therapy, more safe and efficient, that will allow the clinician to select the correct drug, at the adequate dose, for the right patient. In the first part of this review we discuss several aspects of the relationship between genetics and therapeutic response, as well as the concept, history, objectives and different areas of study of pharmacogenetics.
Asunto(s)
Farmacogenética , Bibliometría , Biotransformación/genética , Proteínas Portadoras/genética , Proteínas Portadoras/metabolismo , Enzimas/genética , Enzimas/metabolismo , Variación Genética , Genotipo , Historia del Siglo XX , Historia del Siglo XXI , Historia Antigua , Proyecto Genoma Humano , Humanos , Farmacogenética/historia , Receptores de Droga/genética , Receptores de Droga/metabolismoRESUMEN
Existe una gran variabilidad interindividual en la respuesta a los medicamentos, tanto en lo referente a la efectividad como a la toxicidad, de forma que diferentes pacientes responden de forma dispar a la misma medicación. Esto es debido a factores genéticos y no genéticos. La farmacogenética es el estudio de la respuesta farmacológica del individuo según el genotipo. Su objetivo es optimizar el tratamiento a nivel individual, ir a una terapia personalizada más segura y eficiente que permita al clínico seleccionar el fármaco correcto, a la dosis adecuada, para el paciente indicado. En la primera parte de esta revisión se analizan diferentes aspectos de la relación entre genética y respuesta terapéutica, así como el concepto, historia, objetivos y las diferentes áreas de estudio de la farmacogenética
There is great interindividual variability in the response to drugs, both in effectiveness and toxicity. Different patients respond differently to the same medication as a consequence of genetic and non-genetic factors. Pharmacogenetics represents the study of the individual pharmacological response based on the genotype. Its objective is to optimize treatment in an individual basis, thereby creating an individualized therapy, more safe and efficient, that will allow the clinician to select the correct drug, at the adequate dose, for the right patient. In the first part of this review we discuss several aspects of the relationship between genetics and therapeutic response, as well as the concept, history, objectives and different areas of study of pharmacogenetics
Asunto(s)
Farmacogenética/historia , Farmacogenética/métodos , Farmacogenética/tendencias , Genética/clasificación , Genética/historia , ADN/análisis , ADN/síntesis química , ADN/farmacología , ADN/química , ADN/farmacocinéticaAsunto(s)
Enfermedad de Hodgkin/complicaciones , Enfermedades de la Piel/patología , Piel/patología , Proteínas de la Matriz Viral/análisis , Adulto , Complejo CD3/análisis , Infecciones por Virus de Epstein-Barr/complicaciones , Infecciones por VIH/complicaciones , Humanos , Inmunohistoquímica , Antígenos Comunes de Leucocito/análisis , Leucosialina/análisis , Ganglios Linfáticos/química , Ganglios Linfáticos/patología , Masculino , Piel/química , Enfermedades de la Piel/metabolismoAsunto(s)
Mucinas/metabolismo , Enfermedades del Pene/patología , Pene/patología , Administración Oral , Administración Tópica , Glucocorticoides/administración & dosificación , Glucocorticoides/uso terapéutico , Humanos , Masculino , Metaplasia/patología , Persona de Mediana Edad , Enfermedades del Pene/tratamiento farmacológico , Enfermedades del Pene/metabolismo , Pene/metabolismo , Resultado del TratamientoRESUMEN
Leucocyte infusion from the marrow donor is a new therapeutic option to avoid repeated bone marrow transplants in patients with recurrent leukaemia. The treatment is based on the fact that alloreactive donor immune cells may recognize and eliminate residual leukaemia cells. This phenomenon has been called graft-versus-leukaemia. We describe a patient who received donor leucocyte infusion for a relapsed chronic myeloid leukaemia after his second bone marrow transplant and developed sclerodermatous graft-versus-host disease.