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1.
Colomb. med ; 49(4): 288-291, Oct.-Dec. 2018. graf
Article in English | LILACS | ID: biblio-984310

ABSTRACT

Abstract Introduction: Calciphylaxis is an infrequent disease that almost exclusively affects patients with chronic kidney disease, although cases have been observed in patients without renal function impairment. The diagnosis is mainly made by clinical manifestations and subsequently confirmed by radiological and histological study. The optimal treatment is not known, although there is a consensus that a multifactorial approach is required. Clinical Case: A 68-year-old woman on hemodialysis for 2 years, who presented a painful nodular lesion in the left thigh, a skin biopsy was performed resulting in a diagnosis of calciphylaxis. Treatment and Outcome: Treatment was started with intravenous sodium thiosulfate. Pamidronate is added intravenously, three months later, due to an unfavorable evolution. After 6 months of treatment, improvement in nodular lesions and healing of the ulcerated lesion was observed to be generally well tolerated treatment. Conclusion: The combined treatment of sodium thiosulfate, pamidronate and calcitomimetics has been effectiveand safe for the treatment of calciphylaxis, inducing complete remission.


Resumen: Introducción: La calcifilaxis es una enfermedad infrecuente que afecta casi exclusivamente a pacientes con insuficiencia renal, aunque se han observado casos en pacientes sin deterioro de la función renal. El diagnóstico es clínico confirmándose con estudio radiológico e histológico. No se conoce con exactitud el tratamiento óptimo, aunque hay consenso en que se requiere un abordaje multifactorial. Caso Clínico: Mujer de 68 años en hemodiálisis desde hace 2 años, que presenta una lesión nodular dolorosa en muslo izquierdo, resultando un diagnostico compatible con calcifilaxis, tras biopsia cutánea. Tratamiento y resultado: Inicia tratamiento con tiosulfato de sodio vía venosa. Tres meses más tarde y ante la evolución desfavorable, se añade al tratamiento pamidronato vía intravenosa. Tras 6 meses de tratamiento se observa mejoría de las lesiones nodulares y cicatrización de la lesión ulcerada, habiéndose experimentado buena tolerancia. Conclusión: El tratamiento combinado de tiosulfato de sodio, pamidronato y calcimiméticos ha resultado efectivo y seguro para el tratamiento de la calcifilaxis, induciendo su remisión completa.


Subject(s)
Aged , Female , Humans , Thiosulfates/administration & dosage , Calciphylaxis/drug therapy , Pamidronate/administration & dosage , Kidney Failure, Chronic/complications , Calciphylaxis/etiology , Calciphylaxis/pathology , Chelating Agents/administration & dosage , Renal Dialysis/methods , Treatment Outcome , Drug Therapy, Combination , Administration, Intravenous , Kidney Failure, Chronic/therapy
2.
Actual. osteol ; 14(2): 148-150, Mayo - Ago. 2018. ilus
Article in Spanish | LILACS | ID: biblio-1116417

ABSTRACT

El término "distrofia ósea esclerosante mixta" describe la combinación de las características radiológicas correspondientes a melorreostosis, osteopoiquilosis y osteopatía estriada, como entidades individuales, que ocurren en un mismo paciente. El objetivo de esta comunicación es presentar el caso clínico de una paciente con diagnóstico de distrofia ósea esclerosante mixta y, a partir de este caso, realizar una revisión sobre el tema. (AU)


The term "mixed-sclerosing-bone-dystrophy" describes the combination of the radiological characteristics corresponding to melorheostosis, osteopoikilosis and osteopathia striata, as individual conditions, ocurring in the same patient. The aim of this communication is to present the clinical case of a patient diagnosed with mixed-sclerosing-bone-dystrophy and, based on this case, to undertake a review of this condition. (AU)


Subject(s)
Humans , Female , Adult , Osteopoikilosis/diagnosis , Bone Diseases, Metabolic/diagnosis , Melorheostosis/diagnosis , Osteitis Deformans/diagnosis , Osteitis Deformans/drug therapy , Osteitis Deformans/blood , Osteopoikilosis/blood , Radiology , Tibia/diagnostic imaging , Bone Diseases, Metabolic/blood , Menopause, Premature/metabolism , Femur/diagnostic imaging , Pamidronate/administration & dosage , Melorheostosis/blood
3.
Rev. bras. reumatol ; 57(6): 514-520, Nov.-Dec. 2017. tab, graf
Article in English | LILACS | ID: biblio-899474

ABSTRACT

Abstract Purpose: The use of bisphosphonates for osteoporosis is effective in reducing the risk of fractures. However, oral formulations are sometimes not well tolerated or are contraindicated. Due to its availability in Brazilian public health system, pamidronate is frequently prescribed for osteoporosis, despite the lack of studies demonstrating its anti-fracture efficacy and the absence of FDA or EMEA approval for this purpose. The aim of this study was to evaluate the bone mineral density (BMD) response to pamidronate in a group of women with osteoporosis in a tertiary care hospital. Patients and methods: The medical records of women with osteoporosis who received pamidronate for up to two years of treatment were reviewed. Patients were stratified at high or intermediate risk of fracture. Results: A total of 70 women were in treatment with pamidronate. Among them, 74% were at high risk of fracture. A significant gain in spine BMD after 24 months of treatment was observed (p = 0.012). There was no difference between the groups of high and not high risk of fracture. At the femur, no significant increase in BMD was present, though, a strong negative correlation with high PTH levels (r = −0.61; p = 0.003) was seen. In the multivariate analysis BMI at 12 months had impact in the response to the treatment. Conclusion The intravenous pamidronate in a group of postmenopausal women with predominant high risk of fracture promoted an isolated gain in the spine BMD, even though, clinical randomized trials are needed to confirm its anti-fracture efficacy.


Resumo Justificativa: O uso de bisfosfonatos para a osteoporose é eficaz na redução do risco de fraturas. No entanto, as formulações orais às vezes não são bem toleradas ou são contraindicadas. Em razão da sua disponibilidade no sistema público de saúde brasileiro, o pamidronato é frequentemente prescrito para a osteoporose, apesar da falta de estudos que demonstrem a sua eficácia antifratura e da ausência de aprovação da Food and Drug Administration (FDA) ou da European Medicine Agency (Emea) para essa finalidade. O objetivo deste estudo foi avaliar a resposta da densidade mineral óssea (DMO) ao pamidronato em um grupo de mulheres com osteoporose em um hospital terciário. Pacientes e métodos: Revisaram-se os prontuários médicos de mulheres com osteoporose que receberam pamidronato por até dois anos de tratamento. As pacientes foram estratificadas em risco alto ou intermediário de fratura. Resultados: Estavam em tratamento com pamidronato 70 mulheres. Entre elas, 74% tinham alto risco de fratura. Observou-se um ganho significativo na DMO da coluna vertebral após 24 meses de tratamento (p = 0,012). Não houve diferença entre os grupos de risco de fratura alto e não alto. No fêmur, não foi encontrado aumento significativo na massa óssea; contudo, observou-se uma forte correlação negativa com altos níveis de PTH (r = −0,61; p = 0,003). Na análise multivariada, o IMC aos 12 meses tinha impacto na resposta ao tratamento. Conclusão O pamidronato intravenoso em um grupo de mulheres na pós-menopausa predominantemente com alto risco de fratura promoveu um ganho isolado na DMO da coluna vertebral, embora sejam necessários ensaios clínicos randomizados para confirmar sua eficácia antifratura.


Subject(s)
Humans , Female , Aged , Aged, 80 and over , Bone Density/drug effects , Osteoporosis, Postmenopausal/drug therapy , Bone Density Conservation Agents/administration & dosage , Pamidronate/administration & dosage , Brazil , Logistic Models , Retrospective Studies , Bone Density Conservation Agents/pharmacology , Administration, Intravenous , Pamidronate/pharmacology , Middle Aged
4.
Int. j. odontostomatol. (Print) ; 11(4): 481-485, dic. 2017. tab, graf
Article in Spanish | LILACS | ID: biblio-893292

ABSTRACT

RESUMEN: Los bisfosfonatos son potentes inhibidores de la resorción ósea. El aceite de oliva (O) presenta propiedades anti-inflamatorias y anti-oxidantes. Estudiar el efecto del tratamiento combinado de alendronato (AL) y pamidronato (PA) por vía subcutánea y de O vía oral sobre la regeneración tisular de cavidades óseas neoformadas.: 54 ratas macho de la línea Wistar, se dividieron en 6 grupos. Grupo control (C), recibieron solución salina vía subcutánea. Grupo (AL) recibió 0,5 mg de AL/Kg de peso corporal de por vía subcutánea. Grupo (PA) recibió de igual manera que el grupo anterior. Grupo (O) fue tratado con aceite de oliva con la dieta, 50 g/ Kg de comida. Grupo (ALO) recibió tratamiento combinado con AL y O. Grupo (PAO) recibió de igual tratamiento. Los sacrificios para la toma de muestras fueron a los 15, 30, 60 y 90 días. Para los estudios histopatológicos los cortes fueron teñidos con HE y observados con microscopía óptica. Los estudios estadísticos se realizaron a través del análisis de la variancia. A los quince días las áreas de los osteocitos del grupo PA se diferencian significativamente sólo respecto al grupo AL. En cuanto a la Densidad trabecular se observa un incremento de tejido óseo en todos los grupos. O mejora cualitativamente la estructura del hueso trabecular y cortical, preservando la mineralización, el tamaño y la estructura de los cristales minerales Esto sugiere que O representa una opción terapéutica prometedora para la prevención y tratamiento de las patologías óseas.


ABSTRACT: Bisphosphonates are potent inhibitors of bone resorption. Olive oil (O) has anti-inflammatory and anti-oxidant properties. To study the effect of combined treatment with alendronate (AL) and pamidronate (PA) subcutaneously or orally, and on tissue regeneration of newly formed bone cavities, we divided 54 male Wistar rats into 6 groups. Control group (C) received saline subcutaneously. Group (AL) received 0.5 mg of AL / kg body weight subcutaneously. Group (PA) received the same as the previous group. (O) was treated with olive oil diet, 50 g / kg of food. Group (ALO) received combined treatment with AL and O. Group (PAO) received the same treatment. The animals were euthanized for sampling at 15, 30, 60 and 90 days. For histopathology sections were stained with HE and observed these with light microscopy. Statistical studies were performed by analysis of variance. Fifteen days osteocytes areas of the PA group were significantly different only for the AL group. As the density increased trabecular bone tissue was observed in all groups. O qualitatively improved the structure of trabecular and cortical bone mineralization while preserving the size and structure of the mineral crystals. This suggests that O represents a promising therapeutic option for prevention and treatment of bone diseases.


Subject(s)
Animals , Male , Rats , Dental Implants , Peri-Implantitis , Rats, Wistar , Alendronate/administration & dosage , Alendronate/therapeutic use , Olive Oil/therapeutic use , Pamidronate/administration & dosage , Pamidronate/therapeutic use , Histology
5.
Actual. osteol ; 13(3): 243-250, Sept - DIc. 2017. ilus, tab
Article in Spanish | LILACS | ID: biblio-1117571

ABSTRACT

La hipercalcemia es un trastorno común que representa aproximadamente el 0,6% de todas las admisiones médicas agudas. El hiperparatiroidismo primario (HPTP) y las neoplasias malignas son las dos causas más comunes de elevación de los niveles séricos de calcio; constituyen, en conjunto, alrededor del 90% de todos los casos. La presentación sintomática clásica de la hipercalcemia se observa con relativa poca frecuencia en el mundo desarrollado; la presentación más común es la detección asintomática en las pruebas bioquímicas. Sin embargo, en casos raros, el HPTP puede desarrollar hipercalcemia aguda, grave y sintomática, llamada crisis hipercalcémica (CH). Esta condición se asocia a alteraciones profundas en el estado mental y las funciones cardíaca, renal y gastrointestinal en presencia de concentraciones marcadamente elevadas de calcio sérico y paratohormona (PTH). Mientras que algunas elevaciones en el calcio sérico pueden ser bien toleradas, los síntomas de la CH son severos. Si el tratamiento se retrasa, la CH puede provocar la muerte. Describimos el caso de un paciente masculino que ingresa en la unidad de cuidados críticos por una CH secundaria a un HPTP por adenoma paratiroideo. (AU)


Hypercalcaemia is a most common disorder, accounting for approximately 0,6% of all acute medical admissions. Primary hyperparathyroidism (PHPT) and malignancy are the two most common causes of increased serum calcium levels, together accounting for about 90% of all cases. The classical symptomatic presentation of hypercalcaemia is seen relatively rarely in the developed world, the most common presentation being asymptomatic and detected following on biochemical testing. However, in rare cases HPTP can result in acute, severe and symptomatic hypercalcemia, called hypercalcemic crisis (HC). This condition is associated with profound disturbances in mental status, and cardiac, renal, and gastrointestinal function in the presence of markedly increased serum calcium and parathyroid hormone (PTH) concentrations. While some elevations in serum calcium can be well tolerated, symptoms of HC are severe. If treatment is delayed, HC can result in death. We describe herein a case of a male patient who was admitted to the intensive care unit as a consequence of HC resulting from elevated PTH, secondary to a parathyroid adenoma. We describe the case of a male patient who was admitted to the critical care unit for a HC mediated by PTH secondary to a parathyroid adenoma. (AU)


Subject(s)
Humans , Male , Middle Aged , Parathyroid Neoplasms/complications , Parathyroid Glands/pathology , Hyperparathyroidism, Primary/complications , Hypercalcemia/chemically induced , Parathyroid Hormone/metabolism , Parathyroid Hormone/blood , Parathyroid Neoplasms/surgery , Parathyroid Neoplasms/diagnostic imaging , Parathyroid Glands/surgery , Vitamin D Deficiency/blood , Calcitriol/administration & dosage , Calcium Gluconate/administration & dosage , Weight Loss , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Calcium/administration & dosage , Calcium/blood , Renal Dialysis , Cholecalciferol/administration & dosage , Dehydration , Diuretics/administration & dosage , Hyperparathyroidism, Primary/surgery , Hyperparathyroidism, Primary/diagnosis , Cinacalcet/administration & dosage , Pamidronate/administration & dosage , Crystalloid Solutions/administration & dosage , Hypercalcemia/diagnosis , Hypercalcemia/drug therapy , Hypercalcemia/blood
6.
Rev. colomb. reumatol ; 24(1): 54-59, ene.-mar. 2017. tab, graf
Article in Spanish | LILACS | ID: biblio-900853

ABSTRACT

RESUMEN Los bifosfonatos se utilizan para el manejo de enfermedades con incremento de la resorción ósea como la osteoporosis, la enfermedad metastásica ósea y la hipercalcemia maligna, entre otras patologías. En los últimos años se ha reportado que el uso de bifosfonatos intravenosos como el zoledronato y el pamidronato pueden generar efectos adversos oculares, ocasionados por una reacción de fase aguda mediada por la interleucina-6 (IL-6) y factor de necrosis tumoral alfa (TNF-a). Se reportan 2 casos (una mujer de 71 años y un hombre de 67 años) que entre las 24 a 72 h después de recibir terapia con zoledronato presentaron una uveítis anterior.


ABSTRACT Bisphosphonates are used in the management of diseases characterized by an increase in bone resorption such as osteoporosis, metatasic bone disease, malignant hypercalcemia among others. It has been reported that the use of IV bisphosphonates as zoledronate and pamidronate generate ocular adverse effects by an acute phase reaction mediated by an increase of interleukin 6 (IL-6) and tumoral necrosis factor (TNF-a). We present 2 cases, a woman 71 years old and a 67 years old man that received therapy with bisphosphonates and 24 to 72hours later they presented an anterior uveitis.


Subject(s)
Humans , Male , Female , Aged , Diphosphonates , Zoledronic Acid , Pamidronate , Uveitis, Anterior , Eye Abnormalities
7.
Dental press j. orthod. (Impr.) ; 20(5): 58-65, tab, graf
Article in English | LILACS | ID: lil-764546

ABSTRACT

Introduction: Orthodontic anchorage is one of the most challenging aspects of Orthodontics. Preventing undesired movement of teeth could result in safer and less complicated orthodontic treatment. Recently, several reviews have been published about the effects of different molecules on bone physiology and the clinical side effects in Orthodontics. However, the effects of local application of these substances on the rate of orthodontic tooth movement have not been assessed.Objectives: The aim of this research was to analyze the scientific evidence published in the literature about the effects of different molecules on orthodontic anchorage.Methods: The literature was systematically reviewed using PubMed/Medline, Scopus and Cochrane databases from 2000 up to July 31st, 2014. Articles were independently selected by two different researchers based on previously established inclusion and exclusion criteria, with a concordance Kappa index of 0.86. The methodological quality of the reviewed papers was performed.Results: Search strategy identified 270 articles. Twenty-five of them were selected after application of inclusion/exclusion criteria, and only 11 qualified for final analysis. Molecules involved in orthodontic anchorage were divided into three main groups: osteoprotegerin (OPG), bisphosphonates (BPs) and other molecules (OMs).Conclusions: Different drugs are able to alter the bone remodeling cycle, influencing osteoclast function and, therefore, tooth movement. Thus, they could be used in order to provide maximal anchorage while preventing undesired movements. OPG was found the most effective molecule in blocking the action of osteoclasts, thereby reducing undesired movements.


Introdução: a ancoragem ortodôntica é um dos aspectos mais desafiadores da Ortodontia. A prevenção de movimentos dentários indesejados poderia resultar em um tratamento ortodôntico mais seguro e menos complexo. Recentemente, foram publicadas várias revisões de literatura sobre os efeitos de diferentes substâncias na fisiologia do tecido ósseo e os efeitos colaterais clínicos na Ortodontia. Porém, os efeitos da aplicação local dessas substâncias no grau de movimentação dentária ortodôntica não foram avaliados.Objetivos: o objetivo da presente pesquisa foi analisar a evidência científica publicada na literatura sobre os efeitos de diferentes substâncias na ancoragem ortodôntica.Métodos: a literatura foi sistematicamente revisada utilizando-se as bases de dados PubMed/Medline, Scopus e Cochrane, de 2000 a 31 de julho de 2014. Os artigos foram selecionados, de maneira independente, por dois pesquisadores diferentes, tendo como base critérios de inclusão e exclusão previamente estabelecidos, com um índice Kappa de concordância de 0,86. A qualidade metodológica dos artigos revisados foi analisada.Resultados: a estratégia de pesquisa identificou 270 artigos; 25 artigos foram selecionados após a aplicação dos critérios de inclusão e exclusão, mas apenas 11 foram qualificados para a análise final. As substâncias envolvidas na ancoragem ortodôntica foram divididas em três grupos principais: osteoprotegerina (OPG), bisfosfonatos (BFs) e outras substâncias (OSs).Conclusões: diferentes substâncias são capazes de alterar o ciclo de remodelação óssea, influenciando na função dos osteoclastos e, portanto, na movimentação dentária. Sendo assim, essas substâncias podem ser utilizadas para promover o máximo de ancoragem e prevenir movimentos indesejados. A OPG foi a substância mais eficaz no bloqueio da ação dos osteoclastos, reduzindo os movimentos indesejados.


Subject(s)
Humans , Animals , Rats , Diphosphonates/therapeutic use , Diphosphonates/pharmacology , Anti-Inflammatory Agents/therapeutic use , Anti-Inflammatory Agents/pharmacology , Antioxidants/therapeutic use , Antioxidants/pharmacology , Acetylcysteine/therapeutic use , Acetylcysteine/pharmacology , Diclofenac/therapeutic use , Diclofenac/pharmacology , Bone Remodeling/drug effects , Clodronic Acid/therapeutic use , Clodronic Acid/pharmacology , Orthodontic Anchorage Procedures/methods , Celecoxib/therapeutic use , Celecoxib/pharmacology , Resveratrol , Zoledronic Acid , Pamidronate , Imidazoles/pharmacology
8.
Acta Medica Philippina ; : 35-39, 2011.
Article in English | WPRIM | ID: wpr-631846

ABSTRACT

Objective. To present preliminary data on the effects of intravenous pamidronate in children with moderate to severe Osteogenesis Imperfecta (OI). Methods. This is a restrospective study wherein a review of medical records and available serial radiographs of children (N=14) with moderate to severe IO started on pamidronate from 2006 to 2010 was done. Results. Two children have IO Type I, 8 have IO Type III and 4 have IO Type IV. At baseline, 2 had normal height, 8 had height less than minus 2SD and the rest with less than minus 1SD. Twelve out of 14 had vertebral compression fractures. Mean age at start of pamidronate was 5.4 years (range 0.5-11 years). First infusion fever in five patients and transient generalized macular rash in one child were noted. Serum calcium and phosphorus levels were normal at baseline and remained stable. Based on parental report, improvement of motor function was noted. In the 10 children who had at least a year of treatment, long bone fractures decreased from mean annualized fracture rate of 2.6 at baseline to 0.9. In patients with vertebral compression fractures, serial radiographs showed improvement of vertebral shape. Conclusion. This preliminary study shows that treatment was generally well tolerated and led to decrease in long bone fractures, improved vertebral shape and improved function.


Subject(s)
Humans , Male , Female , Child , Pamidronate , Osteogenesis Imperfecta , Musculoskeletal Diseases , Bone Diseases , Bone Diseases, Developmental , Bone Diseases, Metabolic , Osteochondrodysplasias , Therapeutics , Therapeutics , Osteoporosis
9.
Rev. colomb. reumatol ; 16(2): 146-153, jun. 2009. ilus, tab
Article in Spanish | LILACS | ID: lil-636797

ABSTRACT

Presentamos un paciente con diagnóstico de Osteoporosis Juvenil Idiopática a quien se administró ácido zolendrónico, y una serie de pacientes con diagnóstico de Osteogénesis Imperfecta tratados con pamidronato durante varios años. Se describen las imágenes osteocondensantes que aparecen en los huesos tubulares y la pelvis de estos pacientes a consecuencia de su tratamiento con bisfosfonatos, similares a las líneas de Harris (Growth Arrest Lines) que aparecen eventualmente por diversas causas en el esqueleto inmaduro.


We present one patient with Juvenile Idiopathic Osteoporosis (JIO) who was treated with Zolendronic Acid, and a small series Osteogenesis Imperfecta (OI) patients administered on eyelie Pamidronate proteol. We describe dense lines in radiographs of tubular bones and pelvis of these patients appearing. After bisphosphonates treatment, those images are similar to Harris Lines (Growth Arrest Lines) that appear occasionally by several causes on immature skeletons land through life.


Subject(s)
Humans , Skeleton , Radiography , Diphosphonates , Osteogenesis Imperfecta , Osteoporosis , Bone and Bones , Diagnosis , Pamidronate
10.
Salud(i)ciencia (Impresa) ; 13(4): 5-8, 2005. fot.
Article in Spanish | LILACS | ID: biblio-1434645

ABSTRACT

Collapsing glomerulopathy (CG) is an aggressive type of renal injury first recognized in HIV patients and increasingly seen in non-HIV patients as an idiopathic disease or in various clinical associations. CG shares many clinical and pathologic features in HIV and non-HIV patients. It is characterized by heavy proteinuria frequently combined with rapidly progressive renal failure, and poor outcome. Light microscopy reveals glomerular collapse with prominence and degenerative changes of the podocytes, and frequently a severe tubulointerstitial injury with microcystic tubular changes. Pathogenesis of CG involves a peculiar podocyte injury: podocytes re-enter cell cycle, loose their normal cytoarchitecture, maturity markers, and function. This aberrant proliferative response is observed in both HIV and non-HIV patients with CG but not in other forms of nephrotic glomerulopathies. It becomes apparent that in HIV patients CG is directly caused by the viral infection of the kidney, although unrecognized host factors may play a role. In the population of non-HIV patients, CG mostly remains of un-established origin, however, potential etiologic links with parvovirus B19 and other viral infections, autoimmune and lymphoproliferative disorders as well as therapeutic agents (high-dose pamidronate therapy) are emerging.


La glomerulopatía colapsante (GC) es una forma agresiva de enfermedad renal inicialmente diagnosticada en pacientes con infección por HIV, y crecientemente en pacientes sin HIV, como una enfermedad idiopática o asociada con diferentes cuadros clínicos. La GC comparte varias características clínicas y patológicas en los pacientes HIV+ y HIV-. Se caracteriza por proteinuria grave generalmente asociada con insuficiencia renal rápidamente progresiva y mala evolución. A través del microscopio óptico se observa un colapso glomerular con prominencias y cambios degenerativos en los podocitos y con frecuencia una lesión tubulointersticial grave con cambios tubulares microquísticos. La patogenia de la GC incluye una alteración singular de los podocitos: éstos reingresan en su ciclo celular, pierden su citoarquitectura normal, sus marcadores de maduración y su función. Esta respuesta proliferativa aberrante se observa tanto en pacientes HIV+ como HIV- con GC, pero no en otras formas de glomerulopatías nefróticas. Es posible que en pacientes HIV+ la GC se desencadene directamente por la infección viral del riñón, aunque factores del huésped no reconocidos hasta el momento pueden desempeñar un papel relevante. En la población de pacientes sin HIV aún no se estableció el origen de la GC en su totalidad, sin embargo están surgiendo posibles vínculos etiológicos con el parvovirus B19 y con otras infecciones virales, trastornos autoinmunes y linfoproliferativos, y con agentes terapéuticos como la terapia con pamidronato en dosis elevadas.


Subject(s)
Glomerulonephritis, Membranous , Proteinuria , Therapeutics , HIV , Parvovirus B19, Human , Renal Insufficiency , Pamidronate , Kidney , Kidney Diseases , Lymphoproliferative Disorders
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