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1.
Int J Rheum Dis ; 24(12): 1500-1509, 2021 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-34636151

RESUMEN

INTRODUCTION: Lupus nephritis (LN) is a major manifestation of systemic lupus erythematosus (SLE) which contributes to significant morbidity and mortality. It is unclear whether the timing of LN onset influences renal outcome. This study aimed to investigate differences in clinical features-particularly the relapse-free rate-in remission duration from induction therapies for LN and the onset timing of LN after the development of SLE. METHODS: We enrolled 66 LN patients from January 2004 to March 2020. We collected the following: demographic data, laboratory data, renal histology data, and LN induction therapy data. Renal remission and relapse-free rates were calculated for each group. RESULTS: Patients were first divided into early remission group (achieved renal remission in <12 months [n = 44]) and others (n = 22). There were no significant differences in clinical data, treatments, and relapse-free rate of LN. Patients were then divided into initial-onset LN (<12 months after development of SLE [n = 49]) and delayed-onset LN (≥12 months after development of SLE [n = 17]). Kaplan-Meier analysis showed that the relapse-free rate was significantly higher in all patients with initial-onset LN than those with delayed-onset LN (P = .0094). CONCLUSION: The relapse-free rate was significantly higher in the initial-onset LN group than the delayed-onset LN group of patients with LN of various histopathological backgrounds. These data suggest that delayed-onset LN is a risk factor for the relapse of LN.


Asunto(s)
Nefritis Lúpica/fisiopatología , Inducción de Remisión/métodos , Adulto , Progresión de la Enfermedad , Femenino , Humanos , Inmunosupresores/uso terapéutico , Nefritis Lúpica/tratamiento farmacológico , Masculino , Recurrencia , Estudios Retrospectivos , Factores de Riesgo , Factores de Tiempo
2.
Medicine (Baltimore) ; 97(33): e11449, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-30113451

RESUMEN

INTRODUCTION: Multicentric reticulohistiocytosis (MRH) is a rare histiocytic disorder that involves the skin, joints, and visceral organs. CASE PRESENTATION: We report a 67-year-old woman with MRH who presented with a 2-years history of polyarthralgia and skin nodules. Her symptoms were an inflammatory polyarthropathy with punched-out lesions of the distal interphalangeal (DIP) joints of both hands. Doppler ultrasonography of the hands showed large bone erosions with power Doppler signals in the DIP joints. F-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) demonstrated increased FDG uptake in cutaneous papules surrounding the affected joints, suggesting an inflammatory process. There was no evidence of malignancy. Biopsy samples of skin nodules exhibited dermal infiltration with CD68-positive histiocytes and multinucleated giant cells. The patient was diagnosed with MRH and treated with combination therapy comprising a steroid (prednisolone), tacrolimus, methotrexate, and infliximab, which resulted in clinical improvement. Following infliximab treatment, there was a significant decrease in a bone resorption marker (tartrate-resistant acid phosphatase 5b: TRACP-5b), suggesting that tumor necrosis factor-α targeting therapy may inhibit osteoclast formation and resorption activity in patients with MRH. CONCLUSION: MRH is a progressive destructive arthritic condition, and early diagnostic and therapeutic strategies are necessary to improve the outcome. FDG-PET/CT and joint ultrasonography might be noninvasive imaging modalities that could help diagnose MRH.


Asunto(s)
Artralgia/diagnóstico por imagen , Fluorodesoxiglucosa F18/metabolismo , Histiocitosis de Células no Langerhans/diagnóstico por imagen , Tomografía Computarizada por Tomografía de Emisión de Positrones/métodos , Piel/diagnóstico por imagen , Anciano , Antígenos CD/metabolismo , Antígenos de Diferenciación Mielomonocítica/metabolismo , Antirreumáticos/uso terapéutico , Pueblo Asiatico/etnología , Combinación de Medicamentos , Femenino , Glucocorticoides/uso terapéutico , Mano/diagnóstico por imagen , Mano/patología , Histiocitos/inmunología , Histiocitos/patología , Histiocitosis de Células no Langerhans/tratamiento farmacológico , Histiocitosis de Células no Langerhans/patología , Humanos , Inmunosupresores/uso terapéutico , Infliximab/administración & dosificación , Infliximab/uso terapéutico , Metotrexato/administración & dosificación , Metotrexato/uso terapéutico , Prednisolona/administración & dosificación , Prednisolona/uso terapéutico , Piel/metabolismo , Piel/patología , Tacrolimus/administración & dosificación , Tacrolimus/uso terapéutico , Resultado del Tratamiento , Factor de Necrosis Tumoral alfa/efectos de los fármacos , Ultrasonografía Doppler/métodos
3.
Intern Med ; 56(9): 1101-1106, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28458320

RESUMEN

Pneumatosis cystoides intestinalis (PCI) is a rare disease that involves the presence of gas in the intestinal wall. Connective tissue disease (CTD) is a major cause of secondary PCI. In addition to the nature of CTDs, the use of prednisolone and some immunosuppressants, and the presence of complicating diseases such as diabetes mellitus, constipation and pulmonary diseases are involved in the development of PCI. This report describes four cases of PCI with different CTDs (granulomatosis with polyangiitis, rheumatoid arthritis, dermatomyositis, and overlap syndrome) and discusses the background of each patient and common risk factors for the occurrence of PCI.


Asunto(s)
Antiinflamatorios/uso terapéutico , Enfermedades del Tejido Conjuntivo/complicaciones , Enfermedades del Tejido Conjuntivo/tratamiento farmacológico , Neumatosis Cistoide Intestinal/complicaciones , Neumatosis Cistoide Intestinal/tratamiento farmacológico , Prednisolona/uso terapéutico , Adulto , Anciano , Enfermedades del Tejido Conjuntivo/diagnóstico por imagen , Femenino , Humanos , Masculino , Neumatosis Cistoide Intestinal/diagnóstico por imagen , Enfermedades Raras/diagnóstico , Enfermedades Raras/tratamiento farmacológico , Medición de Riesgo , Factores de Riesgo , Resultado del Tratamiento
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