RESUMEN
BACKGROUND: Bullous lupus is a subepidermal autoimmune bullous dermatosis, a rare entity that forms one of the cutaneous signs of systemic lupus erythematosus. We report on the clinical, immunopathological and progressive features of bullous lupus in three patients. PATIENTS AND METHODS: Our patients consisted of two women and one man aged 34, 22 and 30 years respectively. A diagnosis of bullous lupus erythematosus was evoked by blisters or vesicular blisters and confirmed, in addition to criteria for the diagnosis of systemic lupus erythematosus, by the presence of subepidermal blistering with infiltrate containing neutrophils and eosinophils as revealed by histological analysis, and of deposits of IgG and IgM (two cases) or of IgA (one case) at the dermo-epidermal junction observed under direct immunofluorescence. Indirect immunofluorescence showed anti-collagen VII antibodies. Lupus nephritis was present in two cases. Our patients were treated with corticosteroids and immunosuppressants. CONCLUSION: Bullous lupus erythematosus may be the first sign of systemic lupus erythematosus with severe visceral involvement, especially renal involvement, suggesting that it may be a marker of activity and prognosis.
Asunto(s)
Vesícula/etiología , Lupus Eritematoso Cutáneo/diagnóstico , Lupus Eritematoso Sistémico/diagnóstico , Adulto , Artralgia/etiología , Autoanticuerpos/análisis , Vesícula/diagnóstico , Vesícula/tratamiento farmacológico , Vesícula/inmunología , Vesícula/patología , Colágeno/inmunología , Diagnóstico Diferencial , Progresión de la Enfermedad , Erupciones por Medicamentos/diagnóstico , Femenino , Humanos , Inmunosupresores/uso terapéutico , Lupus Eritematoso Cutáneo/tratamiento farmacológico , Lupus Eritematoso Cutáneo/inmunología , Lupus Eritematoso Sistémico/complicaciones , Lupus Eritematoso Sistémico/tratamiento farmacológico , Lupus Eritematoso Sistémico/inmunología , Nefritis Lúpica/etiología , Masculino , Infiltración Neutrófila , Úlceras Bucales/etiología , Prednisona/uso terapéutico , Piel/inmunología , Piel/patología , Adulto JovenRESUMEN
BACKGROUND: Acute pancreatitis and haemophagocytic syndrome (HS) are rarely seen in systemic lupus erythematosus (SLE). PATIENTS AND METHODS: We report the case of a young female patient without any noteworthy prior history, who was hospitalised for abdominal pain associated with acute pancreatitis possibly related to SLE with associated haemophagocytic syndrome. DISCUSSION: Screening for cutaneous symptoms of lupus in patients with pancreatitis can help avoid diagnostic errors.
Asunto(s)
Lupus Eritematoso Sistémico/complicaciones , Linfohistiocitosis Hemofagocítica/etiología , Pancreatitis Aguda Necrotizante/etiología , Abdomen Agudo/etiología , Autoanticuerpos/sangre , Femenino , Hemorragia Gingival/etiología , Humanos , Hidroxicloroquina/uso terapéutico , Lupus Eritematoso Sistémico/diagnóstico , Lupus Eritematoso Sistémico/tratamiento farmacológico , Activación de Macrófagos , Metilprednisolona/uso terapéutico , Pancreatitis Aguda Necrotizante/diagnóstico por imagen , Pancitopenia/etiología , Tomografía Computarizada por Rayos X , Vómitos/etiología , Adulto JovenAsunto(s)
Intoxicación por Monóxido de Carbono/diagnóstico , Trastornos de la Conciencia/diagnóstico , Urgencias Médicas , Encéfalo/patología , Daño Encefálico Crónico/diagnóstico , Daño Encefálico Crónico/terapia , Intoxicación por Monóxido de Carbono/terapia , Niño , Trastornos de la Conciencia/terapia , Diagnóstico Diferencial , Epilepsia Tónico-Clónica/diagnóstico , Epilepsia Tónico-Clónica/terapia , Humanos , Oxigenoterapia Hiperbárica , Imagen por Resonancia Magnética , Masculino , Pruebas Neuropsicológicas , Terapia por Inhalación de Oxígeno , Admisión del Paciente , Tomografía Computarizada por Rayos XAsunto(s)
Edema/diagnóstico , Enfermedades Musculares/diagnóstico , Dolor/diagnóstico , Aneurisma/complicaciones , Aneurisma/diagnóstico por imagen , Angiografía , Síndrome de Behçet/complicaciones , Síndrome de Behçet/diagnóstico por imagen , Edema/complicaciones , Edema/diagnóstico por imagen , Edema/etiología , Arteria Femoral/diagnóstico por imagen , Arteria Femoral/patología , Humanos , Masculino , Enfermedades Musculares/complicaciones , Enfermedades Musculares/diagnóstico por imagen , Enfermedades Musculares/etiología , Dolor/complicaciones , Dolor/diagnóstico por imagen , Dolor/etiología , Muslo/diagnóstico por imagen , Tromboembolia/complicaciones , Tromboembolia/diagnóstico por imagen , Adulto JovenRESUMEN
INTRODUCTION: Possible adverse complications related to rituximab (RTX) are low, some of which are extremely rare. The authors describe one situation visibly waning exceptional treatment with RTX for SLE refractory to conventional therapies. COMMENT: The authors report a patient of 34 years followed for months for an illness in its bullous lupus, with cutaneous, articular, hematologic and immunologic. Given a corticosteroid resistance, several therapeutic background based hydroxychloroquine, cyclophosphamide and methotrexate, were initiated without any improvement. Immunomodulatory therapy type RTX was introduced to this form refractory at a rate of 375mg/m(2)/week. The waning of the second infusion, the patient presented a sudden intense abdominal pain syndrome, revealing an acute catarrhal appendicitis. At distance from the appendectomy, the consequences of which were favorable, treatment with RTX was resumed. In the aftermath of the third infusion, the patient presented in table tract marked by profuse watery diarrhea whose explorations reveal a morphological endoscopic appearance of erythematous, ulcerative colitis, reversible upon discontinuation of treatment. Histological data revealed important infiltrates composed mainly of CD8T lymphocytes. CONCLUSION: Gastrointestinal immunological consequences to the requirements of the targeted therapies deserved very careful and rigorous monitoring. However, at the slightest sign of digestive, a detailed morphological exploration is essential, to avoid in particular surgical emergency, evolution without treatment could engage in short-term vital prognosis.
Asunto(s)
Anticuerpos Monoclonales de Origen Murino/efectos adversos , Colitis Ulcerosa/inducido químicamente , Factores Inmunológicos/efectos adversos , Dolor Abdominal/etiología , Adulto , Anticuerpos Monoclonales de Origen Murino/uso terapéutico , Linfocitos T CD8-positivos , Colitis Ulcerosa/patología , Colon/patología , Diarrea/inducido químicamente , Humanos , Inmunohistoquímica , Factores Inmunológicos/uso terapéutico , Lupus Eritematoso Sistémico/complicaciones , Lupus Eritematoso Sistémico/tratamiento farmacológico , Masculino , RituximabRESUMEN
INTRODUCTION: The cardiac involvement in hypereosinophilia remains a major cause of morbidity and mortality. Recent advances have identified new molecular mechanisms responsible for the expansion of the eosinophilic lineage, allowing a better classification of the different forms of Hypereosinophilic syndrome (HES) and especially targeted therapy. Since the discovery of the involvement of deregulated tyrosine kinases in the pathophysiology of these diseases, and particularly the identification of the fusion gene FIP1L1-PDGFRA, new molecules inhibiting specifically this signaling pathway (imatinib) were individualized, leading to dramatic therapeutic benefits in proliferative forms of HES considered before that of very poor prognosis. CASE REPORT: We report here the dramatic effectiveness of imatinib used as second line therapy for dilated cardiomyopathy revealing a hypereosinophilic syndrome in a patient in whom the search for FIP1-L1-PDGFRA fusion gene was negative. CONCLUSION: If hypereosinophilia has varied clinical and morphological outcome, its clinical consequences, particularly on heart function, are sometimes dreadful, and are not correlated either with blood eosinophil levels or with a specific etiology. We report here a case of HES lacking the FIP1-L1-PDGFRA fusion gene showing that despite the absence of this molecular defect, imatinib mesylate may have therapeutic interest in those cases of HES resistant to first line therapies.
Asunto(s)
Síndrome Hipereosinofílico/tratamiento farmacológico , Síndrome Hipereosinofílico/genética , Proteínas de Fusión Oncogénica/genética , Piperazinas/uso terapéutico , Inhibidores de Proteasas/uso terapéutico , Pirimidinas/uso terapéutico , Receptor alfa de Factor de Crecimiento Derivado de Plaquetas/genética , Factores de Escisión y Poliadenilación de ARNm/genética , Adulto , Asma/complicaciones , Benzamidas , Electrocardiografía , Eosinófilos/fisiología , Femenino , Humanos , Síndrome Hipereosinofílico/fisiopatología , Hipertensión/fisiopatología , Hipertensión Pulmonar/complicaciones , Mesilato de Imatinib , Recuento de LeucocitosRESUMEN
INTRODUCTION: Autoimmune hemolytic anemia with cold autoantibodies or cold agglutinin disease is a rare chronic disorder in which no treatment has, until now, evidence of its effectiveness. CLINICAL CASE: We report a patient who successfully responded to rituximab for a cold agglutinin disease refractory to conventional therapy with very good tolerance and a complete remission. CONCLUSION: There are only few observations that have been reported in the literature regarding the efficacity of rituximab in the treatment of cold agglutinin disease. This promising therapy could, in the future, constitute a real alternative.