RESUMO
Considering that the prevalence of some hematologic malignancies may have a geographic distribution that could be related with its etiology, a group of 2,387 patients with acute leukemia (1,968 adults and 419 children) was studied along a 5-year period in six different locations within México. Twenty-seven patients (16 males and 11 females) with hairy cell leukemia (HCL) were identified. The adjusted overall proportion of HCL, after excluding data from centers reporting only adults, was 1.12% of all leukemia cases; this figure is lower than that reported in the United States or England. The proportion of adult leukemic patients with HCL was significantly higher in the northern region of the country-where there are more people devoted to farming and agricultural activities-as compared with the central or southeastern regions (3.07 vs. 1.03% vs. 0%; P < 0.05); possible explanations for these differences are briefly discussed.
Assuntos
Leucemia de Células Pilosas/epidemiologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , México/epidemiologia , Pessoa de Meia-IdadeAssuntos
Androgênios/uso terapêutico , Anemia Aplástica/terapia , Transplante de Medula Óssea , Corticosteroides/uso terapêutico , Anemia Aplástica/tratamento farmacológico , Anemia Aplástica/epidemiologia , Anemia Aplástica/etiologia , Anemia Aplástica/cirurgia , Soro Antilinfocitário/uso terapêutico , Transplante de Medula Óssea/efeitos adversos , Transplante de Medula Óssea/mortalidade , Ciclosporinas/uso terapêutico , Doença Enxerto-Hospedeiro/etiologia , Humanos , Terapia de Imunossupressão , Infecções/etiologiaAssuntos
Trombose , Anticoagulantes/uso terapêutico , Antitrombina III/fisiologia , Deficiência de Antitrombina III , Coagulação Sanguínea/fisiologia , Fibrinolíticos/uso terapêutico , Glicoproteínas/deficiência , Glicoproteínas/fisiologia , Heparina/fisiologia , Heparina/uso terapêutico , Humanos , Inibidores da Agregação Plaquetária/uso terapêutico , Proteína C/fisiologia , Deficiência de Proteína C , Proteína S , Fatores de Risco , Trombose/sangue , Trombose/diagnóstico , Trombose/tratamento farmacológico , Trombose/fisiopatologiaRESUMO
Adult patients with chronic autoimmune thrombocytopenic purpura (ATP), which proved refractory to various treatments, received a single dose of autologous in vitro opsonized erythrocytes with 100 micrograms of anti-D IgG. In 1983, 30 of these patients were treated with autologous erythrocytes that had been opsonized and labeled with 25 mCi (740 MBq) of technetium Tc 99m; this treatment was designated as the radioimmune method. Favorable responses were noted in 36% of patients so treated. In 1985, another group of 16 patients with refractory ATP received therapy with autologous opsonized erythrocytes (AOPE) and 55% of these patients showed favorable responses. Five (17%) of the patients treated using the radioimmune method attained a complete, long-term (greater than 35 months) remission of their ATP, and five (31%) of the patients treated using AOPE remained in complete remission over 270 days after cessation of therapy. Major complications were not seen. We concluded that the interaction of macrophages with low-dose AOPE is a successful therapeutic approach in ATP refractory to standard treatment.
Assuntos
Doenças Autoimunes/terapia , Eritrócitos , Imunização Passiva , Proteínas Opsonizantes , Púrpura Trombocitopênica/terapia , Tecnécio/uso terapêutico , Adolescente , Adulto , Idoso , Doenças Autoimunes/sangue , Doenças Autoimunes/tratamento farmacológico , Resistência a Medicamentos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Contagem de Plaquetas , Púrpura Trombocitopênica/sangue , Púrpura Trombocitopênica/tratamento farmacológico , Imunoglobulina rho(D)Assuntos
Fator IX/análise , Fator VIII/imunologia , Transtornos Hemorrágicos/etiologia , Transtornos Puerperais/etiologia , Adulto , Fator IXa , Feminino , Hematoma/sangue , Hematoma/etiologia , Transtornos Hemorrágicos/sangue , Transtornos Hemorrágicos/tratamento farmacológico , Humanos , Metilprednisolona/uso terapêutico , Gravidez , Transtornos Puerperais/sangue , Transtornos Puerperais/tratamento farmacológicoAssuntos
Leucemia Mieloide/cirurgia , Esplenectomia , Adulto , Crise Blástica/prevenção & controle , Bussulfano/uso terapêutico , Terapia Combinada , Seguimentos , Humanos , Leucemia Mieloide/tratamento farmacológico , Leucemia Mieloide/patologia , Pessoa de Meia-Idade , Cromossomo Filadélfia , Esplenectomia/efeitos adversos , Fatores de TempoRESUMO
Idiopathic thrombocytopenic purpura (ITP) is more frequently seen in young females than in any other age or sex group. Danazol, an impeded androgen with a decreased masculinizing potential, has been described as useful in ITP. A total of 25 women 16 to 41 years of age, with chronic ITP were studied. All patients were refractory to treatments with glucocorticoids and splenectomy; 19 were inadequately controlled by immunosuppressants, vinblastine or vincristine-loaded platelets, the radioimmune method, colchicine, plasmapheresis, or surgery for accessory spleens. Danazol was given at a daily dosage of 600 mg for 4 months. All showed clinical improvement, as indicated by cessation or decrease of bleeding, and 12 (48%) cases obtained a drug-dependent excellent or good response of their ITP. Therapy produced amenorrhea or oligomenorrhea in 21 patients (84%) and 7 cases of chronic metrorrhagia were successfully controlled. The drug was well tolerated. Accordingly, danazol may be an effective treatment for ITP or related conditions, especially in adult females with uncontrollable metrorrhagia.
Assuntos
Danazol/uso terapêutico , Metrorragia/tratamento farmacológico , Pregnadienos/uso terapêutico , Púrpura Trombocitopênica/tratamento farmacológico , Adolescente , Adulto , Amenorreia/induzido quimicamente , Danazol/efeitos adversos , Feminino , Humanos , Metrorragia/etiologia , Oligomenorreia/induzido quimicamente , Prednisona/uso terapêutico , Púrpura Trombocitopênica/complicaçõesAssuntos
Megacariócitos/patologia , Púrpura/induzido quimicamente , Adolescente , Adulto , Terapia Combinada , Diazepam/efeitos adversos , Etanol/efeitos adversos , Feminino , Humanos , Inseticidas/efeitos adversos , Masculino , Meprobamato/efeitos adversos , Pessoa de Meia-Idade , Oxifenilbutazona/efeitos adversos , Púrpura/patologia , Púrpura/terapia , Pirazóis/efeitos adversos , Quinina/efeitos adversos , Sulfassalazina/efeitos adversos , Sulfonamidas/efeitos adversos , Tolbutamida/efeitos adversosAssuntos
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Leucemia Linfoide/tratamento farmacológico , Idoso , Ciclofosfamida/administração & dosagem , Feminino , Humanos , Leucemia Linfoide/patologia , Masculino , Pessoa de Meia-Idade , Prednisona/administração & dosagem , Vincristina/administração & dosagemRESUMO
Accessory spleens were sought in 28 patients who had undergone splenectomy for chronic idiopathic thrombocytopenic purpura (ITP), using a variety of techniques. Abdominal scintigraphy with autologous erythrocytes labeled with Tc-99m and opsonized with anti-D IgG (radioimmune method) proved to be most useful, clearly demonstrating one or more accessory spleens in 12 cases (43%). Computed tomography (CT) was also helpful. Four out of five patients demonstrated an increased platelet count following surgery, the effectiveness of which was illustrated by the radioimmune scan. Patients who have had splenectomy for chronic ITP should be scanned using radioimmune techniques and CT to determine whether an accessory spleen is present.
Assuntos
Neoplasias Abdominais/diagnóstico por imagem , Coristoma/diagnóstico por imagem , Púrpura Trombocitopênica/complicações , Baço , Esplenectomia , Neoplasias Abdominais/complicações , Adolescente , Adulto , Idoso , Coristoma/complicações , Eritrócitos , Feminino , Humanos , Imunoglobulina G , Masculino , Pessoa de Meia-Idade , Púrpura Trombocitopênica/sangue , Púrpura Trombocitopênica/terapia , Cintilografia , TecnécioAssuntos
Transtornos da Coagulação Sanguínea/genética , Deficiência do Fator V/complicações , Deficiência do Fator VII/complicações , Adulto , Transtornos da Coagulação Sanguínea/sangue , Criança , Fenda Labial/genética , Consanguinidade , Deficiência do Fator V/genética , Deficiência do Fator VII/genética , Feminino , Genes Dominantes , Heterozigoto , Humanos , Masculino , Tempo de Tromboplastina Parcial , Tempo de ProtrombinaAssuntos
Doenças da Medula Óssea/genética , Aberrações Cromossômicas , Pré-Leucemia/genética , Adulto , Idoso , Doenças da Medula Óssea/induzido quimicamente , Bandeamento Cromossômico , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Síndromes Mielodisplásicas/genética , Transtornos Mieloproliferativos/genética , Doenças Profissionais/induzido quimicamente , Doenças Profissionais/genética , Pré-Leucemia/induzido quimicamente , Prognóstico , Solventes/efeitos adversosRESUMO
In order to analyze the usefulness of different types of treatment in relation to the interval since the onset of idiopathic thrombocytopenic purpura (ITP), a collaborative study of 934 adult patients was undertaken. Prednisone was administered to 818 patients, and 32% of them achieved prolonged complete remission (PCR). However, only 14% of patients who had ITP for more than six months achieved a prednisone-induced PCR (P less than .01). Splenectomy was done in 399 patients, and 65% of them achieved PCR; the remission rate did not vary with the interval since the onset of ITP. Of 120 patients with chronic ITP that was refractory to corticosteroids and splenectomy, 91 received either azathioprine or cyclophosphamide; 21% of them achieved PCR and 55% had a favorable response. None of 19 patients treated with vincristine and only one of ten patients treated with vinblastine-loaded platelets achieved PCR.
Assuntos
Imunossupressores/uso terapêutico , Púrpura Trombocitopênica/terapia , Adolescente , Corticosteroides/uso terapêutico , Adulto , Idoso , Ensaios Clínicos como Assunto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Púrpura Trombocitopênica/mortalidade , Esplenectomia , Vimblastina/uso terapêutico , Vincristina/uso terapêuticoRESUMO
Six patients with acute lymphoblastic leukemia manifested liver dysfunction related to doxorubicin hydrochloride therapy. Other causes, eg, infection, hepatitis, posttransfusion reaction, and leukemic infiltration were ruled out. There was close correlation between the administration of doxorubicin and the appearance of hepatic dysfunction. Doxorubicin may produce an idiosyncratic reaction and must be considered a drug with potential liver toxicity.