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1.
Acta Haematol ; 122(1): 54-7, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19816010

RESUMEN

A 66-year-old Japanese woman was referred to us because of severe anemia and fever and presented at our hospital. She was eventually diagnosed as having acute myeloblastic leukemia (AML; M0) with non-Hodgkin lymphoma (NHL). We investigated the therapeutic efficacy of L-asparaginase (L-Asp), vincristine and prednisolone for both her AML and NHL. Asparagine synthetase (AS) activity in her AML blast cells was undetectable. A lymph node biopsy specimen revealed NHL of the marginal zone B cell type. Complete remission (CR) of AML and NHL was achieved. CR of the AML lasted for 18 months without further consolidation therapy. We conclude that L-Asp can be an effective drug for the treatment of AML in which blasts are negative for AS.


Asunto(s)
Asparaginasa/uso terapéutico , Leucemia Mieloide Aguda/tratamiento farmacológico , Linfoma no Hodgkin/tratamiento farmacológico , Prednisolona/uso terapéutico , Vincristina/uso terapéutico , Anciano , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Aspartatoamoníaco Ligasa/metabolismo , Resultado Fatal , Femenino , Humanos , Inducción de Remisión
2.
Int J Hematol ; 87(2): 118-125, 2008 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18228114

RESUMEN

Twenty-one acute myeloid leukemia (AML) patients were enrolled and received oral induction therapy with cytarabine ocfosfate (SPAC) and etoposide (EP). The median age was 69 years (range: 33-86). There were 11 patients with de novo AML and 10 AML cases that had evolved from myelodysplastic syndromes. Seventeen patients had abnormal karyotypes including eight complex abnormalities, various complications, and 7 of 21 had a poor performance status (PS) with Eastern Cooperative Oncology Group (ECOG) scores of 3-4. All patients completed induction therapy without severe adverse events. Seven achieved complete remission (CR), and two achieved partial remission (PR). Uni- and multivariate analyses demonstrated a positive and significant correlation between the results of therapy (CR +/- PR) and overall survival. The plasma concentrations of cytosine arabinoside (ara-C) in some cases were higher than those previously reported, indicating the accumulation of ara-C with increasing numbers of days of SPAC administration. We conclude that this therapy is well tolerated and useful for refractory and elderly AML patients.


Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica/administración & dosificación , Leucemia Mieloide Aguda/tratamiento farmacológico , Recurrencia Local de Neoplasia/tratamiento farmacológico , Administración Oral , Adulto , Anciano , Anciano de 80 o más Años , Protocolos de Quimioterapia Combinada Antineoplásica/efectos adversos , Protocolos de Quimioterapia Combinada Antineoplásica/sangre , Arabinonucleotidos/administración & dosificación , Arabinonucleotidos/efectos adversos , Arabinonucleotidos/sangre , Citidina Monofosfato/administración & dosificación , Citidina Monofosfato/efectos adversos , Citidina Monofosfato/análogos & derivados , Citidina Monofosfato/sangre , Etopósido/administración & dosificación , Etopósido/efectos adversos , Etopósido/sangre , Femenino , Humanos , Estimación de Kaplan-Meier , Masculino , Persona de Mediana Edad
3.
Intern Med ; 44(4): 335-41, 2005 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-15897648

RESUMEN

A 68-year-old woman with Felty's syndrome was admitted to our hospital due to breathlessness. She was diagnosed as having rheumatoid arthritis at age 59 years. Abdominal computed tomography indicated ascites, splenomegaly and liver atrophy. She had no antigens or antibodies for hepatitis virus, or antibodies for mitochondria with the exception of antinuclear antibody. According to the International Autoimmune Hepatitis (AIH) scoring system, she was diagnosed as having chronic hepatitis, compatible with AIH. The association of Felty's syndrome with AIH is very rare and the most difficult problem to overcome is whether or not steroid therapy is necessary in patients with Felty's syndrome complicated by AIH.


Asunto(s)
Síndrome de Felty/complicaciones , Hepatitis Autoinmune/complicaciones , Anciano , Ascitis/complicaciones , Ascitis/diagnóstico , Biopsia con Aguja/métodos , Diagnóstico Diferencial , Resultado Fatal , Síndrome de Felty/diagnóstico , Femenino , Estudios de Seguimiento , Hepatitis Autoinmune/diagnóstico , Humanos , Laparoscopía , Hígado/diagnóstico por imagen , Hígado/patología , Fallo Hepático/diagnóstico , Fallo Hepático/etiología , Tomografía Computarizada por Rayos X
4.
Artículo en Inglés | MEDLINE | ID: mdl-26185434

RESUMEN

BACKGROUND: Cardiovascular diseases, osteoporosis, and depression are identified comorbidities of chronic obstructive pulmonary disease (COPD), but there have been few reports of chronic kidney disease (CKD) as a comorbidity of COPD. The objective of this study was to investigate the prevalence of CKD in COPD patients using estimated glomerular filtration rate (eGFR) based on creatinine (Cr) and cystatin C (Cys) levels. METHODS: The prevalence of CKD and the values of various CKD-related parameters were compared between 108 stable COPD outpatients (COPD group) and a non-COPD control group consisting of 73 patients aged 60 years or more without a history of COPD or kidney disease. CKD was defined as an eGFR less than 60 mL/min/1.73 m(2). RESULTS: The Cr level was significantly higher in the COPD group, but eGFR based on serum Cr (eGFRCr) was not significantly different between the two groups (73.3±25.3 vs 79.7±15.5 mL/min/1.73 m(2)). The Cys level was significantly higher and eGFR based on serum Cys (eGFRCys) was significantly lower in the COPD group (60.0±19.4 vs 74.0±13.5 mL/min/1.73 m(2), P<0.0001). The prevalence of CKD evaluated based on eGFRCr was 31% in the COPD group and 8% in the non-COPD group with an odds ratio of 4.91 (95% confidence interval, 1.94-12.46, P=0.0008), whereas the evaluated prevalence based on eGFRCys was 53% in the COPD group and 15% in the non-COPD group with an odds ratio of 6.30 (95% confidence interval, 2.99-13.26, P<0.0001), demonstrating a higher prevalence of CKD when based on eGFRCys rather than on eGFRCr. CONCLUSION: CKD is a comorbidity that occurs frequently in COPD patients, and we believe that renal function in Japanese COPD patients should preferably be evaluated based not only on Cr but on Cr in combination with Cys.


Asunto(s)
Creatinina/sangre , Cistatina C/sangre , Tasa de Filtración Glomerular , Riñón/fisiopatología , Enfermedad Pulmonar Obstructiva Crónica/epidemiología , Insuficiencia Renal Crónica/epidemiología , Anciano , Anciano de 80 o más Años , Biomarcadores/sangre , Estudios de Casos y Controles , Comorbilidad , Femenino , Humanos , Japón/epidemiología , Masculino , Persona de Mediana Edad , Modelos Biológicos , Oportunidad Relativa , Valor Predictivo de las Pruebas , Prevalencia , Enfermedad Pulmonar Obstructiva Crónica/diagnóstico , Insuficiencia Renal Crónica/sangre , Insuficiencia Renal Crónica/diagnóstico , Insuficiencia Renal Crónica/fisiopatología , Factores de Riesgo
5.
Rinsho Ketsueki ; 43(11): 993-7, 2002 Nov.
Artículo en Japonés | MEDLINE | ID: mdl-12508485

RESUMEN

We successfully treated a patient with chronic lymphocytic leukemia (CLL) associated with a nephrotic syndrome. An 82-year-old man had been diagnosed as having CLL and been under observation for a year without treatment. In January, 2001, he developed hypoprotenemia, proteinurea, and edema in the extremities and face. With the exacerbation of the symptoms, he was admitted to our hospital in March of the same year. Under the diagnosis of nephrotic syndrome with CLL, the patient underwent induction therapy for CLL with fludarabine (13 mg/m2/day for 4 days), which brought about a complete remission of CLL and the disappearance of the edema. To our knowledge, this was the first case in Japan where fludarabine was dramatically effective in treating both CLL and the nephrotic syndrome. This result indicated that fludarabine is beneficial for not only CLL but also complications like nephrotic syndrome.


Asunto(s)
Antineoplásicos/uso terapéutico , Leucemia Linfocítica Crónica de Células B/tratamiento farmacológico , Síndrome Nefrótico/complicaciones , Vidarabina/análogos & derivados , Vidarabina/uso terapéutico , Anciano , Anciano de 80 o más Años , Humanos , Leucemia Linfocítica Crónica de Células B/complicaciones , Masculino
6.
Respirology ; 8(4): 522-4, 2003 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-14629659

RESUMEN

OBJECTIVE: We evaluated the damage to expandable metallic stents (EMS) based upon analysis of EMS removed at autopsy. METHODOLOGY: Seventeen EMS were obtained during autopsy from the main bronchi of nine patients with lung cancer. Each EMS was categorized into one of the following three groups, according to the degree of EMS damage: no damage at all (ND), damage to part of the EMS (PD), and marked damage (MD) that caused loss of function of the airway stent. The removed EMS were examined using a scanning electron microscope. RESULTS: Of the 17 stents, ND occurred in 13 (7/9 primary, 6/8 secondary), PD in four (all secondary), and MD in none. None of the stents had completely lost the ability to function as an airway stent. Bacterial biofilm formation (BBF) was detected on EMS from four patients. CONCLUSIONS: Bacterial biofilm forms on EMS implanted into the airway. Some physical damage was present in four of 17 EMS, but all remained functional.


Asunto(s)
Obstrucción de las Vías Aéreas/terapia , Biopelículas , Neoplasias Pulmonares/terapia , Infecciones Relacionadas con Prótesis/etiología , Stents/efectos adversos , Adulto , Anciano , Obstrucción de las Vías Aéreas/etiología , Autopsia , Falla de Equipo , Femenino , Humanos , Japón/epidemiología , Neoplasias Pulmonares/complicaciones , Masculino , Microscopía Electrónica de Rastreo , Persona de Mediana Edad , Infecciones Relacionadas con Prótesis/epidemiología , Infecciones Relacionadas con Prótesis/patología
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