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1.
Acta Med Okayama ; 72(5): 515-518, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-30369609

RESUMO

Hepatitis-associated aplastic anemia (HAAA) is an acquired bone marrow failure syndrome that develops after seronegative fulminant hepatitis. Abnormal cytotoxic T-cell activation with cytokine release is a possible pathophysiology. We present the case of a 16-month-old Japanese male who developed HAAA following living-donor liver transplantation for fulminant hepatitis. His aplastic anemia was successfully treated with immunosuppressive therapy. He had been administered tacrolimus for prophylaxis against hepatic allograft rejection. Ten years after the HAAA onset, the patient's bone marrow was found to be slightly hypoplastic. Tacrolimus may be effective in controlling abnormal immune reactions that can cause recurrent impaired hematopoiesis.


Assuntos
Anemia Aplástica/etiologia , Hepatite/complicações , Imunossupressores/efeitos adversos , Transplante de Fígado , Tacrolimo/efeitos adversos , Anemia Aplástica/imunologia , Relação CD4-CD8 , Humanos , Lactente , Ativação Linfocitária , Masculino
2.
Pediatr Int ; 59(5): 624-626, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28417531

RESUMO

Patients with Down syndrome (DS) have a markedly higher incidence of childhood leukemia, but a lower incidence of most solid tumors, compared with age-matched euploid individuals. Trisomy 21 might be protective against tumorigenesis because of several tumor suppressive mechanisms. Desmoid-type fibromatosis (DF) is a rare monoclonal, fibroblastic proliferation characterized by a variable clinical course. In recent reports, almost all cases of DF involved genomic alterations associated with activation of the Wnt/ß-catenin pathway. Here, we report the case of a boy with DS who developed DF without activation of the Wnt/ß-catenin pathway. To the best of our knowledge, this is the first case of DS involving DF.


Assuntos
Síndrome de Down/complicações , Fibromatose Agressiva/diagnóstico , Neoplasias Torácicas/diagnóstico , Pré-Escolar , Fibromatose Agressiva/complicações , Humanos , Masculino , Neoplasias Torácicas/complicações
3.
Pediatr Transplant ; 15(5): E87-91, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20070564

RESUMO

Hepatoblastoma is a rare malignant tumor of the liver in children. Intensive combination chemotherapy has increased the number of surgically resectable cases and improved prognosis markedly. However, unresectable cases and cases with residual metastasis, including lung metastases, have a poor prognosis. In these refractory cases, treatment strategy has not been established. On the other hand, living liver transplantation has been shown to be effective in cases of advanced hepatoblastoma, but its effectiveness in cases with residual distant metastases after chemotherapy remains unclear. We report one successful case of advanced unresectable hepatoblastoma with multiple lung metastases. Intensive chemotherapy consisting of high-dose chemotherapy with autologous hematopoietic stem cell transplantation was not effective. We performed living liver transplantation after surgical resection of residual lung metastases, which were histologically viable. After liver transplantation, the level of tumor marker decreased gradually. The patient experienced no severe complications. This case suggested that living liver transplantation could be effective in cases of advanced refractory hepatoblastoma after control of distant metastases.


Assuntos
Hepatoblastoma/cirurgia , Hepatoblastoma/terapia , Neoplasias Hepáticas/cirurgia , Neoplasias Hepáticas/terapia , Transplante de Fígado/métodos , Neoplasias Pulmonares/patologia , Neoplasias Pulmonares/cirurgia , Pré-Escolar , Veias Hepáticas/patologia , Humanos , Doadores Vivos , Neoplasias Pulmonares/complicações , Masculino , Metástase Neoplásica , Prognóstico , Tomografia Computadorizada por Raios X/métodos , Resultado do Tratamento
4.
Pediatr Transplant ; 12(5): 588-92, 2008 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-18266798

RESUMO

CAEBV is a high mortality and morbidity disease with life-threatening complications. Nevertheless, the treatment regimens for CAEBV have not yet been established. Although some reports have described CAEBV therapy involving treatments such as antiviral drugs, immunomodulatory agents, and immunochemotherapy, none of these treatments have been demonstrated to be effective. The only treatment reported to be effective is allogeneic SCT. However, the complications of SCT are severe, so treatment results have been poor. Recently, immunotherapy has been devised, but this is still in the developmental stage. In this report, two cases of CAEBV in which allogeneic SCT was performed soon after diagnosis are reported. In both cases, a high EBV genome titer in the peripheral blood was detected at onset. After SCT, the EBV genome titer decreased as CTL activity gradually increased. This fact suggested that not only high-dose chemotherapy as a preconditioning treatment of SCT but also increased CTL activity which could eliminate virus-infected cells might be effective, although additional cases should be studied in order to establish effective treatments.


Assuntos
Transplante de Medula Óssea/métodos , Infecções por Vírus Epstein-Barr/sangue , Infecções por Vírus Epstein-Barr/diagnóstico , Linfócitos T Citotóxicos/imunologia , Linfócitos T Citotóxicos/metabolismo , Antineoplásicos/farmacologia , Antivirais/farmacologia , Criança , Pré-Escolar , Feminino , Genoma Viral , Humanos , Fatores Imunológicos/farmacologia , Imunoterapia Adotiva/métodos , Masculino , Transplante Homólogo , Resultado do Tratamento
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