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1.
Gan To Kagaku Ryoho ; 47(13): 1762-1764, 2020 Dec.
Artigo em Japonês | MEDLINE | ID: mdl-33468821

RESUMO

We report a case of a male in his sixties with appendiceal cancer who underwent radical resection following CAPOX plus bevacizumab neoadjuvant chemotherapy. The patient presented to our hospital with a chief complaint of chronic low abdominal pain. Contrast-enhanced CT before neoadjuvant chemotherapy revealed an inhomogeneous tumor in the ileocecal region. Invasion to the bladder and the sigmoid colon was also observed. A colonoscopy showed an elevated lesion, which was caused by extramural invasion to the sigmoid colon. Pathological examination of the sigmoid colon tumor revealed well differentiated tubular adenocarcinoma and KRAS codon13 G13D. Hence, we diagnosed the patient with locally advanced appendiceal cancer with invasion to the bladder and sigmoid colon. We administered CAPOX plus bevacizumab as neoadjuvant chemotherapy. Contrast-enhanced abdominal CT after neoadjuvant chemotherapy revealed shrinkage of the primary tumor and reduction in the invasion to the bladder and sigmoid colon. We performed ileocecal resection(+D3), a partial sigmoidectomy, and partial bladder resection on the 135th day from the diagnosis. The resected specimen showed an appendiceal tumor with invasion to the bladder and sigmoid colon. The pathological diagnosis was Ⅴ, yType 5, tub2>tub1, ypT4b, ypN0, ycH0, ycM0, ycPUL0, Ly1b, V1b(VB), Pn01b, pStage Ⅱa, and the histological treatment effect of preoperative therapy was Grade 1b. Our experience indicates that in patients with locally advanced appendiceal cancer, multimodal treatment with neoadjuvant chemotherapy is an effective option.


Assuntos
Neoplasias do Apêndice , Neoplasias do Colo Sigmoide , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Neoplasias do Apêndice/tratamento farmacológico , Neoplasias do Apêndice/cirurgia , Bevacizumab/uso terapêutico , Humanos , Masculino , Terapia Neoadjuvante , Neoplasias do Colo Sigmoide/tratamento farmacológico , Neoplasias do Colo Sigmoide/cirurgia
2.
No To Hattatsu ; 48(1): 41-4, 2016 Jan.
Artigo em Japonês | MEDLINE | ID: mdl-27012110

RESUMO

We report a case of so-called "surfer's myelopathy" involving a 15-year-old girl. Preceding episodes of vaccination and infection were absent. She experienced back pain during a surfing class for beginners, followed by weakness in both legs, which progressed to paraperesis. Then, 2 days later, sensory disturbance and bladder/rectal disturbance also developed. Spinal MRI revealed a ischemic lesion compatible with anterior spinal cord syndrome. A combination of methylprednisolone pulse therapy and high-dose intravenous immunoglobulin therapy was effective leaving no residual dysfunction. The acute onset during the surfing class and characteristic MRI findings led to the diagnosis of surfer's myelopathy. Although rarely reported, warnings are warranted to prevent surfer's myelopathy and avoid the progressive deterioration of neurological dysfunction.


Assuntos
Exercício Físico , Doenças da Medula Espinal/etiologia , Doenças da Coluna Vertebral/etiologia , Adolescente , Feminino , Humanos , Imageamento por Ressonância Magnética , Doenças da Medula Espinal/terapia , Doenças da Coluna Vertebral/terapia
3.
Tokai J Exp Clin Med ; 40(2): 58-62, 2015 Jun 20.
Artigo em Inglês | MEDLINE | ID: mdl-26150185

RESUMO

We report a case of lip repair surgery performed for bilateral cleft lip and palate in a patient diagnosed with trisomy 13 and holoprosencephaly. At the age of 2 years and 7 months, the surgery was performed using a modified De Hann design under general anesthesia. The operation was completed in 1 h and 21 min without large fluctuations in the child's general condition. The precise measurement of the intraoperative design was omitted, and the operation was completed using minimal skin sutures. It is possible to perform less-invasive and short surgical procedures after careful consideration during the preoperative planning. Considering the recent improvements in the life expectancy of patients with trisomy 13, we conclude that surgical treatments for non-life threatening malformations such as cleft lip and palate should be performed for such patients.


Assuntos
Anormalidades Múltiplas/cirurgia , Transtornos Cromossômicos/complicações , Fenda Labial/complicações , Fissura Palatina/complicações , Procedimentos Cirúrgicos Dermatológicos/métodos , Holoprosencefalia/complicações , Procedimentos de Cirurgia Plástica/métodos , Cirurgia Plástica/métodos , Anestesia Geral , Pré-Escolar , Cromossomos Humanos Par 13 , Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Feminino , Humanos , Lábio/cirurgia , Duração da Cirurgia , Planejamento de Assistência ao Paciente , Cuidados Pré-Operatórios , Técnicas de Sutura , Resultado do Tratamento , Trissomia , Síndrome da Trissomia do Cromossomo 13
4.
No To Hattatsu ; 45(4): 281-7, 2013 Jul.
Artigo em Japonês | MEDLINE | ID: mdl-23951939

RESUMO

OBJECTIVE: We examined the effectiveness of repeated adrenocorticotropic hormone (ACTH) therapy in short-term and long-term seizure control in patients with intractable epileptic spasms. METHODS: Twenty-five patients with intractable spasms, in whom epileptic seizures were not controlled or relapsed after the first ACTH therapy, were given repeated ACTH therapy. The short-term effect (seizure control longer than two months) of repeated ACTH therapy was analyzed, and the long-term effect was estimated by Kaplan-Meier method. RESULTS: Short-term seizure control by repeated ACTH therapy was achieved in 13 of 25 patients (52.0%), and in 5 of 13 patients, seizures were controlled by ACTH therapy at higher doses compared with the first ACTH therapy. Short-term effectiveness was obtained in 76.5% of patients who had epileptic spasms alone at the time of the second ACTH therapy, but was ineffective in all 8 patients who had multiple types of seizures, with relapses within 2 months. Short-term effectiveness was not associated with clinical factors such as onset age, age of repeated ACTH treatment, and EEG findings. Regarding the long-term effect of repeated ACTH therapy, the period until seizure relapse was significantly longer in patients with epileptic spasms alone compared to patients with multiple seizure types. Spasms were controlled in 5 of 25 cases (20.0%) at the final observation. In patients with multiple seizure types and patients with onset age older than eight months, seizure control was not obtained. Long-term outcome was good in patients with treatment lag within 2 months. CONCLUSION: In repeated ACTH therapy, seizure type seems to be one of the major determinants for short- and long-term seizure outcome.


Assuntos
Hormônio Adrenocorticotrópico/uso terapêutico , Epilepsia/tratamento farmacológico , Espasmos Infantis/tratamento farmacológico , Hormônio Adrenocorticotrópico/administração & dosagem , Idade de Início , Pré-Escolar , Epilepsia/diagnóstico , Feminino , Humanos , Lactente , Recém-Nascido , Masculino , Prognóstico , Espasmos Infantis/diagnóstico , Resultado do Tratamento
5.
Brain Dev ; 34(8): 685-90, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22154490

RESUMO

Self-induced seizures by somatosensory stimulation are rare. We describe two epileptic patients with self-induced seizures presumably by peri-orbital somatosensory stimulation. Two infants with severely delayed psychomotor development and poor visual acuity after acute subdural hemorrhage in early infancy had been diagnosed as having West syndrome. They evolutionally became to show serial self-induced seizures preceded by rubbing eye with finger in one case and touching right eyebrow with the back of left hand in the other case. Video-electroencephalography (EEG) monitoring was useful to confirm self-induced seizure by peri-orbital self-stimulation. In patients with serial seizures preceded by peculiar behaviors, we need to consider the possibility of self-induced seizures, even if they have a history of West syndrome and severe psychomotor retardation.


Assuntos
Órbita/inervação , Convulsões/etiologia , Convulsões/fisiopatologia , Autoestimulação/fisiologia , Tato , Pré-Escolar , Eletroencefalografia , Epilepsia/etiologia , Epilepsia/fisiopatologia , Feminino , Humanos , Lactente , Masculino , Espasmos Infantis/complicações , Gravação de Videoteipe
6.
No To Hattatsu ; 42(4): 273-6, 2010 Jul.
Artigo em Japonês | MEDLINE | ID: mdl-20666132

RESUMO

Dravet syndrome is a rare, but highly refractory epilepsy syndrome. As conventional drugs are not effective, introduction of new effective drugs in clinical use will benefit patients with this disease. We assessed the effectiveness of topiramate (TPM) as adjunctive therapy in 11 patients with Dravet syndrome. TPM was started at doses ranging from 10 to 50 mg/day (0.57 to 2.0 mg/kg/day), and the dosage was increased gradually up to the maximum dose (9 mg/kg/day) depending on efficacy and tolerability. The frequencies of convulsive seizures (generalized tonic-clonic seizures, unilateral seizures, partial onset generalized tonic-clonic seizures) during two months before starting TPM, two months after starting TPM, and the fifth and sixth months after starting TPM were determined. The mean dose (mean +/- SD) of TPM at the second month was 2.7 +/- 1.5 mg/kg/day (1.0-5.7 mg/kg/day, n= 11), and that at the sixth month was 4.5 +/- 2.2 mg/kg/day (1.0-7.3 mg/kg/day, n=10). Evaluation at the second month revealed that one of 11 patients (9%) became seizure-free, six patients (54%) showed greater than 50% seizure reduction, three patients (27%) showed less than 50% seizure reduction, and one patient (9%) had aggravation of convulsive seizures resulting in discontinuation of TPM at the first month. Evaluation at the sixth month revealed that one of 10 patients (10%) was seizure-free, seven patients (70%) had greater than 50% seizure reduction, two patients (20%) had less than 50% seizure reduction, and no patient (0%) had aggravation. Adverse effects were observed in five patients; dizziness in three patients, sleepiness in three patients, and oligohidrosis in one patient. In the present study, TPM was useful as an adjunctive therapy to reduce the frequency of convulsive seizures in patients with Dravet syndrome. A large-scale efficacy study of TPM for Dravet syndrome is warranted.


Assuntos
Anticonvulsivantes/uso terapêutico , Epilepsias Mioclônicas/tratamento farmacológico , Frutose/análogos & derivados , Adolescente , Anticonvulsivantes/administração & dosagem , Criança , Pré-Escolar , Feminino , Frutose/administração & dosagem , Frutose/uso terapêutico , Humanos , Lactente , Masculino , Topiramato , Adulto Jovem
7.
Epilepsy Res ; 89(2-3): 303-9, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20227246

RESUMO

Deletion of the terminal end of 17p is responsible for Miller-Dieker syndrome (MDS), which is characterized by lissencephaly, distinctive facial features, growth deficiency, and intractable seizures. Using microarray-based comparative genomic hybridization, 3 patients with epilepsy were revealed to have genomic copy number aberrations at 17p13.3: a partial LIS1 deletion in a patient with isolated lissencephaly and epilepsy, a triplication of LIS1 in a patient with symptomatic West syndrome, and a terminal deletion of 17p including YWHAE and CRK but not LIS1 in a patient with intractable epilepsy associated with distinctive facial features and growth retardation. In this study, it was suggested that the identified gain or loss of genomic copy numbers within 17p13.3 result in epileptogenesis and that triplication of LIS1 can cause symptomatic West syndrome.


Assuntos
1-Alquil-2-acetilglicerofosfocolina Esterase/genética , Deleção Cromossômica , Cromossomos Humanos Par 17/genética , Lissencefalias Clássicas e Heterotopias Subcorticais em Banda/genética , Proteínas Associadas aos Microtúbulos/genética , 1-Alquil-2-acetilglicerofosfocolina Esterase/deficiência , Encéfalo/anormalidades , Lissencefalias Clássicas e Heterotopias Subcorticais em Banda/patologia , Lissencefalias Clássicas e Heterotopias Subcorticais em Banda/fisiopatologia , Anormalidades Craniofaciais/genética , Eletroencefalografia , Feminino , Humanos , Hibridização in Situ Fluorescente , Lactente , Imageamento por Ressonância Magnética , Masculino , Proteínas Associadas aos Microtúbulos/deficiência , Adulto Jovem
8.
Tokai J Exp Clin Med ; 35(1): 25-8, 2010 Apr 20.
Artigo em Inglês | MEDLINE | ID: mdl-21319022

RESUMO

We examined 16 patients with acute cerebellar ataxia (ACA) to determine whether clinical manifestations or laboratory findings could predict the prognosis of ACA. We divided the patients into two groups: a benign group of patients whose cerebellar symptoms completely disappeared within 21 days (9 patients), and a prolonged group of patients whose cerebellar symptoms persisted for more than 22 days (7 patients). The two groups were compared on the basis of demographic and clinical characteristics, and laboratory variables. The cerebellar symptoms did not differ significantly between the two groups, except in duration. The level of neuron-specific enolase (NSE) in the cerebrospinal fluid (CSF) of the prolonged group was significantly higher than that of the benign group (p < 0.01); other parameters, including protein and cell count in the CSF, were not significantly different. The results suggest that the NSE level in CSF is of prognostic value in ACA.


Assuntos
Ataxia Cerebelar/líquido cefalorraquidiano , Ataxia Cerebelar/diagnóstico , Fosfopiruvato Hidratase/líquido cefalorraquidiano , Prognóstico , Criança , Feminino , Humanos , Masculino
9.
No To Hattatsu ; 41(1): 47-51, 2009 Jan.
Artigo em Japonês | MEDLINE | ID: mdl-19172817

RESUMO

We present a 5-year-old boy with recurrent idiopathic cerebral infarction in which analysis of platelet hyperaggregability was useful in choosing appropriate anti-platelet drugs. The patient presented with gait disturbance at the age of 5 years and 1 month. Brain MRI demonstrated multiple infarctions in the right thalamus and left cerebellum. There were no apparent underlying diseases including hematological, cardiac and vascular abnormalities. He was diagnosed as idiopathic cerebral infarction. First, we administered ticlopidine and he remained stable with persistent mild intention tremor in the left upper extremity for 4 months. Then he developed the second stroke at the age of 5 years and 5 months, and multiple infarctions in the right celebellum and cerebellar vermis were demonstrated. On platelet aggregation analysis, adenosine diphosphate (ADP)-induced aggregation was inhibited, probably due to ticlopidine administration. Collagen- and epinephrine-induced platelet aggregation showed hyperaggregation, so we started to administer cilostazol, which inhibits only epinephrine-induced hyperaggregation. We also added aspirin, which inhibits collagen-induced hyperaggregation. The combination of anti-platelet drugs inhibited epinephrine-, collagen- and ADP-induced hyperaggregation in this patient. He has been stable on the triple combination of anti-platelet drugs without further episodes of cerebral infarction or transient ischemic attack for 4 years to date. Appropriate selection of anti-platelet therapy was achieved by the simple and repeatable platelet aggregation analyses, which must be considered even in pediatric patients with cerebral infarction.


Assuntos
Testes de Coagulação Sanguínea , Infarto Cerebral/tratamento farmacológico , Inibidores da Agregação Plaquetária/uso terapêutico , Agregação Plaquetária , Difosfato de Adenosina , Aspirina/uso terapêutico , Infarto Cerebral/sangue , Infarto Cerebral/diagnóstico , Pré-Escolar , Cilostazol , Colágeno , Quimioterapia Combinada , Epinefrina/economia , Epinefrina/genética , Humanos , Masculino , Recidiva , Tetrazóis/uso terapêutico , Ticlopidina/uso terapêutico , Resultado do Tratamento
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