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4.
J Dermatol ; 46(5): 409-412, 2019 May.
Artigo em Inglês | MEDLINE | ID: mdl-30932227

RESUMO

A case of severe fever with thrombocytopenia syndrome (SFTS) in which a skin biopsy from the tick-bite region was analyzed is reported. The patient was a 72-year-old woman who developed fever and thrombocytopenia after a tick bite. SFTS was diagnosed from polymerase chain reaction (PCR) analysis of a blood sample. Histopathological analysis of a skin biopsy specimen from the tick-bite region showed CD20-positive perivascular and interstitial immunoblastic cells, which were positive to anti-SFTS virus (SFTSV) nucleoprotein antibody. In addition, SFTSV RNA was detected by real-time PCR from this biopsy specimen. Moreover, hemophagocytosis was also found in the tick-bite region. To the best of our knowledge, this is the first report to analyze the details of the tick-bite region of skin in SFTS, and the first to detect virus-infected cells in the skin. The present findings may help elucidate the mechanisms of entry of SFTSV.


Assuntos
Coagulação Intravascular Disseminada/virologia , Febre por Flebótomos/virologia , Phlebovirus/isolamento & purificação , Trombocitopenia/virologia , Picadas de Carrapatos/patologia , Idoso , Biópsia , Coagulação Intravascular Disseminada/sangue , Coagulação Intravascular Disseminada/diagnóstico , Evolução Fatal , Feminino , Humanos , Febre por Flebótomos/sangue , Febre por Flebótomos/diagnóstico , Phlebovirus/genética , RNA Viral/isolamento & purificação , Pele/patologia , Pele/virologia , Síndrome , Trombocitopenia/sangue , Trombocitopenia/diagnóstico , Picadas de Carrapatos/sangue , Picadas de Carrapatos/complicações , Picadas de Carrapatos/virologia
7.
Eur J Oncol Nurs ; 28: 28-34, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28478852

RESUMO

PURPOSE: This study was conducted with infants diagnosed with bilateral retinoblastoma (RB) and their mothers. It explored characteristics of the mother-infant interaction, the infants' developmental characteristics and related risk factors. METHOD: Cross-sectional statistical analysis was performed with 18 dyads of one-year-old infants with bilateral RB and their mothers. RESULTS: Using the Japanese Nursing Child Assessment Teaching Scale (JNCATS) results showed that infants with RB had significantly lower scores compared to normative Japanese scores on all of the infants' subscales and "Child's contingency" (p < 0.01). Five infants with visual impairment at high risk of developmental problems had a pass rate of 0% on six JNCATS items. There were positive correlations between Developmental quotients (DQ) and JNCATS score of "Responsiveness to caregiver" (ρ = 0.50, p < 0.05) and DQ and "Child's contingency" (ρ = 0.47, p < 0.05). CONCLUSIONS: Infants with visual impairment were characterized by high likelihood of developmental delays and problematic behaviors; they tended not to turn their face or eyes toward their mothers, smile in response to their mothers' talking to them or the latter's changing body language or facial expressions, or react in a contingent manner in their interactions. These infant behaviors noted by their mothers shared similarities with developmental characteristics of children with visual impairments. These findings indicated a need to provide support promoting mother-infant interactions consistent with the developmental characteristics of RB infants with visual impairment.


Assuntos
Desenvolvimento Infantil/fisiologia , Comportamento do Lactente/fisiologia , Comportamento do Lactente/psicologia , Relações Mãe-Filho/psicologia , Mães/psicologia , Retinoblastoma/complicações , Transtornos da Visão/psicologia , Adolescente , Adulto , Povo Asiático/psicologia , Criança , Pré-Escolar , Estudos Transversais , Feminino , Humanos , Lactente , Japão , Masculino , Pessoa de Meia-Idade , Retinoblastoma/psicologia , Fatores de Risco
8.
J Dermatol ; 43(12): 1429-1432, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27450766

RESUMO

Hereditary lactate dehydrogenase (LDH) M-subunit deficiency is very rare and we have found reports of close to a dozen cases in the published work, two of which were associated with pustular psoriasis-like lesions. We report a third case of pustular psoriasis-like eruptions associated with LDH M-subunit deficiency, which occurred 24 years after the diagnosis of LDH M-subunit deficiency. These cases indicate that abnormal activity of LDH can induce pustular psoriatic lesions in the long term. Some patients with symptoms of hereditary LDH M-subunit deficiency have antecedent annular scaly plaque lesions, that resemble psoriatic lesions. We discuss a hypothesis to explain this scenario.


Assuntos
L-Lactato Desidrogenase/deficiência , L-Lactato Desidrogenase/genética , Psoríase/genética , Doenças Raras/genética , Deleção de Sequência , Adulto , Sequência de Aminoácidos/genética , Biópsia , Éxons/genética , Feminino , Glucocorticoides/uso terapêutico , Humanos , Imuno-Histoquímica , Isoenzimas/deficiência , Isoenzimas/genética , Lactato Desidrogenase 5 , Prednisolona/uso terapêutico , Psoríase/tratamento farmacológico , RNA Mensageiro/genética , Análise de Sequência de DNA , Análise de Sequência de RNA , Pele/patologia , Fatores de Tempo , Valina/genética
10.
Acute Med Surg ; 3(2): 120-127, 2016 04.
Artigo em Inglês | MEDLINE | ID: mdl-29123763

RESUMO

Aim: There has been no indicator that allows an early quantitative evaluation of the severity of a mamushi snake (Gloydius blomhoffii) bite. Because the number of severe mamushi bite cases is much fewer than non-severe cases, a formal case-control study is difficult. Therefore, we tried to generate a preliminary quantitative, real-time index for its severity by referring to published reports of severe mamushi bite cases. Methods: We enrolled patients who presented with a mamushi bite and visited our outpatient clinic. Severe cases were collected from published works. Creatinine kinase levels and white blood cell counts of non-severe and severe cases were compared and analyzed. Results: There was a lag time of 10 h before the creatinine kinase level began to rise. The speed of the increase was higher in severe cases than in non-severe cases, and severe cases were recognized as those showing speeds of above 250 IU/L/h. White blood cell counts increased earlier than creatinine kinase levels without any lag time. Severe cases were recognized as those with the counts of over 1,000 × (h) + 6,000 [/µL] before 5 h and 300 × (h) + 10,000 [/µL] after 5 h. Conclusion: We herein present the creatinine kinase level and white blood cell count trends and demonstrate preliminary cut-off equations. The trends for both parameters serve as quantitative indicators of the severity of a mamushi bite until a large scale case-control study is achieved.

12.
J Med Dent Sci ; 62(4): 103-13, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26984827

RESUMO

This study aimed to clarify the relationships among developmental characteristics of retinoblastoma (RB) infants, mother-infant interaction, and mental health of mothers. Prospective studies were conducted twice with 13 dyads of mothers and infants who were between one (Time 1) and two years old (Time 2). Cross-sectional and longitudinal analyses were performed. The mean Developmental Quotients (DQ) significantly decreased between Time 1 and Time 2 (p < .05). Four (30.8%) infants showed DQ p < 85 at Time 1. They showed a DQ below the borderline at Time 2 and their developmental changes were different from RB infants in the normal DQ range. Infant Behavior Checklist-R (IBC-R) scores negatively correlated with DQ (p < .05). The mothers' Japanese Nursing Child Assessment Teaching Scale (JNCATS) scores were significantly higher than the normative mean. The IBC-R scores negatively correlated with mothers' JNCATS scores at Time 1 (ρ = -.66, p < .05) and positively correlated with the child domain scores on the Parenting Stress Index at Time 2 (ρ = .62, p < .05). Some RB infants showed a developmental delay. Mother-child interactions were negatively affected and mothers recognized their infants' problem. The support needs to be provided in early infancy.


Assuntos
Relações Mãe-Filho/psicologia , Neoplasias da Retina/psicologia , Retinoblastoma/psicologia , Adulto , Desenvolvimento Infantil , Pré-Escolar , Estudos Transversais , Feminino , Humanos , Lactente , Comportamento do Lactente , Japão , Estudos Longitudinais , Mães/psicologia , Poder Familiar/psicologia , Estudos Prospectivos , Estresse Psicológico
14.
Case Rep Dermatol ; 2(2): 110-115, 2010 Jul 02.
Artigo em Inglês | MEDLINE | ID: mdl-20689634

RESUMO

Orbital xanthogranuloma is an uncommon tumor. It is usually associated with a systemic or hematological disease. This report presents a rare case of orbital xanthogranuloma associated with heart disease and thrombocytopenia. A 52-year-old female presented with a bilateral periorbital subcutaneous tumor that had existed for 3 years. Although immunoglobulin levels were within the normal limits, thrombocytopenia, slight anemia and increased levels of C-reactive protein and alkaline phosphatase were observed. The mass was excised successfully. The malar flap elevation technique made it easy to approach the periorbital subcutaneous mass. A histopathological study led to a diagnosis of xanthogranuloma based on the presence of infiltration of histiocytes and Touton-type giant cells.

15.
J Dermatol ; 37(4): 374-7, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-20507410

RESUMO

Drug-induced hypersensitivity syndrome (DIHS) is characterized by a serious adverse systemic reaction that usually appears after a 3-6-week exposure to certain drugs, for example, anticonvulsants. Many different precipitating factors have been reported, but the pathophysiology of DIHS remains unknown. However, reactivation of members of the human herpesvirus (HHV) family, and of HHV-6 in particular, has been reported in patients with DIHS. We report the case of a 64-year-old man who developed a generalized erythematous rash, fever, hepatic failure, lymphadenopathy and an increased number of atypical lymphocytes. In addition, reactivation of HHV-6 and cytomegalovirus (CMV) was demonstrated by real-time quantitative amplification by polymerase chain reaction. The patient was given a diagnosis of DIHS due to carbapenem antibiotics based on his clinical course, laboratory data, and results of lymphocyte-stimulation tests with various drugs. This is the first report, to our knowledge, of DIHS induced by carbapenem antibiotics.


Assuntos
Carbapenêmicos/efeitos adversos , Infecções por Citomegalovirus/etiologia , Citomegalovirus/efeitos dos fármacos , Hipersensibilidade a Drogas/virologia , Herpesvirus Humano 6/efeitos dos fármacos , Infecções por Roseolovirus/etiologia , Ativação Viral/efeitos dos fármacos , Anticorpos Monoclonais/administração & dosagem , Anticorpos Monoclonais Murinos , Protocolos de Quimioterapia Combinada Antineoplásica/administração & dosagem , Carbapenêmicos/administração & dosagem , Ciclofosfamida/administração & dosagem , Infecções por Citomegalovirus/diagnóstico , Infecções por Citomegalovirus/patologia , Doxorrubicina/administração & dosagem , Hipersensibilidade a Drogas/diagnóstico , Hipersensibilidade a Drogas/patologia , Exantema/diagnóstico , Exantema/patologia , Exantema/virologia , Febre/diagnóstico , Febre/virologia , Humanos , Falência Hepática/diagnóstico , Falência Hepática/patologia , Falência Hepática/virologia , Doenças Linfáticas/diagnóstico , Doenças Linfáticas/patologia , Doenças Linfáticas/virologia , Linfoma de Célula do Manto/tratamento farmacológico , Masculino , Pessoa de Meia-Idade , Prednisolona/administração & dosagem , Rituximab , Infecções por Roseolovirus/diagnóstico , Infecções por Roseolovirus/patologia , Síndrome , Vincristina/administração & dosagem
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