RESUMO
Oral squamous cell carcinoma is generally characterized by poor prognosis, and biomarkers are needed for development and selection of therapy. The purpose of this study was to assess expression of actinin-4, which has been implicated in cancer invasion and metastasis, to determine its viability as a prognostic indicator in oral squamous cell carcinoma. Clinical factors and tumor samples immunohistochemically stained for actinin-4 were retrospectively investigated in 55 patients who underwent curative surgery for oral squamous cell carcinoma. Overall survival and disease-free survival were estimated by Kaplan-Meier analysis. Significant differences were detected using the Pearson's chi-square and Fisher's exact tests. Univariate and multivariate analyses were performed with the Cox regression model. No association was found between expression of actinin-4 and clinical factors, including age or sex, or histopathological factors, including vascular invasion, lymphatic invasion, stage, mode of invasion, or histological atypicality. Expression of actinin-4 showed a positive correlation with delayed cervical lymph node metastasis. Disease-free survival was significantly lower in patients who were positive for expression of actinin-4 (p=0.010); overall survival showed no difference between patients with or without expression of actinin-4, however. The results revealed that actinin-4 was an independent prognostic factor for disease-free survival. Expression of actinin-4 showed a 73% sensitivity and 68% specificity for prediction of delayed cervical lymph node metastasis. In conclusion, actinin-4 may potentially be a useful biomarker for prediction of delayed cervical lymph node metastasis.
Assuntos
Carcinoma de Células Escamosas , Neoplasias Bucais , Actinina , Intervalo Livre de Doença , Humanos , Linfonodos , Invasividade Neoplásica , Estadiamento de Neoplasias , Prognóstico , Estudos RetrospectivosRESUMO
This study tests whether comprehensively gathering information from medical records is useful for developing clinical decision support systems using Bayes' theorem. Using a single-center cross-sectional study, we retrospectively extracted medical records of 270 patients aged ≥16 years who visited the emergency room at the Tokyo Metropolitan Tama Medical Center with a chief complaint of experiencing headaches. The medical records of cases were analyzed in this study. We manually extracted diagnoses, unique keywords, and annotated keywords, classifying them as either positive or negative. Cross tables were created, and the proportion of combinations for which the likelihood ratios could be calculated was evaluated. Probability functions for the appearance of new unique keywords were modeled, and theoretical values were calculated. We extracted 623 unique keywords, 26 diagnoses, and 6,904 annotated keywords. Likelihood ratios could be calculated only for 276 combinations (1.70%), of which 24 (0.15%) exhibited significant differences. The power function+constant was the best fit for new unique keywords. The increase in the number of combinations after increasing the number of cases indicated that while it is theoretically possible to comprehensively gather information from medical records in this way, doing so presents difficulties related to human costs. It also does not necessarily solve the fundamental issues with medical informatics or with developing clinical decision support systems. Therefore, we recommend using methods other than comprehensive information gathering with Bayes' theorem as the classifier to develop such systems.
RESUMO
A Peutz-Jeghers polyp (PJP) is a hamartomatous lesion characterized by arborescent smooth muscle bundles covered with mucosa native to the site of involvement. PJPs in the small intestine may represent misplacement of non-neoplastic epithelium into the submucosa, muscularis propria and subserosa. Although epithelial misplacement in PJPs is a well-documented phenomenon, pseudoinvasion even into the vascular space in PJPs has not previously been reported. We report a case of a 22-year-old Japanese woman with a solitary PJP in the ileum. The ileal PJP in this patient showed epithelial herniation even into the vascular space. All the herniated epithelium, including the epithelial components invaginated into the vascular space, demonstrated features of pseudoinvasion, that is, presence of normal small intestinal type mucosa accompanied by the lamina propria, absence of any stromal desmoplastic reaction, and retention of the basal-luminal gradient. Pathologists must be aware of the possibility of vascular pseudoinvasion in small intestinal PJPs to avoid overdiagnosis of carcinoma and resulting unnecessary major surgery.
Assuntos
Neoplasias do Íleo/patologia , Pólipos Intestinais/patologia , Síndrome de Peutz-Jeghers/patologia , Feminino , Humanos , Neoplasias do Íleo/irrigação sanguínea , Neoplasias do Íleo/cirurgia , Pólipos Intestinais/cirurgia , Invasividade Neoplásica/patologia , Síndrome de Peutz-Jeghers/cirurgia , Resultado do Tratamento , Adulto JovemAssuntos
Neoplasias Esofágicas/patologia , Leiomioma/patologia , Neoplasias do Mediastino/patologia , Adulto , Biomarcadores Tumorais/análise , Biópsia , Endoscopia do Sistema Digestório , Endossonografia , Neoplasias Esofágicas/química , Neoplasias Esofágicas/cirurgia , Esofagectomia , Humanos , Imuno-Histoquímica , Leiomioma/química , Leiomioma/cirurgia , Masculino , Neoplasias do Mediastino/química , Neoplasias do Mediastino/cirurgia , Imagem Multimodal , Tomografia por Emissão de Pósitrons , Valor Preditivo dos Testes , Tomografia Computadorizada por Raios X , Carga TumoralAssuntos
Neoplasias Esofágicas/diagnóstico , Neoplasias Esofágicas/patologia , Melanoma/diagnóstico , Melanoma/patologia , Neoplasias Gástricas/diagnóstico , Neoplasias Gástricas/patologia , Endoscopia do Sistema Digestório , Feminino , Histocitoquímica , Humanos , Imuno-Histoquímica , Antígenos Específicos de Melanoma/análise , Microscopia , Pessoa de Meia-Idade , Antígeno gp100 de MelanomaRESUMO
A 72-year-old man visited our hospital due to persistent cough, fever and weight loss. A chest X-ray film revealed a round tumor in the left lower lung field. A specimen obtained by transbronchial lung biopsy demonstrated histiocytic and lymphocytic infiltration in the alveolar space, with spindle myofibroblasts and plasmacytes in the interstitium, Those findings were consistent with inflammatory pseudotumor. Four weeks later, a chest X-ray film showed only scars of the primary lesion, and his symptoms resolved dramatically. He has had no recurrence of symptoms and pulmonary tumor since then. Although spontaneous remission is uncommon in inflammatory pseudotumor of the lung, there are several case reports about spontaneous remission of hepatic inflammatory pseudotumor and autoimmune pancreatitis, parts of IgG4-related sclerosing disease. Recently, inflammatory pseudotumor is thought to be IgG4-related sclerosing disease. We speculate that IgG4 may be associated with spontaneous remission of inflammatory pseudotumor of the lung, and we discuss this issue in relation to the pertinent literature.
Assuntos
Granuloma de Células Plasmáticas/diagnóstico , Imunoglobulina G/análise , Pneumopatias/diagnóstico , Idoso , Humanos , Imuno-Histoquímica , Masculino , Remissão EspontâneaRESUMO
The Tokyo metropolitan hospital society of chief medical technologist has carried out a staining survey once a year since 1992. This staining survey is performed to plan improvements of the staining technology at each hospital and reduction of differences among hospitals. This report describes the examination results for PAS stain, Papanicolaou stain, and PAM stain.
Assuntos
Corantes/normas , Ácido Aminossalicílico , Coleta de Dados , Coloração e Rotulagem/métodos , TóquioRESUMO
A 71-year-old woman was admitted with dyspnea. An electrocardiogram revealed ST-segment elevation, and echocardiography showed akinesis in the left ventricular apex with hyperkinesis of the base. Coronary angiography revealed no stenosis, and left ventriculography indicated ballooning of the left ventricular apex and apical ventricular septal perforation. We diagnosed the patient with Takotsubo syndrome complicated by ventricular septal perforation, which was surgically repaired. Although ventricular septal perforation is recognized as a life-threatening complication after acute myocardial infarction, it can also occur after Takotsubo syndrome. The early recognition and management of this condition can help prevent morbidity and mortality.
Assuntos
Cardiomiopatia de Takotsubo/complicações , Ruptura do Septo Ventricular/etiologia , Idoso , Angiografia Coronária , Ecocardiografia , Feminino , Humanos , Cardiomiopatia de Takotsubo/diagnóstico , Ruptura do Septo Ventricular/diagnósticoAssuntos
Tumores Fibrosos Solitários/diagnóstico , Neoplasias da Língua/diagnóstico , Idoso , Antígenos CD34/análise , Diagnóstico Diferencial , Glossectomia/métodos , Humanos , Imageamento por Ressonância Magnética , Masculino , Neurilemoma/diagnóstico , Proteínas Proto-Oncogênicas c-bcl-2/análise , Neoplasias das Glândulas Salivares/diagnóstico , Vimentina/análiseAssuntos
Doenças Autoimunes/diagnóstico por imagem , Imunoglobulina G/imunologia , Nefrite Intersticial/diagnóstico por imagem , Doenças Autoimunes/tratamento farmacológico , Doenças Autoimunes/imunologia , Glucocorticoides/uso terapêutico , Humanos , Masculino , Pessoa de Meia-Idade , Nefrite Intersticial/tratamento farmacológico , Nefrite Intersticial/imunologia , Tomografia por Emissão de Pósitrons , Tomografia Computadorizada por Raios XRESUMO
A 70-year-old man with diabetes mellitus presented with an enlarged pituitary stalk in 2014. IgG4-related parotitis and submandibular sialoadenitis were diagnosed in 2012. He denied any symptoms related to a pituitary mass. His visual field was intact, and his hypopituitarism was subtle. The serum IgG4 level was elevated. A lip biopsy revealed strong fibrosis and hyper-infiltration of IgG4-positive plasma cells. Based on these findings, IgG4-related hypophysitis was diagnosed. The patient was carefully followed without specific intervention. His clinical condition showed no change until December 2016, suggesting a stable, natural course. Care should be taken when considering glucocorticoid therapy, especially for elderly diabetic patients, given possible side effects.
Assuntos
Hipofisite Autoimune/complicações , Hipopituitarismo/complicações , Imunoglobulina G/imunologia , Idoso , Hipofisite Autoimune/diagnóstico , Biópsia , Humanos , Imunoglobulina G/sangue , Masculino , Hipófise/patologia , PlasmócitosRESUMO
Benign vascular lesions-malformative, reactive, and neoplastic-are fairly common in the oral soft tissues; nevertheless, extravascular papillary endothelial hyperplasia and sinusoidal hemangioma have not been reported in this location. To our knowledge, a single case of intraoral spindle cell hemangioma has appeared in the literature. This report deals with histopathological features of these rare vascular proliferations involving the oral mucosa.
Assuntos
Doenças da Boca/patologia , Mucosa Bucal/patologia , Neoplasias Bucais/patologia , Adulto , Bochecha/patologia , Diagnóstico Diferencial , Endotélio/patologia , Feminino , Hemangioma/patologia , Humanos , Hiperplasia , Masculino , Pessoa de Meia-Idade , Neoplasias Palatinas/patologia , Língua/patologiaRESUMO
We herein describe a case of successful surgical treatment of isolated splenic peliosis presenting with giant splenomegaly and severe coagulopathy. Pathological features of the spleen included multinodular, blood-filled, cyst-like lesions distributed throughout the whole organ. The pathogenesis of isolated splenic peliosis is controversial, and no definitive disease mechanism has been reported. To our knowledge, this is the first report in English of a case like this.
Assuntos
Coagulação Intravascular Disseminada/etiologia , Baço/patologia , Esplenectomia , Esplenopatias/complicações , Esplenopatias/diagnóstico , Esplenomegalia/etiologia , Amiloidose/diagnóstico , Amiloidose/etiologia , Biomarcadores/sangue , Cistos/diagnóstico por imagem , Cistos/cirurgia , Coagulação Intravascular Disseminada/sangue , Humanos , Masculino , Pessoa de Meia-Idade , Tamanho do Órgão , Púrpura/etiologia , Índice de Gravidade de Doença , Baço/diagnóstico por imagem , Baço/cirurgia , Esplenopatias/sangue , Esplenopatias/patologia , Esplenopatias/cirurgia , Esplenomegalia/sangue , Tomografia Computadorizada por Raios X , Resultado do TratamentoRESUMO
An ultrastructural analysis of oral balloon cell nevus of intramucosal type complemented with an immunohistochemical study was performed for the first time. The lesion was composed of large balloon cells with an admixture of small nevus cells and melanophages at the periphery. Balloon cells showed cytoplasmic accumulation of vacuoles of varying sizes and the presence of microgranular and vacuolated melanosomes were found. Residual cytoplasm contained no identifiable organelles. A spectrum of transitional forms between balloon cells and conventional nevus cells with microvacuoles was readily observed. Both cells exhibited intense immunoreactivity to multiple melanocytic markers. Ballooning phenomenon was not evident in melanophages containing a large amount of melanosome complex. It can be inferred, from the present and previous observations, that progressive vacuolization of melanosomes in nevomelanocytes may be responsible for the formation of peculiar ballooning appearance, suggesting an aberrant melanogenesis.