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1.
Interact Cardiovasc Thorac Surg ; 28(4): 652-654, 2019 04 01.
Artículo en Inglés | MEDLINE | ID: mdl-30476087

RESUMEN

Thoracic venous aneurysms are rare, and bleeding is possible. A 9-year-old female patient presented with a thoracic wall mass. No blood flow was observed in the mass, and a chronic expanding haematoma was suspected based on the differential diagnosis. However, the venous structure was identified in the wall of the mass on pathological examination, and the diagnosis of the venous aneurysm was thereby established. Because the venous aneurysm contains fresh blood and bleeding can be profuse when such lesions are not properly handled during a surgical procedure, making the visibility of the surgeon poor, the venous aneurysm must be included in the differential diagnosis.


Asunto(s)
Aneurisma/diagnóstico , Aneurisma/cirugía , Hematoma/diagnóstico , Pared Torácica/irrigación sanguínea , Venas , Niño , Diagnóstico Diferencial , Femenino , Humanos
2.
Gynecol Obstet Invest ; 82(3): 294-302, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-27384958

RESUMEN

BACKGROUND/AIM: The aim of this study was to evaluate the gene and protein expression of angiotensin type (AT) 1, AT2 receptors in endometriotic lesions and its relation to prostaglandin (PG) synthases. MATERIALS AND METHODS: Endometriosis samples were obtained from 32 patients with endometriotic cysts. Endometrial tissues were obtained during operations for benign gynecological conditions. The expression of the AT1 and AT2 receptor mRNA and that of PG-endoperoxide synthase 2 and microsomal PGE2 synthase-1 (mPGES-1) was examined by quantitative RT-PCR. Immunohistochemical staining was performed for these receptors. RESULTS: AT1 and AT2 receptor proteins were mostly located in endometrial glandular epithelium and some stromal cells. Immunoreactivity of the receptor proteins was observed in both the eutopic endometrium and endometriotic lesions. The AT1/AT2 ratio in endometriotic cysts (median 7.29, range 1.88-187.60) was significantly increased compared with that in the eutopic endometrium in the proliferative-phase in controls (median 1.01, range 0.37-2.09, p < 0.001). There was a relationship between the AT1 mRNA expression and that of mPGES-1 mRNA in the endometriotic cysts (r = 0.394089, p < 0.05). There was a significant relationship between the mRNA expression of the AT2 receptor and that of mPGES-1 in eutopic endometrium of non-endometriotic control (r = 0.610714, p < 0.05). CONCLUSION: Renin-angiotensin system may play an important role in the pathophysiology of endometriosis.


Asunto(s)
Endometriosis/metabolismo , Endometrio/química , Endometrio/metabolismo , Expresión Génica , Receptor de Angiotensina Tipo 1/análisis , Receptor de Angiotensina Tipo 2/análisis , Adulto , Angiotensina II , Ciclooxigenasa 2/genética , Endometriosis/patología , Endometrio/patología , Epitelio/química , Femenino , Humanos , ARN Mensajero/análisis , Receptor de Angiotensina Tipo 1/genética , Receptor de Angiotensina Tipo 2/genética , Células del Estroma/química
3.
Int J Clin Exp Pathol ; 10(8): 8925-8927, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-31966761

RESUMEN

We describe a rare intraosseous myoepithelioma, arising in a rib. The patient was a 14-year-old female. The tumor, composed of epitheliod cells and plump spindle cells, was immunopositive for AE1/AE3, S-100 protein, HHF-35, desmin, smooth muscle actin (SMA), CD10, and c-kit, indicating a diagnosis of myoepithelioma. The tumor had invaded surrounding soft tissues, indicating a locally aggressive tumor. Positive staining for CD10 supported the diagnosis of myoepithelioma. To our knowledge, c-kit immunoreactivity has not been reported in intraosseous myoepithelioma. This form of myoepithelioma, arising in a rib and showing c-kit positivity, is very rare.

4.
Virchows Arch ; 465(5): 531-8, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25031015

RESUMEN

Undifferentiated (anaplastic) carcinoma with rhabdoid features is a rare and aggressive subtype of pancreatic carcinoma. Here, we report the clinical, histological, and immunohistochemical phenotypes in six autopsy cases of anaplastic carcinoma with rhabdoid features. The patients ranged between 44 and 76 years of age (median, 61 years) and consisted of four males and two females. All patients except one case died within 3 months of diagnosis, as these tumors were found at an advanced stage and were chemoresistant. At autopsy, tumor masses measuring 4-22 cm in maximum diameter were mainly located in the pancreatic body and tail. Microscopically, all cases showed anaplastic carcinoma with rhabdoid features that were discohesive with round to polygonal eosinophilic cytoplasm with occasional inclusions, and that had vesicular nuclei, and prominent nucleoli. Immunohistochemistry showed that the rhabdoid cells, particularly the inclusions, were strongly positive for pan-cytokeratin (AE1/AE3) and vimentin. Meanwhile, downregulation or aberrant cytoplasmic localization with focal aggregation of E-cadherin, ß-catenin, and EMA were frequently observed in the rhabdoid cells. Moreover, the intracytoplasmic inclusions were labeled with selective autophagy-related molecules including p62/SQSTM1, ubiquitin, and kelch-like ECH-associated protein 1 (KEAP1). In addition, nuclear factor erythroid 2-related factor 2 (NRF2) and overexpression of its target molecule multidrug resistance-associated protein 1 (MRP1) were commonly observed in the rhabdoid cells. Therefore, these results suggest that p62-mediated aggregation of ubiquitinated intermediate filaments and membranous proteins is an important phenomenon in the rhabdoid phenotype. Indeed, the ubiquitinated aggregates of p62 and KEAP1 would induce activation of NRF2 and upregulation of MRP1, leading to potential chemoresistance of anaplastic carcinoma with rhabdoid features.


Asunto(s)
Carcinoma/patología , Neoplasias Pancreáticas/patología , Adulto , Anciano , Autopsia , Biomarcadores de Tumor/biosíntesis , Resistencia a Antineoplásicos , Femenino , Humanos , Inmunohistoquímica , Queratinas/biosíntesis , Masculino , Persona de Mediana Edad , Proteínas Asociadas a Resistencia a Múltiples Medicamentos/biosíntesis , Vimentina/biosíntesis , Neoplasias Pancreáticas
5.
Neurosci Res ; 71(1): 85-91, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21658418

RESUMEN

Spina bifida aperta (SBA) is an open neural tube defect that occurs during the embryonic period. We created SBA chicks by incising the roof plate of the neural tube in the embryo. The area of the dorsal funiculus was smaller in the SBA chicks than in the normal controls. Additionally, the SBA group had fewer nerve fibres in the dorsal funiculus than the normal controls. The pathway of the ascending sensory nerves was revealed by tracing the degenerated nerve fibres using osmification. We cut the sciatic nerve (L5) of the control and SBA chicks at the central end of the dorsal root ganglion 1 day after hatching and fixed the tissue 3 days later. Degenerated sensory nerve fibres were observed in the ipsilateral dorsal funiculus in the control chicks. In contrast, degenerated sensory nerve fibres were observed in the ipsilateral and contralateral dorsal, ventral and lateral funiculi of the spinal cord in the SBA chicks. Consequently, fewer sensory nerve fibres ascended to the thoracic dorsal funiculus in the SBA chicks than in the normal controls. This is the first report of abnormal changes in the ascending sensory nerve fibres in SBA.


Asunto(s)
Axones/patología , Espina Bífida Quística/patología , Médula Espinal/anomalías , Degeneración Walleriana/patología , Vías Aferentes/anomalías , Vías Aferentes/patología , Vías Aferentes/fisiopatología , Animales , Embrión de Pollo , Pollos , Modelos Animales de Enfermedad , Trastornos Neurológicos de la Marcha/etiología , Trastornos Neurológicos de la Marcha/patología , Trastornos Neurológicos de la Marcha/fisiopatología , Conos de Crecimiento/patología , Miembro Posterior/inervación , Miembro Posterior/fisiopatología , Rizotomía/métodos , Células Receptoras Sensoriales/patología , Espina Bífida Quística/fisiopatología , Médula Espinal/patología , Médula Espinal/fisiopatología , Raíces Nerviosas Espinales/patología , Raíces Nerviosas Espinales/fisiopatología , Raíces Nerviosas Espinales/cirugía , Degeneración Walleriana/etiología , Degeneración Walleriana/fisiopatología
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