4 results on '"María Isabel Lavenant-Borja"'
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2. Early diagnosis of Balo's concentric sclerosis by diffusion tensor tractography: a case report and literature review
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Juan Alberto Nader Kawachi, María de la Luz Andrade Magdaleno, Carlos Andrés Peñaherrera, Yeni Fernández De Lara, and María Isabel Lavenant Borja
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Balo’s concentric sclerosis ,demyelination ,tractography ,magnetic resonance imaging ,diffusion tensor imaging ,Medicine ,Medicine (General) ,R5-920 - Abstract
La esclerosis concéntrica de Baló es una variante infrecuente de enfermedad desmielinizante relacionada con la esclerosis múltiple, inicialmente considerada de progresión fatal. En estudios recientes se reportan variantes no fatales de esclerosis concéntrica de Baló en los que se enfatiza la importancia del diagnóstico por medio de la imagen por resonancia magnética, utilizando además la espectroscopia y las secuencias de difusión y perfusión. En los últimos años se ha logrado reproducir la imagen tridimensional de un fascículo en particular y observar la presencia de lesiones por medio de la tractografía por imagen por resonancia magnética mediante la técnica de tensor de difusión. Presentamos el caso de una mujer joven con síntomas neurológicos focales agudos, incluyendo paresia de extremidades derechas, cuyo diagnóstico por biopsia fue de esclerosis concéntrica de Baló, confirmando el resultado de los estudios de imagen. La paciente recibió tratamiento con bolos de metilprednisolona, obteniendo remisión clínica completa a largo plazo. A nuestro entender, este es el primer reporte que describe los hallazgos de la esclerosis concéntrica de Baló utilizando la técnica de tensor de difusión. Consideramos que dicha técnica permitirá en el futuro la detección temprana de la enfermedad, su tratamiento oportuno y permitirá establecer nuevos criterios de clasificación y estratificación. Este caso demuestra la existencia de variantes benignas de esclerosis concéntrica de Baló, que tienen buena respuesta a la terapia con glucocorticoides y donde se logra la recuperación funcional.
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- 2016
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3. Mucinous cystadenoma of the pyelocaliceal system: a report of 3 examples and an analysis of 17 previously published cases
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Jorge Albores-Saavedra, Fredy Chablé-Montero, Marco Aurelio González-Romo, Donald E. Henson, Saulo Mendoza-Ramírez, Virgilia Soto-Abraham, and María Isabel Lavenant-Borja
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Male ,Pathology ,medicine.medical_specialty ,Carcinoid tumors ,Autopsy ,Keratin-20 ,Asymptomatic ,Pathology and Forensic Medicine ,Fatal Outcome ,Cystadenoma, Mucinous ,Biomarkers, Tumor ,medicine ,Humans ,CDX2 Transcription Factor ,Kidney Pelvis ,Mucinous cystadenoma ,Homeodomain Proteins ,Mucin-2 ,Pyelonephritis ,business.industry ,General Medicine ,Middle Aged ,medicine.disease ,Kidney Neoplasms ,Appendix ,medicine.anatomical_structure ,Cystadenoma ,medicine.symptom ,Mucinous cystadenocarcinoma ,business ,Renal pelvis - Abstract
We report 3 patients all men between 45 and 64 years of age with unilocular or multilocular mucinous cystadenomas of the kidney. One tumor arose from the renal pelvis, and 2 involved the entire pyelocaliceal system. The tumors measured between 2.4 and 37 cm in greatest dimension. Two patients were asymptomatic, and 1 had recurrent attack of acute pyelonephritis. Microscopically, the morphology and immunophenotype (CK20, MUC2, and CDX2 positive) of the tumors were similar to the colonic adenomas. Two patients were asymptomatic 24 and 64 months after surgery, including the patient with mucinous cystadenoma and intramucosal carcinoma. One patient died of acute myocardial infarction, and his tumor was an autopsy finding. Only 17 cases of mucinous cystadenomas and 5 cases of mucinous cystadenocarcinomas have been reported. Of the 17 mucinous cystadenomas, 2 arose in horseshoe kidneys. The mean size of these neoplasms was 15 cm (2.4-37 cm). Despite their large size, some patients with mucinous cystadenomas were asymptomatic. Sixty percent were associated with renal lithiasis. Thirty percent progressed to mucinous adenocarcinomas, and only 2 cases showed areas of intramucosal carcinomas. Two cases were associated with carcinoid tumors, similar to those reported in the appendix. Most patients were asymptomatic after surgery, and only 1 patient died by abdominal sepsis related to adenomucinosis. The 3 examples of mucinous cystadenomas of the pyelocaliceal system reported here, and those previously published indicate that they are very uncommon neoplasms with morphology and intestinal immunophenotype similar to the colonic adenomas.
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- 2013
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4. Gastrocolic fistula secondary to adenocarcinoma of the transverse colon: a case report
- Author
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Omar Vergara-Fernández, Ylse Gutiérrez-Grobe, Carlos Rojas, María Isabel Lavenant-Borja, and Nahum Méndez-Sánchez
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Gastric Fistula ,Male ,medicine.medical_specialty ,Abdominal pain ,Pathology ,Colon ,medicine.medical_treatment ,Colonoscopy ,Case Report ,Adenocarcinoma ,Gastrectomy ,Surgical oncology ,Gastroscopy ,Weight Loss ,Intestinal Fistula ,medicine ,Humans ,Medicine(all) ,Chemotherapy ,medicine.diagnostic_test ,business.industry ,Transverse colon ,En bloc ,General Medicine ,Middle Aged ,Resection ,medicine.disease ,digestive system diseases ,Abdominal Pain ,Surgery ,Treatment Outcome ,Gastrocolic fistula ,Chemotherapy, Adjuvant ,Colonic Neoplasms ,Neoplasm Recurrence, Local ,medicine.symptom ,Tomography, X-Ray Computed ,business ,Complication ,Colon, Transverse - Abstract
Introduction Gastrocolic fistula is a rare complication of adenocarcinoma of the colon. Despite radical resections, these patients usually have a poor prognosis with a mean survival of 23 months and long-term survival is rarely reported. Case presentation A 48-year-old Latino-American man presented with watery diarrhea, diffuse abdominal pain and weight loss for 3 months. A computed tomography scan revealed a mass in the splenic flexure that had infiltrated his stomach and diaphragm. Panendoscopy and colonoscopy confirmed the presence of a fistula between the distal transverse colon and the stomach, which was secondary to a colon cancer. His colon, stomach and left diaphragm were resected en bloc. A histological examination revealed a moderately differentiated adenocarcinoma of the colon that had infiltrated the full width of the gastric wall with 37 negative lymph nodes and clear surgical margins. Adjuvant chemotherapy with capecitabine and oxaliplatin was administered after surgery. Our patient is alive and without any recurrence 5 years after surgery. Conclusions En bloc resection with adjuvant chemotherapy offers the best treatment option for gastrocolic fistulas. This is one of the patients with greater survival reported in the medical literature.
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