Presentación atípica del síndrome de Meigs: reporte de caso y revisión de la literatura / Atypical presentation of Meigs syndrome: A case report and literature review

Resumen El síndrome de Meigs (SM) es la asociación de ascitis, derrame pleural y neoplasias ovárica benigna, en el pseudo-Meigs se agrega CA-125 elevado. Presentamos el caso de una mujer de 67 años con masa anexial derecha, marcadores tumorales negativos. Se realiza ooforectomía, reportan cistoadenofibroma seroso. Doce semanas posteriores con distensión abdominal, pérdida de peso, tomografía abdominal con carcinomatosis peritoneal, antígeno CA-125 de 1,063.4 U/l. Segunda visión laparoscopia, sin neoplasia, corroborada por histopatología. Realizar un diagnóstico de SM es sencillo, no así cuando se presenta un caso atípico de pseudo-Meigs. Los artículos mencionan mejoría significativa posterior al manejo quirúrgico.

Abstract Meigs syndrome (MS) is the association of ascites, pleural effusion and benign ovarian neoplasms, the pseudo-Meigs (PMS) adds elevated CA-125. We present the case of a 67-year-old female with a right adnexal mass, negative tumor markers, performed ororectomy reported serous cystadenofibroma. 12 weeks later with abdominal distension, weight loss, abdominal tomography with peritoneal carcinomatosis, CA -125 antigen of 1063.4U/L. Second laparoscopic view, without neoplasia, corroborated by histopathology. Making a diagnosis of MS is simple, but not when an atypical case of Pseudo-Meigs is presented. The articles mention significant improvement after surgical management.

Polycystic ovary syndrome with feasible equivalence to overweight as a risk factor for non-alcoholic fatty liver disease development and severity in Mexican population.

INTRODUCTION AND OBJECTIVES: Polycystic ovary syndrome (PCOS) is the most common endocrinology disorder in women of reproductive age; these patients have a higher risk of suffering from non-alcoholic fatty liver disease (NAFLD). We determine the frequency of NAFLD in Mexican patients with PCOS and matched-controls. PATIENTS AND METHODS: Cross-sectional study, with 98 women of 18-44 years old. Rotterdam 2003 criteria integrated PCOS diagnosis. Those with significant alcohol consumption, chronic liver disease, use of steatogenic drugs, and pharmacological PCOS treatment or fertility protocol were excluded. Controls were matched in a 1:1 ratio by age and body mass index (BMI). The presence of NAFLD was determined by transient elastography performed by a single experienced operator. RESULTS: A total of 98 female volunteers at reproductive age were recruited. NAFLD denoted markedly higher in patients with than without PCOS at 69.3% vs. 34.6%, respectively. Compared to controls, PCOS patients had a significantly higher risk of NAFLD (OR=4.26, 95% CI 1.83-9.93). Severe steatosis was the most frequent NAFLD stage between women with PCOS and NAFLD. Patients with hyperandrogenism have a significantly higher mean CAP 277.83dB/m than controls without hyperandrogenism 191.57dB/m. NAFLD prevalence was 84.3% in PCOS patients with phenotype A, while in another phenotype, it was 41.1%. CONCLUSIONS: PCOS is an independent risk factor for NAFLD development. NAFLD screening needs to be considered in all PCOS patients independently of BMI, except in PCOS patients without hyperandrogenism and BMI<25.

Embarazo ectópico abdominal: protocolo de tratamiento combinado. Reporte de un caso / Ectopic abdominal pregnancy: combined treatment strategy: A case report

Resumen ANTECEDENTES: El embarazo ectópico abdominal es una alteración poco frecuente, sin tratamiento definido hasta ahora. La extracción quirúrgica del feto y la aplicación de metotrexato representan una opción de tratamiento en pacientes con embarazo ectópico abdominal. CASO CLÍNICO: Paciente de 36 años, con 16.2 semanas de embarazo, que acudió al servicio de urgencias por un cuadro de dolor en el epigastrio. El ultrasonido pélvico y la tomografía computada evidenciaron una imagen sugerente de feto sin vitalidad en el hipocondrio derecho. La laparotomía exploradora objetivó un feto masculino, de 115 g, cubierto con epiplón en el mesogastrio, extraído sin dificultad. No se retiró el tejido placentario, pues se encontraba adherido al tejido intestinal. El tratamiento consistió en múltiples dosis de metotrexato. La paciente evolucionó satisfactoriamente y fue dada de alta sin complicaciones. CONCLUSIÓN: El tratamiento combinado (laparotomía para la extracción del feto y administración posterior de metotrexato) es una opción efectiva en pacientes con embarazo ectópico abdominal no complicado, con tejido placentario adherido en zonas sumamente vascularizadas.

Abstract BACKGROUND: Abdominal ectopic pregnancy is a rare entity which treatment has not been clearly stablished. One of the therapeutic alternatives is the surgical extraction of the fetus and the subsequent application of methotrexate in these patients. CLINICAL CASE: A 36-year-old female patient came to the emergency unit complaining of pain in the epigastrium. The patient referred a pregnancy of 16.2 weeks. Pelvic ultrasound and computed tomography were performed, demonstrating a suggestive image of a fetus without vitality at the level of the right hypochondrium. An exploratory laparotomy was performed. A male 115 gram fetus was observed at the level of mesogastrium, and was extracted without difficulty. Placental tissue was not removed because it was adhered to intestinal tissue. The subsequent management consisted of methotrexate. The patient was discharged without complications. CONCLUSION: The combined therapy between laparotomy for the extraction of the fetus and administration of methotrexate may be viable for cases of uncomplicated abdominal ectopic pregnancy in which the placental tissue is adhered to highly vascularized areas.

Tuberculosis pélvica y antecedente de embarazo. Reporte de caso / Pelvic tuberculosis and pregnancy antecedent. Case report

Resumen A lo largo del tiempo, la tuberculosis ha sido un problema de salud pública. La Organización Mundial de la Salud reporta anualmente alrededor de 8 millones de casos nuevos y 3 millones de muertes. En México se estima que anualmente prevalecen cerca de 64,000 casos de esta enfermedad gue puede afectar diferentes órganos con presentaciones clínicas gue simulan otras patologías. Se presenta el caso de una paciente de 22 años de edad con antecedente de embarazo normo evolutivo y parto vaginal 4 meses antes sin complicaciones, gue inició su cuadro clínico en el puerperio con presencia de tos en accesos gue remitió un mes posterior acompañado de síndrome de desgaste, pérdida de peso, dolor abdominal difuso, diarrea y fiebre. Recibió múltiples tratamientos sin mejoría, ingresó a nuestro hospita con cuadro de síndrome abdominal agudo y se le realizó laparotomía exploradora con hallazgos de abdomen congelado, engrosamiento de peritoneo parietal, adherencias fijas, colecciones en hueco pélvico, con material purulento caseoso, blanquecino, poco fétido, tejido friable, presencia de granulomas en asas de intestino; se realizó histerectomía subtotal abdominal con ooforectomía bilateral, la evolución posquirúrgica fue lenta hacia la mejoría tras corroborar por reporte histopatológico y cultivo el diagnóstico de tuberculosis pélvica e iniciar tratamiento específico.

Abstract Tuberculosis has been overtime public health problem. The World Health Organization reports annually about 8 million new cases and 3 million deaths. In Mexico, an estimation of around 64,000 prevalent cases of this disease are reported annually. Tuberculosis can affect different organs with clinica presentations that mimic other diseases. A patient presents a history of normal pregnancy and vaginal delivery without complications for 4 months. The clinical picture begins in the postpartum period with the presence of cough accesses registered a month later accompanied by fatigue, weight loss, diffuse abdominal pain, diarrhea and fever syndrome. She received multiple treatments without improvement. She was ad missioned to our hospital and an acute abdomen laparotomy was performed with findings of abdominal frozen thickened parietal peritoneum, fixed adhesions, collections of pelvic cavity with whitish, slightly fetid pus, friable tissue, presence of granulomas in bowel loop. A subtotal abdominal hysterectomy with bilateral oophorectomy was performed. The postoperative evolution showed a slow improvement after the reportand was corroborated bya histopathological diagnosis of pelvic tuberculosis culture and the initiation of a specific treatment.

[Metastatic choriocarcinoma associated with Wunderlich syndrome: case report and literature review]. / Coriocarcinoma metastásico asociado con síndrome de Wunderlich: presentación de un caso y revisión de la bibliografía.

Choriocarcinoma is a rare condition, with an incidence of 1 in 30 to 40,000 pregnancies in the United States and Europe. In Mexico it is reported in 1 in 10,000 pregnancies. Wunderlich syndrome is a spontaneous perirenal hematoma, a very rare entity. This paper reports the case of a young patient with a history of molar pregnancy one year prior to admission, valuation due to fainting, generalized headache, spontaneous pain in the right flank and data of hypovolemic shock. Computed tomography reported right perirenal hematoma, normal uterus, two annexes with data of tecaluteinic cysts, beta human chorionic gonadotropin greater than 200,000 IU/mL. Patient was stabilized with crystalloid, blood products and right adrenal artery embolization. It was corroborated the brain, mediastinum and abdomen metastases. She was sent to a third level hospital, starting holocraneal radiotherapy, she had retroperitoneal bleeding and died a week later.