ABSTRACT
Mediante un proceso de adaptación de guías de práctica clínica se seleccionaron y evaluaron guías de infección de vías urinarias en mujeres premenopáusicas no embarazadas; se identificaron 3 de alta calidad. Con base en las evidencias y las recomendaciones aportadas por estas guías, se realizó un consenso para realizar recomendaciones para personal de salud -médicos, personal de laboratorio y enfermeros- sobre el diagnóstico de las infecciones urinarias -cistitis y pielonefritis-, sus tratamientos y prevención de la recurrencia.
Using a process of adaptation, guidelines for the diagnosis, treament and prevention of urinary tract infection in premenopausal non-pregnant women were chosen and assessed. Three high quality guidelines were identified. Based on the evidence that supported these guidelines and their recommendations, a consensus was made to do recommendations for healthcare workers (physicians, laboratory personnel and nurses) on the diagnosis of urinary tract infections (cystitis and pyelonephritis), their treatment and the prevention of recurrence.
ABSTRACT
This is a report of an additional patient affected by hemifacial myohyperplasia (HMH). We postulate that this condition originates around the fourth gestational week at any step of cranial muscle development from somitomeres to branchial arches, most probably due to prolonged period of proliferation during cranial muscle development, subsequent abnormal contact between cranial neural crest (CNC) cells and cranial myoblasts, and an impaired interaction among CNC cells and cranial myoblasts derivatives. HMH may represent another example of somatic mosaicism and its features can be explained by a combination of morphostatic and morphodynamic mechanisms of pattern formation during development. Here we suggest that HMH is a sequence in which the primary defect is hyperplasia of the facial muscles and the other findings are secondary to this.
Subject(s)
Craniofacial Abnormalities/pathology , Craniofacial Abnormalities/diagnostic imaging , Facial Asymmetry/pathology , Female , Humans , Infant , Pregnancy , Skull/diagnostic imaging , Tomography, X-Ray ComputedABSTRACT
Se describe un caso de diabetes insípida post parotiditis, entidad sumamente rara en nuestro medio. Se destaca el diagnóstico y la terapéutica de esta entidad, así como la causa etiológico y forma de presentación(AU)
Subject(s)
Humans , Diabetes Insipidus/diagnosis , Diabetes Insipidus/etiology , Diabetes Insipidus/therapy , ParotitisABSTRACT
Se comentan las características clínicas del síndrome de Kartagener. Se analizan sus diferentes corrientes etiopatogénicas presentando un caso clínico que lo ilustra. Se comentan los métodos diagnósticos más importantes y se insiste en el trabajo quirúrgico como terapéutica fundamental en este síndrome(AU)
Subject(s)
Humans , Kartagener Syndrome/diagnosis , Kartagener Syndrome/ethnology , Kartagener Syndrome/pathology , Kartagener Syndrome/surgery , TherapeuticsABSTRACT
Se comentan las características clínicas del síndrome de Kartagener. Se analizan sus diferentes corrientes etiopatogénicas presentando un caso clínico que lo ilustra. Se comentan los métodos diagnósticos más importantes y se insiste en el trabajo quirúrgico como terapéutica fundamental en este síndrome.
Clinical characteristics of Kartageners syndrome are commented. Diferent etiopathogenic currents are analyzed presenting a clinical case that illustrates this topic and the most important diagnostic means. Surgical treatment is stressed as the main therapeutics in this syndrome.
ABSTRACT
Se describe un caso de diabetes insípida post parotiditis, entidad sumamente rara en nuestro medio. Se destaca el diagnóstico y la terapéutica de esta entidad, así como la causa etiológico y forma de presentación.
A case of diabetes insipidus post-parotiditis is described entity totally rare in our midicu. Diagnostics and therapeutics are stressed a well as the ethiologic antecedent and way of presentation.
