ABSTRACT
La duplicación del sistema colector renal es la variación más frecuente del sistema urinário y se puede presentar como duplicación completa o incompleta, así como la inserción ectópica en todas las partes del sistema urinario a partir de la parte distal hacia la vejiga. Este artículo presenta uma duplicación completa no ectópica del ureter en el riñón izquierdo de un cadáver de un individuo brasileño, de sexo masculino. Ambos uréteres tenían origen en el hilio renal y continuaban hasta la vejiga urinaria separadamente, desembocando en ostios diferentes, en el área del trígono vesical, donde el ostio perteneciente al uréter que drenaba el polo superior presentó posición distal y lateral en relación al ostio del uréter que drenaba el polo inferior. Esta disposición es uma excepción a la regla de Weigert-Meyer, que indica que el uréter del polo superior, por el hecho de permanecer fijo por más tiempo al conducto mesonéfrico, presenta mayor migración, terminando medial e inferiormente al uréter que drena el polo inferior en 97 % de los casos.
Duplication of the urinary tract is the most frequent variation of this system and may present as complete or incomplete duplication, as well as ectopic insertion throughout all parts of the urinary system from distal to the bladder. This article presents a complete non-ectopic duplication of the ureter in the left kidney of a cadaver of one Brazilian individual of male sex. In this study, both ureters originated in the renal hilum and continued to the urinary bladder separately, opening into different ostia, in the area of the bladder trigone, where the ostium belonging to the ureter that draining the upper pole presented a distal and lateral position in relation to the ostium of the ureter draining the lower pole. This arrangement is an exception to the Weigert-Meyer rule, which indicates that the ureter of the upper pole, due to its longer fixation to the mesonephric duct, presents a greater migration, ending medial and inferior to the ureter draining the inferior pole in 97 % of cases.
Subject(s)
Humans , Male , Adult , Kidney/abnormalities , Ureter/abnormalities , CadaverABSTRACT
Descrever dois casos de hanseníase em menores de 15 anos, sendo um de paciente com 18 meses de idade e outro de 13 anos, diagnosticados por modos de detecção diferentes, ressaltando a importância de examinar os contatos. DESCRIÇÃO DO CASO: Um dos casos foi diagnosticado precocemente por meio do exame de contatos intradomiciliares, enquanto o outro foi diagnosticado por demanda espontânea após quatro anos de aparecimento das lesões e, apesar de ser contato de um ex-paciente, não foi examinado na época. COMENTÁRIOS: Em países endêmicos, a alta detecção da hanseníase em menores de 15 anos revela a persistência na transmissão do bacilo e as dificuldades dos programas de saúde para o controle da doença. O maior tempo para diagnóstico ocasiona sequelas e deformidades e, dessa forma, a busca dos contatos constitui importante método para o diagnóstico precoce da doença na infância, quando os sinais clínicos nem sempre são fáceis de serem identificados e há grande diversidade de formas clínicas em que a doença pode se apresentar.
To describe two cases of leprosy in children under 15 years old, being one patient aged with 18 months and other 13 years, diagnosed by different modes of detection, emphasizing the importance of examining the contacts. CASE DESCRIPTION: One of the cases was diagnosed early by examining household contacts, while the other was diagnosed by spontaneous demand, after four years of the onset of lesions, although he had been a former patient contact who was not examined at the time. COMMENTS: In endemic countries, the high detection of leprosy in children under 15 years old reveals the persistence of the bacillus transmission and the difficulties encountered by public health programs to control the disease. Delay in leprosy diagnosis leads to sequels and deformities and, thus, the search for contacts is important as an effective method for early diagnosis of the disease in childhood, where clinical signs are not always easy to be identified due to the great variety of clinical forms in which the disease may occur.
Describir dos casos de enfermedad de Hansen en menores de 15 años, siendo uno de paciente con 18 meses de edad y otro de 13 años, diagnosticados por modos de detección distintos, subrayando la importancia de examinar a los contactos. DESCRIPCIÓN DEL CASO: Uno de los casos tuvo diagnóstico temprano mediante examen de contactos intradomiciliares, mientras que el otro fue diagnosticado por demanda espontánea después de cuatro años de surgimiento de las lesiones y, a pesar de ser contacto de un ex-paciente, no fue examinado en la época. COMENTARIOS: En países endémicos, la alta detección de enfermedad de Hansen en menores de 15 años revela la persistencia en la transmisión del bacilo y las dificultades de los programas de salud para el control de la enfermedad. El mayor tiempo para diagnóstico ocasiona secuelas y deformidades y, de ese modo, la búsqueda por los contactos constituye importante método para el diagnóstico temprano de la enfermedad en la infancia, cuando las señales clínicas no siempre son fáciles de identificarse y hay gran diversidad de formas clínicas en que la enfermedad puede presentarse.
Subject(s)
Humans , Male , Infant , Adolescent , Leprosy/diagnosis , Leprosy/epidemiologyABSTRACT
Due to the great importance of the knowledge about variations occurring in the vascular system to surgeons and professionals who work with imaging, we describe in this article a variation of the origin of the occipital artery. 110 cadavers of male and female individuals had they carotid vascular tree in the region of the neck carefully dissected using loupe magnification and its origin and course were measured as well as a simple diameter. This artery usually branches off from the posterior part of the wall of the external carotid artery at the same level of the facial artery branching however, the two cases presented showed the occipital artery branching off very close to the carotid bifurcation, which characterize it as a trifurcation instead. The occipital artery branching off too close to the carotid bifurcation is a rarity as demonstrated by our results and the its literature is insufficient.
Subject(s)
Humans , Male , Female , Carotid Artery, Common/anatomy & histology , Occipital Lobe/anatomy & histology , Cadaver , Dissection , Occipital Lobe/abnormalitiesABSTRACT
Um caso de persistência da artéria ciática com aneurisma associada à artéria femoral hipoplásica no membro inferior direito é relatado. Esta associação é rara, sendo o primero caso descrito na literatura brasileira. As peculiaridades anatômicas, ultra-sonográficas desta observação são revistas