Facial reconstruction of a pathological case.

In this paper, we describe a forensic paleopathology case using findings obtained from images of a skull with leontiasis ossea. This unique specimen is on display in the National Museum of Anthropology and History in Mexico. The skull shows tissue overgrowth, periosteal bone proliferation, which produced a cortical and diploid thickening involving the entire bone matrix. The study of images, X-rays, and helical computed tomography revealed generalized hyperostosis obliterating the maxillary and sphenoid sinuses, and two exuberant bony masses arising from the maxilla with encroachment of the anterior nasal opening. In order to reconstruct an image of the external appearance in life, a copy was obtained in the first place, using a stereolithography machine, after that, three-dimensional (3-D) facial reconstruction technique was applied, thus an approximation of the external appearance of this specimen was obtained. During the process, we encountered several difficulties, mainly when interpreting the cortical topography, the position of eyes and mouth. In this sense, facial reconstruction allows only for a moderate investigation due to the limited information that can be obtained from the skull and the significant alterations observed.

Leontiasis ossea: a paleopathologic case report.

We describe the archeological and imaging findings of a unique specimen (skull and mandible) with leontiasis ossea (LO) that is on display in the National Museum of Anthropology and History in Mexico City. The specimen shows diffuse and irregular periosteal bone proliferation, which produces a grossly nodular appearance involving the neurocranium and the facial skeleton. Plain radiography and helical computed tomography revealed generalized hyperostosis obliterating the maxillary and sphenoidal sinuses and 2 exuberant bony masses arising from the maxilla with encroachment of the anterior nasal aperture.Currently, LO is a purely descriptive term applied to a variety of osseous conditions that have in common hyperostosis of craniofacial bones leading to a leonine appearance. Clinicians who see such lionlike facies should consider the main causes of LO, which include renal osteodystrophy, Paget disease and, as most likely in this specimen, fibrous dysplasia.

Characterization of dental fillings found in skulls from individuals buried in San Jeronimos Church, New Spain: historical and archaeological evidences.

Repair of teeth during the XIX century was often a very costly and painful procedure. During this period, restoration of teeth was a procedure limited only to those who could afford such care. In this study we analyzed teeth from a skull sample found in San Jeronimo's Church. The characterization of molar fillings was made with techniques such as X-ray fluorescence, X-ray diffraction and electron microscopy. The purpose of this investigation was to establish technical procedures for analysis, and to discuss the results within the context of the socioeconomic status of these individuals and the written descriptions of the dental practice during the XIX century.

Osteopoikilosis in an ancient skeleton: more than a medical curiosity.

We describe the palaeopathologic and radiographic findings of the human skeletal remains that belonged to a female who lived in Mexico's viceroyship period (seventeenth and eighteenth centuries A.D.). Radiographic studies showed numerous, radiodense, ovoid, small and well-defined foci in the long tubular bones, sacrum, scapulae and iliac bones. Computed tomography (CT) examination revealed multiple hyperdense foci located in the central marrow portion of the bones. Measurements of attenuation coefficient revealed +1548 HU. The findings are consistent with osteopoikilosis, an uncommon, benign sclerosing bone dysplasia transmitted in an autosomal dominant fashion, which in the clinical setting is important to set apart from different bone pathologies to avoid unnecessary interventions and treatments. To the best of our knowledge, this is the first report of osteopoikilosis in ancient human remains.

Mumps meningoencephalitis. An epidemiological approach.

The aim of this study was to analyse distribution of meningoencephalitis caused by mumps virus in children related to sex, age and seasonal influences. Thirty seven children were evaluated, ages ranging from 2 to 14 years. They were seen at Emergency Unit of Faculdade de Medicina do Triângulo Mineiro and at Hospital da Criança, in Uberaba-MG, Brazil, from March 1st 1991 to February 1st 1993 and they were hospitalized for about 5 days. Through a protocol findings were studied during hospitalization and clinical course stressing epidemiology, symptomatology, cerebrospinal fluid studies, electroencephalogram and cortical function analysis. Only epidemiological data were considered in the present study. Data analysis revealed male predominance, at a range from 5 to 9 years and great number of occurrences at the last quarter of the year.

[Striatocapsular infarction in childhood. Report of 4 cases]. / Infarto estriatocapsular na infância. Relato de quatro casos.

The authors present the study of four children that manifested asymmetric hemiparesis with sudden onset, without consciousness loss. The diagnosis of striatocapsular infarction was confirmed by computed tomography (CT) and magnetic resonance imaging (MRI). The clinical and neurological examination, and laboratorial results are discussed. Familial history of migraine was found in two of the patients. Migraine was diagnosed in two, mild head trauma, viral miocarditis and mitral valve prolapse in one. Left hemiparesis, with brachiofacial features in three, and brachial in one. CT showed lenticular nucleus and internal capsule lesions in all of them, head of caudate nucleus in three, and white substance in two. MRI was done in two and confirmed CT findings. Electroencephalogram, at the acute phase in three, showed abnormalities in all patients.

Infarto estriatocapsular na infância: relato de quatro casos / Striatocapsular infarction in childhood: report of 4 cases

Os autroes apresentam o estudo de quatro crianças que manifestaram hemiparesia desproporcionada de instalaçäo súbita, sem perda da consciência. O diagnóstico de infarto estriatocapsular foi confirmado pela tomografia computadorizada do crânio (TCC) e ressonância magnética (RM). Discutem os achados clínico-neurológicos e de exames complementares. História familiar de migrânea foi relatada em dois dos pacientes. Constatou-se migrânea em dois, trauma craniano, miocardite e prolapso de válvula mitral em um. Hemiparesia esquerda, com predomínio bráquio-facial em três e braquial em um. A TCC demonstrou comprometimento do núcleo lenticular e da cápsula interna nos quatro casos; da cabeça do núcleo caudado em três e da substância branca em dois. A RM foi realizada em dois e confirmou os achados da TCC. O eletrencefalograma, obtido na fase aguda em três, se mostrou alterado nos quatro casos