RESUMO
We reported a case of upper eyelid necrosis initially misdiagnosed as a preseptal cellulitis following a hordeolum externum resulting in great damage to the upper eyelid (anterior lamella). The infection was successfully treated with surgical cleansing, drainage, and endovenous antibiotics. Early treatment may avoid severe complications such as eyelid deformity, systemic involvement, and blindness.
RESUMO
JUSTIFICATIVA E OBJETIVO: A síndrome de Mõbius, evento raro, resulta de uma desordem neurológica que se caracteriza por paralisia congênita do sétimo par de nervos cranianos, acompanhada de mal formações límbicas e das demais estruturas orofaciais. Caracteriza-se clinicamente pela ausência de expressão facial e distúrbios da fala, principalmente. Tais alterações influenciam diretamente na vida social do portador. Trata-se de uma síndrome rara, por isso pouco estudada, sendo o aspecto emocional não abordado pela literatura atual. O objetivo deste estudo foi identificar o sentimento e o significado da síndrome na vida de seus portadores. MÉTODOS: Foram entrevistados portadores da síndrome e, por meio do Discurso do Sujeito Coletivo, buscou-se avaliar o significado da síndrome. RESULTADOS: Evidenciou-se que, apesar das malformações e das dificuldades na fala, que impõem dificuldades no dia a dia, há adaptação por parte dos sindrômicos, que vivem normalmente. CONCLUSÃO: Os portadores da síndrome de Mõbius reconhecem as dificuldades impostas por sua condição, mas se adaptam bem a elas vivendo normalmente.
BACKGROUND AND OBJECTIVE: The Moebius syndrome, a rare disorder, results from a neurological disorder that is characterized by congenital paralysis of the seventh cranial nerve accompanied by limbic and other orofacial structures malformations. It is clinically characterized by the absence of facial expression and speech disorders, especially. These changes directly influence the social life of the patient. This is a rare syndrome, so, little studied, and the emotional aspect not addressed by the current literature. The objective of this article was to identify the feeling and the meaning of the syndrome in the lives of their carriers. METHODS: Patients with the syndrome were interviewed and through the Collective Subject Discourse, we seek to assess the significance of this syndrome. RESULTS: The results showed that despite the defects and difficulties in speech, which imposes difficulties in day-to-day, there is adaptation by the syndromic, which normally live. CONCLUSION: Moebius syndrome carriers recognize the difficulties imposed by their condition, but they adapt well to living normally.
Assuntos
Humanos , Masculino , Feminino , Adulto , Adaptação Psicológica , Exposição Ambiental , Qualidade de Vida , Síndrome de Möbius/etiologia , Síndrome de Möbius/psicologiaRESUMO
Effects of maternal malnutrition during lactation on the kidneys in mice infected with Schistosoma mansoni. Kidneys from programmed infected mice and their respective controls fed a normal diet (23% protein), a protein-restricted group (PR) (8% protein) and a caloric-restricted group (CR) (according to the PR group intake) evaluated by biometry, morphometry and histopathology. Both PR and CR groups showed a reduction in the number of glomeruli when compared with the control group (CR: -29% vs C; PR: -41% vs C; p<0.05) as well as infected mice (ICR: -32% vs IC; IPR: -47% vs IC; p<0.05). Among infected mice, ICR group showed higher kidney weights (+18% vs IC and +12% vs IPR; p<0.01). The ICR and IPR groups showed largest perimeter and area when compared to the corresponding uninfected group (ICR vs CR: +26%; IPR vs PR: +21%, p<0.05) and area (ICR vs CR: +95%; IPR vs PR: +50%, p<0.05). The ICR group showed an increase of within Bowman (CR vs ICR: +56%, p<0.05), whereas Bowman's space was reduced (PR vs IPR, -61%; p<0.05). Conclude that malnutrition during lactation programmed the metabolic state of the host, resulting in the evolution of the histology of the renal parenchyma.
