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1.
Arq. bras. oftalmol ; 84(3): 279-281, May-June 2021. graf
Artigo em Inglês | LILACS | ID: biblio-1248970

RESUMO

ABSTRACT The aim of this study was to discuss a case of late-onset Klebsiella oxytoca keratitis after deep anterior lamellar keratoplasty and its treatment. A 21-year-old female patient presented with redness and effluence in the left eye at 5 months after uncomplicated deep anterior lamellar keratoplasty surgery. In the examination, a single suture was loosened in the superior nasal region and there was an infiltration area and epithelial defect in the graft and recipient bed junction in the area of the loose suture. Topical fortified vancomycin and fortified ceftazidime treatment was started empirically hourly, but there was insufficient response. After K. Oxytoca growth in a swab and suture culture taken from the patient, fortified vancomycin was replaced with fortified imipenem. It was observed that the infiltration area rapidly regressed and the epithelial defect was closed after fortified imipenem treatment. Fortified imipenem may be considered as an alternative treatment, especially in cases in which there is no response to treatment and culture growth is detected.(AU)


RESUMO O objetivo deste estudo é discutir um caso de ceratite tardia por Klebsiella oxytoca, após ceratoplastia lamelar anterior profunda, bem como seu tratamento. Uma paciente de 21 anos apresentou vermelhidão e efluxo no olho esquerdo 5 meses após cirurgia de ceratoplastia lamelar anterior profunda sem complicações. Ao exame, havia uma única sutura solta na região nasal superior e uma área de infiltração com defeito epitelial no enxerto e na junção com o leito receptor na área da sutura solta. Iniciou-se empiricamente um tratamento tópico com vancomicina e ceftazidima fortificada de hora em hora, porém com resposta insuficiente. Após o crescimento de K. oxytoca a partir de cultura de swab e sutura retirados da paciente, a vancomicina fortificada foi substituída por imipenem fortificado. Observou-se que a área de infiltração regrediu rapidamente e que o defeito epitelial foi fechado com o tratamento com imipenem fortificado. O imipenem fortificado pode ser considerado um tratamento alternativo, especialmente nos casos sem resposta ao tratamento e detecção de crescimento na cultura.(AU)


Assuntos
Humanos , Masculino , Adulto , Imipenem/uso terapêutico , Transplante de Córnea , Klebsiella oxytoca/isolamento & purificação , Ceratite/diagnóstico
2.
Clinical and Experimental Otorhinolaryngology ; : 133-137, 2014.
Artigo em Inglês | WPRIM | ID: wpr-173817

RESUMO

OBJECTIVES: To evaluate the effect of weight percentile on deep neck infections in children. METHODS: A retrospective evaluation of 79 patients who were treated for deep neck infections. The patients were divided into six groups according to weight percentile. Patients who had systemic and/or congenital disease were excluded. Their demographics, etiology, localization, laboratory, and treatment results were reviewed. RESULTS: In total, 79 pediatric patients were recorded: 48.1% were females and 51.9% were males, with a mean age of 7.3 years. In total, 60 patients were under the 50th percentile according to their weight versus all children. The anteroposterior triangle (29.1%) and submandibular (26.5%) spaces were most commonly involved with deep neck infection. However, the anteroposterior triangle space was the highest in the group below the 3rd percentile (44.4%). In the blood analysis, white blood cell levels in patients with at percentile values of 75-50 were higher than other groups (P<0.05). Significant differences were found between C-reactive protein and hemoglobin levels and diameter of abscesses. The need for surgical drainage in patients in lower percentiles was higher. The patients who needed surgical drainage consisted of 56 patients (93.3%) below the 50th percentile and 9 patients (100%) below the 3rd percentile. CONCLUSION: Deep neck infection is more insidious and dangerous in low-weight-percentile children, especially those having low white blood cell counts, low hemoglobin levels, and high C-reactive protein in laboratory results.


Assuntos
Criança , Feminino , Humanos , Masculino , Abscesso , Proteína C-Reativa , Demografia , Drenagem , Contagem de Leucócitos , Leucócitos , Pescoço , Estudos Retrospectivos
3.
Pakistan Journal of Medical Sciences. 2010; 26 (3): 634-639
em Inglês | IMEMR | ID: emr-97729

RESUMO

Eagle's Syndrome is caused by elongation of the styloid process or ossification of the stylohyoid ligament. We aimed to evaluate the contribution of 3-Dimensional Multidetector CT findings on Eagle's syndrome. Three-Dimensional Multidetector CT were performed on 13 patients with Eagle's syndrome. Maximum intensity projection [MIP] and volume rendering [VR] images having optimal resolution in all patients were obtained using 3D reconstructions on work-station. Styloid process and its extension, and stylohyoid ligament were evaluated. A styloid processes e"3cm were accepted to be longer than normal. We also had a control group of patients which consisted of ten patients who had no complaints of dysphagia, throat pain, or foreign body sensation in the throat. Elongation of the styloid process was revealed by 3D VR imaging in all patients. We found elongated styloid process bilaterally in two patients. Elongation of the styloid process was clearly revealed by 3D VR imaging in high contrast and spatial resolution under the anatomic orientation like conventional X-ray in all patients. The diagnosis of Eagle's syndrome was confirmed surgically in four of 13 patients. We conclude that 3D VR imaging is a valuable diagnostic method in detecting elongated styloid process


Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Base do Crânio/diagnóstico por imagem , Síndrome , Imageamento Tridimensional , Transtornos de Deglutição/diagnóstico , Dor de Orelha/diagnóstico
4.
Indian J Pediatr ; 2009 Apr; ()
Artigo em Inglês | IMSEAR | ID: sea-79273

RESUMO

An 11-month-old girl who has Dandy-Walker's variant (DWV) associated with tetralogy of Fallot (TOF), atrial septal defect (ASD), patent ductus arteriosus (PDA), and primary hypothyroidy is presented. There has been no report describing a case of DWV associated with TOF, ASD and PDA and primary hypothyroidy. The first case of Dandy-Walker malformation associated with TOF was reported by Kohyama et al in 1988, since then, a few cases were reported in the literature. Our patient is the first reported case.


Assuntos
Encéfalo/diagnóstico por imagem , Síndrome de Dandy-Walker/complicações , Síndrome de Dandy-Walker/diagnóstico , Síndrome de Dandy-Walker/genética , Permeabilidade do Canal Arterial/complicações , Feminino , Comunicação Interatrial/complicações , Humanos , Hipotireoidismo/complicações , Hipotireoidismo/diagnóstico , Tetralogia de Fallot/complicações , Tomografia Computadorizada por Raios X
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