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2.
Braz J Otorhinolaryngol ; 89(5): 101316, 2023.
Article de Anglais | MEDLINE | ID: mdl-37678009

RÉSUMÉ

OBJECTIVE: The present study revisited three classification systems of orbital complications of acute rhinosinusitis (ARS) (Chandler, Mortimore & Wormald, and Velasco e Cruz & Anselmo-Lima) and observed which of them presented the best clinical applicability. METHODS: Clinical data and CT scan findings of patients with orbital infection were retrospectively collected. To compare the three classification systems, we revised and graded all CT images accordingly, and divided the patients into four groups: Eyelid cellulitis (EC), orbital cellulitis (OC), subperiosteal abscess (SA), and orbital abscess (OA). The groups were compared regarding the presence of sinus opacification, the need for hospitalization and/or surgical treatment, and the presence of further complications/sequelae. RESULTS: 143 patients were included. The median number of sinuses involved in patients in the OC, SA, and OA groups was 2.0. ARS was rarely associated with signs of EC (present in both Chandler's and Mortimore & Wormald's classifications. The hospitalization rate was significantly lower in the EC group compared to the other three groups. Surgery was performed in all cases in the OA group, in 58.1% in the SA group, 19.4% in the OC group, and 12.5% in the EC group (p-value < 0.0001). Complications were present at higher rates in the OA group compared to the other three groups. CONCLUSIONS: ARS was rarely associated with Eyelid Cellulitis. The stratification in the other three groups showed to be clinically relevant. Velasco e Cruz & Anselmo-Lima's classification system proved valid, simple, and effective for categorizing orbital complications of ARS.


Sujet(s)
Cellulite orbitaire , Maladies de l'orbite , Rhinite , Sinusite , Humains , Études rétrospectives , Abcès/imagerie diagnostique , Abcès/étiologie , Rhinite/complications , Rhinite/imagerie diagnostique , Rhinite/chirurgie , Cellulite orbitaire/imagerie diagnostique , Cellulite orbitaire/étiologie , Sinusite/complications , Sinusite/imagerie diagnostique , Sinusite/chirurgie , Maladie aigüe , Maladies de l'orbite/étiologie , Maladies de l'orbite/complications
4.
Rev. cir. traumatol. buco-maxilo-fac ; 23(4): 42-47, out.-dez. 2023. ilus
Article de Espagnol | LILACS, BBO - Ondontologie | ID: biblio-1562229

RÉSUMÉ

Apresentamos um caso de tumor fibroso solitário do seio frontal que herniava para a cavidade orbitária. Esta patologia é rara e cerca de trinta casos foram relatados na literatura mundial. O manejo foi feito com um grupo multidisciplinar e uma abordagem combinada transnasal e endoscópica externa através de uma incisão no nível do ângulo interno superior da órbita. A grande maioria da massa tumoral foi retirada e a fístula óssea foi selada com a colocação de uma malha orbital, que foi recoberta por uma membrana autóloga de fatores de crescimento, obtida e processada do sangue do próprio paciente. Os resultados imediatos foram muito bons e o acompanhamento é necessário para o controle do tumor... (AU)


We present a case of a solitary fibrous tumor of the frontal sinus that herniated within the orbital cavity. This pathology is rare and around thirty cases have been reported in the world literature. Management was done with a multidisciplinary group and a combined transnasal endoscopic and external approach through an incision in superior internal angle of the orbit. The tumor mass was removed, and the supraorbital bone was sealed with an orbit mesh, which was covered with an autologous membrane of growth factors, obtained, and processed from the patient's own blood. The immediate result was excellent, and follow-up is required to control the tumor... (AU)


Presentamos un caso de un tumor fibroso solitario de seno frontal que se hernió dentro de la cavidad orbitaria. Esta patología es rara y se han reportado una treintena de casos en la literatura mundial. El manejo se hizo con un grupo multidisciplinario y un abordaje combinado endoscópico transnasal y externo a través de una incisión a nivel de ángulo superior interno de la órbita. Se retiró la masa tumoral en su gran mayoría, y se selló la fístula ósea con la colocación de una malla para órbita, la cual se cubrió con una membrana autóloga de factores de crecimiento, obtenida y procesada de la propia sangre del paciente. Los resultados inmediatos fueron muy buenos y se precisa seguimiento para control de la tumoración... (AU)


Sujet(s)
Humains , Mâle , Sujet âgé , Maladies de l'orbite
5.
Arq Bras Oftalmol ; 86(2): 168-170, 2023.
Article de Anglais | MEDLINE | ID: mdl-35170651

RÉSUMÉ

Sarcoidosis is a generalized systemic chronic inflammation that rarely involves the orbit. As a chronic inflammation, sarcoidosis typically manifests with an insidious onset and slowly progressive course. We report a case of acute-onset proptosis resulting from a rapidly growing diffuse orbital mass that simulated malignant growth, which was biopsy proven to be the first manifestation of systemic sarcoidosis. The patient demonstrated complete resolution of proptosis and systemic involvement with long-term corticosteroid treatment.


Sujet(s)
Exophtalmie , Maladies de l'orbite , Sarcoïdose , Humains , Exophtalmie/étiologie , Exophtalmie/anatomopathologie , Sarcoïdose/complications , Sarcoïdose/traitement médicamenteux , Sarcoïdose/anatomopathologie , Maladies de l'orbite/traitement médicamenteux , Maladies de l'orbite/étiologie , Maladies de l'orbite/anatomopathologie , Orbite , Inflammation/anatomopathologie
7.
Rev. otorrinolaringol. cir. cabeza cuello ; 82(3): 333-337, sept. 2022. ilus
Article de Espagnol | LILACS | ID: biblio-1409942

RÉSUMÉ

Resumen Durante la cirugía endoscópica nasosinusal, la sección inadvertida y retracción hacia la órbita de la arteria etmoidal anterior (AEA) es el mecanismo habitual del hematoma orbitario (HO); éste se manifiesta con proptosis, dolor y déficit visual potencialmente irreversible. El déficit visual es secundario a isquemia del nervio óptico por aumento de la presión intraocular, siendo suficientes treinta minutos para que ocurra daño visual permanente. Por sus secuelas el tratamiento del HO debe ser rápido y agresivo. Presentamos el caso de un varón de 72 años con diagnóstico de rinosinusitis crónica con pólipos nasales refractaria a tratamiento médico que se sometió a cirugía endoscópica nasal y que desarrolló en el posoperatorio inmediato con un HO. Se manejó precozmente con cantotomía-cantolisis, descompresión orbitaria medial endoscópica y control vascular de la AEA. El paciente evoluciona favorablemente, sin déficit visual. En este artículo se discutirán el diagnóstico y manejo oportunos del hematoma orbitario iatrogénico.


Abstract During endoscopic sinonasal surgery, inadvertent section of the anterior ethmoidal artery (AEA) with retraction into the orbit is the usual mechanism of orbital hematoma (OH), leading to proptosis, pain, and potentially irreversible visual loss. Thirty minutes is sufficient for retinal ischemia and permanent visual loss. The explanation for blindness is due to increased intraorbital pressure. The treatment of iatrogenic HO must be quick and aggressive, because if it is not managed in time, it can cause a permanent visual deficit. We present the case of a 72-year-old man with a diagnosis of chronic rhinosinusitis with nasal polyps refractory to medical treatment who underwent nasal endoscopic surgery, evolving in the immediate postoperative period with an HO, requiring canthotomy - cantolysis and early surgical reintervention for endoscopic medial orbital decompression and vascular control of AEA. The patient evolves favorably, without visual deficit. This article will discuss the timely diagnosis and management of iatrogenic orbital hematoma.


Sujet(s)
Humains , Mâle , Sujet âgé , Maladies de l'orbite/étiologie , Polypes du nez/chirurgie , Endoscopie/effets indésirables , Hématome/étiologie , Endoscopie/méthodes , Hémorragie/étiologie
8.
Dermatol Ther ; 35(8): e15655, 2022 08.
Article de Anglais | MEDLINE | ID: mdl-35726592

RÉSUMÉ

Combined vascular malformations are complex vascular anomalies that have high morbidity and therefore, therapeutic strategies are hard to establish. In this report, we aim to present two pediatric cases of ocular combined vascular malformations successfully treated with rapamycin.


Sujet(s)
Maladies de l'orbite , Anomalies vasculaires , Enfant , Humains , Maladies de l'orbite/traitement médicamenteux , Sirolimus/usage thérapeutique , Anomalies vasculaires/traitement médicamenteux
9.
J Pediatr ; 248: 66-73.e7, 2022 09.
Article de Anglais | MEDLINE | ID: mdl-35568061

RÉSUMÉ

OBJECTIVES: To evaluate risk factors associated with surgical intervention and subperiosteal/orbital abscess in hospitalized children with severe orbital infections. STUDY DESIGN: We conducted a multicenter cohort study of children 2 months to 18 years hospitalized with periorbital or orbital cellulitis from 2009 to 2018 at 10 hospitals in Canada. Clinical details were extracted, and patients were categorized as undergoing surgical or medical-only management. Primary outcome was surgical intervention and the main secondary outcome was clinically important imaging. Logistic regression was used to identify predictors. RESULTS: Of 1579 patients entered, median age was 5.4 years, 409 (25.9%) had an orbital/subperiosteal abscess, and 189 (12.0%) underwent surgery. In the adjusted analysis, the risk of surgical intervention was associated with older age (age 9 to <14: aOR 3.9, 95% CI 2.3-6.6; and age 14 to ≤18 years: aOR 7.0, 95% CI 3.4-14.1), elevated C-reactive protein >120 mg/L (aOR 2.8, 95% CI 1.3-5.9), elevated white blood cell count of 12-20 000/µL (aOR 1.7, 95% CI 1.1-2.6), proptosis (aOR 2.6, 95% CI 1.7-4.0), and subperiosteal/orbital abscess (aOR 5.3, 95% CI 3.6-7.9). There was no association with antibiotic use before hospital admission, sex, presence of a chronic disease, temperature greater than 38.0°C, and eye swollen shut. Complications were identified in 4.7% of patients, including vision loss (0.6%), intracranial extension (1.6%), and meningitis (0.8%). CONCLUSIONS: In children hospitalized with severe orbital infections, older age, elevated C-reactive protein, elevated white blood cell count, proptosis, and subperiosteal/orbital abscess were predictors of surgical intervention.


Sujet(s)
Exophtalmie , Cellulite orbitaire , Maladies de l'orbite , Abcès/imagerie diagnostique , Abcès/chirurgie , Adolescent , Antibactériens/usage thérapeutique , Protéine C-réactive , Enfant , Enfant d'âge préscolaire , Études de cohortes , Exophtalmie/complications , Exophtalmie/traitement médicamenteux , Humains , Cellulite orbitaire/imagerie diagnostique , Cellulite orbitaire/chirurgie , Études rétrospectives
10.
Braz. j. otorhinolaryngol. (Impr.) ; Braz. j. otorhinolaryngol. (Impr.);88(2): 257-262, Mar.-Apr. 2022. tab, graf
Article de Anglais | LILACS | ID: biblio-1374726

RÉSUMÉ

Abstract Introduction: The standard management of orbital cellulitis is to administer a combination of intravenous broad-spectrum antibiotics along with treatment of associated sinusitis. Objective: The purpose of this study was to evaluate whether the addition of corticosteroids could lead to earlier resolution of inflammation and improve disease outcome. Methods: We independently searched five databases (PubMed, SCOPUS, Embase, the Web of Science, and the Cochrane database) for studies published as recent as December 2019. Of the included studies, we reviewed orbital cellulitis and disease morbidity through lengths of hospitalization, incidence of surgical drainage, periorbital edema, vision, levels or C-reactive protein, and serum WBC levels in order to focus on comparing steroid with antibiotics treated group and only antibiotics treated group. Results: Lengths of hospitalization after admission as diagnosed as orbital cellulitis (SMD = −4.02 [−7.93; −0.12], p -value = 0.04, I2 = 96.9%) decrease in steroid with antibiotics treated group compared to antibiotics only treated group. Incidence of surgical drainage (OR = 0.78 [0.27; 2.23], p -value = 0.64,I2 = 0.0%) was lower in the steroid with antibiotics treated group compared to the antibiotics only treated group. Conclusion: Use of systemic steroids as an adjunct to systemic antibiotic therapy for orbital cellulitis may decrease orbital inflammation with a low risk of exacerbating infection. Based on our analysis, we concluded that early use of steroids for a short period can help shorten hospitalization days and prevent inflammation progression.


Resumo Introdução: O tratamento padrão da celulite orbitária inicia-se com uma combinação de antibióticos intravenosos de amplo espectro concomitante ao tratamento do seio comprometido. Objetivos: O objetivo deste estudo foi avaliar se a adição de corticosteroides poderia levar a uma resolução mais precoce da inflamação e melhorar o desfecho da doença. Método: Fizemos uma pesquisa independente em cinco bancos de dados (PubMed, SCOPUS, Embase, Web of Science e o banco de dados Cochrane) em busca de estudos publicados até dezembro de 2019. Dos estudos incluídos, revisamos a celulite orbitária e a morbidade da doença através dos períodos de internação, incidência de drenagem cirúrgica, edema periorbital, visão, níveis de proteína C-reativa e níveis séricos de leucócitos com foco na comparação do grupo tratado com esteroides e antibióticos e do grupo tratado apenas com antibióticos. Resultados: Os tempos de internação após a admissão dos diagnosticados com celulite orbitária (SMD = -4,02 [-7,93; -0,12], p-valor = 0,04, I2 = 96,9%) diminuíram no grupo tratado com esteroides e antibióticos em comparação ao grupo tratado apenas com antibióticos. A incidência de drenagem cirúrgica (OR = 0,78 [0,27; 2,23], p-valor = 0,64, I2 =0,0%) foi menor no grupo tratado com esteroides e antibióticos em comparação com o grupo tratado apenas com antibióticos. Conclusão: O uso de esteroides sistêmicos como adjuvante da antibioticoterapia sistêmica para celulite orbitária pode diminuir a inflamação orbitária com baixo risco de agravar a infecção. Com base em nossa análise, concluímos que o uso precoce de esteroides por um curto período pode ajudar a encurtar os dias de internação e prevenir a progressão da inflamação.


Sujet(s)
Humains , Maladies de l'orbite/complications , Maladies de l'orbite/traitement médicamenteux , Cellulite orbitaire/diagnostic , Cellulite orbitaire/étiologie , Cellulite orbitaire/traitement médicamenteux , Stéroïdes , Cellulite sous-cutanée/complications , Cellulite sous-cutanée/traitement médicamenteux , Études rétrospectives , Hormones corticosurrénaliennes/usage thérapeutique , Inflammation , Antibactériens/usage thérapeutique
11.
Arq Bras Oftalmol ; 85(1): 77-81, 2022.
Article de Anglais | MEDLINE | ID: mdl-34468552

RÉSUMÉ

We report the case of a 46-year-old diabetic man receiving treatment for rhino-orbital-cerebral mucormycosis with liposomal amphotericin B and surgical debridement. The patient's condition worsened clinically, accompanied by the loss of ocular motility and a visual acuity of absence of light perception. Radiological extension of the infection was evidenced, with invasion of the cavernous sinus. Based on ophthalmological findings, exenteration (a potentially disfiguring procedure) was indicated, but we opted for wide surgical debridement and administration of amphotericin B via intraconal catheter. Clinical improvement and resolution of inflammation occurred after 2 weeks of treatment. Thus, rhino-orbital-cerebral mucormycosis was effectively controlled through intraconal administration of amphotericin B, while avoiding exenteration. The intervention should be considered as an adjuvant treatment in selected rhino-orbital-cerebral mucormycosis cases before attempting exenteration.


Sujet(s)
Mycoses oculaires , Mucormycose , Maladies de l'orbite , Amphotéricine B/usage thérapeutique , Antifongiques/usage thérapeutique , Mycoses oculaires/traitement médicamenteux , Humains , Mâle , Adulte d'âge moyen , Mucormycose/imagerie diagnostique , Mucormycose/traitement médicamenteux , Maladies de l'orbite/imagerie diagnostique , Maladies de l'orbite/traitement médicamenteux
12.
Braz J Otorhinolaryngol ; 88(2): 257-262, 2022.
Article de Anglais | MEDLINE | ID: mdl-33722520

RÉSUMÉ

INTRODUCTION: The standard management of orbital cellulitis is to administer a combination of intravenous broad-spectrum antibiotics along with treatment of associated sinusitis. OBJECTIVE: The purpose of this study was to evaluate whether the addition of corticosteroids could lead to earlier resolution of inflammation and improve disease outcome. METHODS: We independently searched five databases (PubMed, SCOPUS, Embase, the Web of Science, and the Cochrane database) for studies published as recent as December 2019. Of the included studies, we reviewed orbital cellulitis and disease morbidity through lengths of hospitalization, incidence of surgical drainage, periorbital edema, vision, levels or C-reactive protein, and serum WBC levels in order to focus on comparing steroid with antibiotics treated group and only antibiotics treated group. RESULTS: Lengths of hospitalization after admission as diagnosed as orbital cellulitis (SMD=-4.02 [-7.93; -0.12], p-value=0.04, I2=96.9%) decrease in steroid with antibiotics treated group compared to antibiotics only treated group. Incidence of surgical drainage (OR=0.78 [0.27; 2.23], p-value=0.64, I2=0.0%) was lower in the steroid with antibiotics treated group compared to the antibiotics only treated group. CONCLUSION: Use of systemic steroids as an adjunct to systemic antibiotic therapy for orbital cellulitis may decrease orbital inflammation with a low risk of exacerbating infection. Based on our analysis, we concluded that early use of steroids for a short period can help shorten hospitalization days and prevent inflammation progression.


Sujet(s)
Cellulite orbitaire , Maladies de l'orbite , Hormones corticosurrénaliennes/usage thérapeutique , Antibactériens/usage thérapeutique , Cellulite sous-cutanée/complications , Cellulite sous-cutanée/traitement médicamenteux , Humains , Inflammation , Cellulite orbitaire/diagnostic , Cellulite orbitaire/traitement médicamenteux , Cellulite orbitaire/étiologie , Maladies de l'orbite/complications , Maladies de l'orbite/traitement médicamenteux , Études rétrospectives , Stéroïdes
14.
Rev. argent. reumatolg. (En línea) ; 32(4): 28-37, dic. 2021. ilus, tab
Article de Espagnol | LILACS, BINACIS | ID: biblio-1376441

RÉSUMÉ

Se comunica una serie de tres casos clínicos que consultaron al servicio de Reumatología por compromiso orbitario y renal. Uno de ellos presentó pseudotumor orbitario con proteinuria en rango nefrótico; se realizó biopsia y se encontró infiltrado linfoplasmocitario denso y fibrosis estoriforme con inmunohistoquímica: 15 células IgG4+ por campo de alto poder y relación IgG/IgG4 ≤40%, concluyendo diagnóstico de enfermedad relacionada por IgG4. El segundo y tercer caso presentaron compromiso ocular con "ojos de mapache" y lesiones amarillentas en párpados, ambos con proteinuria >500 mg/24 h, con biopsia de piel rojo Congo positiva y birrefringencia verde manzana con luz polarizada. Se discuten distintos diagnósticos diferenciales poco frecuentes a tener en cuenta en estos pacientes.


A series of three cases that consulted the rheumatology service due to orbital and renal involvement is reported. One of them presented orbital pseudotumor with proteinuria in the nephrotic range, a biopsy was performed, finding dense lymphoplasmacytic infiltrate and storiform fibrosis with immunohistochemistry: 15 IgG4 positive cells per HPF and IgG/IgG4 ratio ≤40%, concluding diagnosis of IgG4 related disease. The second and third cases presented ocular involvement with raccoon eyes and yellowish lesions on the eyelids, both with proteinuria greater than 500 mg/24 h, with apple-green birefringence of amyloid on congo red staining. Different rare differential diagnoses to take into account in these patients are discussed.


Sujet(s)
Humains , Femelle , Adulte , Adulte d'âge moyen , Jeune adulte , Maladies de l'orbite/diagnostic , Maladies de la peau/diagnostic , Maladie associée aux immunoglobulines G4/diagnostic , Amyloïdose/diagnostic , Maladies du rein/diagnostic , Polyarthrite rhumatoïde/diagnostic , Polyarthrite rhumatoïde/traitement médicamenteux , Sarcoïdose/diagnostic , Maladies de la peau/anatomopathologie , Maladies de la peau/traitement médicamenteux , Diagnostic différentiel , Maladie associée aux immunoglobulines G4/anatomopathologie , Maladie associée aux immunoglobulines G4/traitement médicamenteux , Amyloïdose/anatomopathologie , Amyloïdose/traitement médicamenteux , Maladies du rein/anatomopathologie , Maladies du rein/traitement médicamenteux
15.
Int. j. morphol ; 39(6): 1683-1687, dic. 2021. ilus, tab
Article de Anglais | LILACS | ID: biblio-1385553

RÉSUMÉ

SUMMARY: Late orbital reconstruction is a complex and challenge for surgeons. The aim of this article is to present complex orbital reconstruction using patient specific implant (PSI) strategy and polyetheretherketone (PEEK). A literature review and a cases series of sequelae after complex orbital trauma are presented; cases with great middle third deformities showing defect in the maxilla, nasal area, body of the zygoma and zygomatic arch were included; in both cases the sequelae was for more than 10 years. Virtual planning and PEEK implants were manufacture using a puzzle (two or three parts) by 3D print or injection. Patients were treated and their surgeries carried out without complications, using a minimal surgical approach. No infections were observed, and after 12 months follow-up they were stable showing normal function. PSI based-PEEK for orbital reconstruction are safe, efficient, effective and to obtain orbital morphology with low complications.


RESUMEN: La reconstrucción tardía de la órbita es un desafío complejo para cirujanos. El objetivo de este artículo fue presentar la reconstrucción orbitaria compleja utilizando implante paciente específico (PSI) y polietereterketona (PEEK). Son presentados una revisión de literatura y una serie de casos con secuelas posteriores a un trauma orbitario complejo; además, son presentados casos con gran deformidad del tercio medio del rostro mostrando defectos en maxila, área nasal, cuerpo del hueso cigomático y arco cigomático; ambos casos de secuela fueron por más de 10 años. Planificación virtual e implantes en PEEK fueron creados usando una estrategia de puzzle (dos o tres partes) por inyección o impresión 3D. Los pacientes fueron tratados y sus cirugías realizadas sin complicaciones usando accesos quirúrgicos reducidos. No se observaron infecciones y después de 12 meses de seguimiento permanecieron estables mostrando función normal. Los PSI para reconstrucción orbitaria son seguros, eficientes, efectivos y recuperan morfología de órbita con bajas complicaciones.


Sujet(s)
Humains , Mâle , Femelle , Adulte d'âge moyen , Maladies de l'orbite/chirurgie , 33584/méthodes , Impression tridimensionnelle , Orbite/traumatismes , Maladies de l'orbite/complications , Polymères/composition chimique , Benzophénones/composition chimique , Matériaux biocompatibles/composition chimique , Résultat thérapeutique , Implants orbitaires
16.
Arq. bras. oftalmol ; Arq. bras. oftalmol;84(2): 183-185, Mar,-Apr. 2021. graf
Article de Anglais | LILACS | ID: biblio-1153116

RÉSUMÉ

ABSTRACT A 62-year-old woman was admitted to our clinic with the complaints of periorbital ecchymosis and subconjunctival hemorrhage that are visible, especially on the right eye. We noted that her complaints began the day after she underwent leech therapy on the glabella area for headache. On the glabella, 2 leech bites were observed close to the right side. Examination revealed ecchymosis on the bilateral eyelids and subconjunctival hemorrhage on the inferolateral and medial limbus on the right eye. No treatment was initiated, rather control measures were recommended. The follow-up after 1 month revealed that the patient's complaints had disappeared.(AU)


RESUMO Uma paciente de 62 anos procurou nosso ambulatório com queixas de equimose periorbital e hemorragia subconjuntival, visíveis principalmente no olho direito. Descobrimos que suas queixas começaram no dia seguinte a um tratamento para dor de cabeça com sanguessugas na área da glabela. Na glabela, 2 mordidas de sanguessuga foram encontradas próximas ao lado direito. Durante os exames da paciente, foram detectadas equimoses nas pálpebras bilaterais e hemorragia subconjuntival no limbo ínfero lateral e medial do olho direito. Nenhum tratamento foi iniciado, sendo recomendado apenas controle. No acompanhamento, observou-se que as queixas da paciente desapareceram em cerca de um mês.(AU)


Sujet(s)
Adulte d'âge moyen , Hémorragie oculaire/étiologie , Conjonctive/anatomopathologie , Hirudothérapie/effets indésirables , Céphalée/traitement médicamenteux , Maladies de l'orbite , Hématome
17.
Rev. bras. oftalmol ; 80(2): 127-132, Mar.-Apr. 2021. tab, graf
Article de Espagnol | LILACS | ID: biblio-1280102

RÉSUMÉ

RESUMO Objetivo: Conheça as características demográficas e clínicas da Órbita Associada da Tiroide (OAT), bem como a taxa de exigência da cirurgia orbital em pacientes do Centro Médico Nacional do Oeste. Métodos. Estudo observacional, transversal, descritivo e retrospetivo realizado analisando os registos de pacientes diagnosticados com OAT tratados num centro de cuidados de terceiro nível de janeiro de 2005 a julho de 2016. Os resultados. Um total de 236 órbitas de 118 pacientes foram avaliados, com uma idade média de 47,3 (13,2 anos, 74,6% eram do sexo feminino e 25,4% masculinos. 4,2% dos doentes foram tratados com hipotiroidismo, 94,1% com hipertireoidismo e 1,7% com goiter tóxico difuso. 44,9% dos doentes estudados com restrição de movimento ocular,10,2% com queratopatia de exposição e 51,7% com hipertensão intraocular. 34,7% dos doentes avaliados no serviço necessitaram de descompressão orbital, 16,1% de cirurgia palpebral e 8,5% de correção do hatrabisma. Na gestão conservadora destes doentes, 48,3% exigiam o uso de lubrificantes tópicos dos olhos, enquanto 52,5% dos pacientes necessitavam do uso de hipotensivos oculares em número variável. As conclusões. A OAT foi associada principalmente ao hipertiroidismo, sendo mais comum em pacientes do sexo feminino entre os 40 e os 59 anos; mais de 50% dos pacientes necessitaram do uso de hipotensivos oculares. Da mesma forma, a gestão cirúrgica foi realizada em mais de 50% dos pacientes, sendo a descompressão orbital a intervenção mais frequente.


ABSTRACT Objective. To know the demographic and clinical characteristics of Thyroid Associated Orbitopathy (TAO), as well as the requirement rate of orbital surgery in patients of the Orbit Service in the National Medical Center of the West, IMSS. Methods. Observational, cross-cutting, descriptive and retrospective study carried out analyzing the records of patients diagnosed with TAO and treated at a third-level care center from January 2005 to July 2016. Results. A total of 236 orbits of 118 patients were valued, with an average age of 47.3 ± 13.2 years, 74.6% were female and 25.4% male. 4.2% of patients were treated with hypothyroidism, 94.1% with hyperthyroidism and 1.7% with diffuse toxic goiter. 44.9% of patients studied had eye movement restriction,10.2% exposure keratopathy and 51.7% intraocular hypertension. 34.7% of patients valued in the service required orbital decompression, 16.1% palpebral surgery and 8.5% strabism correction. In the conservative management of these patients 48.3% required the use of topical eye lubricants, while 52.5% required the use of eye hypotensives in variable numbers. Conclusions. TAO was mainly associated with hyperthyroidism, being more common in female patients between the age of 40 and 59; more than 50% of patients required the use of eye hypotensives. Likewise, surgical management was performed in more than 50% of patients, with orbital decompression being the most frequent intervention.


Sujet(s)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Sujet âgé , Sujet âgé de 80 ans ou plus , Maladies de l'orbite/chirurgie , Maladies de l'orbite/étiologie , Procédures de chirurgie ophtalmologique/statistiques et données numériques , Maladies de la thyroïde/complications , Exophtalmie/chirurgie , Exophtalmie/étiologie , Orbite/chirurgie , Exophtalmie/diagnostic , Maladie de Basedow/complications , Études transversales , Études rétrospectives , Décompression chirurgicale/méthodes , Pression intraoculaire
18.
J Pediatr ; 230: 174-181.e1, 2021 03.
Article de Anglais | MEDLINE | ID: mdl-33157073

RÉSUMÉ

OBJECTIVE: To evaluate the clinical and imaging characteristics of orbital lesions of pediatric Langerhans cell histiocytosis (LCH). STUDY DESIGN: A retrospective analysis of clinical data and central review of magnetic resonance imaging scans in patients with LCH, enrolled into one of the consecutive international trials LCH I-III, or submitted for a second opinion between 1994 and 2015. RESULTS: Data from 31 children (34 involved orbits) were analyzed. Orbital LCH was the only disease manifestation in 15, part of a multifocal skeletal in 5, or a multisystem LCH in 11 patients. Orbital LCH was part of the initial disease presentation in 23 or developed at relapse in 8 cases. Orbital involvement was unilateral in 28 and bilateral in 3 patients (34 affected orbits). Proptosis was present in 9 patients. Frontal and zygomatic bone were most commonly affected. All orbital lesions were extraconal. Associated extraorbital imaging findings were dural tail sign in 19, neurodegeneration in 8, and hypothalamic-pituitary mass in 3 patients. Sixteen patients (52%) had at least 1 documented disease relapse. Permanent consequences were prominent proptosis in 1, diabetes insipidus in 8, growth hormone deficiency in 2, radiologic neurodegeneration in 8, and clinical neurodegeneration in 3 patients. CONCLUSIONS: Predominantly unilateral orbital LCH can be the only disease manifestation or part of a disseminated disease. Orbital lesions in LCH are exclusively extraconal, typically located at the roof and the lateral wall of the orbit. The optimal treatment approach of unifocal LCH of the orbit remains controversial and warrants a prospective evaluation.


Sujet(s)
Histiocytose à cellules de Langerhans/diagnostic , Imagerie par résonance magnétique , Maladies de l'orbite/diagnostic , Adolescent , Enfant , Enfant d'âge préscolaire , Femelle , Histiocytose à cellules de Langerhans/imagerie diagnostique , Humains , Nourrisson , Mâle , Maladies de l'orbite/imagerie diagnostique , Études rétrospectives
19.
Rev. bras. oftalmol ; 80(3): e0007, 2021. graf
Article de Portugais | LILACS | ID: biblio-1280119

RÉSUMÉ

RESUMO Os diagnósticos diferenciais que compõem as proptoses agudas são, muitas vezes, desafiadores. A anamnese e o exame clínico exigem do oftalmologista atenção especial aos detalhes que permitem diferenciar quadros relativamente benignos e autolimitados de quadros que evoluirão com incapacidades permanentes. Relatamos o caso de uma paciente de 49 anos que, durante viagem de avião, apresentou dor ocular, hematoma periorbitário e proptose do olho esquerdo súbitos. Referia diplopia aguda incapacitante. Exames de tomografia e angiorressonância magnética confirmaram diagnóstico de sinusopatia do seio etmoidal esquerdo e hematoma subperiosteal da órbita esquerda, associado ao barotrauma. Apesar de raro, o diagnóstico de hematoma subperiosteal não traumático deve ser considerado diferencial em relação a proptoses agudas, sendo a anamnese fundamental para essa elucidação diagnóstica.


ABSTRACT Differential diagnoses of acute proptosis are often challenging. History and clinical examination require from ophthalmologists special attention to details, which make it possible to differentiate relatively benign and self-limited conditions from those that will progress to permanent disabilities. We report a 49-year-old female patient who had sudden eye pain, periorbital hematoma and proptosis of the left eye during a commercial flight. She also complained of disabling acute diplopia. Computed tomography and magnetic resonance angiography imaging confirmed the diagnosis of subperiosteal hematoma of the left orbit, associated with left ethmoid sinus disease. Although rare, non-traumatic subperiosteal hematoma should be considered in differential diagnoses of acute proptosis, and history taking is fundamental to elucidate the picture.


Sujet(s)
Humains , Femelle , Adulte d'âge moyen , Maladies de l'orbite/étiologie , Maladies de l'orbite/imagerie diagnostique , Barotraumatismes/complications , Hémorragie oculaire/étiologie , Hémorragie oculaire/imagerie diagnostique , Maladies des sinus/traitement médicamenteux , Maladies des sinus/imagerie diagnostique , Aviation , Tomodensitométrie , Exophtalmie , Angiographie par résonance magnétique , Association amoxicilline-clavulanate de potassium/usage thérapeutique , Diplopie , Voyage aérien
20.
Acta sci. vet. (Impr.) ; 49(supl.1): 715, 2021. ilus
Article de Portugais | VETINDEX | ID: biblio-1363923

RÉSUMÉ

Background: Cryptococcosis is a systemic mycotic disease caused by encapsulated yeasts C. neoformans and C. gattii. Cryptococcus neoformans is predominantly found in soils and feces of pigeons and psittacids. Infection occurs mainly through the respiratory tract, through the inspiration of fungal propagules (basidiospores and/or desiccated yeast cells). The main lesions observed are in the nasal cavity and lungs, but in dogs, the central nervous system and eyes are widely affected. Despite some previously mentioned reports, the retrobulbar form has not been described in the literature. Therefore, the purpose of this report is to describe a case of retrobulbar cryptococcoma mimetizing a tumor in a young bitch. Case: A 2-year-old female Labrador Retriever, was admitted to one Veterinary Hospital with exophthalmia on the left eye for 15 days and other signs included negative retropulsion, mydriasis, and abscence of menace and pupillary reflexes. Ocular ultrasound imaging revealed a hyperecotic and heterogeneous retrobulbar mass in the mid-dorsal region compressing the optic nerve. Computed tomography of the skull showed the presence of proliferation of neoplastic tissue in a locally invasive retrobulbar region promoting moderate rostrolateral displacement of the left ocular bulb, discrete osthelysis in maxillary bone, palatine, medial wall of the orbital bone and frontal bone, with destruction of cribiform plate adjacent to the dorsal region of the orbital wall and presence of mild contrast uptake in the region of the left olfactory bulb lobe, characterizing a picture compatible with neoplasia with malignancy and locally invasive characteristics. Exenteration and excision of part of the frontal bone were performed and histopathological examination revealed granulation with the presence of fibroblasts and numerous typical blastoconidia of Cryptococcus neoformans. The patient was treated with Itraconazole [10 mg/kg, v.o, SID, for 90 days] and one year after diagnosis, X-ray was performed to control the lesion and radiographic aspects were within normal limits. Discussion: Cryptococcus sp. is an environmental fungus that has the potential to be pathogenic to humans and animals. Fungus present as a basidiospores in pigeon droppings. The patient described had a history of contact with free-living pigeons, making it a risk factor for the occurrence of cryptococcosis, being the possible cause of the infection. In dogs, the disease is mainly described in immunosuppressed animals, which was not the case of the patient, who presented clinical and laboratory results within the normal range and without a previous history of use of immunosuppressants. The alterations described in the computed tomography, such as destruction of the cribriform plate adjacent to the dorsal region of the left orbital wall and the presence of slight contrast uptake in the left olfactory bulb lobe region, are compatible with the main entry point for propagules of Cryptococcus sp. In the present case, no periocular and ocular alterations were observed as described in the literature, and the lesion was restricted to the retrobulbar space. Ultrasonography and computed tomography revealed a neoformation mimicking a malignant neoplasm and the diagnosis of cryptococcoma was revealed by histopathology. Based on the present case, cytology through aspiration of retrobulbal neoformations is imperative as a diagnostic method, especially in endemic areas for fungal diseases that can mimic ocular neoplasms.


Sujet(s)
Animaux , Femelle , Chiens , Maladies de l'orbite/médecine vétérinaire , Exophtalmie/médecine vétérinaire , Cryptococcose/médecine vétérinaire , Cryptococcus/isolement et purification , Tomodensitométrie/médecine vétérinaire , Mimétisme moléculaire
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