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1.
J Craniofac Surg ; 26(5): e451-3, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26167999

RESUMO

Juvenile nasopharyngeal angiofibroma (JNA) is a benign, vascular, and locally aggressive tumor that arises in the nasal cavity, extending into the nasopharynx and often in to the orbit. It may rarely present to the ophthalmologist with proptosis and optic neuropathy. Preoperative embolization of JNA is done before surgical resection. In this communication, the authors report a rare occurrence of ipsilateral central retinal artery occlusion (CRAO) following embolization with polyvinyl alcohol in a 13-year-old boy with right-sided JNA. Retrospective review of the angiograms pointed out to a suspicious communication between the external carotid artery and the ophthalmic vessels. Pre-embolization detailed study of the angiograms is necessary to avoid such devastating complications. Although rare, vision loss is a possible complication arising from embolization of nasopharyngeal and intracranial tumors, and all patients undergoing these procedures should be informed of the risk of visual loss because it has a lasting impact on the quality of life.


Assuntos
Angiofibroma/terapia , Cegueira/etiologia , Embolização Terapêutica/efeitos adversos , Neoplasias Nasofaríngeas/terapia , Álcool de Polivinil/efeitos adversos , Oclusão da Artéria Retiniana/complicações , Adolescente , Idoso , Angiografia , Cegueira/diagnóstico , Humanos , Masculino , Oclusão da Artéria Retiniana/induzido quimicamente , Oclusão da Artéria Retiniana/diagnóstico por imagem , Estudos Retrospectivos , Acuidade Visual
2.
BMJ Case Rep ; 13(12)2020 Dec 17.
Artigo em Inglês | MEDLINE | ID: mdl-33334755

RESUMO

Renal biopsy is usually a prerequisite in the diagnosis of adult patients with nephrotic syndrome. Acute Budd Chiari syndrome is a known complication of certain aetiologies of nephrotic syndrome like membranous glomerulopathy and minimal change disease. This complication requires emergent anticoagulation, which would preclude the performance of a renal biopsy. We report the case of a 47-year-old woman who presented with acute Budd Chiari syndrome as the initial presentation of nephrotic syndrome. The difficult situation in which we had to give anticoagulation and also perform a renal biopsy led us to devise a novel way to treat the patient, namely, the initial use of transfemoral thrombolysis and thrombosuction followed by a renal biopsy, which confirmed the diagnosis of primary membranous nephropathy. Anticoagulation was safely instituted 48 hours later with documented clinical and radiological improvement.


Assuntos
Síndrome de Budd-Chiari/terapia , Glomerulonefrite Membranosa/diagnóstico , Síndrome Nefrótica/diagnóstico , Terapia Trombolítica/métodos , Angiografia , Anticoagulantes/administração & dosagem , Biópsia/métodos , Síndrome de Budd-Chiari/etiologia , Feminino , Fibrinólise , Membrana Basal Glomerular/patologia , Glomerulonefrite Membranosa/complicações , Glomerulonefrite Membranosa/patologia , Humanos , Pessoa de Meia-Idade , Síndrome Nefrótica/etiologia , Tomografia Computadorizada por Raios X , Veia Cava Inferior/diagnóstico por imagem
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