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1.
Joint Bone Spine ; 84(5): 615-619, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28499892

RESUMO

BACKGROUND: Giant cell arteritis is an inflammatory disorder of the medium- and large-size arteries. Permanent visual loss related to arteritic anterior ischemic optic neuropathy is among the most serious complications of this disease and initial treatment usually consists of high dose corticosteroids. There is no consensus in the literature concerning the optimal therapeutic approach in giant cell arteritis patients with corticosteroid-resistant arteritic anterior ischemic optic neuropathy. CASE REPORT: A 73-year-old Caucasian female with biopsy-proven giant cell arteritis developed an acute visual loss of the right eye due to arteritic anterior ischemic optic neuropathy. Despite 5 daily methylprednisolone pulses, systemic symptoms persisted and rapid involvement of the controlateral eye was documented. Therefore, tocilizumab (humanised monoclonal antibody binding the human interleukin-6 receptor) was introduced as a potential salvage therapy with a swift consecutive resolution of the systemic symptoms and stabilization of the ophthalmic lesions. CONCLUSIONS: Although a late effect of steroids pulses cannot be formally ruled out in this dramatic situation, tocilizumab likely offered a decisive effect in preventing bilateral blindness and may have contributed to steroid tapering. Tocilizumab may represent a new early effective second-line treatment option in corticosteroid-resistant anterior ischemic optic neuropathy. More data are needed to confirm this observation and to evaluate the safety profile of this treatment.


Assuntos
Anticorpos Monoclonais Humanizados/uso terapêutico , Anticorpos Monoclonais/uso terapêutico , Arterite de Células Gigantes/tratamento farmacológico , Metilprednisolona/uso terapêutico , Neuropatia Óptica Isquêmica/tratamento farmacológico , Idoso , Biópsia por Agulha , Quimioterapia Combinada , Feminino , Angiofluoresceinografia/métodos , Seguimentos , Arterite de Células Gigantes/complicações , Arterite de Células Gigantes/diagnóstico por imagem , Humanos , Imuno-Histoquímica , Neuropatia Óptica Isquêmica/etiologia , Neuropatia Óptica Isquêmica/patologia , Índice de Gravidade de Doença , Resultado do Tratamento
2.
Am J Emerg Med ; 30(8): 1658.e1-3, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22030202

RESUMO

Hiatus hernia (HH) is a frequent condition and is asymptomatic most of the time. Common symptoms can include epigastric pain, postprandial fullness, and nausea. We report a case of postprandial acute right and left heart failure caused by an intrathoracic stomach in a previously asymptomatic woman. Clinical manifestations included acute pulmonary edema and severe hypotension after administration of vasodilators for treatment of acute left heart failure. Chest computed tomography images showed a pre- and afterload compromise caused by a large compressive HH with massive gastric distension. To the best of our knowledge, ours is the first report of both acute right and left heart failure due to an HH. The prompt placement of a nasogastric tube was lifesaving. We believe that the diagnosis of HH ought to be taken into consideration by emergency physicians and included in the differential diagnosis for acute postprandial heart failure.


Assuntos
Insuficiência Cardíaca/etiologia , Hérnia Diafragmática/complicações , Gastropatias/complicações , Idoso de 80 Anos ou mais , Feminino , Hérnia Diafragmática/radioterapia , Humanos , Estômago/diagnóstico por imagem , Estômago/patologia , Gastropatias/diagnóstico por imagem , Gastropatias/patologia , Tomografia Computadorizada por Raios X
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