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1.
Ocul Immunol Inflamm ; 31(8): 1727-1729, 2023 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-35797360

RESUMO

Anti-tumor necrosis factor alpha (TNF- α) biological agents can rarely cause sarcoid-like granulomatosis. A 20-year-old woman presented with a 1-month history of painful left upper eyelid swelling. She was on subcutaneous etanercept and methotrexate for 1 year for juvenile idiopathic arthritis. Imaging showed diffuse enlargement of the left and minimal enlargement of the right lacrimal gland. There was no finding in favor of sarcoidosis on systemic evaluation. Incisional biopsy of the left lacrimal gland revealed non-caseating granulomatous dacryoadenitis. The findings showed significant regression 1 month after cessation of Etanercept therapy. To the best of our knowledge, this report illustrates the first case of an isolated granulomatous dacryoadenitis during TNF-α antagonist therapy.


Assuntos
Dacriocistite , Aparelho Lacrimal , Sarcoidose , Feminino , Humanos , Adulto Jovem , Adulto , Etanercepte/efeitos adversos , Dacriocistite/induzido quimicamente , Dacriocistite/diagnóstico , Dacriocistite/tratamento farmacológico , Sarcoidose/induzido quimicamente , Sarcoidose/diagnóstico , Granuloma , Aparelho Lacrimal/patologia
2.
Ophthalmic Plast Reconstr Surg ; 33(3S Suppl 1): S125-S127, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-26505233

RESUMO

The authors report the case of a 4-year-old boy who presented with unilateral ptosis and a mass lesion of palpebral conjunctiva of the left upper eyelid, that had been present for 2 weeks, and had rapidly enlarged. The lesion was salmon colored and was easily distinguished from the conjunctiva. There was no obvious orbital extension in the MRI studies. Excisional biopsy was performed through a conjunctival approach. The histopathology was consistent with embryonal rhabdomyosarcoma. Thoracoabdominal CT scans revealed nodules in both lungs, indicating stage 4 disease. The patient received chemotheraphy and intensity-modulated radiation therapy. Rhabdomyosarcoma confined to the conjunctiva and distant metastasis without orbital involvement is rare. It should be included in the differential diagnosis of any atypical conjunctival mass lesions in children, and histopathology is necessary to establish proper treatment. As the case indicates, detailed systemic evaluation and careful systemic follow up of these patients are mandatory.


Assuntos
Túnica Conjuntiva/patologia , Neoplasias da Túnica Conjuntiva/patologia , Neoplasias Pulmonares/secundário , Rabdomiossarcoma Embrionário/secundário , Biópsia , Criança , Diagnóstico Diferencial , Humanos , Neoplasias Pulmonares/diagnóstico , Imageamento por Ressonância Magnética , Masculino , Rabdomiossarcoma Embrionário/diagnóstico
3.
Ulus Travma Acil Cerrahi Derg ; 21(4): 271-8, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26374414

RESUMO

BACKGROUND: Cerebrovascular trauma secondary to transorbital intracranial penetrating injury (TIPVI) is rare. Relatively benign initial presentation may mask the underlying life-threatening vascular injury in transorbital intracranial penetrations. The aim of this study was to evaluate clinical features and endovascular treatment of TIPVI. METHODS: Six patients with angiographic documentation of TIPVI in subacute/chronic phase were reviewed retrospectively. Five were treated endovascularly; however endovascular treatment was aborted in one and conservative management was pursued. RESULTS: Except for one case presenting with vision loss and mild stroke, no significant neurologic deficit was present. Vascular lesions included two cases of carotid-cavernous fistulas, three traumatic aneurysms of cavernous carotid, anterior and middle cerebral arteries and a unique case of coalescing cavernous aneurysms following a through-and-through injury in which the aneurysms united within the thrombosed cavernous sinus on follow up. Fistulas were treated with covered stents, aneurysms with parent artery occlusion or flow diverters. All patients had uneventful recoveries. CONCLUSION: TIPVI may present in a delayed fashion after a seemingly benign presentation. A high index of suspicion is critical to rule out TIPVI with vascular imaging. Transcatheter angiographic techniques allow for both diagnosis and treatment of TIPVI with favorable results.


Assuntos
Ferimentos Oculares Penetrantes/terapia , Traumatismos Cranianos Penetrantes/terapia , Aneurisma Intracraniano/terapia , Lesões do Sistema Vascular/terapia , Ferimentos por Arma de Fogo/terapia , Adolescente , Adulto , Angiografia Cerebral , Pré-Escolar , Procedimentos Endovasculares , Ferimentos Oculares Penetrantes/complicações , Ferimentos Oculares Penetrantes/diagnóstico por imagem , Feminino , Traumatismos Cranianos Penetrantes/complicações , Traumatismos Cranianos Penetrantes/diagnóstico por imagem , Humanos , Aneurisma Intracraniano/complicações , Aneurisma Intracraniano/diagnóstico por imagem , Masculino , Estudos Retrospectivos , Resultado do Tratamento , Lesões do Sistema Vascular/complicações , Lesões do Sistema Vascular/diagnóstico por imagem , Ferimentos por Arma de Fogo/complicações , Ferimentos por Arma de Fogo/diagnóstico por imagem
4.
Ophthalmic Plast Reconstr Surg ; 31(6): e150-2, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-24833453

RESUMO

A 6-year-old boy diagnosed with congenital microphthalmic OS was referred for prosthetic eye fitting. He was otherwise healthy without known congenital anomalies. His visual acuity was 20/20 in the OD and no light perception in the OS. His disfigured OS with a conjunctivalized opaque cornea appeared smaller than his OD. He had left esotropia with severely restricted ductions in all directions of gaze. The preoperative orbital MRI of the patient revealed a small orbital cyst posteroinferior to the OS. Because the patient could not tolerate the prosthetic eye worn over his disfigured eye, evisceration was planned. During the surgery, blunt dissection of the conjunctiva and Tenon's capsule uncovered a large orbital cyst that was misdiagnosed as phthisis bulbi preoperatively based on the clinical examination and imaging findings. The structure that was thought to be an orbital cyst on orbital MRI was the microphthalmic eye. Enucleation with cyst excision was performed. Patient had uneventful postoperative course and has been wearing an artificial eye for 1 year since surgery.


Assuntos
Cistos/diagnóstico , Olho/patologia , Microftalmia/diagnóstico , Doenças Orbitárias/diagnóstico , Atrofia , Criança , Cistos/complicações , Diagnóstico Diferencial , Enucleação Ocular , Olho Artificial , Humanos , Imageamento por Ressonância Magnética , Masculino , Microftalmia/complicações , Doenças Orbitárias/complicações , Implantes Orbitários , Ajuste de Prótese
5.
Ulus Travma Acil Cerrahi Derg ; 17(1): 75-8, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21341139

RESUMO

We present the first case of a woman with no significant medical history who developed dissections of bilateral carotid and bilateral vertebral arteries, as well as a retinal artery occlusion, after a roller coaster ride. A 35-year-old woman developed right-sided neck pain followed by a frontal headache immediately after a roller coaster ride. Five days after the incident, she developed complete loss of vision in her right eye for two hours. Subsequently, the vision improved but remained significantly decreased. On presentation, her visual acuity was 20/200 in the right and 20/20 in the left eye. Her fundus exam revealed retinal edema in the superotemporal retinal artery distribution without any visible emboli. Her neurological exam was otherwise normal. The cerebral angiogram showed bilateral internal carotid and vertebral artery dissections. The patient remained stable with conservative therapy without further worsening of vision or any new neurological deficits. Outcomes for cervicocephalic arterial dissection are usually favorable, but early diagnosis is critical for initiation of appropriate treatment of possible complications. Physicians must have a high index of suspicion for arterial dissection when patients note any headache, neck pain or vertigo triggered by violent motion after leisure activities such as roller coaster rides.


Assuntos
Dissecação da Artéria Carótida Interna/etiologia , Oclusão da Artéria Retiniana/etiologia , Dissecação da Artéria Vertebral/etiologia , Adulto , Cegueira , Dissecação da Artéria Carótida Interna/diagnóstico por imagem , Feminino , Cefaleia , Humanos , Atividades de Lazer , Cervicalgia , Radiografia , Oclusão da Artéria Retiniana/diagnóstico por imagem , Dissecação da Artéria Vertebral/diagnóstico por imagem
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