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1.
Orbit ; 38(2): 154-157, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29557698

RESUMO

We report a case of myeloid sarcoma with multifocal skeletal involvement, including the greater wing of the sphenoid bone. A 23-month-old boy presented with left-sided proptosis and fevers, and was found to have an infiltrative mass involving the left sphenoid bone on orbital imaging. Full body imaging further demonstrated multiple bony lesions in the pelvis, thoracic and lumbar vertebrae, bilateral femura, and left humerus, and biopsies of the humerus were consistent with myeloid sarcoma. The patient was started on a standard chemotherapy regimen and is responding well. Myeloid sarcoma presenting with proptosis due to sphenoid bone involvement with simultaneous multifocal skeletal involvement is very uncommon and highlights the importance of biopsy for establishing a definitive diagnosis.


Assuntos
Neoplasias Ósseas/diagnóstico , Exoftalmia/diagnóstico , Febre/diagnóstico , Neoplasias Primárias Múltiplas/diagnóstico , Sarcoma Mieloide/diagnóstico , Neoplasias Cranianas/diagnóstico , Osso Esfenoide/patologia , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Biomarcadores Tumorais/metabolismo , Neoplasias Ósseas/tratamento farmacológico , Neoplasias Ósseas/metabolismo , Humanos , Lactente , Imageamento por Ressonância Magnética , Masculino , Proteínas de Neoplasias/metabolismo , Neoplasias Primárias Múltiplas/tratamento farmacológico , Neoplasias Primárias Múltiplas/metabolismo , Sarcoma Mieloide/tratamento farmacológico , Sarcoma Mieloide/metabolismo , Neoplasias Cranianas/tratamento farmacológico , Neoplasias Cranianas/metabolismo , Tomografia Computadorizada por Raios X
2.
Ophthalmic Plast Reconstr Surg ; 34(3): e79-e81, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29342033

RESUMO

A 51-year-old man who had undergone right orbital decompression 5 months earlier developed a meningoencephalocele extending in the right sphenoid sinus through a skull base defect of the right ethmoid, sphenoid, and frontal bones. The authors report the third case to their knowledge of meningoencephalocele with cerebrospinal fluid leak after orbital decompression and discuss its management and measures that can be taken to prevent this rare but serious complication.


Assuntos
Vazamento de Líquido Cefalorraquidiano/etiologia , Descompressão Cirúrgica/efeitos adversos , Oftalmopatia de Graves/cirurgia , Meningomielocele/etiologia , Complicações Pós-Operatórias/etiologia , Humanos , Masculino , Pessoa de Meia-Idade
3.
Ophthalmic Plast Reconstr Surg ; 33(6): e147-e150, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28328558

RESUMO

Primary orbital natural killer T-cell lymphoma (NKTCL) is a rare condition with only a few published cases in the literature. Over 1 month, an 81-year-old man developed progressive left periocular inflammation unresponsive to treatment. Clinical examination and imaging studies demonstrated a left lacrimal gland enlargement. Bilateral anterior uveitis and erythematous nontender cutaneous lesions were also found. Biopsies of the skin and lacrimal gland on the back revealed histopathologic and immunohistochemical findings confirming Epstein-Barr virus-positive NKTCL. Metastatic work up disclosed multifocal involvement in the pancreas, stomach, and chest wall. Palliative treatment consisting of nonanthracycline-based chemotherapy and radiation was instituted, but the patient died 5 months after the onset of symptoms. This is the first example of acute dacryoadenitis, and the second of bilateral anterior uveitis, in the setting of NKTCL. Absence of naso-sinus involvement in the current case is rare in NKTCL. Despite treatment, the prognosis remains dismal. Orbital specialists should include NKTCL in the differential diagnosis of lacrimal gland/orbital masses and perform an incisional biopsy if the clinical scenario so dictates.


Assuntos
Dacriocistite/etiologia , Aparelho Lacrimal/diagnóstico por imagem , Linfoma Extranodal de Células T-NK/complicações , Órbita/diagnóstico por imagem , Neoplasias Orbitárias/complicações , Idoso de 80 Anos ou mais , Biópsia , Dacriocistite/diagnóstico , Diagnóstico Diferencial , Evolução Fatal , Humanos , Linfoma Extranodal de Células T-NK/diagnóstico , Masculino , Neoplasias Orbitárias/diagnóstico , Tomografia Computadorizada por Raios X
4.
Semin Ophthalmol ; 32(1): 116-124, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-27740876

RESUMO

Natural killer T-cell lymphoma (NKTCL) is a rare and aggressive condition with a high mortality rate. It is most commonly seen in the nasal sinuses, generally affecting the orbit by direct extension. Primary orbital NKTCL is even more rare, with only a few published cases with occasional secondary nasal involvement. This malignancy can present as a "masquerade syndrome," delaying proper diagnosis and treatment. Biopsy is required for diagnosis, which shows specific histopathological characteristics. Radiation and chemotherapy are the mainstay of treatment. Newer chemotherapies show improved prognosis.


Assuntos
Linfoma Extranodal de Células T-NK , Linfoma , Neoplasias Orbitárias , Neoplasias dos Seios Paranasais , Antineoplásicos/uso terapêutico , Biópsia , Terapia Combinada , Diagnóstico por Imagem , Medicina Baseada em Evidências , Humanos , Linfoma/diagnóstico , Linfoma/terapia , Linfoma Extranodal de Células T-NK/diagnóstico , Linfoma Extranodal de Células T-NK/terapia , Neoplasias Orbitárias/diagnóstico , Neoplasias Orbitárias/terapia , Neoplasias dos Seios Paranasais/diagnóstico , Neoplasias dos Seios Paranasais/terapia , Radioterapia
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