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1.
Ophthalmic Plast Reconstr Surg ; 31(1): e18-22, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-24807803

RESUMO

Advantages of transcanalicular laser-assisted dacryocystorhinostomy (TCDCR) over conventional, external, and endonasal dacryocystorhinostomy (DCR) have been purported to include decreased operating time, reduced morbidity, enhanced cosmesis, avoidance of general anesthesia, and a shorter recovery time. However, 1 case of skin necrosis has recently been reported to have occurred following diode laser-assisted TCDCR, and the authors now report 3 additional cases that were evaluated by the Ophthalmic Plastic Surgery services at the University of North Carolina, North Carolina, and the University of California, San Francisco. Three patients developed full-thickness tissue necrosis over the medial canthus following TCDCR, and 2 of these patients experienced persistent tissue breakdown at the site following reconstructive repair.


Assuntos
Dacriocistorinostomia/efeitos adversos , Lasers Semicondutores/efeitos adversos , Pele/patologia , Idoso de 80 Anos ou mais , Feminino , Humanos , Pessoa de Meia-Idade , Necrose/etiologia
2.
Ophthalmic Plast Reconstr Surg ; 28(5): 335-7, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22965013

RESUMO

OBJECTIVE: To describe the complication of anterior filler displacement following injection of calcium hydroxylapatite gel (Radiesse) for anophthalmic enophthalmos correction. METHODS: Retrospective case series of patients who experienced anterior filler displacement following orbital injection of calcium hydroxylapatite. Data includes patient demographics, indication for injection, route and volume of injection, description of postinjection complications, and final outcome. RESULTS: Four cases of anterior filler displacement and expansion following injection of calcium hydroxylapatite were identified. The patients' ages ranged from 33 to 64 years old. All 4 patients underwent multiple prior orbital surgeries and suffered from anophthalmic enophthalmos. Injectable calcium hydroxylapatite was delivered transcutaneously, to the deep extraconal orbital space, via 27-gauge, 1.25-inch retrobulbar needles. Each patient received an initial 1.3 ml of filler, with 1 patient receiving an additional 0.8 ml. Within 1 week, all patients experienced prominent, edematous lower eyelids. A CT scan of 1 patient radiographically documented anterior migration of the filler material. Two patients required transconjunctival excision of the filler and infiltrated orbital fat. Histopathologic examination of 1 specimen revealed chronic foreign body granulomatous inflammation. Two patients were treated medically, with resolution of clinical findings over 6 to 9 months. CONCLUSIONS: Anterior filler displacement is a potential complication of orbital volume augmentation with injectable calcium hydroxylapatite. Patients should be counseled regarding this possibility when considering options for the treatment of anophthalmic enophthalmos. A history of multiple prior orbital surgeries, with associated tissue disruption and scarring, may be a risk factor for filler displacement.


Assuntos
Anoftalmia/terapia , Segmento Anterior do Olho/patologia , Materiais Biocompatíveis/efeitos adversos , Durapatita/efeitos adversos , Oftalmopatias/etiologia , Migração de Corpo Estranho/etiologia , Órbita/efeitos dos fármacos , Adulto , Segmento Anterior do Olho/diagnóstico por imagem , Materiais Biocompatíveis/administração & dosagem , Durapatita/administração & dosagem , Enoftalmia/terapia , Oftalmopatias/diagnóstico por imagem , Oftalmopatias/cirurgia , Enucleação Ocular , Feminino , Migração de Corpo Estranho/diagnóstico por imagem , Géis , Humanos , Injeções Intraoculares , Masculino , Pessoa de Meia-Idade , Tamanho do Órgão , Estudos Retrospectivos , Tomografia Computadorizada por Raios X
3.
Ophthalmic Plast Reconstr Surg ; 23(2): 87-93, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17413619

RESUMO

PURPOSE: To characterize the clinical and imaging features of orbital leukemic tumors in 27 patients seen and treated at St. Jude Children's Research Hospital. METHODS: A retrospective review was performed on the clinical and imaging records of 27 consecutive patients with a diagnosis of orbital leukemic tumors. The following data were extracted from the patients' records: age at diagnosis of orbital leukemic tumors, sex, race, national origin, type of leukemia, temporal relationship of orbital disease to diagnosis of leukemia, survival from diagnosis of orbital leukemic tumor, laterality of the orbital disease, location of the mass within the orbit, imaging features of the mass, chemotherapeutic protocol, treatment with bone marrow transplant, and orbital radiation. RESULTS: The median age at diagnosis of orbital leukemic tumor was 8 years (range, 1-18 years). Nineteen of the 27 patients were male, and 21 patients were born and lived in the United States. Twenty-one patients had acute myeloid leukemia, five had acute lymphoblastic leukemia, and one had chronic myelogenous leukemia. In 85% of patients (n = 23), the diagnosis of leukemia was based on the bone marrow examination findings. Orbital imaging revealed homogenous masses that molded to one or more orbital walls without bony destruction. Nine patients had bilateral orbital involvement. All patients received multiagent systemic chemotherapy, and 14 underwent bone marrow transplantation. Five patients received external beam radiation for the treatment of orbital disease. Fifteen (55.6%) of the 27 patients were alive at the time of the study. The median survival for all patients was 4.75 years (range, 0.1-24 years) after the diagnosis of orbital disease. CONCLUSIONS: Orbital leukemic tumors occur most commonly in the first decade of life, in association with acute myeloid leukemia. They appear as homogenous masses along the orbital walls. Although the overall survival rate for patients with leukemia has improved over the past 3 decades, the mortality of patients who develop orbital leukemic tumors remains high.


Assuntos
Leucemia Linfoide/patologia , Leucemia Mieloide/patologia , Neoplasias Orbitárias/patologia , Doença Aguda , Adolescente , Distribuição por Idade , Criança , Pré-Escolar , Terapia Combinada , Diagnóstico por Imagem , Feminino , Humanos , Lactente , Leucemia Linfoide/diagnóstico , Leucemia Linfoide/mortalidade , Leucemia Linfoide/terapia , Leucemia Mieloide/diagnóstico , Leucemia Mieloide/mortalidade , Leucemia Mieloide/terapia , Imageamento por Ressonância Magnética , Masculino , Neoplasias Orbitárias/diagnóstico , Neoplasias Orbitárias/mortalidade , Neoplasias Orbitárias/terapia , Estudos Retrospectivos , Taxa de Sobrevida , Tomografia Computadorizada por Raios X
4.
Ophthalmic Plast Reconstr Surg ; 19(4): 257-61, 2003 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12878872

RESUMO

PURPOSE: To report 18 cases of unusually large, early conjunctival breakdown occurring with the use of bovine pericardium wrapping material for orbital implants. METHODS: Retrospective case series. The clinical course and histopathologic features of 18 cases of early conjunctival breakdown in patients who had undergone orbital implantation of bovine pericardium-wrapped hydroxyapatite or porous polyethylene are reviewed. RESULTS: Eighteen patients presented with unusually large (average 13.44 mm) conjunctival defects over bovine pericardium-wrapped implants. The average time from enucleation to exposure was approximately 4 months. Implants had to be removed in 8 of 18 cases. There was clinical and histologic evidence of tissue inflammation and conjunctival melting. CONCLUSIONS: The conjunctival melting phenomenon we report herein is alarming. We have abandoned the use of bovine pericardium as a wrapping material for implants after enucleation because of the unfavorable results.


Assuntos
Materiais Revestidos Biocompatíveis/efeitos adversos , Doenças da Túnica Conjuntiva/etiologia , Implantes Orbitários/efeitos adversos , Pericárdio , Complicações Pós-Operatórias , Deiscência da Ferida Operatória/etiologia , Adolescente , Adulto , Idoso , Animais , Bovinos , Pré-Escolar , Doenças da Túnica Conjuntiva/patologia , Feminino , Humanos , Lactente , Masculino , Implantação de Prótese , Estudos Retrospectivos , Deiscência da Ferida Operatória/patologia , Síndrome
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