Neuroblastoma olfatório ectópico: estudo de caso e revisão da literatura / Ectopic olfactory neuroblastoma: case study and literature review

O neuroblastoma olfatório, também conhecido como estesioneuroblastoma (ENB), é tumor maligno de crescimento lento, com origem principalmente na neuroectoderme da cavidade nasal. O pico de incidência do ENB é aos 53 anos, com a maioria dos casos ocorrendo entre os 40 e 70 anos, principalmente em homens. Há poucos relatos de ENB nos seios etmoidal, maxilar e esfenoidal, hipófise e nasofaringe. Esse tumor geralmenteapresenta-se como doença invasiva e tendência a recorrer tardiamente. A disseminação mais frequente do ENB é para os linfonodos cervicais e, se presente, significa pior prognóstico. Seus sintomas são inespecíficos, sendo a obstrução nasal o mais comum. Os exames de imagem são importantes no diagnóstico do ENB, juntamente com o histopatológico e o imuno-histoquímico, que também auxiliam no diagnóstico diferencial. O tratamento cirúrgico de ressecção craniofacial associado à radioterapia apresenta os melhores resultados na sobrevida. Descreve-se seguidamente um caso clínico ilustrativo dessa doença em paciente masculino de oito meses, faixa etária incomum da ENB, com queixa familiar inicial de obstrução nasal e coriza hialina com rajas de sangue...

Olfactory neuroblastoma, also known as esthesioneuroblastoma (ENB), is a slow-growing malignant tumor of that originates mainly in the neuroectodermal cells in the nasal cavity. The peak incidence of ENB is at age 53, with the majority of cases occurring between 40 and 70 years, and mostly among men. There are a few reports of ENB in the ethmoid, maxillary, and sphenoid sinuses, or in the pituitary and nasopharynx. This tumor usually presents as an invasive disease with a tendency for later recurrence. The most frequent dissemination of ENB is to the cervical lymph nodes, which represents a worse prognosis. Its symptoms are nonspecific and nasal obstruction is the most common complaint. Imaging tests are important for the diagnosis of ENB, along with histopathological and immunohistochemical tests to help in the differential diagnosis. Surgical treatment of craniofacial resection associated with radiotherapycan achieve the best results for survival. We present a discussion of an illustrative clinical case of the disease in a male patient aged eight months, an unusual age for ENB, brought to attention by an initial family complaint of nasal obstruction and bloodstained hyaline rhinorrhea...

Endoscopic treatment of esthesioneuroblastoma / Abordagem endoscópica de estesioneuroblastoma

Esthesioneuroblastoma is an uncommon malignant tumor of the nasal vault. Treatment consists of craniofacial resection. As endoscopic techniques have advanced, this approach has been recommended to avoid morbidity and to reduce costs. AIM: To evaluate outcomes in patients with esthesioneuroblastoma treated by an endoscopic technique. METHODS: A prospective study of patients diagnosed with esthesioneuroblatoma and treated by an endoscopic technique. The literature over the past 20 years was reviewed for an update on the pathology. RESULTS: We present 4 patients, 3 males and 1 female, staged according to Kadish and Dulguerov. All were treated surgically with endoscopic techniques, followed by radiotherapy. One patient was also submitted to neck dissection and chemotherapy because of regional metastasis. There were no significant postoperative complications. The mean hospital stay was 3 days; one patient stayed in the ICU for 24 hours after surgery. Follow-up is recent; so far there are no recurrences. CONCLUSION: Esthesioneuroblastoma is a potentially curable malignancy. Endoscopic techniques help reduce hospital costs and decrease the morbidity. Adequate margins of healthy tissue are obtained with endoscopic resection, as with craniofacial resection. The literature suggests that outcomes after endoscopic resection are similar to those of the conventional external approach.

Estesioneuroblastoma é uma neoplasia incomum de linhagem epitelial. Seu tratamento convencional baseia-se na ressecção craniofacial. Técnicas endoscópicas tem sido preconizadas em sua terapia com o intuito de diminuir morbidades e custos. OBJETIVO: Relatar a experiência na abordagem terapêutica do tumor com uso de endoscópio. MATERIAL E MÉTODO: Estudo prospectivo de pacientes com diagnóstico de Estesioneuroblastoma submetidos a tratamento endoscópico. Fez-se revisão de publicações relacionadas ao tumor. RESULTADOS: Apresentamos quatro pacientes, sendo 3 homens e 1 mulher, estadiados de acordo com Kadish e Dulguerov. Foram submetidos a ressecção endoscópica com margem e terapia adjuvante (radio ou quimioterapia). Não se observaram complicações pós-operatórias significativas. O tempo médio de internação foi 3 dias e um paciente permaneceu em observação no CTI por 24 horas. O seguimento é recente e não há relato de recidivas. CONCLUSÃO: Estesioneuroblastoma é um tumor maligno potencialmente curável. O uso da técnica cirúrgica endoscópica nasal traz consigo menor morbidade ao paciente (período de internação e tempo cirúrgico menor) e custos hospitalares diminuídos. Possibilita a ressecção da neoplasia com margens comparáveis à cirurgia convencional. Os resultados em longo prazo descritos na literatura são semelhantes ao tratamento convencional. Nosso seguimento ainda é recente para concluir algo sobre prognóstico.

Estesioneurablastoma y panhipopituitarismo: presentación de un caso / Esthesionerublastoma and panhypopituitarysm: case report

Objetivos: presentar un caso de estesioneuroblastoma que desarrolla hipopituitarismo como complicación grave de su tratamiento. Realizar una revisión de la literatura reciente sobre el tratamiento y pronóstico de estos tumores. Presentar una sistemática de pesquisa de hipipituitarismo en estos pacientes. Descripción: paciente masculino de 68 años que se presenta con metástasis submaxilar de estesioneuroblastoma. La RMN mostraba una masa neoplásica de gran tamaño centrada sobre el etmoides, que comprometía base de cráneo y corteza fronto-orbitaria izquierda. Intervención: se realizó tratamiento combinado de radio y quimioterapia preoperatorios, y cirugía por vía craniofacial. A los 20 meses ingresa con un cuadro convulsivo e hiponatremia grave. Se hace diagnóstico de panhipopituitarismo y el cuadro revierte con la administración de hidrocortisona de 10 mg vía oral. Conclusión: el estesioneuroblastoma es un tumor infrecuente cuyo tratamiento incluye cirugía, radioterapia y quimioterapia. Es necesario un alto índice de sospecha y el seguimiento de por vida para pesquisar la instalación del hipopituitarismo como complicación grave de su tratamiento.

Objectives. To report a case of esthesioneuroblastoma associated to hypopituitarism as a late complication of its treatment, to review the literature regarding treatment and prognosis and to resent a guideline for the diagnosis of hypopituitarism in these patients. Description. A 68-year-old male patient presented with a submaxilar metastasis of a very large esthesioneuroblastoma that involved both ethmoidal bones and invaded left cribiform plate and frontal lobe. Intervention. The patient underwent combined modality treatment with preoperative radio and chemotherapy, and craniofacial sugery of the tumor. Twenty months later he was admitted with a seizure and severe hyponatremia. A diagnosis of panhypopituitarism was made, and his sodium reverted to normal with de administration of 10 mg of hydrocortisone p.o. Conclusions Esthesioneuroblastomas are rare tumours that require multimodality treatment with surgery, radiotherapy and chemotherapy. Hypopituitarism is a late and potentially fatal complication that must be suspected and tested during the patients‘ whole lifespan.

Therapeutic effects of 36 patients with esthesioneuroblastoma and their prognosis / 肿瘤

Objective: To study the different treatment policies for patients with esthesioneuroblastoma (ENB) and their prognosis. Methods: Thirty-six ENB patients included 20 males and 16 females at average age of 46 years old (24-74 years). Two patients received single surgery and 2 patients received single radiotherapy. Thirty-two patients received combined therapy, which included surgery plus radiotherapy (n = 14), radiotherapy plus chemotherapy (n = 6), surgery plus radiotherapy and chemotherapy (n = 12). All the patients were followed up for 2-60 months and the median follow-up period was 48 months. Statistic analysis was performed using software SPSS 13. 0. Results: The overall 5-year survival rate was 55.6%. The 5-year survival rates of patients between patients with and without cervical lymph nodal metastasis were statistically significant (P < 0.05). Conclusion: Early detection and combined therapy are important to improve survival rate. Cervical lymph node metastasis is significantly correlated with the prognosis. Radiotherapy plays an important role in the management of the disease.

Estesioneuroblastoma / Esthesioneuroblastoma

O estesioneuroblastoma é uma neoplasia maligna incomum, que tem origem no epitélio olfatório e corresponde de 4% a 6% dos tumores malignos dos seios paranasais. A última grande revisão sobre esses tumores mostra que, desde sua descoberta, há oitenta anos, menos de mil casos foram publicados na literatura mundial. As manifestações clínicas usuais constituem-se por anosmia, obstrução nasal e epistaxe. Devido às características microscópicas serem bastante variadas e inespecíficas, é importante que o diagnóstico seja bem estabelecido pela histoquímica e imunoistoquímica, pois disso dependerá o prognóstico do paciente. Por se tratar de uma doença rara, ainda não há consenso quanto ao melhor tipo de tratamento, mas os relatos de casos bem sucedidos incluíram tratamento multidisciplinar com quimioterapia, ressecção cirúrgica e radioterapia. Em um período de seis anos (janeiro/ 2000 a janeiro/2006), ocorreram quatro casos no serviço do Hospital e Maternidade Celso Pierro, que são aqui reportados

Esthesioneuroblastoma is an uncommon malignant neoplasm that arises from the olfactory epithelium and corresponds to 4% - 6% of all malignant tumors in the paranasal sinuses. The last extensive review on these tumors reveals that less than one thousand cases have been published in the literature since its discovery eighty years ago. The common clinical manifestations are anosmia, nasal obstruction and epistaxis. Since its microscopic characteristics vary greatly and are unspecific, a precise diagnosis using histochemical and immunohistochemical techniques cannot be overemphasized as the patient?s prognosis depends on the diagnosis. As it is a rare disease, there is no consensus regarding the best treatment, but reports of cases treated successfully cite a multidisciplinary approach, which includes chemotherapy, surgical resection and radiation therapy. Our service has treated four cases over a period of six years (January 2000 - January 2006) that are reported here