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4.
Cir Esp (Engl Ed) ; 100(6): 329-335, 2022 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-35577280

RESUMO

INTRODUCTION: Inflammatory pseudotumor (IPT) and inflammatory myofibroblastic tumor (IMT) are two very rare entities that were formerly included in the same category; however, today they are considered two different diseases due to the neoplastic origin of the IMT. Our objective is to share our experience in the management of these two types of tumors that we must take into account in the differential diagnosis of pulmonary masses or nodules. METHODS: Thirteen patients with a pathological diagnosis of IPT and IMT who underwent surgery between 2008 and 2019 were retrospectively studied. We recorded the pre and postoperative information of each one, as well as the survival analysis. RESULTS: Of the 13 patients, 8 were men and 5 women. The mean age of presentation was 53,5 years. An atypical segmentectomy was performed in 6 patients; a lobectomy was necessary in 6 and a pneumonectomy in 1 case. In all cases a complete resection was achieved. Diagnosis was possible thanks to histology, immunohistochemical (IHQ) and fluorescent in situ hybridization (FISH) techniques determining the expression of IgG4 and the rearrangement of ALK, respectively. After a median follow up of 49 months, we didn't find any loco-regional or distant recurrence in the patients studied. CONCLUSION: IPT and IMT are rare tumors with a very good prognostic. The diagnosis of both entities is based mainly on specific anatomopathological techniques. Surgery has, in most cases, both a diagnostic and therapeutic role.


Assuntos
Granuloma de Células Plasmáticas , Feminino , Granuloma de Células Plasmáticas/diagnóstico , Granuloma de Células Plasmáticas/metabolismo , Granuloma de Células Plasmáticas/cirurgia , Humanos , Imunoglobulina G , Hibridização in Situ Fluorescente , Prognóstico , Estudos Retrospectivos
6.
Cir Esp (Engl Ed) ; 2021 Apr 22.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33896608

RESUMO

INTRODUCTION: Inflammatory pseudotumor (IPT) and inflammatory myofibroblastic tumor (IMT) are two very rare entities that were formerly included in the same category; however, today they are considered two different diseases due to the neoplastic origin of the IMT. Our objective is to share our experience in the management of these two types of tumors that we must take into account in the differential diagnosis of pulmonary masses or nodules. METHODS: Thirteen patients with a pathological diagnosis of IPT and IMT who underwent surgery between 2008 and 2019 were retrospectively studied. We recorded the pre and postoperative information of each one, as well as the survival analysis. RESULTS: Of the 13 patients, 8 were men and 5 women. The mean age of presentation was 53,5 years. An atypical segmentectomy was performed in 6 patients; a lobectomy was necessary in 6 and a pneumonectomy in 1 case. In all cases a complete resection was achieved. Diagnosis was possible thanks to histology, immunohistochemical (IHQ) and fluorescent in situ hybridization (FISH) techniques determining the expression of IgG4 and the rearrangement of ALK, respectively. After a median follow up of 49 months, we didnt find any loco-regional or distant recurrence in the patients studied. CONCLUSION: IPT and IMT are rare tumors with a very good prognostic. The diagnosis of both entities is based mainly on specific anatomopathological techniques. Surgery has, in most cases, both a diagnostic and therapeutic role.

7.
Eur J Cardiothorac Surg ; 60(1): 81-88, 2021 07 14.
Artigo em Inglês | MEDLINE | ID: mdl-33661301

RESUMO

OBJECTIVES: This analysis aimed to evaluate perioperative outcomes of surgical resection following neoadjuvant treatment with chemotherapy plus nivolumab in resectable stage IIIA non-small-cell lung cancer. METHODS: Eligible patients received neoadjuvant chemotherapy (paclitaxel + carboplatin) plus nivolumab for 3 cycles. Reassessment of the tumour was carried out after treatment and patients with at least stable disease as best response underwent pulmonary resection. After surgery, patients received adjuvant treatment with nivolumab for 1 year. Surgical data were collected from the NADIM database and patient charts were reviewed for additional surgical details. RESULTS: Among 46 patients who received neoadjuvant treatment, 41 (89.1%) underwent surgery. Two patients rejected surgery and 3 did not fulfil resectability criteria. There were 35 lobectomies (85.3%), 3 of which were sleeve lobectomies (9.4%), 3 bilobectomies (7.3%) and 3 pneumonectomies (7.3%). Video-assisted thoracoscopy was the initial approach in 51.2% of cases, with a conversion rate of 19% (n = 4). There was no operative mortality at either 30 or 90 days. The most common complications were prolonged air leak (n = 8), pneumonia (n = 5) and arrhythmia (n = 4). Complete resection (R0) was achieved in all patients who underwent surgery, downstaging was observed in 37 patients (90.2%) and major pathological response in 34 patients (82.9%). CONCLUSIONS: Surgical resection following induction therapy with chemotherapy plus nivolumab appears to be safe and offers appropriate oncological outcomes. Perioperative morbidity and mortality rates in our study were no higher than previously reported in this setting. A minimally invasive approach is, therefore, feasible.


Assuntos
Carcinoma Pulmonar de Células não Pequenas , Neoplasias Pulmonares , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Carcinoma Pulmonar de Células não Pequenas/tratamento farmacológico , Carcinoma Pulmonar de Células não Pequenas/cirurgia , Humanos , Neoplasias Pulmonares/tratamento farmacológico , Neoplasias Pulmonares/cirurgia , Terapia Neoadjuvante , Estadiamento de Neoplasias , Pneumonectomia , Resultado do Tratamento
8.
Interact Cardiovasc Thorac Surg ; 32(6): 904-910, 2021 05 27.
Artigo em Inglês | MEDLINE | ID: mdl-33580683

RESUMO

OBJECTIVES: Atypical carcinoids are neuroendocrine neoplasms of intermediate degree and low frequency. The aim of this study is to analyse their clinical characteristics and the importance of different histopathological factors in their prognosis. METHODS: Multicentre cooperative group EMETNE prospectively reviewed 153 patients operated on between 1998 and 2016 with diagnosis of atypical carcinoids. Clinical variables and histopathological features were assessed. RESULTS: Mean age was 54.36 years, similar for both genders. Concerning pathological study, mean tumour size was 31.7 mm. Rosettes were presented in 17% of the cases and tumoural necrosis in 23.3%. The cell proliferation factor Ki-67 index was 10.7%. The 2- and 5-year overall survival rates were 95.8% and 88.9%, respectively. In the univariate study, statistically significant differences in survival were found for each of the categories of T, N and M factors. Mitotic index and quantification of expression of Ki-67 showed influence in overall survival, although without statistical significance. In the multivariate analysis, factors N, M and mitotic index behaved as independent prognostic factors related to survival. Median disease-free interval in the series was 163.35 months. In cases with loco-regional recurrence, 53% had positive hiliar or mediastinal nodal involvement at the time of the surgery. In the univariate analysis, we observed statistically significant differences in disease-free interval in patients with nodal involvement (P = 0.024) and non-anatomical resections (P = 0.04). Histological characteristics showed no statistically significant differences in disease-free interval. CONCLUSIONS: Lymph node involvement, the development of distant metastasis and mitotic index, more than Ki-67 determination, were shown as independent prognostic factors related to survival of these patients.


Assuntos
Tumor Carcinoide , Tumor Carcinoide/cirurgia , Feminino , Humanos , Neoplasias Pulmonares , Masculino , Pessoa de Meia-Idade , Recidiva Local de Neoplasia , Prognóstico , Estudos Retrospectivos
9.
Med. clín (Ed. impr.) ; 152(3): 104-106, feb. 2019. ilus
Artigo em Inglês | IBECS | ID: ibc-181867

RESUMO

Introduction: Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) is a rare disorder characterized by a proliferation of neuroendocrine cells within the lung. It is classically described as a disease with persistent cough, dyspnea and wheezing in non-smoker middle aged females. CT of the chest reveals diffuse air trapping with mosaic pattern. Patients and methods: We present two cases of DIPNECH that were sent to our department to perform a lung biopsy with the diagnostic suspicion of diffuse interstitial disease. Both cases were women with a history of chronic cough and moderate effort dyspnea. Results and discussion: The aim of this paper is that physicians take into account this diagnostic entity before treating as an asthmatic a patient with these characteristics, not forgetting that they are prenoplastic lesions


Introducción: La hiperplasia neuroendocrina difusa pulmonar idiopática (HNDPI) es una patología poco frecuente que se caracteriza por la proliferación de células neuroendocrinas en el parénquima pulmonar. Se describe clásicamente como una enfermedad que afecta a mujeres de mediana edad no fumadoras y que presentan tos persistente, disnea y sibilancias. La TC muestra una imagen de patrón en mosaico como resultado del atrapamiento aéreo. Pacientes y métodos: Presentamos dos casos de HNDPI que fueron enviados a nuestro servicio para realizar una biopsia pulmonar con la sospecha diagnóstica de enfermedad intersticial difusa. Ambos casos fueron mujeres con antecedentes de tos crónica y disnea de esfuerzo moderado. Resultados y discusión: El objetivo de este documento es que los facultativos tengan en cuenta este diagnóstico antes de tratar como asmática a una paciente con estas características, no olvidando además que son lesiones preneoplásicas


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Idoso , Hiperplasia/patologia , Pneumopatias/patologia , Células Neuroendócrinas/patologia , Neoplasias Pulmonares/patologia , Hiperplasia/terapia , Pulmão/citologia , Pulmão/química , Doenças Pulmonares Intersticiais/complicações , Biópsia , Imuno-Histoquímica
10.
Med Clin (Barc) ; 152(3): 104-106, 2019 02 01.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-29789142

RESUMO

INTRODUCTION: Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) is a rare disorder characterized by a proliferation of neuroendocrine cells within the lung. It is classically described as a disease with persistent cough, dyspnea and wheezing in non-smoker middle aged females. CT of the chest reveals diffuse air trapping with mosaic pattern. PATIENTS AND METHODS: We present two cases of DIPNECH that were sent to our department to perform a lung biopsy with the diagnostic suspicion of diffuse interstitial disease. Both cases were women with a history of chronic cough and moderate effort dyspnea. RESULTS AND DISCUSSION: The aim of this paper is that physicians take into account this diagnostic entity before treating as an asthmatic a patient with these characteristics, not forgetting that they are prenoplastic lesions.


Assuntos
Pulmão/patologia , Nódulos Pulmonares Múltiplos/patologia , Células Neuroendócrinas/patologia , Lesões Pré-Cancerosas/patologia , Idoso , Asma/complicações , Asma/diagnóstico , Broncoscopia , Fumar Cigarros , Tosse/etiologia , Diagnóstico Diferencial , Dispneia/etiologia , Feminino , Humanos , Hiperplasia , Pulmão/diagnóstico por imagem , Pessoa de Meia-Idade , Nódulos Pulmonares Múltiplos/complicações , Nódulos Pulmonares Múltiplos/diagnóstico por imagem , Tomografia por Emissão de Pósitrons , Lesões Pré-Cancerosas/complicações , Lesões Pré-Cancerosas/diagnóstico , Lesões Pré-Cancerosas/diagnóstico por imagem , Testes de Função Respiratória , Tomografia Computadorizada por Raios X , Doenças de von Willebrand/complicações
11.
Rev. esp. enferm. dig ; 110(10): 669-671, oct. 2018. ilus, tab
Artigo em Inglês | IBECS | ID: ibc-177824

RESUMO

Several types of thoracic complications can be associated with severe acute pancreatitis. Some are very common, such as pleural effusion, whilst some others are very rare although life threatening, such as enzymatic mediastinitis (EM). Only a few cases of EM (when related to acute pancreatitis) have been described in the literature. Here we describe the case of a 76-year-old female who developed acute respiratory failure and atrial fibrillation during the postoperative period after an open pancreatic necrosectomy, due to an EM episode. The mediastinal collection was drained by thoracotomy, following an improvement of the patient's general condition. This is the first case of EM following surgical management for acute necrotizing pancreatitis. EM is a rare but life threatening complication that usually requires surgery


No disponible


Assuntos
Humanos , Feminino , Idoso , Mediastinite/enzimologia , Pancreatite Necrosante Aguda/cirurgia , Pancreatectomia/efeitos adversos , Necrose/cirurgia , Pancreatite Necrosante Aguda/complicações , Complicações Pós-Operatórias , Drenagem/métodos
12.
Rev Esp Enferm Dig ; 110(10): 669-671, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29931993

RESUMO

Several types of thoracic complications can be associated with severe acute pancreatitis. Some are very common, such as pleural effusion, whilst some others are very rare although life threatening, such as enzymatic mediastinitis (EM). Only a few cases of EM (when related to acute pancreatitis) have been described in the literature. Here we describe the case of a 76-year-old female who developed acute respiratory failure and atrial fibrillation during the postoperative period after an open pancreatic necrosectomy, due to an EM episode. The mediastinal collection was drained by thoracotomy, following an improvement of the patient's general condition. This is the first case of EM following surgical management for acute necrotizing pancreatitis. EM is a rare but life threatening complication that usually requires surgery.


Assuntos
Mediastinite , Pancreatite Necrosante Aguda/cirurgia , Complicações Pós-Operatórias , Idoso , Feminino , Humanos , Mediastinite/diagnóstico , Mediastinite/enzimologia , Mediastinite/terapia , Pâncreas/enzimologia , Complicações Pós-Operatórias/diagnóstico , Complicações Pós-Operatórias/terapia
13.
Cir Esp ; 95(3): 160-166, 2017 Mar.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-28347487

RESUMO

INTRODUCTION: Age has been classically considered as a determining factor for the development of postoperative complications related to lung resection for bronchogenic carcinoma. The Postoperative Complications Study Group of the Spanish Society of Thoracic Surgery has promoted a registry to analyze this factor. METHODS: A total of 3,307 patients who underwent any type of surgical resection for bronchogenic carcinoma have been systematically and prospectively recorded in any of the 24 units that are part of the group. Several variables related to comorbidity and age, as well as postoperative complications, were analyzed. RESULTS: The mean age of patients was 65,44. Men were significantly more common than female. The most frequent complication was prolonged air leak, which was observed in more than one third of patients. In a univariant analysis, air leak presence and postsurgical atelectasis showed statistical association with patient age, when stratified in age groups. In a multivariate analysis, age was recognized as an independent prognostic factor in relation to air leak onset. However, this could not be confirmed for postoperative atelectasis. CONCLUSION: Age is a predisposing factor for the development of postoperative complications after lung resection. Other associated factors also influence the occurrence of these complications.


Assuntos
Carcinoma Broncogênico/cirurgia , Neoplasias Pulmonares/cirurgia , Pneumonectomia , Complicações Pós-Operatórias/epidemiologia , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Causalidade , Feminino , Humanos , Masculino , Estudos Prospectivos
14.
Cir. Esp. (Ed. impr.) ; 95(3): 160-166, mar. 2017. tab
Artigo em Espanhol | IBECS | ID: ibc-162244

RESUMO

INTRODUCCIÓN: La edad del paciente ha sido clásicamente interpretada como un factor condicionante de la aparición de complicaciones postoperatorias en cirugía de resección pulmonar por carcinoma broncogénico. El Grupo de Estudio de Complicaciones Postoperatorias de la Sociedad Española de Cirugía Torácica promovió un registro que permitiera analizar este hecho. MÉTODOS: Se recogieron de forma consecutiva, sistemática y prospectiva los datos de un total de 3.307 pacientes tratados con algún tipo de resección quirúrgica por carcinoma broncogénico en las 24 unidades que forman parte del grupo. Fueron analizadas variables relativas a la comorbilidad y la edad del paciente, así como a las complicaciones postoperatorias acaecidas. RESULTADOS: La edad media de los pacientes intervenidos fue de 65,44 años. La población masculina en la serie era significativamente mayor que la femenina. La complicación más frecuente fue la fuga aérea prolongada, que ocurrió en más de un tercio de los pacientes. En el estudio univariante, la aparición de fugas aéreas y de atelectasias posquirúrgicas mostraron asociación estadística con la edad de los enfermos, analizada por grupos etarios. En el análisis multivariante, la edad se presentó como un factor pronóstico independiente en relación con la aparición de fugas aéreas posquirúrgicas, no así en cuanto a las atelectasias posresección. CONCLUSIÓN: La edad es un factor predisponente para el desarrollo de complicaciones postoperatorias tras resección pulmonar en nuestro medio, si bien otros factores asociados condicionan también la aparición de estas complicaciones


INTRODUCTION: Age has been classically considered as a determining factor for the development of postoperative complications related to lung resection for bronchogenic carcinoma. The Postoperative Complications Study Group of the Spanish Society of Thoracic Surgery has promoted a registry to analyze this factor. METHODS: A total of 3,307 patients who underwent any type of surgical resection for bronchogenic carcinoma have been systematically and prospectively recorded in any of the 24 units that are part of the group. Several variables related to comorbidity and age, as well as postoperative complications, were analyzed. RESULTS: The mean age of patients was 65,44. Men were significantly more common than female. The most frequent complication was prolonged air leak, which was observed in more than one third of patients. In a univariant analysis, air leak presence and postsurgical atelectasis showed statistical association with patient age, when stratified in age groups. In a multivariate analysis, age was recognized as an independent prognostic factor in relation to air leak onset. However, this could not be confirmed for postoperative atelectasis. CONCLUSION: Age is a predisposing factor for the development of postoperative complications after lung resection. Other associated factors also influence the occurrence of these complications


Assuntos
Neoplasias Pulmonares/cirurgia , Carcinoma Broncogênico/cirurgia , 50293 , Complicações Pós-Operatórias , Tempo/estatística & dados numéricos , Estudos Prospectivos , Atelectasia Pulmonar/epidemiologia , Resultado do Tratamento
15.
J Thorac Dis ; 8(11): 3452-3456, 2016 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-28066626

RESUMO

Foreign body (FB) aspiration into the airway is lees common in adults than children. Nevertheless its incidence does not decrease through time. We present clinical relevant aspects of airway FBs on the basis of a selective review of pertinent literature retrieved by a search in the PubMed database. The most common aspirated FBs by adults are organics, especially fragments of bones and seeds. Symptoms usually are cough, chocking and dyspnea. Right localization, especially bronchus intermedius and right lower lobe, is more frequent. Chest radiography can be normal in up to 20% of the cases and FBs can be detected in 26% of the patients. FBs can safely remove in the majority of patients under flexible bronchoscopy. Surgical treatment must be reserved for cases in which bronchoscope fails or there are irreversible bronchial or lung complications.

18.
Arch. bronconeumol. (Ed. impr.) ; 50(12): 557-559, dic. 2014. ilus
Artigo em Espanhol | IBECS | ID: ibc-131002

RESUMO

El timolipoma es una neoplasia benigna infrecuente del timo, formada por tejido tímico y tejido adiposo maduro. El diagnóstico de timolipoma debe considerarse en presencia de una masa mediastínica con densidad de tejido adiposo, sobre todo si está entremezclada con bandas de atenuación de tejido blando en las imágenes de tomografía computarizada. Sin embargo, a veces resulta difícil diferenciar radiológicamente entre un timolipoma y otros tumores adiposos mediastínicos. Presentamos aquí el caso de un paciente con una masa mediastínica enorme que resultó ser un timolipoma (AU)


Thymolipoma is an uncommon benign neoplasm of the thymus composed of mature adipose and thymic tissue. The diagnosis of thymolipoma should be considered in the case of a mediastinal mass with fat density, especially if it is interspersed with strands of soft tissue attenuation on computed tomography scans. However, it is sometimes difficult to differentiate radiologically between a thymolipoma and other mediastinal fatty tumors (AU)


Assuntos
Humanos , Feminino , Idoso , Neoplasias do Mediastino/diagnóstico , Timoma/patologia , Neoplasias do Timo/patologia , Lipoma/patologia
19.
Arch Bronconeumol ; 50(12): 557-9, 2014 Dec.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-24985048

RESUMO

Thymolipoma is an uncommon benign neoplasm of the thymus composed of mature adipose and thymic tissue. The diagnosis of thymolipoma should be considered in the case of a mediastinal mass with fat density, especially if it is interspersed with strands of soft tissue attenuation on computed tomography scans. However, it is sometimes difficult to differentiate radiologically between a thymolipoma and other mediastinal fatty tumors. Here we present a patient with a huge mediastinal mass that proved to be a thymolipoma.


Assuntos
Lipoma/patologia , Timoma/patologia , Neoplasias do Timo/patologia , Idoso , Diagnóstico por Imagem , Feminino , Humanos , Lipoma/diagnóstico , Lipoma/cirurgia , Toracotomia , Timoma/diagnóstico , Timoma/cirurgia , Neoplasias do Timo/diagnóstico , Neoplasias do Timo/cirurgia
20.
Nutr Hosp ; 31(3): 1323-9, 2014 Oct 03.
Artigo em Inglês | MEDLINE | ID: mdl-25726229

RESUMO

BACKGROUND & AIMS: To design and develop a nutritional application for smartphones and tablets with Android operating system for using to in- and outpatients that need a nutritional assessment. To check the validity of the results of such software. METHODS: The application was compiled for version 2.1 of the Android operating system from Google. A cohort of 30 patients was included for evaluating the reliability of the application. The calculations were performed by staff of the Nutrition Unit of the Complexo Hospitalario Universitario de Vigo, manually and through e-Nutrimet software on a smartphone and a tablet. RESULTS: Concordance was absolute between results of different methods obtained using e-Nutrimet on a smartphone and a tablet (Fleiss index κ= 1). The same level of concordance was obtained by comparing handmade and e-Nutrimet made results. CONCLUSIONS: The degree of correlation is good, and it would be extended to all healthcare staff who wants to determine whether a patient has malnutrition, or not. The nutritional assessment software e-Nutrimet does not replace healthcare staff in any case, but could be an important aid in assessing patients who may be in risk of malnutrition, saving time of evaluation.


Introducción y objetivos: Diseñar y desarrollar una aplicación nutricional para smartphones y tablets con Sistema operativo Android® para realizar las valoraciones nutricionales de pacientes ambulatorios y hospitalizados. Verificar y comprobar la validez de los resultados de la aplicación. Métodos: La aplicación se compile para la versión 2.1 del Sistema operativo Android® de Google®. Para evaluar la fiabilidad de la aplicación se incluyeron a 30 pacientes, a los que se le realizó una valoración nutricional. Todos los cálculos fueron efectuados por personal de la Unidad de Nutrición del Complexo Hospitalario Universitario de Vigo, de forma manual y a través del software e-Nutrimet ©, tanto usando un Smartphone como una tablet. Resultados: Se obtuvo una concordancia absoluta entre los resultados de los diferentes métodos obtenidos utilizando la aplicación e-Nutrimet© en smartphones y en tablets (Fleiss index = 1). El mismo nivel de concordancia se obtuvo comparando el método manual como el automatizado mediante el software e-Nutrimet©. Conclusiones: El grado de correlación es muy bueno, permitiendo extender la valoración nutricional usando e-Nutrimet© a todo el personal sanitario que quiera determinar si un paciente presenta malnutrición o no. La aplicación de valoración nutricional e-Nutrimet© no sustituye al personal sanitario en ningún caso, pero podría ser de gran ayuda a la hora de valorar pacientes que pudieran estar en riesgo de malnutrición, ahorrando tiempo en estas valoraciones.


Assuntos
Telefone Celular , Microcomputadores , Aplicativos Móveis , Avaliação Nutricional , Antropometria , Índice de Massa Corporal , Registros Eletrônicos de Saúde , Feminino , Registros de Saúde Pessoal , Nível de Saúde , Humanos , Masculino , Desnutrição/sangue , Desnutrição/diagnóstico , Sobrepeso/sangue , Sobrepeso/diagnóstico , Padrões de Referência , Reprodutibilidade dos Testes , Magreza/sangue , Magreza/diagnóstico
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