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Ectopic thyroid tissue is rare in the general population and more prevalent in people who have existing thyroid disease. Common anatomical sites of ectopic thyroid tissue include the lateral cervical region, thyroglossal duct, mediastinum, lingual, sublingual, and submandibular region. Intrathymic ectopic thyroid tissue is exceedingly rare. The purpose of this report is to describe one such case in a 52-year-old African-American female with Graves' disease. The patient presented for a physical exam and follow-up. During the exam, an incidental mediastinal mass was discovered, which was evaluated by imaging studies and subsequently was resected. Histologically, the mass was composed of variable-sized thyroid follicles lined by a monolayer of cuboidal to columnar follicular epithelial cells and filled with eosinophilic colloid, surrounded by a rim of unremarkable compressed thymic tissue.

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ABSTRACT Ectopic thyroid tissue is rare in the general population and more prevalent in people who have existing thyroid disease. Common anatomical sites of ectopic thyroid tissue include the lateral cervical region, thyroglossal duct, mediastinum, lingual, sublingual, and submandibular region. Intrathymic ectopic thyroid tissue is exceedingly rare. The purpose of this report is to describe one such case in a 52-year-old African-American female with Graves' disease. The patient presented for a physical exam and follow-up. During the exam, an incidental mediastinal mass was discovered, which was evaluated by imaging studies and subsequently was resected. Histologically, the mass was composed of variable-sized thyroid follicles lined by a monolayer of cuboidal to columnar follicular epithelial cells and filled with eosinophilic colloid, surrounded by a rim of unremarkable compressed thymic tissue.

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Resumen: Las grandes masas mediastínicas aumentan los riesgos asociados con la anestesia general. Las complicaciones más temidas en este tipo de pacientes son el colapso de la vía aérea, seguido del colapso cardiovascular. Presentamos el caso de una paciente de 30 años con diagnóstico de sarcoma sinovial con metástasis pulmonar y con la presencia de dos tumores intratorácicos. El objetivo del caso clínico es revisar las implicaciones anestésicas y su manejo en este grupo de pacientes.

Abstract: Large mediastinal masses increase the risks associated with general anesthesia. The most feared complications in this type of patients are the collapse of the airway, leading to cardiovascular collapse. We present the case of a 30-year-old patient diagnosed with synovial sarcoma with pulmonary metastasis, with the presence of two intrathoracic tumors. The objective of the clinical case is to review the anesthetic implications and their management in this group of patients.

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Solitary plasmacytoma is a rare clonal plasma cell tumor, representing 2-5% of plasma cell disorders. The standard treatment is local radiotherapy. However, in some cases, its use is limited by the size and/or location of the mass. Systemic chemotherapy may be a useful therapeutic alternative. We describe a case of a 27-year-old male with a bulky solitary plasmacytoma arising in the posterior mediastinum, causing spinal cord compression. Radiotherapy was considered risky as the mass was located in the heart and left lung fields. Systemic treatment was given. After the first cycle of cyclophosphamide, bortezomib, and dexamethasone (VCD), the patient attained full neurological recovery. After four VCD cycles, complete remission was achieved. Autologous stem cell transplantation was given as consolidation therapy. At 3 months post-transplantation, the patient is in full clinical recovery and complete metabolic remission on 18FDG PET-CT. Although infrequent, plasma cell disorders must be considered in adult patients with a bulky tumoral mass in the posterior mediastinum. PET-CT is the whole-body imaging technique of choice to detect SP, to evaluate response to treatment and during follow-up.

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Mediastinal masses in pregnancy, although rare, can present with life threatening central airway obstruction if general anesthesia is required. In patients with central airway obstruction who are classified as being high risk for anesthesia, specific cardiothoracic interventions are usually required when there is no alternative to general anesthesia. We describe the case of a young female who presented in her second trimester with severe tracheal compression and worsening dyspnea secondary to a mediastinal mass. Intravenous dexamethasone was started, following which her symptoms improved and a drastic reduction in her tracheal compression was observed. The patient subsequently underwent successful vaginal delivery under epidural anesthesia. We discuss the complexities in perioperative decision making for this rare presentation and potential therapeutic options.

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BACKGROUND: Osteosarcoma is a malignant tumor of the bone. The giant cell-rich osteosarcoma (GCRO) is a rare histological variant of the conventional osteosarcoma, accounting for 3% of all osteosarcomas. It has a variable clinical presentation, ranging from asymptomatic to multiple pathological fractures, mainly involving long bones, and less frequently the axial skeleton and soft tissues. CASE PRESENTATION: We present the case of a 25-year-old Hispanic woman, previously healthy, with a 1-month history of dyspnea on exertion, intermittent dry cough, hyporexia, and intermittent unquantified fever. She presented to the emergency department with a sudden increase in dyspnea during which she quickly entered ventilatory failure and cardiorespiratory arrest with pulseless electrical activity. Resuscitation maneuvers and orotracheal intubation were initiated, but effective ventilation was not achieved despite intubation and she was transferred to the intensive care unit of our institution. The chest radiograph showed a mediastinal mass that occluded and displaced the airway. The chest tomography showed a large mediastinal mass that involved the pleura and vertebral bodies. A thoracoscopic biopsy was performed that documented a conventional giant cell-rich osteosarcoma. The patient was considered to be inoperable due to the size and extent of the tumor and subsequently died. CONCLUSIONS: The giant cell-rich osteosarcoma is a very rare histological variant of conventional osteosarcoma. Few cases of this type of osteosarcoma originating from the spine have been reported in the literature, and to our knowledge none of the reported cases included invasion to the chest cavity with airway compression and fatal acute respiratory failure that was present our case. Radiological and histological features of the GCRO must be taken into account to make a prompt diagnosis.

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El schwannoma es un tumor neurogénico que se presenta más frecuentemente en el ángulo costovertebral del mediastino posterior, pero también en otras localizaciones dentro del tórax. Habitualmente suele ser una masa única, encapsulada, bien definida, con un tamaño aproximado 2 a 10 cm. Presentamos el caso de un paciente de 66 años, derivado a nuestro hospital por una masa de 13 cm localizada en el hemitórax inferior izquierdo. Se realizó una biopsia, y la resonancia magnética corroboró el diagnóstico de un tumor mediastínico gigante de la vaina neural. Se procedió a su resección completa sin complicaciones.

Schwannomas are neurogenic tumors, commonly located in the costovertebral angle of the posterior mediastinum, but with many intrathoracic locations. They usually present as a solitary, well-circumscribed and encapsulated mass with a size between 2 and 10 cm. We report a case of a 66-year-old male, referred to our hospital for a mass located at the left lower hemithorax with 13 cm in size. A percutaneous biopsy was performed, and magnetic resonance imaging confirmed the diagnosis of a resectable giant mediastinal nerve sheath tumor. Surgery was performed without complications.

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ABSTRACT The anesthetic management of patients with large mediastinal masses can be complicated due to the pressure effects of the mass on the airway or major vessels. We present the successful anesthetic management of a 64-year-old female with a large mediastinal mass that encroached on the great vessels and compressed the trachea. A tracheal stent was placed to relieve the tracheal compression under general anesthesia. Spontaneous ventilation was maintained during the perioperative period with the use of a classic laryngeal mask airway. We discuss the utility of laryngeal mask airway for anesthetic management of tracheal stenting in patients with mediastinal masses.

RESUMO O manejo anestésico de pacientes com grandes massas situadas no mediastino pode ser complicado por causa dos efeitos da pressão da massa sobre as vias aéreas ou grandes vasos. Relatamos o manejo anestésico bem-sucedido de uma paciente de 64 anos com uma grande massa mediastinal que invadiu os grandes vasos e comprimiu a traqueia. Um stent traqueal foi colocado para aliviar a compressão da traqueia, sob anestesia geral. A ventilação espontânea foi mantida durante o período perioperatório com o uso de uma máscara laríngea clássica. Discutimos a utilidade da máscara laríngea para o manejo da colocação de stent traqueal em pacientes com massas situadas no mediastino.

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The anesthetic management of patients with large mediastinal masses can be complicated due to the pressure effects of the mass on the airway or major vessels. We present the successful anesthetic management of a 64-year-old female with a large mediastinal mass that encroached on the great vessels and compressed the trachea. A tracheal stent was placed to relieve the tracheal compression under general anesthesia. Spontaneous ventilation was maintained during the perioperative period with the use of a classic laryngeal mask airway. We discuss the utility of laryngeal mask airway for anesthetic management of tracheal stenting in patients with mediastinal masses.

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Neste trabalho é relatado o caso de uma mulher de 51 anos de idade, com dor torácica, dispneia e engurgitamento de vasos do tórax superior, sem evidências clínicas de doença granulomatosa. O estudo por imagem do tórax revelou massa mediastinal com calcificações, abordada por mediastinoscopia com biópsia. A análise histopatológica mostrou padrão inflamatório crônico sem etiologia definida, compatível com mediastinite fibrosante.

The present study reports the case of a 51-year-old woman with chest pain, dyspnea and upper chest vessels engorgement, with no clinical evidence of granulomatous disease. Chest imaging study revealed a mediastinal mass with calcifications that was approached by mediastinoscopy with biopsy. Histopathological study demonstrated an etiologically undefined chronic inflammatory pattern compatible with fibrosing mediastinitis.

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The left brachiocephalic vein occasionally follows an aberrant course. It is usually associated with congenital cardiac anomaly. We present a case of anomalous left brachiocephalic vein which followed a sub aortic course, with no cardiac abnormality. Multi detector computed tomography is very useful in accurate diagnosis of this condition and prevents any further investigation in cases of isolated abnormalities.

A veia braquiocefálica esquerda, ocasionalmente, segue curso aberrante. Esta variação freqüentemente está associada com anomalias congênitas do coração. Neste trabalho é apresentado um caso de veia braquiocefálica esquerda anômala, com trajeto subaórtico, sem anormalidade cardíaca. A tomografia computadorizada com multidetectores é muito útil no correto diagnóstico dessa condição e permite a conclusão diagnóstica, sem quaisquer outras investigações.

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Introducción. El quiste broncogénico es una estructura quística limitada por epitelio bronquial de incidencia desconocida, pocas veces diagnosticado en el período neonatal. Caso clínico. Feto con masa quística en hemitórax izquierdo arriba de la silueta cardiaca con sospecha diagnóstica de hernia diafragmática izquierda vs enfermedad adenomatoidea quística con base a ultrasonido prenatal. Al nacimiento, recién nacido femenino de término eutrófico, con peso de 3 030 g, talla 49 cm, calificación de Apgar de 8-9 en tiempos convencionales. La radiografía antero posterior y lateral de tórax confirmaron masa mediastinal izquierda, arriba de la silueta cardiaca, la tomografía axial computada corroboró la presencia de masa quística en mediastino hacia el lado izquierdo a nivel de T4 y T5. Se sometió a toracotomía izquierda para resección de quiste de 3 x 3 cm adherido a pared antero lateral izquierda de la tráquea, no tenía comunicación con ésta. El reporte histopatológico fue de quiste broncogénico. Se egresó al sexto día de vida, sin complicaciones. Conclusiones. El diagnóstico prenatal y la confirmación postnatal inmediata del quiste broncogénico permitió el tratamiento oportuno, lo que previene complicaciones pulmonares posteriores.

Introduction. The bronchogenic cyst is a cystic structure limited by bronchial epithelium the incidence is unknown and it is not very often diagnosed in the neonatal period. Case report. Fetus with cystic mass in the left hemithorax above the cardiac silhouette with suspicion of the left diaphragmatic hernia vs cystic adenomatoid disease based on prenatal ultrasound.At birth female eutrofic term newborn with birth weight of 3 030 g, length 49 cm, Apgar 8-9.The AP and lateral chest x ray confirmed a left mediastinal mass, above the cardiac silhouette, a CT scan confirmed the presence of a cystic mass in the left mediastinum at the level of T4 and T5.A left thoracotomia was performed to remove the 3 by 3 cm cyst adhered the left antherolateral wall of the trachea. There was no communication with it The histopathologic report was positive for a bronchogenic cyst.The patient was discharged on day 6 with no complications. Conclusions. The prenatal diagnosis and the immediate postnatal confirmation of the bronchogenic cyst allowed for a prompt treatment, preventing further complications.