Lobectomia total como tratamento de hemangiossarcoma hepático em um cão - relato de caso / Total lobectomy as treatment of hepatic hemangiosarcoma in a dog - case report / Lobectomía total como tratamiento de hemangiosarcoma hepático en un perro - reporte de caso

O hemangiossarcoma é uma neoplasia mesenquimal maligna agressiva com elevada taxa de morbidade e de mortalidade em cães e gatos; que se desenvolve mais frequentemente em baço, fígado, coração, ossos além de poder manifestar metástases regionais. O presente relato tem por objetivo descrever um caso de um canino diagnosticado com hemangiossarcoma hepático em lobo caudado submetido a uma lobectomia total. A técnica cirúrgica consistiu na utilização da sutura de guilhotina modificada na base do lobo acometido utilizando fio de polidioxanona e, com o auxílio de um bisturi elétrico unipolar, e respeitando o distanciamento de 0,5 cm da sutura, foi realizada a lobectomia. Após a remoção do lobo, foi fixada uma esponja hemostática de colágeno na região da incisão como forma de auxílio no controle hemorrágico. Foi indicado também a realização de tratamento quimioterápico adjuvante, entretanto o tutor do animal optou pela não realização da mesma. Ainda assim, o paciente do presente relato obteve uma boa resposta ao procedimento, e o tutor ficou muito satisfeito, relatando que houve uma grande melhora na qualidade de vida do animal e que ele não sentia mais dor, voltando a ter o seu comportamento habitual.(AU)

Hemangiosarcoma is an aggressive malignant mesenchymal neoplasm with a high rate of morbidity and mortality in dogs and cats; which develops more frequently in the spleen, liver, heart, bones, in addition to being able to manifest regional metastases. The present report aims to describe a case of a canine diagnosed with hepatic hemangiosarcoma in the caudate lobe submitted to a total lobectomy. The surgical technique consisted of using a modified guillotine suture at the base of the affected lobe using polydioxanone thread and, with the aid of a unipolar electric scalpel, and respecting the distance of 0.5 cm from the suture, lobectomy was performed. After removing the lobe, a hemostatic collagen sponge was fixed in the region of the incision as an aid in hemorrhagic control. Adjuvant chemotherapy treatment was also indicated, however the animal's tutor chose not to perform it. Even so, the patient in the present report had a good response to the procedure, and the tutor was very satisfied, reporting that there was a great improvement in the animal's quality of life and that he no longer felt pain, returning to his usual behavior.(AU)

El hemangiosarcoma es una neoplasia mesenquimatosa maligna agresiva con una alta tasa de morbilidad y mortalidad en perros y gatos; la cual se desarrolla con mayor frecuencia en bazo, hígado, corazón, huesos, además de poder manifestar metástasis regionales. El presente reporte tiene como objetivo describir un caso de un canino con diagnóstico de hemangiosarcoma hepático en el lóbulo caudado sometido a una lobectomía total. La técnica quirúrgica consistió en utilizar una sutura de guillotina modificada en la base del lóbulo afectado con hilo de polidioxanona y, con la ayuda de un bisturí eléctrico unipolar, y respetando la distancia de 0,5 cm de la sutura, se realizó la lobectomía. Después de retirar el lóbulo, se fijó una esponja hemostática de colágeno en la región de la incisión como ayuda para el control hemorrágico. También se indicó tratamiento de quimioterapia adyuvante, sin embargo el tutor del animal optó por no realizarlo. Aun así, el paciente del presente reporte tuvo una buena respuesta al procedimiento, y el tutor quedó muy satisfecho, informando que hubo una gran mejoría en la calidad de vida del animal y que ya no sintió dolor, volviendo a su comportamiento habitual.(AU)

Intra-Axial Metastatic Angiosarcoma of the Central Nervous System Associated with Anemia, Pulmonary Tuberculosis and Short Survival

Introduction Angiosarcoma (AG) is a malignant mesenchymal neoplasm that predominantly affects the soft tissues and, to variable degrees, expresses themorphological and functional characteristics of the endothelium. The incidence of sarcomas of the central nervous system(CNS) is low (0.5% to 2.7%), and AGs involving the brain are even rarer. Case Description A 45-year-old male patient presented with complaints of headache, nausea, and vomiting. An examination showed bilateral papilledema and a right lung pleurotomy. The patient's previous history included drug addiction, pulmonary tuberculosis, lung abscess, pleural empyema, and pulmonary artery embolization for severe hemoptysis. Computed tomography/magnetic resonance imaging scans revealed a large intra-axial lesion extending into the right parietal and temporal lobes, with hemorrhagic zones. The patient underwent surgical resection of the lesion. Microscopy showed a poorly-differentiated, high-grade malignant tumor composed of plump/epithelioid cells forming small vascular spaces and solid nests, compatible with AG.In the postoperative period, the patient developed recurrent hemoptysis. A biopsy of the tissues adjacent to the pleurotomy determined the diagnosis of pulmonary AG. At 30 days after the resection, the patient died from hemoptysis, hemothorax, lung atelectasis, and intracranial hypertension related to the recurrence of the brain tumor. Conclusion Angiosarcoma is a rare neoplasia related to short survival due to the high proliferative index, which must be considered in patients presenting hemorrhagic tumors. No specific genetic abnormalities have been described for this neoplasia.

Use of video laryngoscope for tracheal intubation in patient with oral cavity mass: case report / Uso de videolaringoscópio para intubação traqueal em paciente com massa tumoral na cavidade oral: relato de caso

Abstract Background and objectives When planning the management of a predicted difficult airway, it is important to determine which strategy will be followed. Video laryngoscopy is a major option in scenarios with factors suggesting difficult airway access. It is also indicated in rescue situations, when there is tracheal intubation failure with direct laryngoscopy. The objective of the present report was to show the efficacy of using the video laryngoscope as the first device for a patient with a large tumor that occupied almost the entire anterior portion of the oral cavity. Case report An 85 year-old male patient, 162 cm, 70 kg, ASA Physical Status II, Mallampati IV classification, was scheduled for resection of an angiosarcoma located in the right maxillary sinus that invaded much of the hard palate and the upper portion of the oropharynx. He was conscious and oriented, with normal blood pressure, heart and respiratory rates and, despite the large tumor in the oral cavity, he showed no signs of respiratory failure or airway obstruction. After intravenous cannulation and monitoring, sedation was performed with 1 mg of intravenous midazolam, and a nasal cannula was placed to provide oxygen, with a flow of 2 L min−1. Then, the target-controlled infusion of remifentanil with an effect site concentration of 2 ng mL−1 was initiated, according to Minto's pharmacokinetic model. Ventilation was maintained spontaneously during airway handling. A trans-cricothyroid block was performed, with 8 mL of 1% lidocaine solution injected into the tracheal lumen. Slight bleeding did not prevent the use of an optical method for performing tracheal intubation. The entire oral cavity was sprayed with 1% lidocaine. The McGraph video laryngoscope with the difficult intubation blade was used, and an armored tube with a guide wire inside was used for tracheal intubation, performed on the first attempt with appropriate glottis visualization. Conclusion The video laryngoscope occupies a prominent position in cases in which access to the airway is difficult. In the present case it was useful. It can be used as first choice or as a rescue technique. The video laryngoscope is an appropriate alternative and should be available for facing the ever-challenging difficult airway patient.

Resumo Justificativa e objetivos No planejamento da abordagem a uma via aérea difícil prevista, é importante determinar qual será a estratégia a ser seguida. A videolaringoscopia é uma ótima opção em situações em que existam fatores indicadores de dificuldade de acesso à via aérea. Também é indicada em situações de resgate, quando houve insucesso na tentativa de intubação com a laringoscopia direta. O objetivo deste relato é mostrar a eficácia da utilização do videolaringoscópio como primeiro dispositivo diante de paciente com grande tumor que ocupava quase a totalidade da porção anterior da cavidade oral. Relato do caso Paciente com 85 anos, sexo masculino, 162 cm, 70 kg, estado físico ASA II, classificação de Mallampati IV, foi escalado para a ressecção de um angiossarcoma localizado no seio maxilar direito que invadia grande parte do palato duro e da porção superior da orofaringe. Apresentava-se lúcido, consciente e orientado, com valores de pressão arterial, frequência cardíaca e respiratória normais e, apesar do grande tumor na cavidade oral, não apresentava qualquer sinal de insuficiência respiratória ou de obstrução das vias aéreas. Após venóclise, foi feita monitorização e sedação com 1 mg de midazolam, por via venosa, e colocado cateter nasal para administração de oxigênio, com fluxo de 2 L.min-1. Em seguida, foi iniciada a infusão alvo-controlada de remifentanil com concentração efeito de 2 ng.mL-1 segundo o modelo farmacocinético de Minto. A ventilação foi mantida em espontânea durante a manipulação da via aérea. Foi realizado bloqueio transcricotireóideo, sendo injetados 8 mL de solução de lidocaína a 1% na luz traqueal. Um pequeno sangramento não impediu que um método óptico fosse utilizado para realizar a intubação traqueal. Toda a cavidade oral recebeu o spray de lidocaína tópica a 1%. Foi utilizado o videolaringoscópio McGraph com a lâmina de intubação difícil, e um tubo aramado com fio guia no seu interior, foi utilizado para a intubação traqueal, que foi realizada na primeira tentativa, com boa visualização da glote. Conclusão O videolaringoscópio ocupa uma posição de destaque nos casos em que o acesso à via aérea é difícil. No presente caso, a sua utilização foi útil. Ele pode ser utilizado como primeira opção ou como técnica de resgate. Nas condições sempre preocupantes diante de um paciente com via aérea difícil, o videolaringoscópio deve estar disponível, constituindo-se uma boa opção.

Radiation-induced angiosarcoma: case report / Angiossarcoma induzido por radiação: relato de caso

ABSTRACT Angiosarcoma of the breast accounts for less than 1% of breast tumors. This tumor may be primary or secondary to previous radiation therapy and it is also named "radiogenic angiosarcoma of the breast", which is still a rare entity with a poor prognosis. So far, there are only 307 cases reported about these tumors in the literature. We present a case of a 73-year-old woman with a prior history of breast-conserving treatment of right breast cancer, exhibiting mild pinkish skin changes in the ipsilateral breast. Her mammography was consistent with benign alterations (BI-RADS 2). On incisional biopsy specimens, hematoxylin-eosin showed atypical vascular lesion and suggested immunohistochemisty for diagnostic elucidation. Resection of the lesions was performed and histology showed radiogenic angiosarcoma. The patient underwent simple mastectomy. Immunohistochemistry was positive for antigens related to CD31 and CD34, and C-MYC oncogene amplification, confirming the diagnosis of angiosarcoma induced by breast irradiation. A delayed diagnosis is an important concern. Initial skin changes in radiogenic angiosarcoma are subtle, therefore, these alterations may be confused with other benign skin conditions such as telangiectasia. We highlight this case clinical aspects with the intention of alerting to the possibility of angiosarcoma of the breast in patients with a previous history of adjuvant radiation therapy for breast cancer treatment. Sixteen months after the surgery the patient remains asymptomatic.

RESUMO Os angiossarcomas de mama representam menos de 1% dos tumores da mama e podem ser primários ou secundários à radioterapia prévia. Tais tumores são chamados de "angiossarcomas radiogênicos da mama" e representam uma entidade mais rara ainda e de prognóstico ruim. Atualmente, na literatura, são encontrados apenas 307 casos desses tumores. Relatamos o caso de uma mulher de 73 anos, com história prévia de tratamento conservador de câncer de mama direita, apresentando alteração rósea discreta em pele da mama homolateral. A mamografia demostrou resultado compatível com alterações benignas (BI-RADS 2). No material de biópsia incisional, a hematoxilina-eosina demonstrou lesão vascular atípica e sugeriu imuno-histoquímica para elucidação diagnóstica. A paciente foi submetida à ressecção de lesões, e a histologia demonstrou angiossarcoma radiogênico. Em seguida, mastectomia simples foi realizada. A imuno-histoquímica demonstrou positividade para os antígenos relacionados a CD31 e CD34, e a amplificação do oncogene C-MYC confirmou o diagnóstico de angiossarcoma induzido por radiação mamária. O atraso no diagnóstico constitui questão importante. Considerando que as alterações iniciais da pele do angiossarcoma radiogênico são sutis e podem ser confundidas com outras condições benignas da pele, como telangiectasias, neste relato destacamos os aspectos clínicos, no intuito de alertar sobre a possibilidade de angiossarcoma de mama em pacientes com história prévia de radioterapia adjuvante para tratamento de câncer de mama. A paciente permaneceu assintomática 16 meses após a cirurgia.

Reconstrução de couro cabeludo após ampla ressecção de angiossarcoma / Scalp reconstruction after wide resection of an angiosarcoma

Introdução: O couro cabeludo é uma área de difícil reconstrução devido à sua pouca elasticidade e por sobrepor-se a uma estrutura rígida e convexa. Existem diferentes técnicas cirúrgicas para reparação dos defeitos, que podem ser produto de diversas etiologias, como: traumas, deformidades e consequência de doenças, principalmente oncológicas, como é o caso do paciente apresentada neste trabalho. O angiossarcoma cutâneo é um tumor vascular maligno raro e extremamente agressivo, que afeta principalmente idosos. É caracterizado clinicamente pelo aparecimento de placas eritêmato-violáceas e de rápida evolução. O tratamento depende da extensão da doença. A maioria dos casos são tratados com ampla ressecção cirúrgica e reconstrução. O objetivo é relatar um caso de reconstrução de grande defeito do couro cabeludo depois de uma dissecção oncológica, realizado no Hospital Central do Exército (HCE) - RJ. Métodos: O caso foi tratado com enxerto autólogo e uso de matriz dérmica, em 2 tempos cirúrgicos, até a total cobertura da área lesionada. Resultados: Obteve-se resultado satisfatório após as cirurgias de enxertia de pele na área ressecada. Conclusão: O enxerto autólogo, juntamente a matriz dérmica mostrou-se uma opção viável na reconstrução do couro cabeludo.

Introduction: It is difficult to reconstruct the scalp due to its poor elasticity and presence of layers over a rigid convex structure. Different surgical techniques are used to repair defects that may develop due to several etiologies, such as trauma, deformities, and disease sequelae, especially cancer, as noted in the present case. Cutaneous angiosarcoma, a rare and extremely aggressive malignant vascular tumor that mainly develops in elderly individuals, is clinically characterized by the onset of rapidly evolving erythematous purple plaques. The treatment depends on disease extent. Most patients are treated with wide surgical resection and reconstruction. The objective is to report a case of reconstruction of a major scalp defect after an oncologic dissection performed at the Hospital Central do Exército in Rio de Janeiro. Methods: An autologous graft and dermal matrices were applied during two surgical periods till the damaged area was fully covered. Results: Satisfactory results were obtained after performing skin grafting surgery in the resected area. Conclusion: The autologous graft and dermal matrix proved to be a viable option for scalp reconstruction.

Primary cardiac angiosarcoma with rare presenting feature and successful surgical treatment

Abstract Primary angiosarcoma is a rare clinical entity, it's typically located within the right atrium and known to be rapidly fatal. A 37-year-old female was presented with a history of recurrent facial paralysis and left hemiparesis. A cranial mass was identified at cranial magnetic resonance imaging and she underwent neurosurgery operation. The immunohistochemical examination was determined as metastatic cardiac angiosarcoma. The tumor, as well as part of the right pericardium, were resected. A piece of bovine pericardium was used to reconstruct the right atrial wall. Tricuspid valve was reconstructed with ring annuloplasty. Due to resection of right coronary artery with the tumor, coronary bypass surgery was performed successfully. The patient is currently healthful without any recurrence and complaint 12 months after the diagnosis as followed up.

Hemangiossarcoma de terceira pálpebra em uma cadela da raça boxer - Relato de caso / Third-eyelid hemangiosarcoma in a boxer bitch - Case report / Hemangiosarcoma en tercer párpado en una perra de la raza boxer - Relato de caso

O hemangiossarcoma é a neoplasia maligna originária do endotélio vascular. Os sítios primários mais comuns são baço, fígado, coração e pele, sendo considerado raro o acometimento da pálpebra e demais componentes oculares. Neste relato, descreve-se o caso de uma cadela da raça Boxer, de dez anos de idade, que apresentou aumento de volume, na borda livre da terceira pálpebra, de cor vermelho escuro. O tratamento de escolha foi a remoção cirúrgica e o diagnóstico de hemangiossarcoma foi confirmado ao exame histopatológico.(AU)

Hemangiosarcoma is malignant neoplasm originating from the vascular endothelium. The most common primary sites of this neoplasia are the spleen, liver, heart and skin. The involvement of the eyelid and other ocular components is unusual. In this report, we describe the case of a 10-year-old Boxer bitch who presented an increase in volume, at the free edge of the third eyelid, a deep red color. The mass was surgically removed and the diagnosis of hemangiossarcoma was confirmed by histopathological exam.(AU)

El hemangiosarcoma es una neoplasia maligna originada en el endotelio vascular, encontrado principalmente en el bazo, hígado, corazón y piel. Su presencia en párpados y otros componentes oculares es poco común. En este relato se describe el caso de una perra de la raza Boxer, de diez años, que presentó aumento de volumen, en el borde libre del tercer párpado, de color rojo oscuro. El tratamiento escogido fue la remoción quirúrgica y el diagnóstico de hemangiosarcoma fue confirmado por examen histopatológico.(AU)

A rare cause of abdominal pain in childhood: cardiac angiosarcoma

Abstract Cardiac angiosarcomas are extremely rare in childhood, they are rapidly progressive tumours that often present themselves as diagnostic dilemmas, resulting in delayed diagnosis. Also, extracardiac manifestations, including abdominal pain, are extremely rare in patients with intracardiac tumors. We herein present the case of a 15-year-old girl who presented with abdominal pain. Echocardiography and thoracic computed tomography showed right atrial mass. The patient underwent surgery, chemotherapy, and radiotherapy. Eight months after treatment, abdominal recurrence was detected. The abdominal mass was resected, and radiotherapy and new chemotherapy protocol were given. The present case illustrates a rare case of primary cardiac angiosarcoma posing a diagnostic dilemma in an adolescent girl.

Angiosarcoma of the head and neck

Introduction Angiosarcoma of the head and neck is a rare vascular sarcoma associated with high rates of local recurrence and distant metastasis and a poor prognosis. Objective We describe our experience treating patients with angiosarcoma of the head and neck to evaluate the outcomes, patterns of failure, and current treatments. Methods We identified six patients with angiosarcoma of the head and neck and treated at our institution between 2000 and 2013. We compared our results to the literature from 1979 to 2013. Results Mean follow-up was 42 months. Local recurrence rate was 50% with diseasespecific survival and 2-year disease-free survival rates of 33.3 and 20%, respectively. Prognostic factors included tumor size > 5 cm and surgical margin status, with no correlation between histologic grade and survival. Combined-modality therapy was only used for aggressive tumors with positive surgical margins but is suggested to improve local control and overall survival. Conclusions Our data series supports that angiosarcoma of the head and neck has a high rate of recurrence and is associated with a poor prognosis, despite current combined-modality therapy. The study highlights the importance of attaining negative margins during surgical resection, the utility of adjuvant therapies, as well as the need for continued research in developing new management strategies.

Stewart Treves Syndrome

Stewart-Treves Syndrome is characterized by the presence of lymphangiosarcoma on limb extremities. Rare, it occurs in 0.5% of patients who have undergone radical mastectomy with axillary node dissection. The main cause is chronic lymphedema with endothelial and lymphatic differentiation, with no direct relationship to breast cancer. Seven years after a radical right-side mastectomy with lymph node dissection and adjuvant therapy, the patient developed a lesion on her right arm. The dermatological examination revealed an erythematous nodule with bleeding surface on chronic right forearm lymphedema. After the biopsy, a lymphangiosarcoma on chronic lymphedema was diagnosed. Infrequent, this syndrome is relevant because of its associated mortality. Early diagnosis is important to improve survival and reduce complications.

Hemangiossarcoma corneal em cão / Corneal hemangiosarcoma in a dog

O hemangiossarcoma é uma neoplasia maligna e sua apresentação corneal é rara em cães. Relata-se um caso de hemangiossarcoma corneal primário, em uma fêmea canina, sem raça definida, de 20kg, nove anos de idade e com histórico de crescimento progressivo de massa em bulbo ocular direito há dois meses. Ao exame oftálmico do olho direito, foram observados blefarospasmo, hiperemia conjuntival moderada e presença de nódulo avermelhado, irregular em região dorsal de córnea direita, ocupando cerca de 60% dela. A ultrassonografia ocular foi realizada, e constatou-se que a neoplasia acometia apenas a córnea. Por meio do exame citológico, foi diagnosticada neoplasia mesenquimal maligna. O paciente foi submetido à ceratectomia seguida de flap de terceira pálpebra. Encaminhou-se o material excisado para análise histopatológica, e foi diagnosticado hemangiossarcoma. Após 15 dias, o flap de terceira pálpebra foi retirado, e, ao exame oftálmico, notou-se a recidiva da neoplasia, que recobria toda a córnea e parte da conjuntiva bulbar, procedendo-se à enucleação. O paciente foi submetido à ultrassonografia abdominal e à radiografia torácica sem nenhuma alteração evidente, o que caracterizou o caráter primário da afecção. Após dois anos do procedimento cirúrgico, o paciente encontra-se bem clinicamente, sem qualquer sinal de recidiva ou metástase. Apesar da exérese cirúrgica da neoplasia com margens limpas, em casos de hemangiossarcoma com comportamento agressivo, a enucleação deve ser considerada uma opção viável para um protocolo terapêutico de sucesso e melhor prognóstico do paciente.(AU)

Hemangiosarcoma is a malignant neoplasm and its corneal presentation is uncommon in the dog. The present work reports a case of primary corneal hemangiosarcoma on a mongrel female dog, 20kg, nine years old with a 2 month history of a mass with progressive growth in the right eye. The ophthalmic examination of the right eye showed blepharospasm, moderated conjunctival hyperemia and the presence of a reddish irregular nodule on the dorsal region of the cornea, occupying approximately 60% of the cornea. The ocular ultrasound revealed that the neoplasm affected only the cornea and the cytological examination diagnosed a malignant mesenchymal neoplasm. The patient was submitted to keratectomy followed by a third eyelid flap. The excised material was sent for histopathological analysis that diagnosed hemangiosarcoma. Fifteen days after surgery the third eyelid flap was removed and the ophthalmic examination revealed recurrence of the tumor, with the mass occupying the entire cornea and part of the bulbar conjunctiva. The patient was submitted to enucleation. No alterations were observed on the abdominal ultrasound and thoracic radiography, showing the primary characteristics of the disease. Two years after surgery the patient is clinically healthy, without any signs of recurrence or metastasis. Despite the surgical excision of the tumor with free margins, in cases of hemangiosarcoma with aggressive behavior, the enucleation should be considered as a viable option for a successfull therapeutic protocol and better prognosis of the patient.(AU)

Angiosarcoma cardíaco: una neoplasia infrecuente / Cardiac angiosarcoma: an infrequent neoplasia

Los tumores cardíacos son infrecuentes, siendo los más comunes los metastásicos. De los primarios, sólo el 25 por ciento son malignos, donde el angiosarcoma es el más frecuente. Este corresponde a un tumor de alto grado de malignidad, caracterizado por un rápido crecimiento, obstrucción de válvulas y metástasis principalmente pulmonares. Es más frecuente entre los 30 y 50años, especialmente en el género masculino, con una relación de2:1. Su clínica es de naturaleza cardiovascular inespecífica y su pronóstico es malo, con una supervivencia de entre nueve a doce meses a partir del diagnóstico. Presentación del caso: Paciente de género femenino, de 50 años de edad, con antecedentes de hipertensión arterial y artritis reumatoide. Consultó por disnea y deterioro de capacidad funcional. Ecocardiograma transtorácico mostró masa de seis centímetros de diámetro, que ocupa toda la aurícula derecha y que generaba obstrucción al flujo tricuspídeo, asociado a derrame pericárdico masivo con taponamiento cardíaco. Tomografía computada (TC) de cerebro, tórax, abdomen y pelvis descartan lesiones metastásicas. Se decidió conducta quirúrgica. Se resecó el tumor y el 70 por ciento de la pared libre de la aurícula y se instaló prótesis valvular biológica; con pericardio autólogo se reconstruyó la aurícula derecha. Evolucionó favorablemente, sin incidentes. Estudio histopatológico concluyó angiosarcoma cardíaco. Discusión: Los tumores cardíacos son infrecuentes. Se deben sospechar en pacientes con clínica cardiovascular, asociada a masa intracavitaria, derrame pericárdicono explicable por otra causa, así como la presencia de metástasis torácicas de un tumor primario desconocido...

Introduction: Cardiac tumors are rare; of them, the metastatic tumors are the most frequent. Of the primary tumors, only 25 percent are malignant, being the angiosarcoma the most common. It is a tumor of high malignancy, characterized by rapid growth, obstruction of cardiac valves and lung metastases. It is most common between 30 and 50 years, especially in men, with a ratio of 2:1. Its symptoms are nonspecific cardiovascular and its prognosis is poor, with a survival of nine to twelve months from diagnosis. Case report: A 50 years old woman with a history of hypertension and rheumatoid arthritis. She presented with dyspnea and impaired functional capacity. Transthoracic echocardiogram showed a mass of 6 cm in diameter, occupying the entire right atrium with tricuspid flow obstruction, associated with massive pericardial effusion with cardiac tamponade. Computed tomography (CT) of the brain, thorax, abdomen and pelvis discarded metastatic lesions. Surgical treatment was decided. The tumor and 70 percent of the free wall of the atrium were resected and biological prosthetic valve was installed, and the righ tatrium was reconstructed with autologous pericardium. She evolved favorably, without incident. Histopathological reports confirmed cardiac angiosarcoma. Discussion: Cardiac tumors are rare. They should be suspected in patients with cardiovascular symptoms, associated with intracavitary mass, pericardial effusion not explained by other causes, as well as the presence of thoracic metastases from an unknown primary tumor...

Angiossarcoma pouco diferenciado primário de glândula salivar parótida: relato de caso / Primary poorly differentiated angiosarcoma of the parotid gland

As neoplasias mesenquimais primárias das glândulas salivares são raras. Os autores descrevem um caso de angiossarcoma primário da glândula parótida em um homem com 84 anos (AU)

Primary mesenchymal neoplasms of the salivary glands are rare. The authors report a case of primary angiosarcoma of the parotid gland in a 84-year old male (AU)

Angiosarcoma primario de mama y carcinoma papilar de tiroides sincrónico: presentación de un caso / Primary angiosarcoma of breast and synchronous thyroid papillary carcinoma: a case report

Antecedentes: El angiosarcoma primario de mama constituye un tumor infrecuente que se desarrolla de forma predominante en mujeres en la tercera y cuarta décadas de la vida. Los nódulos tiroideos incidentales son aquellos que se objetivan en pruebas de imagen realizadas por otra causa y se observan en menos de un 10 por ciento con la tomografía por emisión de positrones (PET). Objetivo: Presentar el caso excepcional de una paciente con angiosarcoma primario de mama y un carcinoma papilar de tiroides sincrónicos. Caso clínico: Mujer de 34 años con angiosarcoma primario en la mama derecha sometida a mastectomía simple. En el estudio de extensión se halló un incidentaloma tiroideo derecho compatible con carcinoma papilar que requirió tiroidectomía total y linfadenectomía del compartimento central cervical en un segundo tiempo. Comentarlo: Los angiosarcomas primarios suponen menos del 0,05 por ciento de todos los tumores primarios malignos de la mama. El diagnóstico definitivo de estos tumores viene definido por el estudio anatomopatológico, que establece tres grados: alto, bajo e intermedio, los cuales se relacionan de forma directa con la supervivencia. La prevalencia de los incidentalomas malignos tiroideos objetivados por PET varía del 14-30,9 por ciento, según diferentes estudios. La planificación del tratamiento quirúrgico de las neoplasias incidentales tiroideas en pacientes con otro tumor primario debe analizarse de forma individualizada, según la supervivencia esperada del tumor primario.

Background: The primary angiosarcoma of breast is a rare tumor that develops predominantly in women in the third and fourth decades of life. Incidental thyroid nodules are observed in imaging tests performed for other reasons and it's observed in less than 10 percent with the positron emission tomography (PET). Aims: To report the exceptional case of a patient with primary angiosarcoma of the breast and synchronous thyroid papillary carcinoma. Clinical case: Female patient 34 year old with primary angiosarcoma in the right breast, submitted to a simple mastectomy. In the extension study we found an incidental thyroid papillary carcinoma that required a total thyroidectomy and central cervical lymphadenectomy in a second time. Comments: The primary angiosarcoma are less than 0.05 percent of all primary malignant tumors of the breast. The definitive diagnosis is determined by the pathology, which defines three grades: high, low and intermediate, which relate directly to survival. Prevalence of malignant thyroid incidentalomas observed by PET varies from 14 to 30.9 percent, according different studies. Planning the surgical treatment of incidental thyroid malignancies in patients with other primary tumor should be analyzed individually, according the expected survival of the primary tumor.

Eyelid angiosarcoma: a case report and review of the literature

A 77-year-old woman presented with a 3-month history of a lesion on her left lower eyelid. External examination showed a tan-colored nodule with an overlying crust-covered ulcer on the left lower eyelid, nasally. The ulcer measured 12 mmx7 mm. Complete surgical excision with a frozen section margin control was performed. Histopathological examination showed islands and sheets of spindle and epithelioid cells with little intervening stroma. The cells had copious amounts of either rounded or tapered eosinophilic cytoplasm with occasional intracytoplasmic lumina and large vesicular nuclei with prominent nucleoli. There was intense immunoreactivity for CD34, CD31, factor VIII, and Ki-67. The diagnosis was eyelid angiosarcoma. The patient refused any further therapy. At 1-year follow-up, there was no recurrence or development of metastasis. In conclusion, tan-colored eyelid nodules with overlying ulcer are usually a basal cell carcinoma; however, rarely it can be an eyelid angiosarcoma

Angiosarcoma de mama: a propósito de un caso / Angiosarcoma of the breast: apropos of one case

El angiosarcoma de mama constituye una neoplasia vascular maligna muy poco frecuente en la mama, con una incidencia inferior al 0,05 por ciento de entre todos los tumores primarios que asientan en la mama. Teniendo en cuenta que su edad de aparición es a partir de la tercera-cuarta década de la vida, resulta preocupante la aparición de casos a edades cada vez más tempranas. Se presenta el caso clínico de una paciente de 25 años de edad con antecedente de fibroma mamario benigno desde los 17 años que degenera en un angiosarcoma mamario...

Breast Angiosarcoma is a malignant vascular neoplasm rare in the breast with an incidence of less than 0.05 percent of all primary tumors in the breast that seat. Given its age of onset is from the third to fourth decade of life, it is disturbing to the occurrence of increasingly early ages. We describe the case of a patient 25 years old with a history of benign breast fibroid from the 17 years that degenerates into a breast angiosarcoma...

Angiosarcoma primario uterino: revisión de la literatura y presentación de caso / Primary uterine angiosarcoma: clinical case and literature review

Antecedentes: Los angiosarcomas son infrecuentes y corresponden a menos del 1 por ciento de tumores de tejidos blandos, pueden presentarse en cualquier localización fundamentalmente en la piel. El angiosarcoma primario uterino fue por primera vez reportado en 1902 por Silberberg con informes ulteriores esporádicos que suman un total de 33 casos incluyendo el presente. Objetivo: Exponer un caso diagnosticado en el Departamento de Patología de la Universidad Industrial de Santander (Bucaramanga-Colombia), y revisar la literatura de los casos previamente descritos. Caso clínico: Paciente de 25 años, con 2 años de evolución de menometrorragias y dolor pélvico crónico. Se realiza ablación endometrial encontrándose tumor maligno de endometrio pobremente diferenciado, infiltrante, el cual no es posible categorizar. Se efectúa una histerectomía ampliada, salpingooforectomía bilateral, linfadenectomía pélvica y omentectomía. El examen microscópico reveló lesión tumoral pobremente diferenciada compatible con un angiosarcoma uterino de alto grado.

Background: Angiosarcomas are rare and account for less than 1 percent of soft tissue tumors can occur at any location primarily in the skin. The primary uterine angiosarcoma was first reported in 1902 by Silberberg with sporadic subsequent reports, with a total of 33 cases including the present. Objective: To present a case diagnosed in the Department of Pathology, Universidad Industrial de Santander (Bucaramanga, Colombia) and review the literature of the cases previously described. Case report: A 25 years old woman, with 2 years of chronic pelvic pain and menometrorrhagia. Endometrial ablation is performed and an endometrial malignancy was found, poorly differentiated and infiltrating, which is not possible to categorize. It makes an extended hysterectomy, bilateral salpingo-oophorectomy, pelvic lymphadenectomy, and omentectomy. Microscopic examination revealed poorly differentiated tumor, compatible with a high-grade uterine angiosarcoma.