[Ischemic stroke due to paradoxical embolism through pulmonary arteriovenous malformation in a young patient]. / ACV isquémico debido a embolia paradojal a través de malformación arteriovenosa pulmonar en paciente joven.

Paradoxical embolism due to an isolated pulmonary arteriovenous malformation (PAVM) is a rare cause of ischemic stroke. PAVMs are abnormal high-flow connections between pulmonary arteries and veins, diverting deoxygenated blood into the systemic circulation and they represent a less common source of paradoxical embolisms, especially in young individuals. Endovascular embolization is the preferred treatment for clinically significant PAVMs. We present the case of a 34-year-old woman with a left thalamic ischemic stroke. Severe contrast passage was detected in cerebral arteries through transcranial Doppler. Intracardiac ultrasound did not reveal a patent foramen ovale, prompting further investigation with pulmonary CT angiography, confirming the presence of PAVM. The patient underwent successful endovascular treatment. It is essential to consider PAVM in the etiological diagnosis of ischemic stroke, especially in young patients with signs of abnormal right-to-left communication. Periodic follow-up imaging is recommended to assess potential recurrence or changes in PAVM, emphasizing the importance of appropriate management of these malformations.

La embolia paradojal debido a una malformación arteriovenosa pulmonar (MAVP) aislada es una causa infrecuente de accidente cerebrovascular (ACV) isquémico. Las MAVP son conductos anómalos de alta circulación entre arterias y venas pulmonares, desviando sangre desoxigenada hacia la circulación sistémica y representan una fuente menos común de embolias paradojales, especialmente en personas jóvenes. La embolización endovascular es el tratamiento preferido para MAVP clínicamente significativas. Presentamos el caso de una mujer de 34 años con ACV isquémico talámico izquierdo. Se detectó pasaje de burbujas "en cortina" en arterias cerebrales mediante Doppler transcraneal. En ecografía intracardíaca no se encontró foramen oval permeable, motivo por el cual se avanzó con realización de angiotomografía pulmonar, la cual confirmó la presencia de MAVP. La paciente recibió tratamiento endovascular exitoso. Es esencial considerar la MAVP en el diagnóstico etiológico del ACV isquémico, especialmente en pacientes jóvenes con signos de comunicación anormal de derecha a izquierda. Se recomienda un seguimiento periódico mediante imágenes para evaluar la posible recurrencia o cambios en la MAVP, resaltando la importancia del manejo adecuado de estas malformaciones.

Prevalence and Predictors of Hereditary Hemorrhagic Telangiectasia and Capillary-Malformation Arteriovenous Malformation Syndrome Among Children with Neurovascular Malformations.

OBJECTIVE: To investigate the prevalence and predictors of hereditary hemorrhagic telangiectasia (HHT) and capillary-malformation arteriovenous malformation (CM-AVM) syndrome among children with no prior personal or family history of these diseases who presented with an arteriovenous shunt lesion. STUDY DESIGN: A retrospective chart review was completed on patients aged 0 through 21 years with arteriovenous shunt lesions evaluated at our Cerebrovascular Center. Diagnosis of definite or suspected HHT or CM-AVM was based on clinical features and genetic testing. Associations between final diagnosis and type and number of lesions, epistaxis, telangiectasias, CM, and pulmonary AVMs were assessed. RESULTS: Eighty-nine patients were included. Thirteen (14.6%) had definite HHT, 11 (12.4%) suspected HHT, and 4 (4.5%) definite CM-AVM. Having ≥2 episodes of epistaxis/year and ≥ 2 sites with telangiectasias were each associated with definite HHT (P < .001). Having ≥ 2 CM was associated with definite CM-AVM (P < .001). Pulmonary AVM was associated with increased odds of having definite HHT (OR = 6.3, 95% CI: 1.2-33.4). Multiple lesions (OR = 24.5, 95% CI: 4.5-134.8) and arteriovenous fistulas (OR = 6.2, 95% CI: 1.9-20.3) each increased the likelihood of having definite HHT or CM-AVM. Genetic testing was positive in 31% of patients tested. CONCLUSIONS: We recommend that children with neurovascular shunt lesions be offered genetic testing and undergo further evaluation for HHT and CM-AVM. Awareness and early diagnosis of these conditions is a critical step toward improving long-term outcomes and preventing disease-associated complications.

Aneurisma venoso yuxta-anastomótico en fístula arterio-venosa para hemodiálisis / Juxtaanastomotic venous aneurysm in arteriovenous fistula for hemodialysis

Introducción: A pesar del gran avance técnico que representan las fístulas arterio-venosas internas para la hemodiálisis, estas no están exentas de complicaciones que comprometen su durabilidad. Entre ellas se encuentran los aneurismas venosos yuxta-anastomóticos. Objetivo: Presentar el tratamiento quirúrgico utilizado para reparar los aneurismas venosos yuxta-anastomóticos. Presentación del caso: Paciente de 54 años, de género femenino y color de piel negra. Presentó antecedentes de padecer insuficiencia renal crónica de 12 años de evolución, con transplante renal fallido, la cual tuvo un aneurisma venoso yuxta-anastomótico, localizado en una fístula arterio-venosa húmero-cefálica en miembro superior izquierdo, que fue confirmado por eco-doppler. Se emplearon como tratamiento quirúrgico la aneurismectomía y el injerto por sustitución con prótesis vascular expandible de poli-tetrafluoretileno. Finalmente, se preservó la fístula arterio-venosa, así como su permeabilidad. Conclusiones: La evolución fue satisfactoria en cuanto a su durabilidad y utilización como vía de acceso para la hemodiálisis(AU)

Introduction: Despite the great technical advance represented by internal arterio-venous fistulas for hemodialysis, these are not exempt from complications that compromise their durability. Among them are juxtaanastomotic venous aneurysms. Objective: Present the surgical treatment used to repair juxtaanastomotic venous aneurysms. Case presentation: 54-year-old patient, female and black skin color. She presented a history of chronic renal failure of 12 years of evolution, with failed kidney transplant, which had a juxtaanastomotic venous aneurysm, located in a humerus-cephalic arterio-venous fistula in the left upper limb, which was confirmed by Doppler echo. Aneurysmectomy and replacement grafting with expandable polytetrafluorethylene vascular prostheses were used as surgical treatment. Finally, the arterio-venous fistula was preserved, as well as its permeability. Conclusions: The evolution was satisfactory in terms of durability and use as an access route for hemodialysis(AU)

Safety and efficacy of arteriovenous fistula angioplasties performed by nephrologists: report from a Brazilian interventional nephrology center.

INTRODUCTION: Arteriovenous fistulas (AVF) are the first choice vascular access for hemodialysis. However, they present a high incidence of venous stenosis leading to thrombosis. Although training in interventional nephrology may improve accessibility for treatment of venous stenosis, there is limited data on the safety and efficacy of this approach performed by trained nephrologists in low-income and developing countries. METHODS: This study presents the retrospective results of AVF angioplasties performed by trained nephrologists in a Brazilian outpatient interventional nephrology center. The primary outcome was technical success rate (completion of the procedure with angioplasty of all stenoses) and secondary outcomes were complication rates and overall AVF patency. FINDINGS: Two hundred fifty-six angioplasties were performed in 160 AVF. The technical success rate was 88.77% and the main cause of technical failure was venous occlusion (10%). The incidence of complications was 13.67%, with only one patient needing hospitalization and four accesses lost due to the presence of hematomas and/or thrombosis. Grade 1 hematomas were the most frequent complication (8.2%). The overall patency found was 88.2 and 80.9% at 180 and 360 days after the procedure, respectively. CONCLUSION: Our findings suggest that AVF angioplasty performed by trained nephrologists has acceptable success rates and patency, with a low incidence of major complications as well as a low need for hospitalization.

An unusual case of femoral arteriovenous fistula associated with acute limb ischemia following femoral vein catheterization for hemodialysis / Um caso incomum de fístula arteriovenosa femoral associada a isquemia aguda de membro após cateterização da veia femoral para hemodiálise

Abstract Co-occurrence of acute limb ischemia (ALI) and arteriovenous fistula (AVF) as a manifestation of inadvertent arterial injury during percutaneous femoral vein dialysis catheter insertion is a rare and dangerous, but preventable complication. Iatrogenic femoral AVF commonly presents late, with leg swelling or high output cardiac failure. However, the co-occurrence of a femoral AVF with both progressive leg swelling, and acute thromboembolism has not been previously reported. We report the case of an iatrogenic femoral AVF with superficial femoral artery (SFA) thrombosis and distal embolism in a 53-year-old female who underwent percutaneous femoral access for temporary hemodialysis. Both the SFA and AVF were managed with open surgical repair.

Resumo A coocorrência de isquemia aguda de membro (IAM) e fístula arteriovenosa (FAV) como uma manifestação de lesão arterial inadvertida durante a inserção de cateter para hemodiálise por via femoral percutânea é uma complicação rara e perigosa, porém evitável. A FAV femoral iatrogênica geralmente tem apresentação tardia, com edema dos membros inferiores ou insuficiência cardíaca de alto débito. No entanto, a coocorrência de FAV femoral com edema progressivo dos membros inferiores e tromboembolismo agudo não foi previamente relatada. Relatamos o caso de uma FAV femoral iatrogênica com trombose da artéria femoral superficial (AFS) e embolia distal em uma paciente do sexo feminino, 53 anos, submetida à acesso femoral percutâneo para hemodiálise temporária. Tanto a AFS quanto a FAV foram manejadas com reparo cirúrgico aberto.

Secondary stabbing headache associated with intracranial tumors, aneurysms, and arteriovenous malformation: An alarming warning sign.

BACKGROUND: Stabbing headache (SH) is considered as a pure primary headache, but according to a few clinical observations it could also be secondary. Over the past decades, we have been observing the complaint of SH in patients with intracranial vascular and neoplastic lesions. OBJECTIVE: To describe a series of patients with intracranial lesions who experienced SH. METHODS: This is a cross-sectional, retrospective study of 34 patients with intracranial lesions associated with SH, admitted at Hospital das Clínicas, Federal University of Pernambuco, Brazil. RESULTS: In this series of 34 patients [29 women, 44 ± 12 years (mean ± SD)] with secondary SH, the causes were intracranial neoplasms (n = 31), cerebral aneurysms (n = 2), or arteriovenous malformation (n = 1). Pituitary tumor (n = 18), meningioma (n = 6), and vestibular schwannomas (n = 4) were the most prevalent types of intracranial neoplasms. All these lesions had intimate contact with the dura mater, including an oligodendroglioma, the only intra-axial tumor in the series. A characteristic in the secondary SH is the crescendo pattern (12/34, 35%), progressing from infrequent attacks to recurrent crises occurring several times a day. The SH lasted from 5 days to 60 months (15 ± 18 months, mean ± SD) until the correct diagnosis [16/34 (47%) of the patients ≤6 months]. The SH was triggered by the movement of the head (5/34, 15%) or Valsalva maneuver (1/34). After surgery, suppression of the SH was observed. In a few of the patients to whom dexamethasone was prescribed, the SH subsided within a few days. CONCLUSION: This study was able to identify clinical red flags associated with intracranial lesions and secondary SH, for example, recent onset of SH, exclusively unilateral (ipsilateral) at the same location, crescendo pattern, triggered by head movements, or Valsalva maneuver.

Tratamento endovascular com endoprótese aórtica para aneurisma de artéria subclávia secundário à fístula arteriovenosa axilo-axilar traumática tardia / Endovascular treatment with aortic endoprostheses for subclavian artery aneurysm secondary to late traumatic axillary-axillary arteriovenous fistula

Resumo As fístulas arteriovenosas (FAVs) traumáticas envolvendo os vasos axilares e subclávios são incomuns e correspondem de 5 a 10% de todos os traumas arteriais. A anatomia complexa dessa região torna desafiador o tratamento desse segmento. Neste desafio terapêutico, descrevemos o caso de um homem de 73 anos, encaminhado por edema progressivo e úlcera no membro superior direito, com história pregressa de ferimento por arma de fogo na região infraclavicular direita há cerca de 50 anos. Foi realizada angiotomografia e identificou-se FAV axilo-axilar associada à tortuosidade e dilatação aneurismática de artéria subclávia a jusante. O paciente foi submetido à intervenção endovascular com endoprótese cônica (monoilíaca) 26 × 14 × 90 mm Braile® na artéria subclávia aneurismática, posterior à saída da artéria vertebral direita, e endoprótese monoilíaca 16 × 16 × 95 mm Excluder® com sobreposição na primeira prótese, apresentando resultado satisfatório. Portanto, descreve-se a possibilidade de utilização de endoprótese aórtica em situação incomum e de exceção, com sucesso.

Abstract Traumatic arteriovenous fistulas (AVFs) involving the axillary and subclavian vessels are uncommon and account for 5 to 10% of all arterial traumas. The complex anatomy of this region makes treatment of this segment challenging. In this therapeutic challenge, we describe the case of a 73-year-old man, referred for progressive edema and ulceration involving the right upper limb and with a history of gunshot wound to the right infraclavicular region about 50 years previously. Angiotomography was performed and an axillary-axillary AVF was found, associated with tortuosity and aneurysmatic dilation of the subclavian artery downstream. He underwent endovascular intervention and a conical (monoiliac) 26 × 14 × 90 mm Braile® endoprosthesis was used in the aneurysmatic subclavian artery, posterior to the exit of the right vertebral artery and a 16 × 16 × 95mm Excluder® monoiliac endoprosthesis was placed overlapping the first prosthesis, showing a satisfactory result. Therefore, the possibility of successfully using aortic endoprostheses in an unusual and exceptional situation is described.

[Congenital renal arteriovenous fistula: a rare cause of acute abdomen and a review of its literature]. / Fístula arteriovenosa renal congénita: una causa rara de abdomen agudo y revisión de la literatura.

Introduction: Congenital renal arteriovenous fistula is an abnormal connection between the arterial and venous system. Since the first case described in 1928 by Varela et al, no more than 200 cases have been published. Material and methods: A 45-year-old woman consulted for severe abdominal and low-back pain associated with arterial hypertension. The CT scan showed an infrarenal retroperitoneal lesion with invasion of neighboring structures. Results: During the abdominal exploration, a vascular-looking lesion of 60 x 34 x 41 mm was identified. It was associated with right nephrectomy. Discussion: The etiology of congenital fistulas remains unknown; it is believed that a congenital arterial aneurysm erodes into an adjacent vein and gradually increases its size. Other authors believe that the fistula exists since birth and gradually increases its size until it causes symptoms. Conclusion: Congenital arteriovenous fistulas are rare entities, representing less than 25% of all renal arteriovenous malformations.

Introducción: La fístula arteriovenosa renal congénita es una conexión anómala entre el sistema arterial y venoso. Desde el primer caso descrito en 1928 por Varela y cols, no más de 200 casos han sido publicados. Material y Método: Mujer de 45 años consultó por dolor abdominal y lumbar severo, asociado a hipertensión arterial. En tomografía computada se observó lesión retroperitoneal infrarrenal con invasión de estructuras vecinas. Resultados: En exploración abdominal se identificó lesión de aspecto vascular de 60 x 34 x 41 mm. Se asoció a nefrectomía derecha. Discusión: La etiología de las fístulas congénitas sigue siendo desconocida, se cree que un aneurisma arterial congénito erosiona hacia una vena adyacente y aumenta su tamaño lentamente. Otros autores creen que la fístula existe desde el nacimiento e incrementa progresivamente de tamaño hasta producir síntomas. Conclusión: Las fístulas arteriovenosas congénitas son entidades raras, representando menos del 25% del total de las malformaciones arteriovenosas renales.

Repercusión hemodinámica del cierre de la fístula arteriovenosa sobre el corazón derecho en trasplantados renales / Hemodynamic impact of arteriovenous fistula closure on the right heart in kidney transplant patients

Introducción: Las complicaciones cardiovasculares constituyen la primera causa de morbilidad y mortalidad en el receptor de trasplante renal. Objetivo: Caracterizar la repercusión de la fístula arteriovenosa sobre variables hemodinámicas del corazón derecho en trasplante renal. Métodos: Estudio prospectivo, longitudinal. Se incluyeron 52 pacientes, evaluados clínica y ecocardiográficamente. Se compararon cinco variables hemodinámicas en el corazón derecho, previos y seis meses posteriores al cierre de la fístula arteriovenosa. Resultados: La edad promedio 46,02 años, 29 masculinos (55,8 por ciento). El diámetro de la aurícula derecha en las fístulas cerradas en la muñeca izquierda 8805; 6 años disminuyó (p=0,044), al igual que en el ventrículo derecho <6 años a nivel del pliegue del codo izquierdo (p=0,004). La presión sistólica de la arteria pulmonar descendió tras el cierre en el codo izquierdo lt;6 años (p=0,002), en las 8805;6 (p=0,05) y en el derecho (p=0,006). La presión media de la arteria pulmonar se redujo en las cerradas en pliegue del codo izquierdo <6 años (p=0,001) y 8805;6 años (p=0,017) al igual que en el derecho (p=0,009). La fracción de eyección del ventrículo derecho se incrementó al cierre en muñeca izquierda ;6 años (p=0,046) y en el codo derecho 8805;6 años (p=0,027). Conclusiones: La permanencia de la fístula arteriovenosa en el receptor de trasplante renal contribuye a la perpetuación y progresión de la disfunción cardiovascular preexistente(AU)

Introduction: Cardiovascular complications are the leading cause of morbidity and mortality in kidney transplant recipients. Objective: To describe the consequence of arteriovenous fistula on hemodynamic variables of the right heart in kidney transplantation. Methods: We conducted a prospective, longitudinal study. Fifty two patients were included, and they were clinically and echocardiographically assessed. Five hemodynamic variables were compared in the right heart, prior to the closure of the arteriovenous fistula and six months after. Results: The average age was 46.02 years, 29 were male (55.8 percent). The diameter decreased in the right atrium in closed fistulas in the left wrist #8805; 6 years (p = 0.044). The same occurred in the right ventricle <6 years at the level of the left elbow crease (p = 0.004). The systolic pressure of the pulmonary artery decreased after closure in the left elbow <6 years (p = 0.002), in ≥6 (p = 0.05) and in the right (p = 0.006). The mean pressure of the pulmonary artery was reduced in those closed in the crease of the left elbow <6 years (p = 0.001) and ≥6 years (p = 0.017) as well as in the right (p = 0.009). The right ventricular ejection fraction increased at closure in the left wrist <6 years (p = 0.046) and in the right elbow ≥6 years (p = 0.027). Conclusions: The permanence of arteriovenous fistula in the kidney transplant recipient contributes to the perpetuation and progression of the pre-existing cardiovascular dysfunction(AU)

The influence of a doppler ultrasound in arteriovenous fistula for dialysis failure related to some risk factors / Influência da Ultrassonografia Doppler nas Falhas de Fístulas Arteriovenosas de Diálise Relacionada a Alguns Fatores de Risco

ABSTRACT Introduction: The increasing prevalence of chronic kidney disease has increased the demand for arteriovenous fistula (AVF) care. The objective of this study was to assess the relationship between some risk factors for AVF failure (advanced age, female sex, diabetes, obesity, central venous catheter, previous fistula, and hospitalization) and having a Doppler ultrasound performed preoperatively. Methods: A prospective study was performed with 228 dialysis patients from Imperatriz, Maranhão. Half of the sample was randomly selected to receive preoperative Doppler ultrasound and the other half did not, from the period of October 2016 to September 2018. Results: There were 53 total failures corresponding to 23.2% of our sample, which is almost double that of the patients in the clinical group. Considering the failures and risk factors associated with the overall sample, there was a statistically significant association between a central venous catheter on the same side of the AVF with P = 0.04 (Odds Ratio 1.24) and obesity with P = 0.05 (Odds Ratio 1.36), which was not repeated in the Doppler ultrasound group individually. There was no statistically significant difference between the Doppler group and clinical group with respect to the amount of days of previous AVF hospitalization and failure. Conclusions: We concluded that the reduction of failures with an introduction of the Doppler was statistically significant in the overall sample, but establishing a relationship between specific risk factors and failure was only possible with two of the risk factors in the study - obesity and central venous catheter on the same side of the AVF.

RESUMO Introdução: A crescente prevalência de doença renal crônica aumentou a demanda por confecção de fístula arteriovenosa (FAV). O objetivo do presente estudo foi avaliar a relação entre alguns fatores de risco para falha da FAV (idade avançada, sexo feminino, diabetes, obesidade, cateter venoso central, fístula prévia e hospitalização) e a realização de ultrassonografia Doppler no pré-operatório. Métodos: Estudo prospectivo com 228 pacientes em diálise em Imperatriz, MA. Metade da amostra foi randomizada para receber ultrassonografia Doppler no pré-operatório. A outra metade dos pacientes não foi submetido a exame ultrassonográfico. O estudo incluiu pacientes atendidos no período de outubro de 2016 a setembro de 2018. Resultados: Houve 53 falhas (23,2%) em nossa amostra, quase o dobro do número dos pacientes no grupo clínico. Considerando as falhas e os fatores de risco associados à amostra geral, houve associação estatisticamente significativa entre catéter venoso central do mesmo lado da FAV (P = 0,04; Razão de Chances: 1,24) e obesidade (P = 0,05; Razão de Chances: 1,36), o que não foi reproduzido no grupo de ultrassonografia Doppler individualmente. Não houve diferença estatisticamente significativa entre o grupo Doppler e o grupo clínico em relação à quantidade de dias de internação e falha da FAV. Conclusões: A redução de falhas com a introdução do Doppler foi estatisticamente significativa na amostra geral, mas só foi possível estabelecer uma relação entre fatores de risco específicos e falha em dois dos fatores estudados, obesidade e catéter venoso central no mesmo lado da FAV.

The influence of a doppler ultrasound in arteriovenous fistula for dialysis failure related to some risk factors.

INTRODUCTION: The increasing prevalence of chronic kidney disease has increased the demand for arteriovenous fistula (AVF) care. The objective of this study was to assess the relationship between some risk factors for AVF failure (advanced age, female sex, diabetes, obesity, central venous catheter, previous fistula, and hospitalization) and having a Doppler ultrasound performed preoperatively. METHODS: A prospective study was performed with 228 dialysis patients from Imperatriz, Maranhão. Half of the sample was randomly selected to receive preoperative Doppler ultrasound and the other half did not, from the period of October 2016 to September 2018. RESULTS: There were 53 total failures corresponding to 23.2% of our sample, which is almost double that of the patients in the clinical group. Considering the failures and risk factors associated with the overall sample, there was a statistically significant association between a central venous catheter on the same side of the AVF with P = 0.04 (Odds Ratio 1.24) and obesity with P = 0.05 (Odds Ratio 1.36), which was not repeated in the Doppler ultrasound group individually. There was no statistically significant difference between the Doppler group and clinical group with respect to the amount of days of previous AVF hospitalization and failure. CONCLUSIONS: We concluded that the reduction of failures with an introduction of the Doppler was statistically significant in the overall sample, but establishing a relationship between specific risk factors and failure was only possible with two of the risk factors in the study - obesity and central venous catheter on the same side of the AVF.

[Pulmonary arteriovenous fistulas in a pediatric patient: a case report]. / Fístulas arteriovenosas pulmonares en un paciente pediátrico: un reporte de caso.

Pulmonary arteriovenous fistulas are congenital malformations due to anomalous direct communication between arteries and veins; the incidence is 2-3 : 100,000 inhabitants. This condition is usually asymptomatic and incidentally appearing in adult imaging findings. Transcutaneous endovascular embolization is the technique of choice for treatment. The unusual presentation in a 10-year-old patient is described; she was presented to the Emergency Department with dyspnea, cough, central cyanosis and digital clubbing; chest X-ray with images suggestive of parahilar nodules, arterial blood gases with increased alveolar arterial gradient. The high resolution computed tomography of the thorax revealed pulmonary arteriovenous malformation in the right parahilar region not associated with Rendu-Osler- Weber disease. The patient was treated with transcutaneous endovascular embolization, and after a year and a half of follow-up there were no relapses. There are few reported cases of pulmonary arteriovenous fistulas in the pediatric age.

Las fístulas arteriovenosas pulmonares son malformaciones congénitas dadas por la comunicación directa anómala entre arterias y venas, con una incidencia mundial de 2-3 : 100 000 habitantes. La presentación es, en general, única, asintomática, y aparecen en forma incidental como hallazgo imagenológico en la adultez, y su tratamiento de elección es la embolización endovascular. Se describe la inusual presentación clínica en una paciente de 10 años, que ingresó por disnea, tos, cianosis central y cefalea. Se encontró hipoxemia persistente, hipocratismo digital, nódulos parahiliares pulmonares, gases arteriales con gradiente alvéolo-arterial aumentado. La tomografía axial computarizada de tórax de alta resolución confirmó la presencia de una malformación arteriovenosa pulmonar en la región parahiliar derecha, la cual no se asociaba con la enfermedad de Rendu-Osler-Weber. La paciente fue tratada con embolización endovascular transcutánea. Tras 1,5 años de seguimiento, no hubo recaídas. Son pocos los casos reportados de estas fístulas en la edad pediátrica.

Embolia colesterínica en miembro superior izquierdo asociado a fístula arteriovenosa / Cholesterol embolism in the left upper limb associated with venous artery fistula

RESUMEN El embolismo por cristales de colesterol (ECC) es una complicación de la enfermedad arterioesclerótica en la que el desprendimiento de fragmentos de placa de ateroma, principalmente de grandes arterias, provoca oclusión de pequeños vasos. Esta entidad, también llamada ateroembolia o síndrome de los dedos del pie azules, es más frecuente en pacientes de edad avanzada y después de procedimientos invasivos intravasculares. Se manifiesta con cianosis, livedo reticularis, necrosis y úlceras asociado a manifestaciones renales y gastrointestinales. Se presenta un paciente trasplantado renal y portador de fístula arteriovenosa trombosada izquierda con ateroembolia localizada en mano homolateral.

ABSTRACT The cholesterol crystal embolism (ECC) is a complication of arteriosclerotic disease in which the detachment of fragments of atheromatous plaque mainly from large arteries, causes occlusion of small vessels. This entity, also called atheroembolism or blue toe syndrome, is more common in elderly patients and after intravascular invasive procedures. It manifests with cyanosis, livedo reticularis, necrosis and ulcers associated with renal and gastrointestinal manifestations. We present a renal transplant patient with a left thrombosed arteriovenous fistula with atheroembolism located in homolateral hand.

Cerebellar Arteriovenous Malformation with Coexistent Hemangioblastoma.

BACKGROUND: This is a case of a man aged 40 years with a past medical history of smoking, hypertension, polycythemia vera, intellectual disability, and schizophrenia who presented with generalized headaches, progressive loss of balance, and visual disturbance for 1 month. CASE DESCRIPTION: Head computed tomography and magnetic resonance imaging revealed a right cerebellar hematoma associated to heterogenous lesion with cystic components and flow-voids in the right cerebellar hemisphere. A ventriculoperitoneal shunt was placed with partial improvement of symptoms. Further vascular studies confirmed presence of a vascular nidus with significant arteriovenous shunting. The patient later required intervention for cerebellar arteriovenous malformation (AVM) removal. Microscopic evaluation of the lesion showed the AVM nidus, as well as large, vacuolated stromal cells and numerous thin-walled vessels. Immunostaining with inhibin and S-100 highlighted the stromal cells with numerous lipid-containing vacuoles. The earlier mentioned findings were consistent with the diagnosis of an AVM with coexistent hemangioblastoma of the right cerebellar hemisphere. CONCLUSIONS: Coexistence of hemangioblastomas and AVMs are extremely rare, and only 3 cases have been reported previously in the literature.

Tratamento endovascular da hipertensão portal e da hemorragia digestiva recorrente e secundária à síndrome da fístula arterioportal: complicação tardia de trauma abdominal penetrante / Endovascular treatment of portal hypertension and recurrent digestive hemorrhage secondary to arterioportal fistula syndrome: late complication of penetrating abdominal trauma

Resumo A síndrome da fístula artério-portal (FAP) é uma rara e reversível causa de hipertensão portal pré-sinusoidal, ocasionada pela comunicação de uma artéria visceral com o sistema venoso portal. A maioria dos pacientes é assintomática, mas quando desenvolvem sintomas, estes são mais relacionados com sangramento gastrointestinal, ascite, insuficiência cardíaca congestiva e diarreia. Este desafio terapêutico apresenta um caso de FAP decorrente de ferimento antigo por arma branca e subsequente evolução clínica desfavorável, com grave desnutrição e frequentes hemorragias digestivas. O caso foi solucionado através de oclusão da FAP por meio de tratamento endovascular.

Abstract The arterioportal fistula (APF) syndrome is a rare and reversible cause of pre-sinusoidal portal hypertension, caused by communication between a visceral artery and the portal venous system. Most patients are asymptomatic, but when they do develop symptoms, these are mainly related to gastrointestinal bleeding, ascites, congestive heart failure, and diarrhea. This therapeutic challenge presents a case of APF caused by a 20-year-old stabbing injury with unfavorable late clinical evolution, including significant malnutrition and severe digestive hemorrhages. The patient was treated using an endovascular procedure to occlude of the fistula.

Fatores de risco para pacientes com falência recorrente de fístula arteriovenosa / Risk factors for patients showing arteriovenous fistula recurrent failure / Factores de riesgo para pacientes con falencia recorrente de fiesta arteriovenosa

Objetivo: Identificar os fatores de risco/condicionantes para a falência da fístula arteriovenosa e analisar os cuidados necessários para manutenção da fístula arteriovenosa. Métodos: Estudo piloto realizado com 10 participantes com histórico de falência de fístula arteriovenosa, com dados coletados por meio de formulário e analisados por estatística descritiva, aceito pelo Comitê de Ética em Pesquisa do Hospital Universitário Pedro Ernesto, com número do CAAE nº 64150117.2.0000.5259. Resultados: A idade média foi de 57,3 anos. A hipertensão arterial foi a doença prévia mais comum encontrada entre os participantes. A hipotensão e as punções repetidas foram os fatores de risco/condicionantes com maior ocorrência. Conclusão: a maioria dos participantes possuíam baixa escolaridade e informaram ter tido alguma complicação na FAV. A hipotensão como fator condicionante para falência das FAV, permaneceu de forma frequente entre os participantes. Observou-se que grande parte já realizava tratamento dialítico prévio

Objective: The study's purpose has been to identify the risk/conditioning factors for Arteriovenous Fistula Failure (AVF), and also to analyze the care required for handling the arteriovenous fistula. Methods: It is a pilot study that was carried out with 10 participants showing a history of AVF. The data were collected through a form and analyzed by descriptive statistics. This research was accepted by the Research Ethics Committee from the Pedro Ernesto University Hospital, under the Certificado de Apresentação para Apreciação Ética (CAAE) [Certificate of Presentation for Ethical Appreciation] No. 64150117.2.0000.5259. Results: The average age was 57.3 years old. Arterial hypertension was the most common prior disease among the participants. Hypotension and repeated punctures were the most frequent risk/conditioning factors. Conclusion: A relevant percentage of the participants had little education and reported having had some complication in the AVF. Hypotension, as a conditioning factor for AVF failure, remained frequent among the participants. It was observed that a large part of the participants have undergone dialysis treatment previously

Objetivo: Identificar los factores de riesgo / condicionantes para la quiebra de la fístula arteriovenosa y analizar los cuidados necesarios para el mantenimiento de la fístula arteriovenosa. Métodos: Estudio piloto realizado con 10 participantes con historial de fallo de fístula arteriovenosa, con datos recogidos por medio de formulario y analizados por estadística descriptiva, aceptado por el Comité de Ética en Investigación del Hospital Universitario Pedro Ernesto, con número del CAAE nº 64150117.2.0000.5259 . Resultados: La edad media fue de 57,3 años. La hipertensión arterial fue la enfermedad previa más común entre los participantes. La hipotensión y las punciones repetidas fueron los factores de riesgo / condicionantes con mayor ocurrencia. Conclusión: la mayoría de los participantes tenían baja escolaridad e informaron haber tenido alguna complicación en la FAV. La hipotensión como factor condicionante para la quiebra de las FAV, permaneció de forma frecuente entre los participantes. Se observó que gran parte ya realizaba tratamiento dialítico previo

Growth of Pulmonary Arteriovenous Malformations in Pediatric Patients with Hereditary Hemorrhagic Telangiectasia.

The evolution of pulmonary arteriovenous malformations (PAVMs) over time in children with hereditary hemorrhagic telangiectasia (HHT) is not well-defined. Herein we demonstrate that, although new PAVMs did not evolve in children with HHT, existing PAVMs exhibit quantitative growth over time highlighting the need for ongoing follow-up throughout childhood.

Acceso venoso para hemodiálisis y repercusión crónica en el sistema cardiovascular / Hemodialysis venous access and chronic impact on cardiovascular system

En el tratamiento de enfermos renales en fase terminal, se realizan accesos vasculares para hemodiálisis. Son hechos habitualmente, en las venas de los miembros superiores, especialmente la técnica de Brecia y Cimino (fístula arteriovenosa latero lateral de la cefálica y la radial en la muñeca). La mayor complicación, directamente relacionada con un flujo excesivo por la fístula arteriovenosa, es la insuficiencia cardíaca congestiva. Se presenta el caso de un paciente con una fístula arteriovenosa (iatrogénica) que causó una insuficiencia cardiaca congestiva. El paciente, hipertenso conocido, tuvo un acceso venoso de más de 10 años de evolución (por un aparente diagnóstico y para una futura hemodiálisis que nunca fue efectuada). Acudió a consulta con disnea y edemas periféricos. Al examen físico se encontró la tensión arterial en 160 y 100 mm Hg, signos clínicos de cardiomegalia, edemas periféricos, ingurgitación yugular y hepatomegalia. Se palpó un thrill sistodiastólico en la muñeca izquierda, donde presentaba una cicatriz. Pudo observarse marcada dilatación y endurecimiento de todas las venas superficiales del plexo braquial de ese lado, (arterialización del árbol venoso del miembro superior izquierdo hasta las venas superficiales del hemitórax). Se diagnosticó una insuficiencia cardiaca de gasto alto, mejoró con el tratamiento habitual, pero continuó con la malformación venosa adquirida. Fue un caso muy llamativo, que muestra una complicación poco frecuente de los accesos venosos para hemodiálisis y también una causa mencionada, pero escasamente vista, de insuficiencia cardiaca de gasto elevado(AU)

In the treatment of renal patients in terminal phase. Vascular accesses are used for hemodialysis. They are usually performed in the veins of the upper limbs, especially using Brecia and Cimino technique (lateral arteriovenous fistula of the cephalic and radial at the wrist). The major complication, directly related to an excessive flow of arteriovenous fistula, is congestive heart failure. We present the case of a patient with an arteriovenous (iatrogenic) fistula that caused a congestive heart failure. He is hypertensive and had venous access for over 10 years of evolution (for an apparent diagnosis and for future hemodialysis, which was never performed). He went to the clinic with dyspnea and peripheral edema. Physical examination revealed blood pressure of 160 and 100 mm Hg, clinical signs of cardiomegaly, peripheral edema, jugular engorgement and hepatomegaly. We found a systodiastolic thrill on his left wrist, where there is a scar. A marked dilation and hardening of all the superficial veins of the brachial plexus on that side was observed, that is arterialization of the venous tree of the left upper limb to the superficial veins of hemitorax. The diagnosis was high output heart failure. He improved with the usual treatment, but the acquired venous malformation continued in an iatrogenic manner. It was a very striking case because of the infrequent complication of venous accesses for hemodialysis and because for rarely seen elevated heart failure(AU)