Successful Endovascular Treatment of a Traumatic Cervical Arteriovenous Fistula After a Carotid Paraganglioma Resection: A Case Report.

Traumatic cervical arteriovenous fistulas are rare, accounting for only 4% of all arteriovenous fistulas. They can be caused by penetrating, or rarely, blunt trauma, resulting in high-pressure arterial blood draining directly into a vein, decreasing distal perfusion. They are seldom reported as a complication of a carotid paraganglioma surgical resection. Historically, arteriovenous fistulas were treated initially conservatively, after that, surgically; nowadays, endovascular treatment, when feasible, is the preferred method as it offers advantages over surgery. This case report describes a rare traumatic cervical arteriovenous fistula that developed after a carotid paraganglioma resection and was successfully treated using coils and Onyx embolic agent via endovascular embolization. After successful embolization, the patient had a smooth recovery and remained stable. In conclusion, vascular injury seems to be the only constant in all acquired cervical arteriovenous fistulas independent of the trauma mechanism; and endovascular treatment, when feasible, is preferred over surgery as it offers superior advantages.

Epithelioid hemangioendothelioma of the parotid gland: a case report in an unusual location with a review of the literature / Hemangioendotelioma epitelioide de la glándula parótida: reporte de un caso de una localización inusual y revisión de la literatura

Epithelioid hemangioendothelioma (EHE) is a malignant vascular tumor that usually affects the liver, lung, bone and deep soft tissues of the extremities or trunk. To our knowledge, only 3 cases in the parotid gland have been reported to date. We report a case of a 62-year-old woman who presented with a 1-year history of a slow-growing, painless mass over the left mandibular angle. Imaging studies showed a 2cm mass over the left parotid gland with peripheral calcifications. The patient underwent a superficial parotidectomy. Sections displayed neoplastic epithelioid cells with cytoplasmic vacuoles containing erythrocytes, surrounded by a myxohyaline stroma. Immunohistochemistry was positive for CD31, CD34, ERG, and factor VIII, but negative for cytokeratin AE1/AE3, CK7, EMA, SMA, and S100. The findings were those of an EHE involving the parotid gland. This case demonstrates an EHE in a rare location and emphasizes the need to consider this tumor when diagnosing uncommon soft tissue tumors of salivary glands

El hemangioendotelioma epitelioide (HEE) es un tumor vascular maligno, que generalmente afecta el hígado, los pulmones, los huesos y los tejidos blandos profundos de las extremidades o el tronco. Por lo que sabemos, solo 3 casos reportados en la literatura han descrito este tumor en la glándula parótida. Presentamos el caso de una mujer de 62 años que presentó una historia de un año, de una masa indolora, de crecimiento lento sobre el ángulo mandibular izquierdo. Los estudios de imagen mostraron una masa de 2cm sobre la glándula parótida izquierda con calcificaciones periféricas. La paciente se sometió a una parotidectomía superficial. Los cortes mostraron células epitelioides neoplásicas con vacuolas citoplasmáticas que contenían eritrocitos, rodeadas por un estroma mixohialino. Se demostró mediante técnicas de inmunohistoquímica positividad en la celularidad neoplásica para CD31, CD34, ERG y factor VIII, pero negatividad para la citoqueratina AE1/AE3, CK7, EMA, SMA y S100. Estos hallazgos fueron los de un HEE comprometiendo la glándula parótida. Este caso demuestra un HEE en una localización rara y enfatiza la necesidad de considerar este tumor al diagnosticar tumores raros de tejidos blandos de glándulas salivales

Epithelioid hemangioendothelioma of the parotid gland: A case report in an unusual location with a review of the literature.

Epithelioid hemangioendothelioma (EHE) is a malignant vascular tumor that usually affects the liver, lung, bone and deep soft tissues of the extremities or trunk. To our knowledge, only 3 cases in the parotid gland have been reported to date. We report a case of a 62-year-old woman who presented with a 1-year history of a slow-growing, painless mass over the left mandibular angle. Imaging studies showed a 2cm mass over the left parotid gland with peripheral calcifications. The patient underwent a superficial parotidectomy. Sections displayed neoplastic epithelioid cells with cytoplasmic vacuoles containing erythrocytes, surrounded by a myxohyaline stroma. Immunohistochemistry was positive for CD31, CD34, ERG, and factor VIII, but negative for cytokeratin AE1/AE3, CK7, EMA, SMA, and S100. The findings were those of an EHE involving the parotid gland. This case demonstrates an EHE in a rare location and emphasizes the need to consider this tumor when diagnosing uncommon soft tissue tumors of salivary glands.