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1.
Am J Case Rep ; 25: e942839, 2024 Mar 31.
Article in English | MEDLINE | ID: mdl-38555492

ABSTRACT

BACKGROUND An arteriovenous malformation (AVM) is an abnormal connection between an artery and a vein, bypassing the capillary network. An AVM of the superficial temporal artery (STA) can occur after trauma, iatrogenic injury, infection, or spontaneously. Spontaneous, or iatrogenic, presentations of STA AVM are thought to be rare, with very few reported cases. Symptoms include local pain, headache, tinnitus, or paresthesia, in addition to a palpable mass associated with thrill on palpation. Options for diagnosis include intra-arterial angiography, doppler ultrasound, magnetic resonance angiography (MRA), and computed tomography angiography (CTA). Current management options include surgical excision, ligation, and embolization; however, it is unknown which treatment is superior in terms of recurrence and which carries a lower risk of complications. CASE REPORT We present a case of a spontaneous STA AVM in a 76-year-old woman with past medical history significant for seasonal allergies and hyperlipidemia, who presented with pulsatile tinnitus and a palpable, tender mass located to the left temporal area. The mass had been present for several years, with gradual increase in size two to three years prior to presentation. She denied any history of trauma or procedure prior to presentation of the pulsatile mass. She underwent open excision with complete resolution of symptoms and no recurrence at 11-month follow-up. CONCLUSIONS AVM of the STA is a condition that can occur secondary to trauma, infection, iatrogenic injury, or spontaneously. Spontaneous, or iatrogenic, presentations of STA AVM are thought to be rare, with very few cases documented in the literature. Surgical treatment remains the standard of management, with options including surgical excision, ligation, or embolization.


Subject(s)
Arteriovenous Malformations , Temporal Arteries , Female , Humans , Aged , Temporal Arteries/surgery , Temporal Arteries/abnormalities , Arteriovenous Malformations/surgery , Magnetic Resonance Angiography , Tomography, X-Ray Computed , Iatrogenic Disease
2.
Plast Reconstr Surg ; 148(1): 19e-27e, 2021 Jul 01.
Article in English | MEDLINE | ID: mdl-34003805

ABSTRACT

BACKGROUND: Anatomical knowledge of the zygomatico-orbital artery and its most relevant clinical applications is essential for ensuring the safety of filler injection into the temporal region. The purpose of this study was to provide the precise position, detailed course, and relationship with surrounding structures of the zygomatico-orbital artery. METHODS: Fifty-eight patients who underwent head contrast-enhanced three-dimensional computed tomography and 10 fresh frozen cadavers were investigated. RESULTS: The zygomatico-orbital artery was identified in 93 percent of the samples in this work. Ninety-four percent of the zygomatico-orbital arteries derived directly from the superficial temporal artery, and the remaining arteries started from the frontal branch of the superficial temporal artery. According to the origin of the zygomatico-orbital artery, it was classified into type I and type II. Type I arteries were then classified into three subtypes. The trunk of the zygomatico-orbital artery was located between the deep temporal fascia and the superficial temporal fascia. Deep branches of the zygomatico-orbital artery pierced the superficial layer of the deep temporal fascia. The zygomatico-orbital artery originated from 11.3 mm in front of the midpoint of the apex of the tragus, and most of its trunks were located less than 20.0 mm above the zygomatic arch. The mean diameter of the zygomatico-orbital artery was 1.2 ± 0.2 mm. There were extensive anastomoses between the zygomatico-orbital artery and various periorbital arteries at the lateral orbital rim. CONCLUSION: The precise anatomical knowledge of the zygomatico-orbital artery described in this study could be helpful for cosmetic physicians for improving the safety of temporal augmentation.


Subject(s)
Anatomic Variation , Cosmetic Techniques/adverse effects , Forehead/blood supply , Temporal Arteries/abnormalities , Vascular System Injuries/prevention & control , Adult , Aged , Cadaver , Contrast Media/administration & dosage , Dermal Fillers/administration & dosage , Female , Humans , Imaging, Three-Dimensional , Injections, Subcutaneous/adverse effects , Male , Middle Aged , Orbit/blood supply , Temporal Arteries/diagnostic imaging , Temporal Arteries/injuries , Tomography, X-Ray Computed , Vascular System Injuries/etiology , Zygoma/blood supply
4.
Int J Med Sci ; 16(10): 1377-1385, 2019.
Article in English | MEDLINE | ID: mdl-31692910

ABSTRACT

The superficial temporal artery (STA) plays a very important role in neurovascular diseases and procedures. However, until now, no comprehensive review of the role of STA in neurovascular diseases from a neurosurgical perspective has ever been published. To review research on the clinical importance of STA in neurovascular diseases, a literature search was performed using the PubMed database. Articles were screened for suitability and data relevance. This paper was organized following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. According to the literature, STA is one of the terminal branches of the external carotid artery and can give off scalp, muscle, and transosseous branches. STA-middle cerebral artery (MCA) bypass is very useful for intracranial ischemic diseases, including moyamoya disease, chronic ICA and MCA insufficiency, and even acute ischemic stroke. For intracranial complex aneurysms, STA bypass remains a major option that can serve as flow replacement bypass during aneurysmal trapping or insurance bypass during temporary parent artery occlusion. Occasionally, the STA can also be involved in dural AVFs (DAVFs) via to its transosseous branches. In addition, the STA can be used as an intraoperative angiography path and the path to provide endovascular treatments. Therefore, STA is a very important artery in neurovascular diseases.


Subject(s)
Cerebral Revascularization/methods , Neurosurgical Procedures/methods , Temporal Arteries/abnormalities , Temporal Arteries/surgery , Arteriovenous Fistula/etiology , Arteriovenous Fistula/surgery , Brain Ischemia/surgery , Cerebral Angiography/methods , Humans , Intracranial Aneurysm/surgery , Intraoperative Care/methods , Middle Cerebral Artery/surgery , Stroke/surgery , Temporal Arteries/diagnostic imaging
5.
J Med Invest ; 66(1.2): 209-210, 2019.
Article in English | MEDLINE | ID: mdl-31064944

ABSTRACT

An arteriovenous fistula of the superficial temporal artery (STA) is a direct and abnormal communication between the STA, feeding artery, and superficial temporal vein, draining veins that bypass the capillary network. Several cases of trauma-induced or iatrogenic-induced arteriovenous fistula (AVF) of the STA have been reported ; however, spontaneous AVF of the STA not associated with trauma or medical treatment are extremely rare. Herein, we present a case of spontaneous AVF of the STA diagnosed in old age. J. Med. Invest. 66 : 209-210, February, 2019.


Subject(s)
Arteriovenous Fistula/etiology , Temporal Arteries/abnormalities , Aged , Humans , Male
6.
Ophthalmic Plast Reconstr Surg ; 35(3): e57-e59, 2019.
Article in English | MEDLINE | ID: mdl-30844909

ABSTRACT

Intraorbital arteriovenous fistula is a rare vascular disease characterized by an acquired arteriovenous communication without direct cavernous sinus involvement. Intraorbital arteriovenous fistula may develop slowly and present similarly to other insidious orbitopathies, such as carotid-cavernous fistula. The authors present a case of a superficial temporal artery to superior ophthalmic vein fistula arising in the absence of trauma or prior surgery. This is the first report of a spontaneous intraorbital arteriovenous fistula arising between these vessels and further describes the rare occurrence of intraorbital arteriovenous fistula.


Subject(s)
Arteriovenous Fistula/diagnosis , Cavernous Sinus/abnormalities , Intracranial Arteriovenous Malformations/diagnosis , Temporal Arteries/abnormalities , Aged, 80 and over , Arteriovenous Fistula/therapy , Cerebral Angiography , Embolization, Therapeutic/methods , Female , Humans , Intracranial Arteriovenous Malformations/therapy , Tomography, X-Ray Computed
9.
Turk Neurosurg ; 27(5): 671-681, 2017.
Article in English | MEDLINE | ID: mdl-27593841

ABSTRACT

The middle cerebral artery (MCA) covers a large part of the cerebral hemispheres and is therefore exposed during surgical intervention in this area. Aspects of cerebral branches tend to vary, different branching patterns can be described, and several anomalies can be observed. Knowledge of these variations and anomalies is important and can be helpful to neurosurgeons and clinicians. The aim of this manuscript was to review the available literature on the cortical branches, branching pattern and anomalies of the MCA, to identify the gaps in the literature, and to fill these gaps by including the results of a pilot study. Twenty hemispheres were perfused with colored silicone and the MCA was dissected. For the cortical branches, the diameter, length, presence, duplication and origins were noted. Most commonly duplicated was the anterior parietal artery in 30.0%, and most commonly absent was the common temporal artery in 65.0%. A detailed description on the origins is given. Criteria were described for the bifurcation subtypes and medial bifurcation (50.0%) was most commonly observed. No anomalies were observed. Aspects previously neglected of the MCA cortical branches were reported in the pilot study. The branching subtypes were identified and criteria are given. Illustrations of the different branching subtypes and anomalies are provided. Certain aspects of the MCA anatomy have been neglected, and future studies should give adequate descriptions of the MCA cortical branches, MCA branching pattern, and any anomalies observed.


Subject(s)
Middle Cerebral Artery/anatomy & histology , Temporal Arteries/anatomy & histology , Humans , Middle Cerebral Artery/abnormalities , Temporal Arteries/abnormalities
10.
J Emerg Med ; 51(5): 572-575, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27599616

ABSTRACT

BACKGROUND: Emergency bedside point-of-care ultrasound provides an extremely fast and cost-effective diagnostic modality for the diagnosis of vascular abnormalities, such as pseudoaneurysms. The cost-benefit and timing advantages of ultrasound are increasingly apparent when compared to more conventional diagnostic tests, such as computed tomography angiography and magnetic resonance angiography scans. CASE REPORT: A 33-year-old man with no medical history presented to our emergency department complaining of a constant, throbbing, left-sided headache over his temple with an associated mass. The physical examination revealed a 0.5-cm, tender, flesh-colored, pulsatile mass over his left temple. The tender mass was evaluated at the bedside by an emergency physician with a linear array L-14 probe on the ZONARE ultrasound system (ZONARE Medical Systems, Inc., Mountain View, CA). A small anechoic collection adjacent to the superficial temporal artery was identified with a sac containing flow in a prototypical "yin and yang" pattern. These findings were consistent with a superficial temporal artery pseudoaneurysm. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: We present this case report because of the implications of missing the diagnosis. Emergency physicians should be aware of the possible diagnosis of pseudoaneurysm of the temporal artery because of the plethora of head injuries that we evaluate on a regular basis. Missing the diagnosis can lead to delayed neurologic sequela and potential life-threatening bleeding in patients presenting with what appears to be a minor complaint.


Subject(s)
Aneurysm, False/diagnosis , Temporal Arteries/abnormalities , Ultrasonography/standards , Wounds and Injuries/complications , Adult , Aneurysm, False/surgery , Headache/etiology , Humans , Male , Point-of-Care Systems/trends , Temporal Arteries/physiopathology , Ultrasonography/instrumentation , Ultrasonography/methods
11.
J Craniofac Surg ; 27(4): 1065-7, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27213745

ABSTRACT

Aplasia cutis congenita with or without congenital anomalies is a rare congenital disorder most commonly involving the skin of the scalp, as well as the skull and dura.The etiology is uncertain, and several theories, including vascular accident intrauterine period, vascular anomaly, intrauterine infection, teratogen, and aminiotic adhesion, have been proposed. One theory is that lesions of the scalp are usually caused by vascular anomalies.The authors report on a patient with aplasia cutis congenita presenting with a huge skin and skull defect combined with aplasia of the superficial temporal artery, which was thought to be the etiology.


Subject(s)
Ectodermal Dysplasia/diagnosis , Temporal Arteries/abnormalities , Humans , Infant, Newborn , Male , Skull/diagnostic imaging , Temporal Arteries/diagnostic imaging , Tomography, X-Ray Computed
12.
Clin Rheumatol ; 35(7): 1817-22, 2016 Jul.
Article in English | MEDLINE | ID: mdl-26925851

ABSTRACT

The diagnosis of giant cell arteritis (GCA) is based on clinical grounds and confirmed by characteristic histological findings on temporal artery biopsy (TAB). Patients may be diagnosed with GCA based on clinical grounds only, despite negative histological findings. We aimed to investigate which baseline clinical and laboratory features best predict an ultimate diagnosis of giant cell arteritis among patients referred to TAB. We retrospectively analyzed 224 patients who underwent TAB in our hospital between 2000 and 2014. Patients were diagnosed with GCA if TAB was positive for GCA, or by clinical grounds only despite a negative biopsy, provided they fulfilled the American College of Rheumatology 1990 criteria. Baseline clinical and laboratory features were obtained from medical records. Predictors of an ultimate GCA diagnosis were investigated. Overall, 82 patients were diagnosed with GCA-57 had histological evidence of GCA and 25 were diagnosed with GCA despite a negative biopsy. One hundred and forty-two patients were not diagnosed with GCA. Predictors of an eventual diagnosis of GCA in a multivariate logistic regression analysis were headache (OR = 6; p < 0.001), jaw claudication (OR 4.5; p = 0.007), erythrocyte sedimentation rate (ESR) (OR = 1.5; p = 0.032) and platelet count (OR = 1.74; p = 0.004). Among patients referred to TAB, headache, jaw claudication, ESR, and thrombocyte levels are predictors for an ultimate diagnosis of GCA. These clinical and laboratory features should be considered when contemplating the diagnosis and treatment of GCA.


Subject(s)
Facial Pain/etiology , Giant Cell Arteritis/diagnosis , Headache/etiology , Temporal Arteries/abnormalities , Temporal Arteries/pathology , Adult , Aged , Aged, 80 and over , Biopsy , Blood Sedimentation , Female , Humans , Israel , Logistic Models , Male , Middle Aged , Multivariate Analysis , Retrospective Studies
17.
J Laryngol Otol ; 126(9): 923-7, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22874530

ABSTRACT

OBJECTIVE: We report an interesting case of a right temporal pre-auricular arteriovenous fistula (cirsoid aneurysm) causing intractable tinnitus successfully managed by transarterial n-butyl cyanoacrylate glue embolisation. CASE REPORT: A 52-year-old female presented with a one-year history of tinnitus and pulsatile swelling in the right pre-auricular region. A colour Doppler ultrasound test and magnetic resonance angiography revealed a high-flow scalp arteriovenous fistula with a feeder vessel from the distal superficial temporal artery, which drained into the corresponding, dilated, tortuous vein. The patient underwent diagnostic digital subtraction angiography. This was followed by transarterial embolisation of the fistula using a 50 per cent mixture of n-butyl cyanoacrylate glue and Lipiodol®, with manual distal venous occlusion. A successful outcome was achieved with instant relief of symptoms. CONCLUSION: Cirsoid aneurysms of the facial region, an uncommon cause of tinnitus, can be effectively managed by endovascular embolisation. This treatment obviates the need for surgery, which is associated with an increased risk of complications such as scarring, deformity and bleeding.


Subject(s)
Arteriovenous Fistula/complications , Embolization, Therapeutic/methods , Temporal Arteries/abnormalities , Tinnitus/etiology , Angiography/methods , Arteriovenous Fistula/diagnosis , Arteriovenous Fistula/therapy , Enbucrilate/therapeutic use , Ethiodized Oil/therapeutic use , Female , Humans , Middle Aged , Scalp/blood supply , Tinnitus/therapy , Treatment Outcome , Ultrasonography, Doppler, Color
18.
J Stroke Cerebrovasc Dis ; 21(8): 918.e1-5, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22721822

ABSTRACT

Recently, intraoperative indocyanine green (ICG) videoangiography has become a common technique for treating cerebrovascular diseases. We report a case of dural arteriovenous fistula (AVF) treated with direct surgery using intraoperative ICG videoangiography. A 41-year-old man with right hemiplegia caused by a left subcortical hemorrhage was transferred to our hospital. Digital subtraction angiography (DSA) revealed a left convexity parasagittal dural AVF. Surgical resection of the dural AVF was performed using step-by-step ICG videoangiography 4 times in each dissection procedure, which precisely delineated the structure of the dural AVF. After a circular incision of the dura around the fistular point, repeated ICG videoangiography identified the residual fistula between the pial artery from the middle cerebral artery and the draining vein. Complete disappearance of the AVF was confirmed by ICG videoangiography after this pial fistula was removed. Postoperative DSA revealed no residual AVF. Accurate detection of all fistular points and complete resection, including the dura mater and pial vessels, are necessary to avoid rebleeding caused by the residual dural AVF due to incomplete obliteration of the fistular points. Intraoperative ICG videoangiography could provide information on angiographically occult vascular malformation, such as pial fistulas, that cannot be detected by preoperative DSA. Our findings suggest that multistage intraoperative ICG videoangiography can be quite useful for complete resection of a dural AVF with angiographically occult pial fistula.


Subject(s)
Brain/blood supply , Central Nervous System Vascular Malformations/diagnosis , Central Nervous System Vascular Malformations/surgery , Cerebral Angiography/methods , Fluorescent Dyes , Indocyanine Green , Neurosurgical Procedures , Vascular Surgical Procedures , Video Recording , Adult , Angiography, Digital Subtraction , Central Nervous System Vascular Malformations/complications , Cerebral Veins/abnormalities , Cerebral Veins/surgery , Humans , Intracranial Hemorrhages/diagnosis , Intracranial Hemorrhages/etiology , Intraoperative Care , Male , Middle Cerebral Artery/abnormalities , Middle Cerebral Artery/surgery , Predictive Value of Tests , Temporal Arteries/abnormalities , Temporal Arteries/surgery , Tomography, X-Ray Computed
19.
Neurosurgery ; 67(2): 314-21, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20644416

ABSTRACT

BACKGROUND: The external carotid artery (ECA) anastomoses in many distal territories supplied by the internal carotid artery (ICA) and is an important source of collateral circulation to the brain. Stenosis of the ECA in ipsilateral ICA occlusion can produce ischemic sequelae. OBJECTIVE: To examine the effectiveness of ECA stenting in treating symptomatic ipsilateral ICA occlusion. METHODS: We retrospectively reviewed patient databases from 5 academic medical centers to identify all individuals who underwent ECA stenting after 1998. For all discovered cases, coinvestigators used a common submission form to harvest relevant demographic information, clinical data, procedural details, and follow-up results for further analysis. RESULTS: Twelve patients (median age, 66 years; range, 45-79 years) were identified for our cohort. Vessel disease involvement included severe ECA stenosis >or= 70% in 11 patients and ipsilateral ICA occlusion in all patients. Presenting symptoms included signs of transient ischemic attack, stroke, and amaurosis fugax. ECA stenting was associated with preservation of neurological status in 11 patients and resolution of symptoms in 5 patients at a median follow-up time of 26 months (range, 1-87 months; mean, 29 months). Symptomatic in-stent restenosis did not occur within any patient during the follow-up course. CONCLUSION: We found ECA stenting in symptomatic ipsilateral ICA disease to be a potentially effective strategy to preserve neurological function and to relieve ischemic symptoms. Further investigation with larger studies and longer follow-up periods is warranted to elucidate the true indications of this management strategy.


Subject(s)
Carotid Artery, External/surgery , Carotid Artery, Internal , Carotid Stenosis/surgery , Stents , Aged , Carotid Artery, External/pathology , Carotid Artery, Internal/pathology , Cerebrovascular Disorders/complications , Cohort Studies , Female , Follow-Up Studies , Humans , Magnetic Resonance Angiography , Magnetic Resonance Imaging , Male , Middle Aged , Middle Cerebral Artery/abnormalities , Prospective Studies , Retrospective Studies , Stents/adverse effects , Temporal Arteries/abnormalities , Tomography, X-Ray Computed , Treatment Outcome
20.
Congenit Anom (Kyoto) ; 50(1): 68-70, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20201971

ABSTRACT

The pinna is the second most common site for external ear vascular malformation in the head and neck. These malformations are relatively uncommon in adults and can pose difficult therapeutic challenges. We hereby present a case of a 69-year-old man with a congenital lesion in the right pinna consistent with an arteriovenous malformation. The lesion was complicated by ulceration and bleeding for 6 months prior to presentation. Resection of pinna was carried out, and satisfactory functional and esthetic results were obtained. There was no recurrence at 22 months of regular follow up.


Subject(s)
Arteriovenous Malformations , Ear Auricle/blood supply , Aged , Angiography , Arteriovenous Malformations/diagnostic imaging , Arteriovenous Malformations/surgery , Humans , Male , Temporal Arteries/abnormalities
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