Evaluation of a large adrenal carcinoma with 3D reconstruction of computed tomography images: A case report and literature review

2016 ◽  
Vol 24 (5) ◽  
pp. 665-671 ◽  
Author(s):  
Liang Chen ◽  
Xiaoyong Zeng ◽  
Shuang Li ◽  
Chengliang Gong ◽  
Ejun Peng ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Literature Review ◽  
3D Reconstruction ◽  
Adrenal Carcinoma ◽  
Computed Tomography Images

scholarly journals Idiopathic ovarian vein thrombosis causing pulmonary embolism: case report and literature review

2021 ◽  
Vol 49 (6) ◽  
pp. 030006052110106
Author(s):  
Wenrui Li ◽  
Saisai Cao ◽  
Renming Zhu ◽  
Xueming Chen
Keyword(s):  
Computed Tomography ◽  
Pulmonary Embolism ◽  
Abdominal Pain ◽  
Case Report ◽  
Literature Review ◽  
Ovarian Vein ◽  
Review Of Literature ◽  
Vein Thrombosis ◽  
Medical Disorder ◽  
Ovarian Vein Thrombosis

Ovarian vein thrombosis (OVT) is a rare medical disorder, which is most often found in the immediate postpartum period. OVT is rarely considered idiopathic. We report a case of idiopathic OVT with pulmonary embolism in a 33-year-old woman who presented with abdominal pain. Computed tomography and postoperative pathology confirmed the diagnosis of idiopathic OVT. To date, only 12 cases of idiopathic OVT have been reported. In this case report, we present a summary of these cases and a review of literature regarding management of idiopathic OVT.

scholarly journals Percutaneous transgluteal computed tomography-guided aspiration of obturator internus pyomyositis in adolescent athlete: A case report and literature review

2018 ◽  
Vol 13 (6) ◽  
pp. 1123-1127
Author(s):  
Anthony Chuprin ◽  
Nicholas Tyler Beavers ◽  
Victor Fong ◽  
Harlan Vingan ◽  
Abhimanyu Aggarwal
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Literature Review ◽  
Adolescent Athlete ◽  
Obturator Internus

scholarly journals A rare case of accessory maxilla: a case report and literature review of Tessier no. 7 clefts

2020 ◽  
Vol 48 (5) ◽  
pp. 030006052092568
Author(s):  
Ming Sun ◽  
Na Lv ◽  
Ya Xiao ◽  
Jiabin Li ◽  
Guangzhao Guan
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Rare Case ◽  
Clinical Presentation ◽  
Craniofacial Abnormalities ◽  
Supernumerary Teeth ◽  
Computed Tomography Images ◽  
Facial Clefts ◽  
Patient Prognosis ◽  
Patient’S History

Bilateral Tessier no. 7 clefts are rarely reported in the literature. Here, we describe the presence of accessory maxilla with supernumerary teeth in a patient who exhibited bilateral Tessier no. 7 clefts; the diagnosis was established based on the patient’s history, clinical presentation, and computed tomography images. A review of the available literature revealed 24 patients with Tessier no. 7 clefts from 2000 to 2020, including our patient. The most common clinical manifestation in patients with Tessier no. 7 clefts comprises bilateral facial clefts. Additionally, Tessier no. 7 clefts are more frequently found in boys or men, rather than in girls or women. The presence of an accessory maxilla with supernumerary teeth in a patient with bilateral Tessier no. 7 clefts is extremely rare. Early detection of craniofacial abnormalities is important, because it may influence patient prognosis and management.

scholarly journals Angioembolization of Scrotal Arteriovenous Malformations: A Case Report and Literature Review

2020 ◽  
Vol 2020 ◽  
pp. 1-8
Author(s):  
Ammar Mohammad ◽  
Wael Sahyouni ◽  
Taisser Almeree ◽  
Bayan Alsaid
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Literature Review ◽  
Digital Subtraction Angiography ◽  
Acute Pain ◽  
Arteriovenous Malformations ◽  
Duplex Ultrasound ◽  
Digital Subtraction ◽  
Acute Bleeding ◽  
Scrotal Mass

Arteriovenous malformations (AVMs) of the scrotum are rare lesions, usually diagnosed incidentally during the evaluation of scrotal masses or infertility. It could be presented with acute bleeding or acute pain. We are presenting a case of painless bilateral infiltrated scrotal mass (more advanced in the left side) developed dramatically over a year, no other symptoms existed. The diagnosis was made using duplex ultrasound (DUS), computed tomography arteriography (CTA), and digital subtraction angiography (DSA). Three sessions of angioembolization were performed and followed by surgical resection of the left side of the scrotum.

scholarly journals Severe and persistent facial nerve stimulation after cochlear implantation in a patient with cochlear–facial dehiscence: a case report

2021 ◽  
Vol 49 (11) ◽  
pp. 030006052110578
Author(s):  
Jingyuan Chen ◽  
Biao Chen ◽  
Lifang Zhang ◽  
Yongxin Li
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Facial Nerve ◽  
Inner Ear ◽  
Cochlear Implants ◽  
Nerve Stimulation ◽  
Cochlear Implantation ◽  
Computed Tomography Images ◽  
Ear Malformations ◽  
Facial Nerve Stimulation

Generally, cochlear implants (CIs) are effective in helping patients improve their hearing performance; however, some patients have poor hearing performance owing to facial nerve stimulation (FNS), which is often associated with cochlear anomalies. We report a case with a normal cochlea and severe and persistent FNS owing to cochlear–facial dehiscence (CFD) that affected the CI outcomes. Preoperatively, a careful review of the computed tomography images before CI surgery is necessary not only for patients with otosclerosis and inner ear malformations but also for patients with normal cochlear structures because facial nerve anomalies could be present.

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