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Radiology Case Reports

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https://read.qxmd.com/read/30766648/rare-malignant-glomus-tumor-of-the-stomach-with-liver-metastases
#1
Luca Toti, Tommaso Maria Manzia, Silvia Roma, Rosaria Meucci, Francesca Blasi, Amedeo Ferlosio, Giuseppe Tisone, Antonio Orlacchio
We report a case of a 72-year-old male admitted in our Unit with anemia and a 10 cm liver neoplasm. Computed tomography scan showed 2 lesions respectively in the II, III and, VIII segment of the liver. Surgical resection of the larger liver mass was performed and the tumor appeared as a solid-cystic mass and a diagnosis of malignant mesenchymal tumor not otherwise specified, was made. One month later a Computed tomography scan detected a dishomogeneous gastric mass, 6 cm in diameter, in the greater curvature, confirmed by esophagogastroduodenoscopy...
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30740191/pediatric-idiopathic-retroperitoneal-fibrosis
#2
Ashwin V Subramani, Gina M Lockwood, Jennifer G Jetton, Neha Dhungana, T Shawn Sato
Retroperitoneal fibrosis (RPF) is a very rare disease that is even more rare in the pediatric population. Even less common are idiopathic pediatric cases of retroperitoneal fibrosis, with a majority of reported pediatric retroperitoneal fibrosis cases being associated with secondary etiologies. We present an 11-year-old Caucasian female that was diagnosed with idiopathic retroperitoneal fibrosis using magnetic resonance imaging (MRI) to work-up severe bilateral hydronephrosis that was identified with retroperitoneal ultrasound...
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30733848/iliocaval-fistula-with-high-output-cardiac-failure
#3
Mohammed A Ismail, Tracy Van Meter
Fistulous communications between the common iliac arteries and inferior vena cava are very uncommon and usually occur as a result of trauma, aneurysmal rupture, or endovascular repair. They can present with signs of high output cardiac failure including hypotension, venous congestion, and pulmonary hypertension. This case outlines the utility of CTA in diagnosing iliocaval fistulas and the importance of considering this diagnosis in a patient with signs of right heart strain and high output cardiac failure.
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30733847/internal-jugular-vein-agenesis-a-rare-vascular-abnormality-and-incidental-finding-a-case-of-internal-jugular-vein-agenesis-in-a-52-years-old-male
#4
Laura Filograna, Antonello Calcagni, Giorgia Rossi, Carla Di Stefano, Emanuela Beninati, Alberto Collura, Roberto Floris
We report a case of vascular malformation arising from internal jugular vein discovered during radiological investigations for restaging of metastatic colon carcinoma of an adult male patient. Congenital absence of internal jugular vein is extremely uncommon. These developmental anomalies in general population are seen in about 0.05%-0.25%. The awareness of these vascular anomalies is extremely important to avoid unsafe complications, primarily in oncological patients, whom usually require the incannulation of neck veins for diagnostic procedures or intravenous therapy administration...
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30728880/radiography-of-chitayat-syndrome-in-an-infant-male
#5
Seong Hwan Shin, Emma StJoseph, Khalid Mannan, Khalid Khan
Chitayat syndrome is a rare genetic syndrome characterised by bilateral hyperphalangism, bronchomalacia, hallux valgus, and other facial dysmorphism including large anterior fontanelle, hypertelorism, and anteverted nostrils. Since the initial discovery, only few cases of Chitayat syndrome have been reported in the literature. Previous literatures showed the genetic link between 5 case reports, showing that a unique link of recurrent c.266A>G p.(Tyr89Cys) variant in the ERF gene may be the contributory genetic cause of Chitayat syndrome...
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30728879/dolichoectasia-of-the-right-internal-carotid-artery-diagnosed-incidentally-by-mr-angiography-in-a-17-year-old-girl
#6
Akira Uchino, Masayuki Ohira
Dolichoectasia of the cerebral artery, a rare disorder of arterial elongation, dilatation, and tortuosity, usually involves the vertebrobasilar system in elderly patients with hypertension and is associated with the development of atherosclerosis in the aging process. We present a very rare case in a 17-year-old girl with multiple sclerosis of dolichoectasia of the supraclinoid segment of the internal carotid artery that was found incidentally on magnetic resonance angiography and seems to represent a congenital arterial malformation...
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30728878/multimodality-appearance-of-multiple-endocrine-neoplasia-type-1-a-case-report
#7
John Monge, Daniel Homuth, Loren Zuiderveld
Multiple endocrine neoplasia type 1 is a rare autosomal dominant disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary, and enteropancreatic endocrine cells. We present the clinical details of a patient with diarrhea, nephrolithiasis, erectile dysfunction, and new onset abdominal pain, as well as a discussion of the etiology, pathophysiology, and classical imaging findings of this condition.
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30701012/round-pneumonia-due-to-chlamydia-pneumoniae-in-a-child
#8
Goro Koinuma, Masayoshi Shinjoh, Tomoka Kageyama, Maki Nakazawa, Isamu Kamimaki
Round pneumonia is a disease commonly recognized in the pediatric age group, especially under the age of 8 years. Streptococcus pneumoniae is the most common agent causing this characteristic type of pneumonia. We herein report a case of a 6-year-old boy with only mild cough and low-grade fever who was then diagnosed with round pneumonia due to Chlamydia pneumoniae . He had multiple round opacities in the right lower lung field, and the symptoms subsided soon after oral administration of antibiotics.
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30701011/breast-involvement-in-mixed-connective-tissue-disease
#9
Ross Varma, Sandor Szilagyi, Manju Harshan
To date, mammographic involvement in mixed connective tissue disease has not been described in the literature to the authors' knowledge. In addition, only 2 case reports have described panniculitis in mixed connective tissue disease. We present a patient with mixed connective tissue disease with coarse sheet-like calcifications on mammography bilaterally, which increased over time corresponding to rise in levels of anti-dsDNA. Biopsy showed fat necrosis with calcifications, chronic inflammation and fibrosis, vasculitis, as well as CD3, CD4, and CD8+ T cells and CD20+ B cells...
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30701010/breast-hemangioma-in-a-male-patient-report-of-a-case
#10
Sebastian Isaza Zapata, Ricardo Uribe González, Carlos Mario González Vasquez
Breast hemangioma is a rare benign tumor in female and extremely rare in males. They are part of vascular tumors. Here, we described the case of a male patient who had a breast hemangioma for 30 years that was diagnosed incidentally in a thorax and abdomen tomography. We briefly review epidemiology, histopathology, clinical, and imaging findings related to breast hemangioma.
April 2019: Radiology Case Reports
https://read.qxmd.com/read/30766647/paucisymptomatic-pulmonary-and-right-ear-tuberculosis-in-young-woman-suffering-from-anorexia-and-bulimia-nervosa
#11
Francesco Giuseppe Garaci, Erald Vasili, Francesco Bocchinfuso, Adriano Lacchè, Vittorio Nardone, Carlo Di Donna, Luigi Spiritigliozzi, Roberto Floris
Nowadays tuberculosis has become a reemerging infectious disease due to the many forms of immunodeficiency. Patients with eating disorders like anorexia nervosa and bulimia are a susceptible group due to the immune impairment correlated with severe malnutrition and their prevalence and incidence is growing. We describe the case of a 31-year-old woman, with long-standing history of anorexia nervosa and bulimia, diagnosed with advanced pulmonary tuberculosis. This case underlines the importance on never neglecting even the slightest symptoms in patients with malnutrition and never excluding this pathology without a proper investigation...
March 2019: Radiology Case Reports
https://read.qxmd.com/read/30766646/confusing-radiographic-appearance-of-a-central-venous-split-tip-hemodialysis-catheter
#12
Priya Sarv, Kao C Simon
Long-term cuffed hemodialysis catheters are being increasingly used in the management of patients with chronic kidney disease. These tunneled catheters are available in different types and characteristics. Patients undergo imaging, primarily chest radiographs to confirm the position of the catheter tip. It is essential to be aware of the normal imaging appearances of these catheters as they may simulate pathological appearance due to the shape of their tips. This knowledge will help avoid misdiagnosis and unnecessary medical interventions...
March 2019: Radiology Case Reports
https://read.qxmd.com/read/30766645/remote-cerebellar-hemorrhage-a-case-report
#13
Adil Omer, Ester Engelman, Khushbir Bath, Alan V Krauthamer, Leszek Pisinski
Remote Cerebellar Hemorrhage is a rare entity that manifests spontaneously after supratentorial craniotomy and spinal surgeries. We present a 53-year-old male who was admitted due to subdural hematoma along the left frontoparietotemporal convexity. After treatment of the subdural hematoma with craniotomy and evacuation, he developed remote cerebellar hemorrhage 1 week later. Brain computed tomography demonstrated the zebra sign. Follow-up imaging showed complete recovery without any neurologic symptoms or signs...
March 2019: Radiology Case Reports
https://read.qxmd.com/read/30705710/ethmoid-pneumatization-and-a-large-frontal-orbital-ethmoid-mucocele
#14
Mainak Dutta
Frontal-orbital-ethmoid mucocele is a slow-growing retention cyst of the fronto-ethmoid complex secondary to blockage of the sinus ostia. It may produce significant disfigurement of the periorbital region necessitating surgical intervention. Prior to surgery, it is imperative to study the mucocele's extent through the variable patterns of ethmoid pneumatization as evident from clinical, imaging (computed tomogram) and endoscopic evaluation. This is illustrated in a case study of a 41-year-old woman presenting with fullness below the right eyebrow, progressive proptosis, and gaze restriction...
March 2019: Radiology Case Reports
https://read.qxmd.com/read/30705709/association-of-klippel-feil-syndrome-dandy-walker-malformation-spina-bifida-a-case-report
#15
Alessio Pirino, Maria Alessandra Sotgiu, Erich Cosmi, Andrea Montella, Pasquale Bandiera
Klippel-Feil syndrome is a congenital malformation characterized by the fusion of at least 2 cervical vertebrae. It may occur in association with other clinical syndromes and disorders. We describe a case of prenatal diagnosis of a Klippel-Feil syndrome with Dandy-Walker malformation, and spina bifida, proved by ultrasound examination. A postmortem x-ray and autopsy were performed in a female fetus of 16 + 6 weeks of gestation: several malformations have been discovered. To the best of our knowledge, no similar cases have been reported in the medical literature...
March 2019: Radiology Case Reports
https://read.qxmd.com/read/30627299/superior-bearing-dislocation-in-a-unicompartmental-total-knee-prosthesis
#16
Thea De Geus, Terence Farrell, Eoin Kavanagh
The mobile bearing Oxford Unicompartmental Knee Prosthesis (OUKP) is the most commonly used treatment of osteoarthritis confined to 1 compartment of the knee. Dislocation of the mobile bearing is an uncommon but recognized complication of the OUKP. Patients typically present with severe pain and reduced range of motion of the affected knee. Radiological evaluation of OUKP can be challenging and requires knowledge of the prosthesis components and common complication patterns. Dislocation of the bearing can easily be overlooked on plain radiographs as the bearing is radiolucent, distinguished only by radiopaque markers...
March 2019: Radiology Case Reports
https://read.qxmd.com/read/30627298/ct-guided-percutaneous-cryoablation-of-an-osteoid-osteoma-of-the-rib-%C3%A2
#17
Eric Basappa, Joshua Rabang, William Anderson, Randy Richardson, Ryan Scott
An osteoid osteoma is a benign bone tumor that arises from osteoblastic dysfunction and usually presents as nonspecific, nocturnal pain located in the diaphysis of long bones, with <1% occurring in the ribs. It is most commonly treated with nonsteroidal anti-inflammatory drugs or merely observed; when these treatments do no prove efficacious, either open surgery or interventional ablation are pursued. Herein, we report a rare case of an osteoid osteoma located in the rib of a 19-year-old male that was histologically diagnosed through computed tomography (CT)-guided biopsy...
March 2019: Radiology case reports
https://read.qxmd.com/read/30627297/a-case-of-post-angiography-subdural-collection-contrast-enhancement-time-course-of-attenuation-reduction
#18
Abhi Jain, Seyedmehdi Payabvash
The leakage of contrast material into the subdural space following intra-arterial or intravenous administration can present as hyperattenuating subdural collections on noncontrast head computed tomography (CT) scan, mimicking subdural hematomas. Such a finding can potentially initiate erroneous intervention or hinder thromboprophylaxis treatment. We report the time course of attenuation changes in enhancing subdural collections of a patient with suspected stroke following percutaneous coronary intervention...
March 2019: Radiology Case Reports
https://read.qxmd.com/read/30627296/splenic-angiosarcoma-diagnosed-on-bone-marrow-biopsy-case-report-and-literature-review
#19
Asaph C J Levy, Miriam DeFilipp, Morgan Blakely, Saeed Asiry, Susan Jormark, Allen Goodman
Primary splenic angiosarcoma carries a poor prognosis and is among the rarest forms of malignancy. An overwhelming majority of patients with splenic angiosarcoma will develop metastases. However, osseous metastatic disease is rare. We present an 83 year old hispanic female who was diagnosed with primary splenic angiosarcoma on bone marrow biopsy performed for a hematologic workup. We highlight key historical, laboratory, imaging, and pathological features of splenic angiosarcoma. The synthesis of both imaging features and clinical history is essential for establishing early diagnosis in these patients...
March 2019: Radiology Case Reports
https://read.qxmd.com/read/30627295/endovascular-management-of-the-peripherally-inserted-central-venous-catheter-iatrogenic-pinch-off-syndrome-a-case-report
#20
Sergey V Vlasenko, Maksim V Agarkov, Anton A Khilchuk, Sergey G Scherbak, Andrey M Sarana, Evgeniy G Karmazanashvili, Linda P Kalinina, Vladislav G Volkov
The recent increase in the number of patients with implanted peripherally inserted central catheters (PICCs) requires physicians to be familiar with rare and unusual complication-pinch-off syndrome (POS). We present a case of a 40-years-old female with human epidermal growth factor receptor type 2 (HER2)-positive breast cancer and implanted Groshong PICC (BARD). The patient was admitted for an elective chest and abdomen CT angiography control after finishing her trastuzumab and paclitaxel chemotherapy course a month earlier...
March 2019: Radiology case reports
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