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2.
Radiographics ; 42(5): 1265-1282, 2022.
Article de Anglais | MEDLINE | ID: mdl-35960666

RÉSUMÉ

The lymphatic system plays an important role in balancing fluid compartments in the body. It is disrupted by various disease processes in the thorax, including injury to the thoracic lymphatic duct after surgery, as well as malignancy and heart failure. Because of the small size of lymphatic vessels, imaging of the lymphatics is relatively difficult, and effective imaging methods are still being optimized and developed. The standard of reference for lymphatic imaging has been conventional lymphangiography for several decades. Other modalities such as CT, noncontrast or contrast-enhanced MRI, and lymphoscintigraphy can also demonstrate lymphatic abnormalities and help in treatment planning. Imaging findings associated with lymphatic abnormalities can be seen in the pulmonary parenchyma, pleural space, and mediastinum. In the pulmonary parenchyma, common findings include interlobular septal thickening as well as reversal of lymphatic flow with intravasation of contrast material into pulmonary lymphatics. In the pleural space, findings include chylous pleural effusion and occasionally nonchylous pleural effusion. In the mediastinum, thoracic duct leak, plexiform thoracic duct, lymphatic malformations, and lymphangiectasis may occur. Management of chylothorax includes conservative or medical treatment, surgery, and interventional radiology procedures. The authors discuss thoracic lymphatic anatomy, imaging manifestations of lymphatic abnormalities in the various anatomic compartments, and interventional radiology treatment of chylothorax. Radiologists should be familiar with these imaging findings for diagnosis and to help guide appropriate management. ©RSNA, 2022.


Sujet(s)
Chylothorax , Malformations lymphatiques , Épanchement pleural , Chylothorax/imagerie diagnostique , Chylothorax/thérapie , Humains , Lymphographie/méthodes , Conduit thoracique/imagerie diagnostique , Conduit thoracique/chirurgie
3.
J Med Case Rep ; 16(1): 102, 2022 Mar 03.
Article de Anglais | MEDLINE | ID: mdl-35241158

RÉSUMÉ

BACKGROUND: The current coronavirus disease pandemic has brought recognition of multisystem inflammatory syndrome in adults as a de novo entity, temporally associated with severe acute respiratory syndrome coronavirus 2 viral infection in adults. Hypothesis about its true pathophysiology remains controversial. CASE REPORT: The patient was a 22-year-old African American female presenting to the emergency department with fever, sore throat, and neck swelling for the past 3 days. During her initial emergency department visit, her blood pressure was stable at 110/57 mmHg, temperature of 39.4 °C, and heart rate of 150 beats per minute. While in the emergency department, she received broad-spectrum antibiotics (vancomycin and ceftriaxone) and 30 cc/kg bolus of normal saline. Originally, she was admitted to a telemetry floor. The following night, a rapid response code was called due to hypotension. At that time, her blood pressure was 80/57 mmHg. She appeared comfortable without signs of respiratory distress. She received intravenous fluids and vasopressors, and was transferred to the intensive care unit. The patient had reported a previous coronavirus disease infection a few weeks prior. She was diagnosed and treated for multisystem inflammatory syndrome in adults. Intravenous immunoglobulin infusion was initiated and completed on hospital day 5. She was weaned off vasopressors by day 6, and discharged home on day 11. CONCLUSION: Our case report is an example of the presentation, diagnosis, and management of multisystem inflammatory syndrome. Our research into previous case reports illustrates the wide range of presentations, degree of end organ damage, and treatment modalities. This diagnosis needs to be considered in the presence of recent coronavirus disease infection with new-onset end organ failure, as prompt diagnosis and treatment is crucial for better outcomes.


Sujet(s)
COVID-19 , Adulte , COVID-19/complications , Femelle , Fièvre/étiologie , Humains , Immunoglobulines par voie veineuse , Pandémies , SARS-CoV-2 , Syndrome de réponse inflammatoire généralisée/diagnostic , Syndrome de réponse inflammatoire généralisée/thérapie , Jeune adulte
4.
Neurosci Insights ; 16: 26331055211007445, 2021.
Article de Anglais | MEDLINE | ID: mdl-34485912

RÉSUMÉ

Hypertrophic olivary degeneration is a rare condition caused by a lesion in the Guillain-Mollaret triangle which leads to trans-synaptic degeneration resulting in the degenerative hypertrophy of the inferior olivary nucleus. This condition presents clinically with palatal tremor but can also produce ocular myoclonus or cerebellar signs. While any lesion that occurs within the Guillian-Mollaret triangle and results in the deafferentation of the inferior olive can lead to hypertrophic olivary degeneration, the most common etiologies include ischemic and hemorrhagic stroke, vascular malformation, neoplasm, and iatrogenic injury related to surgery. We report a series of 7 patients who presented with this condition bilaterally on MRI imaging, including 1 case which represents the first report of toxoplasmosis leading to the development of bilateral hypertrophic olivary degeneration and only the third reported case, unilateral or bilateral, related to an infectious etiology.

5.
J Neuroradiol ; 48(5): 369-378, 2021 Sep.
Article de Anglais | MEDLINE | ID: mdl-33516733

RÉSUMÉ

This systematic review aims to clarify and comprehensively detail the sometimes variable published imaging features as well as the pathogenesis, clinical diagnostic criteria, and treatment options of IgG4-Related Diseases (IgG4-RD) in the head and neck to aid the radiologist in diagnosing relapse and new sites of disease. A literature search in PubMed and EMBASE for reported cases of IgG4-RD was performed in December 2019. Case reports or series of IgG4-RD in the head and neck in adults that included sufficient imaging and pathology findings were included. This yielded 50 reports. IgG4-RD locations included the orbits, thyroid, pituitary gland, paranasal sinuses, salivary and parotid glands, larynx, pharynx, cervical lymph nodes, meninges, and skull base. Most lesions demonstrated non-specific homogenous CT attenuation, diffuse enhancement, isointense/low T2 signal intensity, and low T1 signal intensity. 6 cases from our institution followed previously reported imaging patterns.


Sujet(s)
Maladie associée aux immunoglobulines G4 , Adulte , Imagerie diagnostique , Tête/imagerie diagnostique , Humains , Maladie associée aux immunoglobulines G4/imagerie diagnostique , Base du crâne
6.
Curr Probl Diagn Radiol ; 50(6): 899-904, 2021.
Article de Anglais | MEDLINE | ID: mdl-33279307

RÉSUMÉ

Radiation induced oral mucositis (RIOM) is a common and debilitating complication of radiation therapy for head and neck cancers. RIOM can lead to oral pain, dysphagia, and reduced oral intake, which can be severe enough to necessitate placement of a feeding tube or utilization of total parenteral nutrition. When severe, RIOM can cause premature termination of radiation therapy and can alter treatment plans leading to suboptimal treatment doses. While patient reporting of RIOM symptoms has been the gold standard of documenting RIOM progression, little has been described in the radiology literature concerning the typical imaging findings of RIOM. Herein, we review the pathophysiology and clinical presentation that underlies the development of RIOM with illustrative cases to highlight the relevant imaging findings related to RIOM for the practicing radiologist.


Sujet(s)
Tumeurs de la tête et du cou , Inflammation muqueuse , Lésions radiques , Stomatite , Tumeurs de la tête et du cou/imagerie diagnostique , Tumeurs de la tête et du cou/radiothérapie , Humains , Inflammation muqueuse/imagerie diagnostique , Inflammation muqueuse/étiologie , Lésions radiques/imagerie diagnostique , Radiologues , Stomatite/imagerie diagnostique , Stomatite/étiologie
7.
Skeletal Radiol ; 49(8): 1183-1193, 2020 Aug.
Article de Anglais | MEDLINE | ID: mdl-32162049

RÉSUMÉ

Temporomandibular disorders encompass multiple pathologies of the temporomandibular joint that manifest as middle/inner ear symptoms, headache, and/or localized TMJ symptoms. There is an important although somewhat limited role of imaging in the diagnostic evaluation of temporomandibular disorders. In this manuscript, we provide a comprehensive review of TMJ anatomy, outline potentially important features of TMJ disc ultrastructure and biochemistry in comparison with the intervertebral disc and knee meniscus, and provide imaging examples of the TMJ abnormalities currently evaluable with MRI and CT. In addition, we provide an overview of emerging and investigational TMJ imaging techniques in order to encourage further imaging research based on the biomechanical alterations of the TMJ disc.


Sujet(s)
Disque intervertébral/imagerie diagnostique , Ménisques de l'articulation du genou/imagerie diagnostique , Troubles de l'articulation temporomandibulaire/imagerie diagnostique , Articulation temporomandibulaire/imagerie diagnostique , Humains , Disque intervertébral/anatomie et histologie , Disque intervertébral/composition chimique , Imagerie par résonance magnétique , Ménisques de l'articulation du genou/anatomie et histologie , Ménisques de l'articulation du genou/composition chimique , Articulation temporomandibulaire/anatomie et histologie , Articulation temporomandibulaire/composition chimique , Troubles de l'articulation temporomandibulaire/métabolisme , Tomodensitométrie
8.
Radiol Case Rep ; 14(12): 1561-1565, 2019 Dec.
Article de Anglais | MEDLINE | ID: mdl-31737136

RÉSUMÉ

Primary bone lymphoma (PBL) is rare bone disease that accounts for very small number of all primary bone tumors. Among the described sites of PBLs, the patella is an extremely rare example. To date, only a few cases of PBL affecting the patella have been reported. Clinically, these tumors have very similar presentation of pain, decreased range of motion and swelling and, sometimes, pathologic fractures. On radiographs, skeletal lymphoma commonly manifests as osteolytic lesions with ill-defined margins affecting the metaphysis of axial long bones. We present a rare case of patellar adult T-cell lymphoma/leukemia in a 58-year-old female who presented with left-knee pain and swelling. Computed tomography and magnetic resonance imaging revealed diffuse marrow replacement by a lesion with aggressive features. PET scan demonstrated neoplastic range hypermetabolic FDG uptake within this lesion. Ultrasound-guided biopsy was consistent with PBL.

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