Bilateral IgG4-related Ophthalmic Disease With Diffuse Large B-cell Lymphoma of the Right Eye: A Case Report

2020 ◽  
Vol 36 (4) ◽  
pp. e84-e85 ◽  
Author(s):  
Xiaolin Peng ◽  
Hou Jing ◽  
Weimin He
2018 ◽  
Vol 71 (3-4) ◽  
pp. 121-124
Author(s):  
Aleksandra Ilic ◽  
Ivanka Savic ◽  
Aleksandra Fejsa-Levakov ◽  
Branislav Bajkin

Introduction. Lymphomas are a group of neoplasms of the lymphatic and reticuloendothelial system. The two main types are Hodgkin lymphoma and non-Hodgkin lymphoma, depending on the immunohistological characteristics of malignant lymphocytes. B-cell lymphomas are more frequent than T-cell lymphomas. In this case report we present a male patient with diffuse large B-cell lymphoma localized in the maxilla. Case Report. A 59-year-old man presented with a painless swelling in the right posterior region of the maxilla. A solid tumor was found in the right posterior maxillary region by intraoral examination, firstly suspected as a dental infection. Since the symptoms did not improve a month after the first dental treatment, he was referred for further diagnostic evaluation. The established diagnosis was diffuse large B-cell lymphoma. The patient received standard therapy for diffuse large B-cell lymphoma - rituximab-cyclophosphamide, hydroxydaunomycin, oncovin, prednisolone, six cycles and regression of the oral lesion was noticed. Conclusion. Lymphoma of the oral cavity usually presents as a swelling and may mimic odontogenic infection. Dentists should be aware of this possibility especially if the swelling is painless and if the initial treatment has failed.


Skull Base ◽  
2009 ◽  
Vol 19 (03) ◽  
Author(s):  
Gopi Shah ◽  
Marc Rosen ◽  
James Evans

2019 ◽  
Vol 9 (1) ◽  
pp. 59-61
Author(s):  
Bala Koteswara Rao P ◽  
◽  
Jayshree C Awalekar ◽  
Ajinkye Nashte ◽  
Rahul Surve ◽  
...  

2021 ◽  
Vol 25 ◽  
pp. 200530
Author(s):  
Amintas Samuel ◽  
Laurent Elodie ◽  
Gros Audrey ◽  
Sesboue Come ◽  
Merlio Jean-Philippe ◽  
...  

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Lilla Prenek ◽  
Klára Csupor ◽  
Péter Beszterczán ◽  
Krisztina Boros ◽  
Erika Kardos ◽  
...  

Abstract Background Cardiac tumors are very uncommon compared to other cardiac diseases. Their clinical symptoms can vary from absent to non-specific. The most common symptoms are arrhythmias, blood flow obstruction due to valvular dysfunction, shortness of breath, systemic embolization, and accumulation of pericardial fluid. Hereby, we describe a very rare case of a diffuse large B cell lymphoma patient who presented with the symptoms and signs of acute coronary syndrome (ACS) but the patient’s complaints were caused by his intramyocardial lymphoma metastasis. Case presentation Forty-eight-year-old diffuse large B cell lymphoma patient was admitted to our emergency department with chest pain, effort dyspnea, and fever. The patient had normal blood pressure, blood oxygen saturation, sinus tachycardia, fever, crackles over the left lower lobe, novum incomplete right bundle branch block with Q waves and minor ST alterations, elevated C-reactive protein, high-sensitivity troponin-T, and d-dimer levels. Chest X-ray revealed consolidation on the left side and enlarged heart. Bed side transthoracic echocardiography showed inferior akinesis with pericardial fluid. Coronary angiography showed no occlusion or significant stenosis. Chest computed tomography demonstrated the progression of his lymphoma in the myocardium. He was admitted to the Department of Hematology for immediate chemotherapy and he reached complete metabolic remission, followed by allogeneic hematopoietic stem cell transplantation. Unfortunately, about 9 months later, he developed bone marrow deficiency consequently severe sepsis, septic shock, and multiple organ failure what he did not survive. Conclusions Our case demonstrates a very rare manifestation of a heart metastasis. ACS is an unusual symptom of cardiac tumors. But our patient’s intramyocardial lymphoma in the right atrium and ventricle externally compressed the right coronary artery and damaged the heart tissue, causing the patient’s symptoms which imitated ACS. Fortunately, the quick diagnostics and immediate aggressive chemotherapy provided the patient’s remission and suitability to further treatment.


2019 ◽  
Vol 69 (5) ◽  
pp. 312-314 ◽  
Author(s):  
Kenji Yorita ◽  
Yu Tanaka ◽  
Koki Hirano ◽  
Miki Mizobuchi ◽  
Kei Kohno ◽  
...  

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