scholarly journals Acute kidney injury and cardiac arrhythmia as the presenting features of widespread diffuse large B-cell lymphoma

2019 ◽  
Vol 9 (3) ◽  
Author(s):  
Anthony Jacob Emanuel ◽  
Susan Erin Presnell
Keyword(s):  
Acute Kidney Injury ◽  
B Cell ◽  
Cardiac Arrhythmia ◽  
Cell Lymphoma ◽  
Kidney Injury ◽  
B Cell Lymphoma ◽  
Large B Cell Lymphoma ◽  
Large B Cell

Acute kidney injury secondary to renal large B-cell lymphoma: role of early renal biopsy

2010 ◽  
Vol 43 (1) ◽  
pp. 237-240 ◽  
Author(s):  
Suhail Al-Salam ◽  
Ahmad Shaaban ◽  
Maha Alketbi ◽  
Naveed U. Haq ◽  
Samra Abouchacra
Keyword(s):  
Acute Kidney Injury ◽  
B Cell ◽  
Renal Biopsy ◽  
Cell Lymphoma ◽  
Kidney Injury ◽  
B Cell Lymphoma ◽  
Large B Cell Lymphoma ◽  
Large B Cell

scholarly journals Diffuse large B-cell lymphoma presenting as bilateral renal infiltration leading to acute kidney injury

2017 ◽  
Vol 6 (2) ◽  
pp. 140-147
Author(s):  
Tomoe Okubo ◽  
Shuma Hirashio ◽  
Minako Shimizu ◽  
Yoshiaki Kuroda ◽  
Shigehiro Doi ◽  
...  
Keyword(s):  
Acute Kidney Injury ◽  
B Cell ◽  
Cell Lymphoma ◽  
Kidney Injury ◽  
B Cell Lymphoma ◽  
Large B Cell Lymphoma ◽  
Large B Cell

scholarly journals Acute Kidney Injury and Electrolyte Abnormalities After Chimeric Antigen Receptor T-Cell (CAR-T) Therapy for Diffuse Large B-Cell Lymphoma

2020 ◽  
Vol 76 (1) ◽  
pp. 63-71 ◽  
Author(s):  
Shruti Gupta ◽  
Harish Seethapathy ◽  
Ian A. Strohbehn ◽  
Matthew J. Frigault ◽  
Elizabeth K. O’Donnell ◽  
...  
Keyword(s):  
Acute Kidney Injury ◽  
B Cell ◽  
Chimeric Antigen Receptor ◽  
Cell Lymphoma ◽  
Kidney Injury ◽  
B Cell Lymphoma ◽  
Large B Cell Lymphoma ◽  
Car T ◽  
Large B Cell ◽  
Electrolyte Abnormalities

scholarly journals Acute Kidney Injury as Presenting Symptom of Primary Lymphoma of the Uterus: Uncommon Presentation of a Rare Disease

2021 ◽  
Author(s):  
Alexandra Snyder ◽  
Ida Dhanuka ◽  
Haiyan Li ◽  
Fouzia Shakil ◽  
Liying Han ◽  
...  
Keyword(s):  
Acute Kidney Injury ◽  
B Cell ◽  
Rare Disease ◽  
Cell Lymphoma ◽  
Kidney Injury ◽  
B Cell Lymphoma ◽  
Diagnosis And Treatment ◽  
Bilateral Hydronephrosis ◽  
Large B Cell Lymphoma ◽  
Large B Cell

Abstract Background: Primary uterine lymphoma is a rare disease, with diffuse large B cell lymphoma being the most common subtype. There are a limited number of reports, series, and reviews in the literature on this disease and its variable clinical presentations. Further data is needed to prevent delay in diagnosis and treatment.Case: We present the case of a 73-year-old with acute kidney injury secondary to severe bilateral hydronephrosis in setting of an enlarged uterus, confirmed to be primary uterine diffuse large B cell lymphoma.Conclusion: Acute kidney injury secondary to severe bilateral hydronephrosis is an uncommon clinical presentation of primary uterine lymphoma. This case highlights the importance of heightened awareness of such rare presentations so not to delay diagnosis and treatment of this disease, and emphasizes benefit of surgical resection in the diagnosis and treatment of this disease.

Acute kidney injury as a presentation of primary renal diffuse large B-cell lymphoma in HIV

2013 ◽  
Vol 25 (5) ◽  
pp. 380-382 ◽  
Author(s):  
DJ Hughes ◽  
N Fitzgerald ◽  
H Sran ◽  
M Konig ◽  
R Moore-Moffatt ◽  
...  
Keyword(s):  
Acute Kidney Injury ◽  
B Cell ◽  
Cell Lymphoma ◽  
Kidney Injury ◽  
B Cell Lymphoma ◽  
Large B Cell Lymphoma ◽  
Large B Cell

scholarly journals Fatal cardiac arrhythmia caused by tumor lysis in a patient with diffuse large B-cell lymphoma upon start of R-CHOP

2018 ◽  
Vol 6 (3) ◽  
pp. 490-493 ◽  
Author(s):  
Nina Sørensen ◽  
Paw Jensen ◽  
Erik Clasen-Linde ◽  
Jacob Moesgaard Larsen ◽  
Tarec El-Galaly
Keyword(s):  
B Cell ◽  
Cardiac Arrhythmia ◽  
Cell Lymphoma ◽  
B Cell Lymphoma ◽  
Tumor Lysis ◽  
Large B Cell Lymphoma ◽  
Fatal Cardiac Arrhythmia ◽  
Large B Cell

scholarly journals Nephrotic syndrome without kidney injury revealing intravascular large B cell lymphoma

2019 ◽  
Vol 12 (6) ◽  
pp. e229359
Author(s):  
Lucie Pothen ◽  
Selda Aydin ◽  
Alessandra Camboni ◽  
Philippe Hainaut
Keyword(s):  
Nephrotic Syndrome ◽  
B Cell ◽  
Cell Lymphoma ◽  
Biological Evolution ◽  
Kidney Injury ◽  
Unknown Origin ◽  
B Cell Lymphoma ◽  
Cell Transplant ◽  
Large B Cell Lymphoma ◽  
Large B Cell

We describe the case of a 64-year-old woman admitted for fever of unknown origin, who developed nephrotic syndrome during hospitalisation and pulmonary infiltrates. Renal biopsy disclosed intracapillary glomerular invasion by intravascular large B cell lymphoma. Clinical and biological evolution was favourable after rituximab, cyclophosphamide, doxorubicine, vincristine and prednisone (R-CHOP) treatment and autologous stem cell transplant. Two years after diagnosis the patient was considered in remission.

scholarly journals Primary renal diffuse large B-Cell lymphoma causing haemodialysis-dependent nephromegaly in a child

2018 ◽  
pp. bcr-2018-226328 ◽  
Author(s):  
Andrew Michael South
Keyword(s):  
B Cell ◽  
Estimated Glomerular Filtration Rate ◽  
Cell Lymphoma ◽  
Kidney Injury ◽  
B Cell Lymphoma ◽  
Intrathecal Methotrexate ◽  
Renal Ultrasound ◽  
Large B Cell Lymphoma ◽  
Corticomedullary Differentiation ◽  
Large B Cell

A 4-year-old boy presented with fatigue and was found to have severe kidney injury requiring haemodialysis. A renal ultrasound demonstrated bilateral nephromegaly with mild loss of corticomedullary differentiation but preserved echogenicity. He had a persistent isolated monocytosis. Renal biopsy revealed extensive infiltration by primary renal diffuse large B-cell lymphoma. He required haemodialysis for 18 days and received chemotherapy with cyclophosphamide, doxorubicin, vincristine, prednisone, rituximab and intrathecal methotrexate. He achieved remission with an estimated glomerular filtration rate of 50 mL/min/1.73 m2, and his kidneys returned to normal size. Nephromegaly due to renal-limited haematolymphoid disease is extremely rare, especially in children.

scholarly journals Colonic Diffuse Large B-Cell Lymphoma in a Liver Transplant Patient with Historically Very Low Tacrolimus Levels

2012 ◽  
Vol 2012 ◽  
pp. 1-4
Author(s):  
Christopher M. Moore ◽  
Ihab Lamzabi ◽  
Anne K. Bartels ◽  
Shriram Jakate ◽  
David H. Van Thiel
Keyword(s):  
Liver Transplant ◽  
B Cell ◽  
Cell Lymphoma ◽  
Wide Spectrum ◽  
Kidney Injury ◽  
B Cell Lymphoma ◽  
Virus Genotype ◽  
Genotype 4 ◽  
Large B Cell Lymphoma ◽  
Large B Cell

Posttransplant lymphoproliferative disorders (PTLDs) comprise a wide spectrum of hematologic malignancies that are found increasingly in orthotopic liver transplant (OLT) patients given the rising frequency of these surgeries and their long-term success. PTLDs are highly correlated with both the Epstein-Barr virus (EBV) infection and the degree of immunosuppression involved. Herein is reported a case of a 53-year-old male with successfully treated hepatitis C virus genotype 4 and hepatocellular carcinoma who underwent OLT and developed symptoms of weakness and poor appetite 4 years later while on tacrolimus 3 mg b.i.d. with historically very low plasma levels. He was found to be anemic and colonoscopy revealed a 4.5 cm cecal diffuse large B-cell lymphoma (DLBCL). Further workup revealed mesenteric lymph node enlargement consistent and nodal DLBCL dissemination. He was treated with cyclophosphamide-hydroxyldaunorubicin-oncovin-prednisone-rituximab (CHOP-R) chemotherapy and his tacrolimus dose was lowered. Additionally, he manifested PTLD-associated cryoglobulinemia leading to acute kidney injury. After a prolonged hospitalization he was discharged with close followup.

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