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
2010 ◽  
Vol 43 (1) ◽  
pp. 237-240 ◽  
Author(s):  
Suhail Al-Salam ◽  
Ahmad Shaaban ◽  
Maha Alketbi ◽  
Naveed U. Haq ◽  
Samra Abouchacra

2017 ◽  
Vol 6 (2) ◽  
pp. 140-147
Author(s):  
Tomoe Okubo ◽  
Shuma Hirashio ◽  
Minako Shimizu ◽  
Yoshiaki Kuroda ◽  
Shigehiro Doi ◽  
...  

2020 ◽  
Vol 76 (1) ◽  
pp. 63-71 ◽  
Author(s):  
Shruti Gupta ◽  
Harish Seethapathy ◽  
Ian A. Strohbehn ◽  
Matthew J. Frigault ◽  
Elizabeth K. O’Donnell ◽  
...  

2021 ◽  
Author(s):  
Alexandra Snyder ◽  
Ida Dhanuka ◽  
Haiyan Li ◽  
Fouzia Shakil ◽  
Liying Han ◽  
...  

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.


2013 ◽  
Vol 25 (5) ◽  
pp. 380-382 ◽  
Author(s):  
DJ Hughes ◽  
N Fitzgerald ◽  
H Sran ◽  
M Konig ◽  
R Moore-Moffatt ◽  
...  

2018 ◽  
Vol 6 (3) ◽  
pp. 490-493 ◽  
Author(s):  
Nina Sørensen ◽  
Paw Jensen ◽  
Erik Clasen-Linde ◽  
Jacob Moesgaard Larsen ◽  
Tarec El-Galaly

2019 ◽  
Vol 12 (6) ◽  
pp. e229359
Author(s):  
Lucie Pothen ◽  
Selda Aydin ◽  
Alessandra Camboni ◽  
Philippe Hainaut

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.


2018 ◽  
pp. bcr-2018-226328 ◽  
Author(s):  
Andrew Michael South

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.


2012 ◽  
Vol 2012 ◽  
pp. 1-4
Author(s):  
Christopher M. Moore ◽  
Ihab Lamzabi ◽  
Anne K. Bartels ◽  
Shriram Jakate ◽  
David H. Van Thiel

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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