Diffuse Large B-cell Lymphoma with Renal Involvement Presenting with Multiple Cranial Nerve Palsy in a Frail Older Adult: a Case Report

Author(s):  
Manicka Saravanan Subramanian ◽  
Abhijith Rajaram Rao ◽  
Urza Bhattarai ◽  
Naren Hemachandran ◽  
Mohamad Sulaiman ◽  
...  
2012 ◽  
Vol 52 (4) ◽  
pp. 245-250 ◽  
Author(s):  
Akira Yokote ◽  
Yoshio Tsuboi ◽  
Kousuke Fukuhara ◽  
Jun Tsugawa ◽  
Hirosato Inoue ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Guillermo Enrique Quintero Vega ◽  
Daniel Osorio ◽  
José Antonio de la Hoz Valle ◽  
Daniela Rodríguez Feria

Intravascular large B-cell lymphoma (IVLBCL) is a rare subtype of non-Hodgkin lymphoma. It is characterized by the proliferation of cancerous cells into the intraluminal space of the blood vessels. It has a low incidence rate of 0.095 cases per 1,000,000. The clinical presentation is insidious and unspecific, often delaying the diagnosis. IVLBCL can be diagnosed through body images and histopathology analysis. This neoplasm averages a 60% response rate to current chemotherapy treatment, favoring rituximab, and doxorubicin-based regimen if it is diagnosed in time. Here, we present the case of a 56-year-old man admitted to our hospital with a fever who was eventually diagnosed with IVLBCL. He presented to the consultation with anemia, fever, and splenomegaly. An infection panel, a bone marrow biopsy, and a PET-CT scan were performed and ruled out the possibility of infections and neoplasms. The patient later developed edematous syndrome. As a result, a renal biopsy was performed which tested positive for intravascular large B-cell lymphoma. Currently, the patient has been in complete remission for 33 months. Along with presenting this specific case, we also reviewed previously published cases of IVLBCL to illustrate the renal involvement of this pathology.


2012 ◽  
Vol 113 (1) ◽  
pp. 103-104 ◽  
Author(s):  
Chih-Hung Tsai ◽  
E-Jian Lee ◽  
Yi-Sheng Liu ◽  
Ying-Chen Chen ◽  
Yu-Hsiang Shih ◽  
...  

2021 ◽  
Vol 429 ◽  
pp. 118435
Author(s):  
Dulmini Weerathunga ◽  
P. Manokaran ◽  
Arjuna Fernando ◽  
Nethini Wijesinghe ◽  
Gamini Pathirana

2021 ◽  
Vol 39 (15_suppl) ◽  
pp. 7542-7542
Author(s):  
Xavier Andrade-Gonzalez ◽  
Antoine N Saliba ◽  
Harry E Fuentes ◽  
Zhuoer Xie ◽  
Thomas Matthew Habermann ◽  
...  

7542 Background: 60-70% of patients with newly diagnosed diffuse large B-cell lymphoma (DLBCL) can be cured with R-CHOP or R-CHOP-like immunochemotherapy. However, patients ≥80 years of age were either excluded or underrepresented in modern DLBCL trials, and their outcomes are understudied. The aim of this study is to define the survival trends and risk factors for inferior survival in older adult patients with DLBCL. Methods: Patients with newly diagnosed DLBCL were identified from the National Cancer Database (2004-2017, representing the rituximab era). Clinical characteristics, treatment, and outcomes were compared between patients ages ≥ 80, 65-79, and < 65 years. The Kaplan-Meier method and Cox proportional hazards model were used for survival analysis. Results: A total of 231,756 patients with newly diagnosed DLBCL were identified; 46,250 (20%) were ≥80 years, 87,702 (38%) were 65-79 years, and 97,904 (42%) were < 65 years. Patients ≥80 years were more likely to have a higher Charlson-Deyo Comorbidity Index score (CDS) (CDS ≥2, 12% vs 11% vs 8%, p = 0.001), less likely to receive systemic chemotherapy (63% vs 83% vs 89%, p < 0.001), and more likely to receive treatment at a non-academic center (71% vs 65% vs 48%, p < 0.001), compared to patients 65-79 and < 65 years, respectively. Median overall survival (OS) was significantly worse for patients ≥80 years compared to patients 65-79 years (11.6 vs 61.0 months, p = 0.001) and patients < 65 years (11.6 vs 178.1 months, p = 0.001). During the study period, the median OS had only minimally improved for patients ≥80 years (10.6 months in 2004-2007 vs 11.5 months in 2008-2011 vs 12.3 months in 2012-2016, p = 0.006). In contrast, the OS improvement appears more meaningful in patients 65-79 years (median in months: 51 vs 61.2 vs 65.9, p = < 0.001) and patients < 65 years (median in years: 14.6 vs 11.3 vs not reached, p < 0.001) in the prespecified intervals (2004-07, 2008-11, and 2012-16). In multivariate analysis, the most substantial risk factor for worse survival in patients ≥80 years was not receiving systemic therapy (hazard ratio [HR] = 3.26, 95%CI = 3.01-3.54, p = 0.001). Other risk factors associated with worse survival included high-risk IPI score (HR = 2.16, 95%CI = 1.96-2.39, p = 0.001), CDS score ≥2 (HR = 1.56, 95%CI = 1.40-1.73, p = 0.001), male sex (HR = 1.16, 95%CI = 1.09-1.24, p = 0.001), B symptoms at diagnosis (HR = 1.16, 95%CI = 1.08-1.25, p = 0.001), and treatment at a non-academic center (HR = 1.1, 95%CI = 1.01-1.20, p = 0.001). Conclusions: Patients ≥ 80 years of age with DLBCL have a significantly inferior survival which has not meaningfully improved in recent years. More than 1/3 of patients ≥ 80 years did not receive systemic therapy. Older adult patients with DLBCL should be assessed for fitness for chemotherapy using validated geriatric assessment tools. Novel therapeutic strategies with favorable safety profiles are urgently needed for this expanding patient population.


2014 ◽  
Vol 8 (5) ◽  
pp. 1983-1985 ◽  
Author(s):  
SHANG-YIH YAN ◽  
YI-JEN PENG ◽  
CHUN-SHU LIN ◽  
GIIA-SHEUN PENG ◽  
PING-YING CHANG

2013 ◽  
Vol 35 (1) ◽  
pp. 103-104 ◽  
Author(s):  
Tsukasa Saito ◽  
Takayuki Katayama ◽  
Katsuya Ikuta ◽  
Yutaka Kohgo ◽  
Naoyuki Hasebe

Sign in / Sign up

Export Citation Format

Share Document