Vasculitis Diagnosed on Fluorine-18 Labelled-2-Deoxy-2-Fluoro-D-Glucose Uptake in A Patient With Fever of Unknown Origin and A History of Non Hodgkin’s Lymphoma

2015 ◽  
Vol 2 (1) ◽  
pp. 16-18
Author(s):  
Artor Asabella ◽  
◽  
Alessandra Palo ◽  
Corinna Altini ◽  
Cristina Ferrari ◽  
...  
Blood ◽  
1990 ◽  
Vol 75 (4) ◽  
pp. 831-838 ◽  
Author(s):  
GL Phillips ◽  
JW Fay ◽  
RH Herzig ◽  
HM Lazarus ◽  
SN Wolff ◽  
...  

Abstract Intensive chemoradiotherapy, with or without additional local radiotherapy, and unpurged autologous marrow transplantation was given to 68 patients with progressive non-Hodgkin's lymphoma. Responses were attained in 44 patients (65%, 95% confidence intervals [CI], 52% to 76%), including 37 who achieved complete responses. Fifteen patients (22%, 95% C.I. 13% to 34%) remain free of disease (including 11 continuously) at a median of 5.3 (range 3.1 to 9.1) years later. Higher Karnofsky scores (P less than .01, Mann-Whitney U test) and the absence of a history of prior radiotherapy (P = .02, chi 2 test) were associated with achievement of complete plus partial responses. Higher Karnofsky scores (P less than .01, Mann-Whitney U test) and less resistant disease status at transplantation (P = .04, chi 2 test) were significant when calculations were limited to complete responses. Karnofsky scores were also associated with the probability of freedom from progression (P = .02, log-rank) for responding patients. Also, Karnofsky scores and the absence of prior radiotherapy (P less than .01 and P = .01, respectively, log-rank) were associated with improved survival. Progressive lymphoma was the chief cause of failure; progression usually occurred less than 6 months after transplantation, most often at the sites of active disease before the transplant. However, five patients (including four with high-grade non-Hodgkin's lymphoma) suffered hematogenous patterns of relapse; four of these five patients had no prior history of marrow involvement. Other causes of mortality included interstitial pneumonitis, sepsis, hemorrhage and renal failure. Intensive chemoradiotherapy and autologous marrow transplantation produces durable remissions in some patients with progressive non-Hodgkin's lymphoma. Since such therapy is more effective when given to patients with signs of less advanced disease, earlier treatment would be the simplest way to produce improved results. However, improved conditioning regimens will also be needed, and measures to reduce occult lymphoma stem cell contamination with the autograft may also be required to increase the likelihood of cure in some patients.


2003 ◽  
Vol 107 (1) ◽  
pp. 99-105 ◽  
Author(s):  
Ikuko Kato ◽  
Karen L. Koenig ◽  
Mark S. Baptiste ◽  
Patricia P. Lillquist ◽  
Glauco Frizzera ◽  
...  

2009 ◽  
Vol 100 (3) ◽  
pp. 524-526 ◽  
Author(s):  
Y Lu ◽  
J Sullivan-Halley ◽  
W Cozen ◽  
E T Chang ◽  
K Henderson ◽  
...  

2002 ◽  
Vol 20 (20) ◽  
pp. 4255-4260 ◽  
Author(s):  
Shin-ichi Nakatsuka ◽  
Masayuki Yao ◽  
Yoshihiko Hoshida ◽  
Satoru Yamamoto ◽  
Keiji Iuchi ◽  
...  

PURPOSE: Pyothorax-associated lymphoma (PAL) is a non-Hodgkin’s lymphoma developing in the pleural cavity after a long-standing history of pyothorax. Full details of PAL are provided here.PATIENTS AND METHODS: Clinical and pathologic findings were reviewed in 106 patients with PAL collected through a nationwide survey in Japan.RESULTS: Age of the patients with PAL was 46 to 82 years (median, 64 years), with a male/female ratio of 12.3:1. All patients had a 20- to 64-year (median, 37-year) history of pyothorax resulting from artificial pneumothorax for treatment of pulmonary tuberculosis (80%) or tuberculous pleuritis (17%). The most common symptoms on admission were chest and/or back pain (57%) and fever (43%). Laboratory data showed that the serum neuron-specific enolase level was occasionally elevated (3.55 to 168.7 ng/mL; median, 18.65 ng/mL), suggesting a possible diagnosis of small-cell lung cancer. Histologically, PAL usually showed a diffuse proliferation of large cells of B-cell type (88%). In situ hybridization study showed that PAL in 70% of the patients was Epstein-Barr virus (EBV)-positive. PAL was responsive to chemotherapy, but the overall prognosis was poor, with a 5-year survival of 21.6%.CONCLUSION: This study established the distinct nature of PAL as a disease entity. PAL is a non-Hodgkin’s lymphoma of exclusively B-cell phenotype in the pleural cavity of patients with long-standing history of pyothorax, and is strongly associated with EBV infection. Development of PAL is closely related to antecedent chronic inflammatory condition; therefore, PAL should be defined as malignant lymphoma developing in chronic inflammation.


2006 ◽  
Vol 165 (2) ◽  
pp. 126-133 ◽  
Author(s):  
F. Mensah ◽  
E. Willett ◽  
P Ansell ◽  
P. Adamson ◽  
E Roman

Blood ◽  
1990 ◽  
Vol 75 (4) ◽  
pp. 831-838 ◽  
Author(s):  
GL Phillips ◽  
JW Fay ◽  
RH Herzig ◽  
HM Lazarus ◽  
SN Wolff ◽  
...  

Intensive chemoradiotherapy, with or without additional local radiotherapy, and unpurged autologous marrow transplantation was given to 68 patients with progressive non-Hodgkin's lymphoma. Responses were attained in 44 patients (65%, 95% confidence intervals [CI], 52% to 76%), including 37 who achieved complete responses. Fifteen patients (22%, 95% C.I. 13% to 34%) remain free of disease (including 11 continuously) at a median of 5.3 (range 3.1 to 9.1) years later. Higher Karnofsky scores (P less than .01, Mann-Whitney U test) and the absence of a history of prior radiotherapy (P = .02, chi 2 test) were associated with achievement of complete plus partial responses. Higher Karnofsky scores (P less than .01, Mann-Whitney U test) and less resistant disease status at transplantation (P = .04, chi 2 test) were significant when calculations were limited to complete responses. Karnofsky scores were also associated with the probability of freedom from progression (P = .02, log-rank) for responding patients. Also, Karnofsky scores and the absence of prior radiotherapy (P less than .01 and P = .01, respectively, log-rank) were associated with improved survival. Progressive lymphoma was the chief cause of failure; progression usually occurred less than 6 months after transplantation, most often at the sites of active disease before the transplant. However, five patients (including four with high-grade non-Hodgkin's lymphoma) suffered hematogenous patterns of relapse; four of these five patients had no prior history of marrow involvement. Other causes of mortality included interstitial pneumonitis, sepsis, hemorrhage and renal failure. Intensive chemoradiotherapy and autologous marrow transplantation produces durable remissions in some patients with progressive non-Hodgkin's lymphoma. Since such therapy is more effective when given to patients with signs of less advanced disease, earlier treatment would be the simplest way to produce improved results. However, improved conditioning regimens will also be needed, and measures to reduce occult lymphoma stem cell contamination with the autograft may also be required to increase the likelihood of cure in some patients.


1991 ◽  
Vol 5 (1) ◽  
pp. 5-10
Author(s):  
Brian H Weinerman ◽  
Brendan MacDougall ◽  
Ian Carr

Forty-one individuals who presented with symptoms referable to the gastrointestinal tract were extracted from the authors’ total review of non-Hodgkin’s lymphoma in Manitoba from 1968 through 1978. Only cases at stages I to III were included, and there were 22 males and 19 females. Sixteen non-Hodgkin’s lymphomas arose in the small bowel, 15 in the stomach and 10 in the colon. The natural history of this group of gastrointestinal non-Hodgkin’s disease is described, and univariate and multivariate analyses were done using the variables of sex, pathology, stage, resection, site of disease and initial chemotherapy. The median survival of the group was 28 months. Sex and stage appeared to be important prognostically, but after multivariate analysis, only the female sex appear to be a good prognostic variable. There was a suggestion that resection should be attempted in these lesions, but there was not a large sample size in this group. In addition, it was felt that this group of individuals followed the same survival pattern as did poor prognosis non-Hodgkin’s lymphomas of nongastrointestinal origin.


2006 ◽  
Vol 15 (2) ◽  
pp. 245-250 ◽  
Author(s):  
Eva Negri ◽  
Renato Talamini ◽  
Maurizio Montella ◽  
Luigino Dal Maso ◽  
Anna Crispo ◽  
...  

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