scholarly journals Successful Outcome of Patellectomy Plus Chemotherapy for Primary Bone Lymphoma of the Patella: A Case Report and Literature Review

2021 ◽  
Vol 11 ◽  
Author(s):  
Xin Cao ◽  
Hui-Jin Chen

Primary bone lymphoma (PBL) is a rare but distinct clinicopathological disease, usually occurring in the pelvis, spine, and ribs. To date, only a few cases have been reported as beginning in the patella. Due to the lack of clinical evidence, the optimal treatment strategy has not been established. Here, we report a case that presented unexplained right knee pain. The case was diagnosed with the non-germinal center, diffuse large B cell lymphoma in the patella by imaging examinations and bone biopsy. Then, the patient received a patellectomy and eight cycles of R-CHOP chemotherapy. After treatment, the patient achieved a favorable prognosis and satisfactory functional recovery.

2020 ◽  
Vol 13 (1) ◽  
pp. 276-280
Author(s):  
Tala Batia ◽  
Mohamed A. Yassin ◽  
Deena S. Mudawi ◽  
Omnia A. Hamid ◽  
Ahmed M.A. Abdalhadi

Primary bone lymphoma (PBL) is a peculiar extranodal presentation of non-Hodgkin’s lymphoma. Primary bone diffuse large B-cell lymphoma (DLBCL) is the most common pathological type, comprising about 80% of PBL. The diagnosis of PBL depends on the combined clinical examination and imaging studies and is confirmed with immunohistochemical examination. Due to the rarity of this disease, more relative studies and case reports are needed to provide insight into this obscure lymphoproliferative malignancy. Here, we report one rare case of primary bone DLBCL involving the axial skeleton in a 37-year-old female.


2020 ◽  
Vol 7 (10) ◽  
pp. C133-136
Author(s):  
Cyrus Dara Jokhi ◽  
Kalpesh V Vaghela ◽  
Pruthvi Damor

Primary bone lymphoma is rare, among which commonly involved site at time of presentation are femur, pelvic bones, tibia and most common type is Large B cell lymphoma which usually occurs in adults.  Cases of large B cell lymphoma in clavicle as primary bone lymphoma is extremely rare finding. According to our knowledge this case may be first reported case of world. We are here reporting a case of 62-year female presented as sternoclavicular joint swelling, without fever or pain in local area. Patient was diagnosed on X ray by radiologist, as well as by clinician as, osteosarcoma of right clavicle. Patient came to Department of Cytopathology for FNA for confirmation of X ray finding. On FNA diagnosis of Non-Hodgkin lymphoma was given, and advise for biopsy and immunohistochemistry (IHC) was given for confirmation of diagnosis and to subtype NHL. On IHC Ki67 index was 85%, with diffuse positivity noted for MUM1, CD79a, and CD138 along with cytoplasmic positivity for ALK 1 and patchy positivity for PAX 5. Tumor was negative for BCL6, BCL2, CD20, CD5, CD23, CD10, CD19, CD4, CD8, CD7, CD3. Diagnosis of ALK positive DLBCL was given on biopsy after IHC. Patients with PBL treated with combined modality were found to have a superior outcome, with a significantly better survival (5-year cause-specific survival 95%). So correct and timely pathological diagnosis of DLBCL as PBL is significantly important for prognosis.


2007 ◽  
Vol 127 (1) ◽  
pp. 47-54 ◽  
Author(s):  
X. Frank Zhao ◽  
Ken H. Young ◽  
Dale Frank ◽  
Ami Goradia ◽  
Michael P. Glotzbecker ◽  
...  

Author(s):  
abbas mofidi ◽  
Mohsen Esfandbod ◽  
Ehsan Pendar ◽  
Masoud Mortezazadeh ◽  
Alireza hadizadeh

In this article, we report a 34-year-old man who presented with progressive hip pain and osteolytic bone lesions . Primary workup included Core needle biopsies manifested as osteomyelitis; however as no sign of remission was observed, an open biopsy considered which revealed primary bone lymphoma.


2018 ◽  
Vol 43 (8) ◽  
pp. 779.e1-779.e4 ◽  
Author(s):  
Virginia Galati ◽  
Friederike Wortmann ◽  
Felix H. Stang ◽  
Christoph Thorns ◽  
Peter Mailänder ◽  
...  

Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 4874-4874
Author(s):  
Anna Morozova ◽  
Eugene Zvonkov ◽  
Vasilii Mamonov ◽  
Alla M. Kovrigina ◽  
Sergei Kravchenko ◽  
...  

Abstract Abstract 4874 Background Primary bone lymphoma (PBL) is a rare extranodal type of tumor. A diagnosis of diffuse large B-cell lymphoma (DLBCL) is made in 90% of all cases. The treatment standard for PBL is ÑÍÎ−D chemotherapy (CT) combined with radiation therapy. In the group of PBL patients with a local (IE) stage and without any unfavourable prognostic factors (elevated lactate dehydrogenase (LDH) concentrations, Â-symptoms, tumor size ≥10 cm) treated with standard chemotherapy and radiation, the relapse-free 5-year survival rate is as high as 80% to 100%. In advanced disease stages (stage II, IVE and any unfavourable prognostic factor) this treatment strategy leads to a remission in just 20% of patients (Ramadan KM, Shenkier T et al. Ann Oncol 18:129–135, 2007). Therefore, the results achieved with the ÑÍÎ−D regimen and radiation therapy in the treatment of adult patients with advanced PBL are unsatisfactory. Further research is thus needed to boost treatment efficacy for patients with advanced PBL. One of the ways to overcome the chemotherapy resistance of the tumor is primary intensification of CT. For instance, according to Children's Cancer Group data, high-dose CT was effective in children suffering from advanced PBL (Lones MA, Perkins SL et al. Clin Oncol 20:2293–2301, 2002). Intensive CT has not been used previously in adult patients with PBL. Purpose To evaluate the efficacy of intensive CT according to the mNHL-BFM-90 program in adult patients with advanced-stage PBL. Materials and methods The study enrolled all patients (22 subjects in total) with advanced-stage PBL monitored by the Research Centre of Haematology in the period from 2007 to 2012; 13 were male and 9 female, aged from 16 to 69 years (median age, 39 years). According to the WHO classification, all patients were diagnosed with DLBCL. The following evaluations were performed for disease staging: physical examination and medical history, complete blood count and blood chemistry, chest and abdominal computed tomography, whole-body positron emission tomography using 18F-fluorodeoxyglucose, magnetic resonance imaging and computed tomography of affected bones. Tumor staging was done according to the Ann-Arbor classification. Local IÅ stage (involvement of 1 bone) was verified in 6 cases (27%), stage IIÅ (involvement of regional lymph nodes) in 3 subjects (13%), and stage IVÅ (multiple bone involvement) in 13 patients (60%). Patients with the IIIÅ stage (distant nodal disease) were not recruited in this study. The main symptoms of the disease included pain and swelling. LDH elevation was observed in 13 cases (60%), Â-symptoms were found in 15 patients (68%), and large-size tumors were seen in 20 subjects (90%). The most common tumor sites were the skull bones, vertebrae, and femur. The average ECOG score for global condition assessment was 2 at the time of CT initiation. All patients received treatment according to the mNHL-BFM-90 intensive CT program (Reiter A, Schrappe M. et al. Blood 94(10): 3294–3306, 1999). This program was modified: adriamycin was administered on the 3rd day of course ÀÀ at a dose of 50 mg/m2. Methotrexate was administered on the 1rd day of course C. The dose of methotrexate was reduced to 1.0 g/m2 and the administration time shortened to 12 hours. Leucovorin was administered in 6 hours after the end of the methotrexate infusion until the serum methotrexate concentration fell below 0.1 μmol/L. The toxicity of this treatment was assessed using the NCIC Common Toxicity Criteria. Results Complete remissions were achieved in 20 patients (90%; 95th% CI, 70% to 95%). The mean follow-up period was 23 months (range, 1 to 68 months). Relapses were observed in two patients for 6 and 40 months. Grades 3, 4 haematological toxicity was observed in all study subjects. Non-haematological toxicities were not life-threatening (grades 1, 2). Blood component replacement therapy and administration of leukopoiesis stimulators were required in all patients. No deaths related to mNHL-BFM-90 treatment occurred. No patient was withdrawn from the treatment program. No second malignancies were observed. Conclusion The obtained results indicate a high chemosensitivity of PBL. The mNHL-BFM-90 program is the therapy of choice for patients with advanced PBL. Adult patients tolerate the intensive CT program well with complex accompanying therapy being administered. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 5404-5404
Author(s):  
Katie Guo ◽  
Melissa Boileau ◽  
Bernard Fortin ◽  
Francine Aubin ◽  
Tony Petrella ◽  
...  

Abstract Introduction Primary bone lymphoma (PBL) is an uncommon form of lymphoma. Diffuse large B-cell lymphoma (DLBCL) represents the main histology associated with PBL. Clinicopathological understanding and management of PBL rely only on retrospective series. Methods Cases of DLBCL diagnosed by bone biopsy treated in one referring center between 1993 and 2014 were retrospectively reviewed (Montreal, Canada). Bone biopsies done as part of the bone marrow analysis were excluded. Patients files were analyzed to determine if patient had primary bone lymphoma or systemic lymphoma with bony involvement. We excluded patient with distant lymph node or other extranodal involvement. Data on clinical presentation, staging procedures and treatment management including use of radiotherapy was collected. Staging was performed according to WHO classification of soft tissue tumors (2002). Survival time and time to recurrence were calculated from the date of the first documented treatment until recurrence or death with the Kaplan-Meier method. Prognostic factors of recurrence or death were explored with log-rank tests and Cox proportional hazards models. Competing risks analysis was attempted to isolate deaths from lymphoma and death from other causes. Our study was approved by local research and ethic committees. Results We retrieved 42 cases of PBL with a median age of 63 years (23-83) treated between October 1995 and April 2014. We identified 3/14 (21%) GCB and 11/14 (79%) non-GCB subtypes based on the modified Hans algorithm (Meyer et al., JCO 2011). The most common presenting symptom was pain (88%). 12/42 (33%) patients had an IPI score ≥ 3. We identified 18 (43%) stage I, 11 (26%) stage II and 13 (31%) stage IV. 20/42 (48%) had bulky disease (≥ 10cm). Among the 37 patients treated with curative intent, 36 (97%) received CHOP-based regimen and 23 (62%) received rituximab. 30 of these 37 (81%) patients received additional radiotherapy of which 67% received a dose of radiotherapy between 36-50 Gy. Overall response rate for patients treated with curative intent was 86%. With a median follow up of 64.8 months for the whole cohort, the 5- and 10-year overall survival was 73% and 54%, respectively. The 5- and 10-year progression-free survival was 70% and 49% respectively. Age, LDH, stage (I-II vs IV), ECOG (0-1 vs 2-4), IPI (0-2 vs 3-5), use of radiotherapy or addition of rituximab were associated with differences in survival and progression rates that did not reach statistical significance given the limited number of patients in our cohort and the fact that half of the deaths were attributed to other causes. A larger cohort would be required to demonstrate a benefit with rituximab. Response was based on positron emission tomography-computed tomography (TEP-CT) imaging in 12 patients. There was an insufficient number of patients to evaluate the role of adding radiotherapy in patient complete remission defined by PET-CT. Conclusion Our survival rates reproduce published data from series of PBL (Ramadan et al., Ann Oncol 2007; Bruno Ventre et al., Oncologist 2014), although the benefit of adding rituximab did not reach statistical significance in our cohort. The role of radiotherapy in the era of response defined by PET-CT remains to be defined. Disclosures Fleury: Gilead: Consultancy, Speakers Bureau; Amgen: Consultancy, Speakers Bureau; Roche: Consultancy, Speakers Bureau; Novartis: Consultancy, Speakers Bureau; Lundbeck: Consultancy, Speakers Bureau; Seattle Genetics: Consultancy, Speakers Bureau.


2013 ◽  
Vol 2013 (may22 1) ◽  
pp. bcr2013009809-bcr2013009809 ◽  
Author(s):  
M. Mohamed ◽  
T. Brain ◽  
S. Sharma

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