scholarly journals Testicular lymphoma in inguinal hernia

Author(s):  
Eduardo Poblano Olivares ◽  
Jorge L. Olmos Gonzalez

Primary testicular lymphoma is a rare disease that has a higher incidence in patients over 60 years of age, presenting as an increase in volume in the inguinal region, which is usually painless and slow-growing. In the case that we present, it is a patient who was initially diagnosed with an indirect inguinal hernia due to the findings on examination and ultrasound, without presenting relevant findings in the laboratory studies, during the trans-operative we found testicular tumor compatible with diffuse large B-cell lymphoma, this being the most common variant of testicular lymphoma. This case emphasizes on importance of pre-operative suspicion in older age patients with increased volume in the groin region and without a clear diagnosis.

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 2697-2697
Author(s):  
Ali Mazloom ◽  
Nathan Fowler ◽  
Puneeth Iyengar ◽  
Bouthaina S. Dabaja

Abstract Abstract 2697 Poster Board II-673 Background: Primary testicular lymphoma (PTL) is the most common testicular neoplasm in males over the age of 60, representing 1% to 7% of all testicular malignancies. Histologically, the most common subtype of PTL is diffuse large B-cell lymphoma (DLBCL) representing 80–90% of diagnosed tumors. Primary testicular lymphoma has a tendency to disseminate to the contralateral testis and the central nervous system. Treatment approaches can include loco-regional treatment regimens (orchiectomy, radiotherapy) and systemic chemotherapy with or without intra-thecal chemoprophylaxis. The purpose of this study is to determine the clinical characteristics, patterns of failure, and survival of patients with PTL at our institution and to determine any correlation between outcome and treatment strategies. Methods: We retrospectively reviewed the medical records of patients with diffuse large B cell lymphoma of the testis. All patients were diagnosed and managed at the University of Texas MD Anderson Cancer Center between 1964 and 2008. Pathological diagnosis of DLBCL of the testis was made from orchiectomy specimens or fine needle aspiration of the testis. Factors analyzed included: age, stage at diagnosis, presence of b-symptoms, serum lactate dehydrogenase (LDH), beta-2 microglobulin, and modality of treatment. Cox proportional hazards model was used to generate hazard ratios for prognostic factors that affect the overall survival (OS) and disease free survival (DFS). Estimates of survival were calculated using the Kaplan-Meier method and the log-rank test was used to compare OS and DFS by the type of treatment. Results: Seventy-five patients with DLBCL of the testis were identified. The median age at diagnosis was 64 years (range 22 – 82). Ann Arbor stage I was present in 34 (45%), stage II in 13 (17%), stage III in 4 (5%), stage IV in 23 (31%), and unknown in 1 (1%). On univariate analysis, patients with advanced stage disease (stage III and IV; p = 0.042), elevated serum LDH levels (p = 0.029), B-symptoms at presentation (p = 0.003), and high-intermediate and high IPI score (p = 0.013), had a significantly decreased OS and DFS. The 5-years OS and DFS for all patients was 53.3%, and 45.9%, respectively. Treatment details are described in Table 1. A greater proportion of patients who received trimodality regimen (doxorubicin based chemotherapy, scrotal RT, and intrathecal methotrexate) had limited stage disease compared to those receiving less than a trimodality approach, however this variation was not statistically significant (71% vs 60%; p = 0.374, chi-square test). The 5-year OS and DFS for those treated with trimodality regimen was 90.4% and 79.5%, respectively, while for those treated with doxorubicin-based chemotherapy and testicular irradiation but without intrathecal chemotherapy it was 63.5%, and 55.6%, respectively, and for those treated with doxorubicin-based chemotherapy alone it was 39.3%, and 28.6% (p = 0.009 for OS and p = 0.012 for DFS). Figures 1 & 2 Conclusion: Prognostic factors for DLBCL of the testis include stage, LDH, B-symptoms, and IPI score. Patients with DLBCL of the testis who received trimodality regimen (doxorubicin based chemotherapy combined with scrotal RT and intrathecal chemotherapy) had significantly improved OS and DFS, which support the use of this approach as standard of care. Disclosures: No relevant conflicts of interest to declare.


Folia Medica ◽  
2020 ◽  
Vol 62 (1) ◽  
pp. 200-203
Author(s):  
Yavuz Guler ◽  
Burak Ucpinar ◽  
Akif Erbin

Introduction: Testicular cancers detected in older males are mostly testicular lymphomas. Primary testicular lymphoma (PTL) is a rare, clinically aggressive form of extranodal lymphoma. In population-based studies, the  incidence of PTL is 0.09-0.26/100.000. The vast majority of PTL are diffuse large B-cell lymphoma (DLBCL).   Case presentation: We present a case of PTL diagnosed in a 68-year-old male patient and also, we discuss the incidence, clinical presentation, prognostic factors and management of this rare pathology in the light of current literature. Histopathological and immunohistochemical exams of the patient confirmed the diagnosis of DLBCL after radical orchiectomy. According to the internal prognostic index (IPI), patients’ IPI score was evaluated as 5 and according to Ann Arbor staging, patients’ stage was interpreted as grade 3E. Cyclophosphamide, vincristine, etoposide, and prednisolone chemotherapy was planned for the patient and until now, the patient received his first chemotherapy regimen.   Discussion: Primary testicular lymphoma should be kept in mind for every patient who admits with a testicular mass, especially in advanced age.  Misinterpreatation of the clinical findings can delay the definitive diagnosis. Primary testicular lymphoma should be managed with a multi-disciplinary team including urologists, medical and radiation oncologists. 


Blood ◽  
2014 ◽  
Vol 123 (4) ◽  
pp. 486-493 ◽  
Author(s):  
Chan Y. Cheah ◽  
Andrew Wirth ◽  
John F. Seymour

Abstract Primary testicular lymphoma (PTL) is a rare, clinically aggressive form of extranodal lymphoma. The vast majority of cases are histologically diffuse large B-cell lymphoma, but rarer subtypes are clinically important and must be recognized. In this review, we discuss the incidence, clinical presentation, and prognostic factors of PTL and present a summary of the recent advances in our understanding of its pathophysiology, which may account for the characteristic clinical features. Although outcomes for patients with PTL have historically been poor, significant gains have been made with the successive addition of radiotherapy (RT), full-course anthracycline-based chemotherapy, rituximab and central nervous system–directed prophylaxis. We describe the larger retrospective series and prospective clinical trials and critically examine the role of RT. Although rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone given every 21 days with intrathecal methotrexate and locoregional RT is the current international standard of care, a substantial minority of patients progress, representing an unmet medical need. Finally, we discuss new treatment approaches and recent discoveries that may translate into improved outcomes for patients with PTL.


Author(s):  
R. Anantharamakrishnan ◽  
Senthil Kumar ◽  
K. Pranay ◽  
Rekadi Srinivasa Rao

Primary testicular lymphoma is a collection of neoplasms that constitutes only 1–9% of testicular tumors. Although uncommon in the general population, it is the most common type of malignant testicular tumor in men ≥50 years of age. There are various subtypes, including diffuse large B-cell lymphoma (DLBCL), Burkitt’s lymphoma and follicular lymphoma. In the adult testis, primary DLBCL represents the most frequent subtype of lymphoma (80–90%), whereas the majority of testicular lymphomas in children consist of secondary involvement by Burkitt’s lymphoma, DLBCL or lymphoblastic lymphoma. The typical clinical sign is a painless testicular mass of variable size that is usually unilateral. Primary testicular lymphoma may be identified during the initial presentation of primary or systemic malignant lymphomas, or during a clinical follow-up of patients with lymphoma. Historically, primary testicular lymphoma has been reported to exhibit a poor prognosis with an overall 5-year survival rate of 17–48%, particularly primary testicular DLBCL, whose clinical behavior has been reported to be aggressive and to demonstrate a high propensity to disseminate to the central nervous system (CNS) and skin at presentation and relapse. The underlying mechanisms responsible for this aggressive behaviour have yet to be elucidated. In the present study, a patient with primary testicular DLBCL was examined from histological examination and immunohistochemical staining in the diagnosis of testicular DLBCL.


2021 ◽  
Vol 8 (1) ◽  
pp. 1
Author(s):  
Nicholas Haslett ◽  
Adam Ulano ◽  
John C. DeWitt

Neurolymphomatosis is a rare manifestation of lymphoma presenting as diffuse invasion and involvement of peripheral and spinal nerves. Due to the common presenting symptomatology of neurologic complaints localizing to the affected peripheral nerve, lymphoma as the underlying etiology can be diffificult to diagnose. Here we present the case of a gentleman presenting with right extremity neuropathic symptoms, subsequently discovered to have diffuse large B-cell lymphoma of testiticular orgin after nerve biopsy revealed neurolymphomatous involvement of a spinal nerve. This case highlights the importance of the consideration of neurolymphomatosis in the work up of neuropathic symptoms, as well as the full assessment for the site of primary involvement.


Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 4161-4161
Author(s):  
Hany R.Y. Guirguis ◽  
Mervat Mahrous ◽  
Matthew Cheung ◽  
Liying Zhang ◽  
Rena Buckstein

Abstract Abstract 4161 Background: While some clinical characteristics/sites of diffuse large B-cell lymphoma (DLBCL) are associated with increased rates of central nervous system (CNS) relapse, the role/benefits of CNS prophylaxis are controversial, particularly in the era of better disease control with R-CHOP chemotherapy. We evaluated the benefits of high dose methotrexate (HDMTX 3 g/m2) and intrathecal (IT) chemotherapy (MTX 12 mg) as primary CNS prophylaxis (CNSPr) in patients with DLBCL (de novo or transformed) treated with curative intent R-CHOP chemotherapy between the years of January 2002-December 2008. During this period, we adopted a local ‘informal' clinical practice recommendation for CNS prophylaxis for patients with testicular involvement, increased lactate dehydrogenase enzyme (LDH) and greater than 1 extranodal (EN) site, epidural disease, invasive sinus or skull involvement. Compliance with and efficacy of this treatment recommendation was the catalyst for this retrospective audit. Methods: Using the cancer pharmacy database, we retrospectively identified 214 patients who received 1–8 cycles of R-CHOP chemotherapy (median 6) for DLBCL. Patients with transformed histologies were included if they had not yet received R-CHOP chemotherapy. Patients with HIV or CNS involvement at diagnosis were excluded. Results: The median age was 64 with 54% male patients. 71% had stage III-IV disease, 49% had an elevated LDH, 57% EN disease (35% >1 EN site), 49% had high or high-intermediate international prognostic index scores (IPI), 14% had transformed disease, 8 patients had testicular lymphoma, 11% had increased LDH + > 1 EN site. 27 patients (12.6%) received some form of CNS prophylaxis (37% IT MTX alone (median 1.5 times (1-3)); 7% with HDMTX 3g/m2 alone (median 1.5 times (1-3)) and 56% with both HDMTX and IT chemotherapy (median 2 HDMTX (1-6) and 3 IT chemotherapy (1-9)). Compared with patients that did not receive CNSPr, patients that did had higher stage disease (p=.0061), more EN disease (P <0.0001), more testicular involvement (p<0.0001), higher IPI (p=.029), age adjusted IPI (aaIPI) (p=.048) and revised international prognostic index (R-IPI) (p=.016). Of those deemed to be at higher risk of CNS relapse defined by high IPI (20%; Haioun et al. 2000), high-intermediate and high aaIPI (52%; Feugier et al. 2004), or increased LDH and > 1 EN site (11%; Van Besien et al. 1998), 23%, 18% and 29% received CNSPr respectively, demonstrating imperfect compliance with local practice guidelines. 75% of patients with testicular lymphoma received CNSPr, 83% inclusive of both HDMTX (median 2) and IT chemotherapy (median 3). Eight patients (3.7% of all patients) relapsed in the CNS at a median time of 17 months (6-35 months range). Five patients developed parenchymal CNS relapse, 2 had leptomeningeal disease and 1 had both parenchymal and leptomeningeal involvement. The relapse rates in those that received or did not receive prophylaxis were 7.4% (2/27) and 3.2% (6/187) respectively. Six out of the 8 relapses were isolated relapses in the CNS and 4/8 were in testicular lymphoma patients. If the 8 testicular lymphoma patients were excluded, the overall rate of CNS relapse was 1.9% (0% in the 21 with prophylaxis and 2% in the 185 that did not). 62% (5/8) of those with CNS relapse have died with a median survival post CNS relapse of 2 months (range 0.5–16). Of the 4/8 patients with testicular involvement that relapsed, 3 had received CNS prophylaxis with HDMTX and IT chemotherapy (median 2 (range 1–5)). By multivariate analysis, testicular involvement was the only negative risk factor for CNS relapse (HR 33.5, p<.0001 (95% CI 8.3–135). Conclusion: R-CHOP chemotherapy may negate the need for CNS prophylaxis in patients with DLBCL, even those formerly identified as higher risk using standard prognostic scoring systems with the exception of testicular lymphoma. Better forms of CNS prophylaxis are needed in these patients. CNS relapses appear to occur later as isolated parenchymal events compared with the pre rituximab era, but survival post CNS relapse remains short. Disclosures: No relevant conflicts of interest to declare.


Praxis ◽  
2016 ◽  
Vol 105 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Andreas Lohri

Zusammenfassung. Maligne Lymphome unterteilen sich zwar in über 60 Entitäten, das grosszellige B-Zell-Lymphom, das follikuläre Lymphom, der Hodgkin und das Mantelzell-Lymphom machen aber mehr als die Hälfte aller Lymphome aus. Im revidierten Ann Arbor staging system gelten die Suffixe «A» und «B» nur noch für den Hodgkin. «E» erscheint nur noch bei Stadien I und II. Eine Knochenmarksuntersuchung wird beim Hodgkin nicht mehr verlangt, beim DLBCL (Diffuse large B cell lymphoma) nur, falls das PET keinen Knochenmark-Befall zeigt. Der PET-Untersuchung, speziell dem Interim-PET, kommt eine entscheidende Bedeutung zu. PET-gesteuerte Therapien führen zu weniger Toxizität. Gezielt wirkende Medikamente mit eindrücklicher Wirksamkeit wurden neu zugelassen. Deren Kosten sind hoch. Eine strahlen- und chemotherapiefreie Behandlung maligner Lymphome wird in Zukunft möglich sein.


Sign in / Sign up

Export Citation Format

Share Document