scholarly journals Diagnostic and Management Difficulty of Bleeding Aorto-Duodenal Fistula Associated with Hodgkin’s Lymphoma

Diagnostics ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 389
Author(s):  
Boaz Nachmias ◽  
Allan I. Bloom ◽  
Alexander Gural

Primary aorto-enteric fistula (AEF) resulting from abdominal malignancy is a rare and often fatal complication. The few reports to date are mostly secondary to solid tumors. We present a case of a patient with refractory Hodgkin’s lymphoma who developed life-threatening AEF. We describe the diagnostic and therapeutic efforts, requiring a multi-disciplinary team of interventional radiology, gastroenterology, and transfusion medicine, resulting in a favorable outcome. Importantly, we offer several insights regarding the identification and management of high-risk patients, with an emphasis on pre-treatment considerations and urgent diagnosis and intervention.

Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 1818-1818
Author(s):  
Luis P Monteiro ◽  
Catia L Gaspar ◽  
Margarida Fevereiro ◽  
Ana L Tome ◽  
Nuno Almeida ◽  
...  

Abstract Introduction: the shortage of some anticancer drugs has forced their substitution in established combination chemotherapy regimens, but the replacement may have critical effects on the results of treatment and need careful evaluation. Since 1996 we treat Hodgkin's lymphoma (HL) with the Stanford V (SV) regimen, which achieves the same results as the more widely employed ABVD regimen with the benefits of a shorter duration (12 weeks) and lower cumulative doses of bleomycin and doxorubicin. When mechlorethamine became unavailable in 2008, we substituted cyclophosphamide at a dose of 650 mg/m2 for mechlorethamine 6 mg/m2. In 2012 the Pediatric Hodgkin Lymphoma Consortium, which had adopted the same policy, suggested in a retrospective analysis that the modification could lead to an inferior event-free survival (EFS). To assess the impact of the substitution, we retrospectively compared our results with the original SV (SVo) and the modified SV (SVm). Methods: we evaluated the 265 patients consecutively treated in our center with SV between Nov/96 and Dec/14. We compared the pre-treatment characteristics, the complete remission (CR) rate, EFS and overall survival (OS) of the 184 patients who received SVo to those of the 81 patients treated with SVm. Radiotherapy indications and supportive measures were unchanged between the 2 periods. Results: median age of the 2 groups was identical: 31 (16-69) for SVo and 31 (15-72) for SVm. No differences were found in histologic subtypes (nodular sclerosis 76/74%), frequency of B symptoms (36/47%, p=0.09), proportion of advanced stages (32/33%) or International Prognostic Score (≥3 in 20/13%, p=0.22). The CR rate was 89% for SVo and 86% for SVm. With a median follow up of 9 years for the SVo group and 4.6 years for the SVm group, there were no significant differences in EFS (76/73%, p=0.66) and OS (89%/85%, p=0.63) at 5 years. Conclusion: the impact of forced substitutions in components of combination chemotherapy regimens due to drug shortage must be carefully scrutinized, notably in first line protocols for curable diseases. In the case of HL treated with the SV regimen, the present study is the first, to our knowledge, to evaluate the impact of replacing mechlorethamine by cyclophosphamide in adults. We found no difference in OS nor, unlike the pediatric study, in EFS. The substitution can be considered safe, since the modified version of SV achieves the same favorable results as the original SV. Disclosures No relevant conflicts of interest to declare.


Hematology ◽  
2015 ◽  
Vol 2015 (1) ◽  
pp. 74-81 ◽  
Author(s):  
Patrick Stiff

Abstract The role of autologous hematopoietic stem cell transplantation (ASCT) in the management of non-Hodgkin's lymphoma (NHL) is evolving, in the era of novel agents. Multiple histologies and remission stages have been impacted with changing outcomes. In the 1990s, ASCT could cure 50% of relapsed chemosensitive aggressive NHL; now the percentage maybe as low as 20% for patients relapsing within 1 year of completing rituximab-containing induction. Yet recent trials have clarified the value of first remission ASCT for high-grade NHL, the utility of augmented preparative regimens, the efficacy of ASCT in primary CNS lymphoma and in the elderly and analyses have defined strategies to reduce transplant related myeloid malignancies. In addition, optimizing nontransplant induction therapy for mantle cell and double-hit NHL is leading to improved outcomes and a re-examination of the use of ASCT in first complete remission. Caution is needed, however, as delaying transplants may mean that patients will need more morbid allogeneic transplants to achieve long-term control of refractory disease. As an alternative, maintenance therapy trials to improve ASCT outcome in high-risk patients are starting, based on the efficacy of lenolidomide and brentuximab in myeloma and Hodgkin's lymphoma, respectively. In addition, efforts to define early high-risk patients by minimal residual disease (MRD) assessments and genetic profiling, are beginning even for those with “indolent” phenotypes not currently autotransplanted. These efforts should not only refine but also enhance the value of early potentially curative ASCT, especially if novel agents only delay but do not prevent relapse for patients with NHL.


2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Sarra Benmiloud ◽  
Mohamed Hbibi ◽  
Sana Chaouki ◽  
Sana Abourazzak ◽  
Moustapha Hida

Hemophagocytic lymphohistiocytosis (HLH) is a severe life-threatening disorder, responsible for extensive phagocytosis of hematopoietic cells and causing a multisystem organ failure. If lymphomas are common causes of HLH, the association with Hodgkin’s lymphoma is rarely described in children. We report a case of a 9-year-old boy presenting with HLH as an initial manifestation of Hodgkin’s lymphoma. He has been suffering from persistent high fever, asthenia, weight loss, and hepatosplenomegaly with no lymphadenopathy. The diagnosis of HLH secondary to infectious disease was initially worn. The patient received high-dose intravenous immunoglobulin with broad-spectrum antibiotics. However, his state got worse with the onset of dry cough and pleural effusion. Histopathologic examination of pleural fluid showed the presence of Reed-Sternberg cells. The outcome was favorable after treatment by corticosteroid and chemotherapy. Hodgkin’s lymphoma revealed by HLH is a source of delayed diagnosis and should be borne in mind in children.


2020 ◽  
Vol 16 (2) ◽  
Author(s):  
Abdul Azih MN ◽  
Rahman AA ◽  
Hin HS ◽  
Chunn KY ◽  
Kori AN

We report a 26-year old lady who presented with chronic cough and breathlessness associated with subtle TB symptoms for 1 year. Her CT thorax showed multiple cavitating pulmonary nodules with mediastinal and cervical lymphadenopathy. Cervical lymph node biopsy and CT-guided pulmonary biopsy at our centre confirmed the diagnosis of Hodgkin’s lymphoma with pulmonary infiltrations. She was successfully treated with ABVD regime but later developed life-threatening bleomycin-induced pulmonary fibrosis. Sadly, she succumbed to respiratory failure due to severe pneumonia with possibility of bleomycin-induced pulmonary fibrosis. Multiple cavitating pulmonary nodules secondary to lymphoma is rare and in TB endemic area, it may result in delayed diagnosis and treatment.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 2079-2079
Author(s):  
Asad Bashey ◽  
Oralia Loza ◽  
Bridget Medina ◽  
Katherine Keesee ◽  
Sue Corringham ◽  
...  

Abstract High-dose chemotherapy (HDC) with autologous stem-cell support (ASCS) is commonly used to treat patients with relapsed or high risk but chemosensitive non-Hodgkin’s lymphoma (NHL) and Hodgkin’s Disease (HD). However, the optimum HDC regimen for these patients has not been defined. CEB or BEAM are among the most commonly used regimens, but they have not been compared in a randomized prospective study. At our center, CEB was the preferred regimen until Dec 2002 and BEAM has been the preferred regimen since. We compared pre-treatment characteristics and post HDC outcomes in 219 consecutive patients undergoing single HDC+ASCS for NHL/HD at our center who received BEAM or CEB as the HDC regimen. BEAM (BCNU 300mg/m2, Etoposide 800 mg/m2, Cytarabine 1600 mg/m2, Melphalan 140 mg/m2) was used in 110 patients and 109 patients received CEB (Cyclophosphamide 6000mg/m2, Etoposide 2000mg/m2, BCNU 600mg/m2). The groups were comparable with respect to pre-treatment characteristics: median age (48 vs 52), gender (M 66% vs 64%), diagnosis (NHL 75% vs 81%), number of prior regimens (median=2 for both),stage at diagnosis, disease status pre-HDC, and median CD34+ cell dose/kg infused (5.6 x 10e6 vs 5.4x 10e6), KPS (≥90 vs <90) (p=NS for all). Median follow-up from HDC was longer in CEB patients (841 days) than in BEAM patients (443 days). Estimated Kaplan-Meier probabilities of progression-free survival (PFS) at 12 months and 24 months post HDC were 66.3%, 49.3% for BEAM and 60.2%, 55.1% for CEB (p=NS). The probability of overall survival (OS) at 12 and 24 months was 79.2%, 68.7% respectively for BEAM and 68.6%, 62.9% for CEB (p=NS). Transplant-related mortality (TRM) at 12m was 4.5% for BEAM versus 6.4% for CEB (p=NS). A Cox proportional hazards analysis was performed to assess the effect on OS, PFS and TRM of the following variables: regimen (BEAM vs CEB), diagnosis (HD vs NHL), age, gender, KPS, number of prior Rx regimens,stage at diagnosis, stage at treatment, disease status at transplant, CD34+ cell dose. On multivariate analysis, the following statisically significant associations were observed for the three outcome variables. PFS: age, gender, number of prior regimens,disease status at transplant. OS: age, gender, diagnosis, disease status at transplant. TRM: none. Females and patients with HD had better OS and PFS than males and NHL patients respectively. Conditioning regimen did not correlate with outcome for PFS, OS or TRM.The rate of severe mucositis (as defined by use of infusional opiate therapy during the first 25 days following HDC+ASCS) was significantly higher with CEB than BEAM (53% vs 47%, p=0.040). The rate of BCNU induced pnemonitis syndrome (as measured by prednisone use during first 30–120 days following HDC+ASCS and/or hospital readmission before day +120) was not significantly different between the two regimen groups. In summary, analysis of this sequential series of well matched patients receiving BEAM or CEB for HDC+ASCS for NHL or HD indicates that survival outcomes are comparable and BEAM is associated with a significant lower incidence of mucositis


2017 ◽  
Vol 10 (4) ◽  
pp. 183-185 ◽  
Author(s):  
Rhiannon George-Carey ◽  
Maryam Parisaei ◽  
Wiece Koniman ◽  
Micaela Pluckinski ◽  
Jonathan Lambert

Hodgkin’s lymphoma is rarely diagnosed in pregnancy, occurring in 1:6000 deliveries. However, improvements in survival and the use of less gonadotoxic treatments have increased the number of Hodgkin’s lymphoma survivors becoming pregnant. Both de novo and relapsed Hodgkin’s lymphoma in pregnancy pose difficult decisions for both clinicians and patients. This review discusses important diagnostic and treatment considerations of relapsed Hodgkin’s lymphoma in pregnancy. We discuss a difficult case which illustrates these particular dilemmas and suggests the evidence behind different modalities of investigation and management.


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