Mantle Cell Lymphoma of the Gastrointestinal Tract in a Patient with Renal Cell Carcinoma

2016 ◽  
Vol 111 (7) ◽  
pp. 922 ◽  
Author(s):  
Homayoun Shojamanesh ◽  
Frank Melgoza
Keyword(s):  
Renal Cell Carcinoma ◽  
Gastrointestinal Tract ◽  
Cell Carcinoma ◽  
Mantle Cell Lymphoma ◽  
Renal Cell ◽  
Cell Lymphoma ◽  
Mantle Cell

Mantle Cell Lymphoma in Lymph Nodes with Metastatic Small Cell Carcinoma of Lung: A Diagnostic and Treatment Dilemma

2004 ◽  
Vol 45 (2) ◽  
pp. 409-414 ◽  
Author(s):  
Bal Kampalath ◽  
Nashwa Abed ◽  
Christopher R Chitambar ◽  
Peter vanTuinen ◽  
Gargi Chakrabarty ◽  
...  
Keyword(s):  
Lymph Nodes ◽  
Cell Carcinoma ◽  
Mantle Cell Lymphoma ◽  
Small Cell Carcinoma ◽  
Cell Lymphoma ◽  
Small Cell ◽  
Mantle Cell

scholarly journals 2586 Renal Cell Carcinoma Presenting as Paraneoplastic Syndrome Involving the Gastrointestinal Tract

2019 ◽  
Vol 114 (1) ◽  
pp. S1422-S1423
Author(s):  
Barrett Attarha ◽  
Satish Maharaj ◽  
Ciel Harris ◽  
Ron Schey ◽  
Ammar Nassri ◽  
...  
Keyword(s):  
Renal Cell Carcinoma ◽  
Gastrointestinal Tract ◽  
Cell Carcinoma ◽  
Paraneoplastic Syndrome ◽  
Renal Cell

scholarly journals Mantle Cell Lymphoma of the Gastrointestinal Tract (Lymphomatous Polyposis)

1996 ◽  
Vol 10 (3) ◽  
pp. 144-148
Author(s):  
Hugh James Freeman
Keyword(s):  
Gastrointestinal Tract ◽  
Mantle Cell Lymphoma ◽  
Cell Lymphoma ◽  
Mantle Cell ◽  
History Of ◽  
Postmortem Studies ◽  
Gastrointestinal Lymphomas ◽  
Aggressive Clinical Course ◽  
Widespread Dissemination ◽  
Entire Gastrointestinal Tract

A74-year-old male with a history of a tonsillar lymphoma developed diarrhea. Investigations led to detection of extensive intestinal lymphomatous polyposis (mantle cell lymphoma). After an aggressive clinical course with associated nodal and peripheral blood involvement, death followed within three months. Postmortem studies revealed widespread dissemination within the entire gastrointestinal tract, including the esophagus, stomach, and small and large intestines. Although this type of lymphoma is rare and accounts for only about 1% to 8% of all forms of primary B cell gastrointestinal lymphomas in North America, separation from other subtypes has become more important because of reported responses of mucosa-associated lymphoid tissue-lymphomas to antibiotics aimed atHelicobacter pylorieradication.

scholarly journals Diagnosis of Therapy-related Acute Myeloid Leukemia with t(8;21)(q22;q22.1) after Treatment for Mantle Cell Lymphoma and Oral Squamous Cell Carcinoma

2019 ◽  
pp. 1-7
Author(s):  
Patrícia Colombo Corrêa ◽  
Íris Mattos Santos-Pirath ◽  
Chandra Chiappin Cardoso ◽  
Camila Mattiolo ◽  
Bruno Vieira Dias ◽  
...  
Keyword(s):  
Squamous Cell Carcinoma ◽  
Oral Squamous Cell Carcinoma ◽  
Cell Carcinoma ◽  
Mantle Cell Lymphoma ◽  
Squamous Cell ◽  
De Novo ◽  
Cell Lymphoma ◽  
Correct Diagnosis ◽  
Treatment Strategies ◽  
Mantle Cell

Aims: We report a rare case of therapy-related AML with t(8;21)(q22;q22.1) that occurred after treatment for mantle cell lymphoma (MCL) and oral squamous cell carcinoma (OSCC). Presentation of Case: A 52 years-old male patient was diagnosed with MCL in leukemic phase. The treatment consisted in R-CHOP rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone, then patient experienced remission. Three months later, he presented a lump that was diagnosed as OSCC, which was surgically removed and treated with cisplatin and radiotherapy. Then, the patient’s hemogram presented 35.0% of blasts and, after morphologic, phenotypic and molecular analysis, it was classified as AML with t(8;21)(q22;q22.1). However, due to the previous historic of chemotherapy and radiotherapy, the final diagnosis was t-AML. Discussion: The correct diagnosis of therapy related malignancies is important due to its severity as they are very aggressive and, usually, considered incurable. t-AMLs with t(8;21)(q22;q22.1) is considered as favorable karyotype, still, it has a poorer outcome compared with its de novo counterpart. Conclusion: t-AML with t(8;21)(q22;q22.1) is rare and few cases are described in the literature. More reports are necessary to better elucidate the mechanisms involved in this disease to define better treatment strategies to prevent these events and to improve the poor outcomes.

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