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Anaplastic lymphoma kinase protein positive diffuse large B cell lymphoma; A developing world experience
Huzaifah Salat1, Nasir Ud Din2, Tariq Moatter2
1Vanderbilt University Medical Centre, Division of Medicine, 116121st Ave. SMCN S-3223, Nashville, TN, 37232, United States.
Pathology, Research and Practice
|May 29, 2017
Summary
Anaplastic lymphoma kinase (ALK) positive diffuse large B-cell lymphoma (ALK+DLBCL) is a rare aggressive non-Hodgkin
Area of Science:
- Hematology
- Oncology
- Pathology
Background:
- Anaplastic lymphoma kinase (ALK) positive diffuse large B-cell lymphoma (ALK+DLBCL) is a rare, aggressive non-Hodgkin's lymphoma (NHL).
- ALK+DLBCL presents unique diagnostic challenges due to its aberrant immunophenotype and differential diagnosis with other lymphomas and carcinomas.
- Conventional diffuse large B-cell lymphoma treatments lack clinical or prognostic significance in ALK+DLBCL.
Purpose of the Study:
- To present a series of 7 ALK+DLBCL cases from Aga Khan University Hospital.
- To review existing literature on ALK+DLBCL.
- To contribute to the understanding of this rare lymphoma subtype in the South Asian population.
Main Methods:
- Case series reporting 7 ALK+DLBCL cases diagnosed between 2009 and 2015.
- Comprehensive literature review on ALK+DLBCL.
- Analysis of diagnostic challenges and treatment implications.
Main Results:
- The study presents the second-largest reported series of ALK+DLBCL cases globally.
- This is the first reported series from the South Asian subcontinent.
- The findings highlight the diagnostic complexities and the need for specific management strategies.
Conclusions:
- ALK+DLBCL is a distinct and aggressive lymphoma subtype requiring careful diagnosis.
- Further research is needed to establish optimal treatment protocols for ALK+DLBCL.
- This study provides valuable data on ALK+DLBCL in a previously underrepresented region.

