Abstract
Comparison of LyP and HD suggests that these are closely related lymphoproliferative disorders that may occur in the same patient, share similar histologic features, and have the same immunologic phenotype. Recent studies of the molecular biology of both disorders confirm a similar distribution of T-cell receptor gene rearrangement patterns. The study of LyP, although a rare and benign disorder, has improved our understanding of HD, which appears, in some cases, to be a proliferation of malignant activated T lymphocytes. Further analysis of LyP may lead to a better understanding of the spontaneous regression of this disorder and result in new methods for treatment of HD.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
