A rare type of cancer called Hodgkin lymphoma (HL) arises in the lymphatic system. Thomas Hodgkin, a British physician who was discovered in 1832, suggested the name. Under a microscope, Reed-Sternberg cells—abnormal cells that are present in this kind of lymphoma—are easily visible.
Hodgkin lymphoma can be classified into two basic categories: nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) and classical Hodgkin lymphoma (cHL).
There are multiple histological subtypes of classical Hodgkin lymphoma, each with unique characteristics. Among these subtypes are:
Unlike classical Hodgkin lymphoma, nodular lymphocyte-predominant Hodgkin lymphoma is a less prevalent variation. Popcorn cells, which have a unique look and are huge, multi-lobed cells, are what define it. Compared with common Hodgkin lymphoma, NLPHL typically has a more indolent outcome.
Although HL may affect individuals at any age, its typical mixed-age distribution indicates that it most frequently strikes early and late adulthood. Common signs of Hodgkin lymphoma include painless swelling of lymph nodes, tiredness, fever, night sweats, and unexplained weight loss.
Chemotherapy, radiation therapy, and even stem cell transplantation are used in the treatment of Hodgkin lymphoma. Hodgkin lymphoma has an excellent prognosis these days, with high cure rates, particularly in situations detected early in the disease. Improvements in diagnosis and therapy are contributing to our growing understanding of Hodgkin lymphoma and providing hope for better prognoses and a higher standard of living for people afflicted with the illness.
A wide range of blood malignancies known as non-Hodgkin lymphoma (NHL) originates from lymphocytes, a subset of white blood cells. In comparison with Hodgkin lymphoma, NHL is more common, making up over 90% of all lymphomas, and does not feature Reed-Sternberg cells. Both B cells and T cells are susceptible to NHL, and their subtypes are distinguished by many characteristics such as cell type, growth pattern, and genetic traits.
Here is an overview of some common subtypes of Non-Hodgkin lymphoma
B cells are the main target of the closely related diseases CLL and SLL. CLL often manifests in the blood and bone marrow, while SLL affects the lymph nodes. Both are seen as distinct symptoms of the same illness and have similar therapeutic strategies.
Mature T cells give rise to a variable group of aggressive lymphomas known as PTCL. Compared to B-cell lymphomas, these lymphomas are less prevalent and can be difficult to cure. Anaplastic large cell lymphoma (ALCL), angioimmunoblastic T-cell lymphoma (AITL), and other subtypes are examples of PTCL subtypes.
An aggressive B-cell lymphoma called Burkitt lymphoma frequently appears as a fast-growing tumour in the jaw or other facial bones. It is more common in regions with a high incidence of malaria and is linked to the Epstein-Barr virus (EBV). Chemotherapy is one of the intensive treatment options for Burkitt lymphoma.
Anaplastic huge Cell Lymphoma (ALCL) is a kind of lymphoma defined by the presence of anaplastic cells, which are huge, damaged cells. Both T cells and null cells—those without T or B cell markers—may be impacted. ALK-positive and ALK-negative subtypes are the two further classifications for ALCL. Compared to ALK-negative ALCL, ALK-positive ALCL frequently has a better prognosis.
Non-Hodgkin lymphoma can cause several symptoms, including fever, fatigue, night sweats, painless lymph node swelling, and unexplained weight loss. The exact subtype, disease stage, and unique patient characteristics all influence the NHL therapy plan. Chemotherapy, immunotherapy, targeted therapy, radiation therapy, and stem cell transplantation are examples of common treatments.
Lymphoma, a diverse group of cancers affecting the lymphatic system, comprises various subtypes with distinct characteristics. Each type and sub-type exhibit unique clinical behaviours, necessitating tailored treatment approaches. Diagnoses rely on biopsy, imaging and molecular analysis. Advances in targeted therapies and immunotherapies have improved outcomes, emphasizing personalized treatment strategies. Ongoing research aims to enhance understanding and refine therapeutic interventions for these complex malignancies. The multifaceted nature of lymphoma underscores the importance of precise diagnosis and evolving treatment paradigms for improved patient outcomes.
Q1: What is the most rare type of lymphoma?
A: Extranodal NK/T-cell lymphoma, nasal type.
This is a serious kind of lymphoma more common in Asian and Hispanic groups but very rare in the US and Europe overall. It can affect both adults and children, usually affecting the sinuses and nasal cavity.
Q2: Is lymphoma a blood disease?
A: White blood cells form the majority of the fluid known as lymph, and lymphomas are malignancies that originate in these cells. Your body uses lymph to fight infections. One type of blood cancer is lymphoma. It happens when abnormal white blood cells dominate your lymphatic system and grow.