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Duodenal-type follicular lymphoma (DFL) is a form of lymphoma in which certain lymphocyte types, the B-cell-derived centrocytes and centroblasts, form lymph node follicle-like structures principally in the duodenum and other parts of the small intestine. It is an indolent disease which on rare occasions progresses to a more aggressive lymphoma ...
In situ follicular lymphoma is an accumulation of monoclonal B cells (i.e. cells descendent from a single ancestral cell) in the germinal centers of lymphoid tissue. These cells commonly bear a pathological genomic abnormality, i.e. a translocation between position 32 on the long (i.e. "q") arm of chromosome 14 and position 21 on chromosome 18's q arm.
May progress to follicular lymphoma or mantle cell lymphoma; may be associated with the development of certain other lymphoid malignancies: Duration: Chronic: Types: In situ follicular lymphoma; in situ mantle cell lymphoma: Treatment: Follow-up tests for the development of follicular or mantle cell lymphoma, or other lymphoid malignancies
Patients normally present with painless, swollen lymph nodes, often in the neck, armpit, or groin. [1] Some have swollen lymph nodes inside their body, such as in the chest or abdomen, which can go undetected until they become very large and cause symptoms like cough or abdominal pain. [1]
Pediatric-type follicular lymphoma (PTFL) is a disease in which malignant B-cells (i.e. a lymphocyte subtype originating from the bone marrow) accumulate in, overcrowd, and cause the expansion of the lymphoid follicles in, and thereby enlargement of the lymph nodes in the head and neck regions [1] and, less commonly, groin and armpit regions. [2]
Follicular hyperplasia (FH) is a type of lymphoid hyperplasia and is classified as a lymphadenopathy, which means a disease of the lymph nodes. It is caused by a stimulation of the B cell compartment and by abnormal cell growth of secondary follicles .
Peripheral T-cell lymphoma subtype peripheral T-cell lymphoma not otherwise specified (PTCL-NOS): Unlike ITCLD-GT, PTCL-NOS a) is a heterogenous disease that typically involves peripheral lymph nodes but only rarely develops in the GI tract [15] and b) is characterized by the rapid proliferation of CD4+ T cells that overexpress either GATA3 or ...
In Type II RCD, the same types of abnormal ILE found in the small intestine may be detected in the colon, stomach, [9] mesenteric lymph nodes, blood, bone marrow, and epithelium of the airways and skin. [9] Finally, the small intestinal lesions in Type II RCD contain IL-2 and IL-21 [18] as well as increased levels of IL-15. [3]