2007
DOI: 10.1186/1477-7819-5-119
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Primary gastric Hodgkin's lymphoma

Abstract: Background: Primary Hodgkin's disease of the stomach is an extremely rare entity. Nearly all cases of primary gastric lymphoma are of the non-Hodgkin's variety. Diagnoses in such cases are difficult due to considerable histological similarities between the 2 disease entities.

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Cited by 18 publications
(17 citation statements)
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“…In most of the gastric Hodgkin lymphoma cases, preoperative diagnosis of gastric Hodgkin lymphoma could not be made [10], as in our patient. This can be due to the relatively low rate of Reed-Steinberg cells in biopsy specimens and increasing prevalence of histologically similar diseases.…”
Section: Discussioncontrasting
confidence: 55%
“…In most of the gastric Hodgkin lymphoma cases, preoperative diagnosis of gastric Hodgkin lymphoma could not be made [10], as in our patient. This can be due to the relatively low rate of Reed-Steinberg cells in biopsy specimens and increasing prevalence of histologically similar diseases.…”
Section: Discussioncontrasting
confidence: 55%
“…However, in some cases, careful differential diagnosis through the use of a full panel of immunohistochemical markers is necessary to exclude other disease entities, in which there are similarities with both histopathological features and the presence of HRS-like cells in tumors [4,8]. Phenotypically, the HRS cells were positive for CD30 in nearly all cases, for CD15 in the majority (75 to 85%) of cases and variable expressions of B-cell markers such as CD20 and CD79a [4,8]. In addition, these cells are negative for EMA, T-cell markers and ALK-1.…”
Section: Discussionmentioning
confidence: 99%
“…Gastric infiltration with malignancy is a relatively commonly encountered scenario observed in clinical practice with gastric adenocarcinoma (90% of cases) and PGL (less than 5% of cases and usually of the non-Hodgkin's variety) being the more prevalent histological considerations; however, PGHL remains a rare clinical entity, prior to confirmation by histology and immunohistochemistry, and is reported as being less than 1% of all PGLs 57. The demographic profile for patients with PGHL with mediastinal involvement in the literature shows a female preponderance and tends to occur in older patients; the median age listed in pooled data in the literature ranges from 27–50 years of age 8.…”
Section: Discussionmentioning
confidence: 99%