1999
DOI: 10.5858/1999-123-0335-ailclo
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Angiotropic (Intravascular) Large Cell Lymphoma of T-Cell Phenotype Presenting as Acute Appendicitis in a Patient With Acquired Immunodeficiency Syndrome

Abstract: We describe a patient with acquired immunodeficiency syndrome who presented with acute appendicitis but was found to have angiotropic large cell lymphoma (ALCL) by pathologic examination of the appendectomy specimen, without acute inflammation. Very rare cases of angiotropic large cell lymphoma have been reported in patients with human immunodeficiency virus infection, and most cases of this rare lymphoma are of B-cell origin, but in this instance immunohistochemical analysis showed a T-cell phenotype.

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Cited by 27 publications
(1 citation statement)
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“…10 According to the literature we collected, there are 12 reports of IVLBCL occurring in the gastrointestinal system, involving 15 cases, of which 5 occurred in the small intestine. 10,[22][23][24][25][26][27][28][29][30][31][32] The clinicopathological characteristics of IVLBCL in the gastrointestinal tract are described in Supplemental Table 1. The pathogenesis of IVLBCL in the gastrointestinal tract is complex, and the clinical symptoms almost always present as acute abdominal pain.…”
Section: Discussionmentioning
confidence: 99%
“…10 According to the literature we collected, there are 12 reports of IVLBCL occurring in the gastrointestinal system, involving 15 cases, of which 5 occurred in the small intestine. 10,[22][23][24][25][26][27][28][29][30][31][32] The clinicopathological characteristics of IVLBCL in the gastrointestinal tract are described in Supplemental Table 1. The pathogenesis of IVLBCL in the gastrointestinal tract is complex, and the clinical symptoms almost always present as acute abdominal pain.…”
Section: Discussionmentioning
confidence: 99%