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Idelalisib-associated Enterocolitis: Clinicopathologic Features and Distinction From Other Enterocolitides
Christine Y Louie1, Michael A DiMaio, Karen E Matsukuma
1Departments of *Pathology ‡Medicine (Hematology), Stanford University School of Medicine, Stanford †Department of Pathology, University of California Davis, Sacramento, CA.
Idelalisib treatment for certain leukemias can cause enterocolitis. Histologic analysis revealed apoptosis, cryptitis, and increased intraepithelial lymphocytes, aiding diagnosis and differentiation from other conditions.
Area of Science:
- Oncology
- Gastroenterology
- Pathology
Background:
- Idelalisib, a phosphoinositide-3-kinase δ inhibitor, is approved for chronic lymphocytic leukemia/small lymphocytic lymphoma and follicular lymphoma.
- Idelalisib is associated with severe diarrhea and colitis as known side effects.
Purpose of the Study:
- To describe the histologic findings of idelalisib-associated enterocolitis.
- To aid in differentiating idelalisib-associated enterocolitis from other gastrointestinal conditions.
Main Methods:
- Retrospective review of colon biopsies from 11 patients treated with idelalisib for leukemia.
- Histologic examination including apoptosis assessment, cryptitis, architectural distortion, and inflammatory cell analysis.
- Immunohistochemical stains for cytomegalovirus were performed in a subset of cases.
Main Results:
- All biopsies showed apoptosis within crypts; 5 had moderate to severe apoptosis with goblet cell loss.
- Focal acute cryptitis was present in all cases, with 8 showing mild architectural distortion.
- Increased lamina propria inflammation and intraepithelial lymphocytes (predominantly CD8 T cells) were observed in most cases.
Conclusions:
- Histologic features of idelalisib-associated enterocolitis include apoptosis, cryptitis, and increased intraepithelial lymphocytes.
- Recognizing these features is crucial for distinguishing idelalisib-associated enterocolitis from mimics like graft-versus-host disease and infectious enterocolitis.
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