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Epstein-Barr virus-associated smooth muscle tumors in immunocompromised patients: Six case reports.
Khan, Afshin A; Estfan, Bassam N; Yalamanchali, Anirudh; Niang, Djibril; Savage, Erica C; Fulmer, Clifton G; Gosnell, Hailey L; Modaresi Esfeh, Jamak.
Afiliación
  • Khan AA; Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH 44195, United States. khana13@ccf.org.
  • Estfan BN; Department of Solid Tumor Oncology, Taussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, United States.
  • Yalamanchali A; Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH 44195, United States.
  • Niang D; Department of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH 44195, United States.
  • Savage EC; Department of Pathology, Cleveland Clinic, Cleveland, OH 44195, United States.
  • Fulmer CG; Department of Pathology, Cleveland Clinic Foundation, Cleveland, OH 44195, United States.
  • Gosnell HL; Department of Pathology, Cleveland Clinic Foundation, Cleveland, OH 44195, United States.
  • Modaresi Esfeh J; Department of Gastroenterology, Hepatology and Nutrition , Cleveland Clinic, Cleveland, OH 44195, United States.
World J Clin Oncol ; 13(6): 540-552, 2022 Jun 24.
Article en En | MEDLINE | ID: mdl-35949429
BACKGROUND: Epstein-Barr virus associated smooth muscle tumor (EBV-SMT) is a rare oncological entity. However, there is an increasing incidence of EBV-SMTs, as the frequency of organ transplantation and immunosuppression grows. EBV-SMT diagnosis relies on histopathology and immunochemical staining to distinguish it from post-transplant lymphoproliferative disorder (PTLD). There is no clear consensus on the treatment of EBV-SMTs. However, surgical resection, chemotherapy, radiation therapy, and immunosuppression reduction have been explored with varying degrees of success. CASE SUMMARY: Our case series includes six cases of EBV-SMTs across different age groups, with different treatment modalities, adding to the limited existing literature on this rare tumor. The median latency time between immunosuppression and disease diagnosis is four years. EBV-SMTs present with variable degrees of aggressiveness and seem to have worse clinical outcomes in patients with tumor multiplicity and worse immunocompetency. CONCLUSION: It is imperative to continue building on this knowledge and keeping EBV-SMTs on the differential in immunocompromised individuals.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: World J Clin Oncol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: World J Clin Oncol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos