Chronic Epstein-Barr virus infection causing both benign and malignant lymphoproliferative disorders / 소아과
Korean Journal of Pediatrics
;
: 420-424, 2014.
Artículo
en Inglés
| WPRIM
| ID: wpr-96674
ABSTRACT
The Epstein-Barr virus (EBV) is oncogenic and can transform B cells from a benign to a malignant phenotype. EBV infection is also associated with lymphoid interstitial pneumonia (LIP). Here, we report the case of a 14-year-old boy who was diagnosed with a latent EBV infection and underlying LIP, without any associated immunodeficiency. He had been EBV-seropositive for 8 years. The first clinical presentations were chronic respiratory symptoms and recurrent pneumonia. The symptoms worsened in the following 2 years. The results of in situ hybridization were positive for EBV, which led to a diagnosis of LIP. The diagnosis was confirmed by the results of a thoracoscopic lung biopsy. The EBV titer of the bronchoalveolar lavage specimens obtained after acyclovir treatment was found to be fluctuating. The patient had latent EBV infection for 8 years, until presented at the hospital with intermittent abdominal pain and distension. Physical examination and pelvic computed tomography revealed a large mesenteric mass. A biopsy of the excised mass led to a diagnosis of Burkitt's lymphoma (BL). The patient received combination chemotherapy for 4 months, consisting of vincristine, methotrexate, cyclophosphamide, doxorubicin, and prednisolone. He is now tumor-free, with the LIP under control, and is being followed-up at the outpatient clinic. This is the first report of a Korean case of chronic latent EBV infection that developed into LIP and BL in a nonimmunocompromised child.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Fenotipo
/
Examen Físico
/
Neumonía
/
Vincristina
/
Biopsia
/
Aciclovir
/
Prednisolona
/
Linfocitos B
/
Doxorrubicina
/
Dolor Abdominal
Tipo de estudio:
Estudio diagnóstico
Límite:
Adolescente
/
Niño
/
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Korean Journal of Pediatrics
Año:
2014
Tipo del documento:
Artículo
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