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Secondary bilateral adrenal Burkitt lymphoma with hepatic and renal involvement in a 17-year-old patient: A rare case report and literature review.

증례보고 1/5 보강
Radiology case reports 📖 저널 OA 100% 2021: 2/2 OA 2022: 4/4 OA 2023: 5/5 OA 2024: 9/9 OA 2025: 21/21 OA 2026: 64/64 OA 2021~2026 2026 Vol.21(1) p. 214-219 OA
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
추출되지 않음
I · Intervention 중재 / 시술
the pediatric-adapted Lymphomes Malins B (LMB) chemotherapy protocol
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
The patient received the pediatric-adapted Lymphomes Malins B (LMB) chemotherapy protocol. This case highlights the diagnostic challenges and aggressive behavior of adrenal Burkitt lymphoma in young patients and emphasizes the importance of early recognition, biopsy, and prompt initiation of intensive therapy.

Elmassoudi N, Aznague Y, Ayez M, Adnor S, Maouelainin ML, Saalaoui A

📝 환자 설명용 한 줄

Secondary adrenal involvement by lymphoma is rare in adolescents, and Burkitt lymphoma in this location is exceptional.

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↓ .bib ↓ .ris
APA Elmassoudi N, Aznague Y, et al. (2026). Secondary bilateral adrenal Burkitt lymphoma with hepatic and renal involvement in a 17-year-old patient: A rare case report and literature review.. Radiology case reports, 21(1), 214-219. https://doi.org/10.1016/j.radcr.2025.09.063
MLA Elmassoudi N, et al.. "Secondary bilateral adrenal Burkitt lymphoma with hepatic and renal involvement in a 17-year-old patient: A rare case report and literature review.." Radiology case reports, vol. 21, no. 1, 2026, pp. 214-219.
PMID 41142855 ↗

Abstract

Secondary adrenal involvement by lymphoma is rare in adolescents, and Burkitt lymphoma in this location is exceptional. We report a 17-year-old male with no prior medical history who presented with 3 months of persistent bilateral flank pain and significant unexplained weight loss. Contrast-enhanced computed tomography (CT) demonstrated large bilateral adrenal masses with central necrosis and direct contiguous extension into the adjacent liver and kidneys, while adrenal function remained preserved. No residual adrenal parenchyma was identifiable. CT-guided biopsy and immunohistochemistry confirmed Burkitt lymphoma with diffuse CD20 expression and a Ki-67 proliferation index approaching 100%. The patient received the pediatric-adapted Lymphomes Malins B (LMB) chemotherapy protocol. This case highlights the diagnostic challenges and aggressive behavior of adrenal Burkitt lymphoma in young patients and emphasizes the importance of early recognition, biopsy, and prompt initiation of intensive therapy.

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