본문으로 건너뛰기
← 뒤로

Rare diagnosis: the second documented report of primary diffuse large B-cell lymphoma of the fallopian tube.

1/5 보강
BMJ case reports 📖 저널 OA 40.9% 2021: 14/14 OA 2022: 17/17 OA 2023: 7/7 OA 2024: 2/12 OA 2025: 7/73 OA 2026: 4/71 OA 2021~2026 2026 Vol.19(1)
Retraction 확인
출처

Lane EJ, Watmore S

📝 환자 설명용 한 줄

Primary non-Hodgkin's lymphoma is a highly prevalent haematologic malignancy but contrarily, primary lymphoma of the female genital tract (PLFGT) is extremely rare.

이 논문을 인용하기

↓ .bib ↓ .ris
APA Lane EJ, Watmore S (2026). Rare diagnosis: the second documented report of primary diffuse large B-cell lymphoma of the fallopian tube.. BMJ case reports, 19(1). https://doi.org/10.1136/bcr-2025-269103
MLA Lane EJ, et al.. "Rare diagnosis: the second documented report of primary diffuse large B-cell lymphoma of the fallopian tube.." BMJ case reports, vol. 19, no. 1, 2026.
PMID 41611332 ↗

Abstract

Primary non-Hodgkin's lymphoma is a highly prevalent haematologic malignancy but contrarily, primary lymphoma of the female genital tract (PLFGT) is extremely rare. The most common histological subtype of PLFGT is diffuse large B-cell lymphoma (DLBCL), which most commonly arises from the ovary, cervix, uterus or vagina. It is rarer still for DLBCL to arise from the fallopian tube, and therefore, we present the second case ever reported. A woman in her 30s presented with abdominal pain and a pelvic mass on CT. The mass was laparoscopically excised, which allowed the histological diagnosis to be made, and the patient was subsequently treated with chemotherapy. This report aims to contribute to existing knowledge of this rare condition because, although unusual, PLFGT is a potential diagnosis to consider when managing pelvic masses.

🏷️ 키워드 / MeSH 📖 같은 키워드 OA만

🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반