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Lymph node core biopsies reliably permit diagnosis of lymphoproliferative diseases. Real-World Experience from 554 sequential core biopsies from a single centre.
Cohen, Oliver C; Brodermann, Maximillian H; Dervin, Aoife; Raja, Neel; Marafioti, Teresa; Otero, Sofia; Beale, Tim; Jawad, Susan; Ramsay, Alan; Pomplun, Sabine; Ardeshna, Kirit M; Proctor, Ian; Townsend, William; Morley, Simon.
Afiliación
  • Cohen OC; University College London Hospitals NHS Foundation Trust, London, UK.
  • Brodermann MH; University College London Hospitals NHS Foundation Trust, London, UK.
  • Dervin A; University College London Hospitals NHS Foundation Trust, London, UK.
  • Raja N; University College London Hospitals NHS Foundation Trust, London, UK.
  • Marafioti T; University College London Hospitals NHS Foundation Trust, London, UK.
  • Otero S; University College London Hospitals NHS Foundation Trust, London, UK.
  • Beale T; University College London Hospitals NHS Foundation Trust, London, UK.
  • Jawad S; University College London Hospitals NHS Foundation Trust, London, UK.
  • Ramsay A; University College London Hospitals NHS Foundation Trust, London, UK.
  • Pomplun S; University College London Hospitals NHS Foundation Trust, London, UK.
  • Ardeshna KM; University College London Hospitals NHS Foundation Trust, London, UK.
  • Proctor I; University College London Hospitals NHS Foundation Trust, London, UK.
  • Townsend W; University College London Hospitals NHS Foundation Trust, London, UK.
  • Morley S; University College London Hospitals NHS Foundation Trust, London, UK.
Eur J Haematol ; 106(2): 267-272, 2021 Feb.
Article en En | MEDLINE | ID: mdl-33159689
INTRODUCTION: Whilst excision biopsy is traditionally preferred, advances in radiological and histological techniques warrant a re-look at core biopsy as a viable primary diagnostic method. METHOD: Over a 3-year period, all patients who underwent core biopsy to investigate lymphoma at our centre were included. RESULTS: 554 consecutive patients were included (40.1% prior lymphoma and 59.4% new presentations). Three or more cores were taken in 420 (75.8%) cases. Median time from request to biopsy and biopsy to histology report was 2 (0-40) days and 7 (1-24) days, respectively. 510/544 (93.8%) biopsies were diagnostic. There was no difference in whether the biopsy was diagnostic based on indication (new vs. relapsed lymphoma) (P = .445), whether biopsy was PET-directed (P = .507), for T-cell lymphoma (P = .468) or nodal vs. extra-nodal (P = .693). Thirty-eight patients (6.9%) required a second biopsy due to inadequate tissue. In a patient experience survey, only 13.9% reported any complications (1 self-limiting minor bleeding, 4 bruising) whilst 16.7% reported any discomfort beyond 12 hours. CONCLUSION: Core biopsy performed by experienced radiologists and analysed by expert haemato-pathologists is a reliable, well-tolerated method for diagnosing lymphoma and confirming relapse. Multiple cores can be obtained under local anaesthetic yielding sufficient material in the majority of cases.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Biopsia con Aguja Gruesa / Ganglios Linfáticos / Trastornos Linfoproliferativos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Eur J Haematol Asunto de la revista: HEMATOLOGIA Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Biopsia con Aguja Gruesa / Ganglios Linfáticos / Trastornos Linfoproliferativos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Eur J Haematol Asunto de la revista: HEMATOLOGIA Año: 2021 Tipo del documento: Article