Evidence map›Paper›PMID 16672329›Full record

ArticleThe British journal of ophthalmology2006

Primary lymphoma of the lacrimal sac: an EORTC ophthalmic oncology task force study.

L D Sjö, E Ralfkiaer, B R Juhl, J U Prause, T Kivelä, C Auw-Haedrich, F Bacin, M Carrera, S E Coupland, B Delbosc and 7 more

Open access · greenAbstract read
In one paragraph

Article in The British journal of ophthalmology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Exclusive or combined endoscopic approach to tumours of the lower lacrimal pathway: review of the literature.Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Lacrimal sac diffuse large B-cell lymphoma: A case report.Indian journal of ophthalmology · 2022
    Article
  9. Lacrimal Sac Tumors: A Case Series.Ocular oncology and pathology · 2022
    Article
  10. Lacrimal sac lymphoma: a case report.Archives of craniofacial surgery · 2022
    Article
  11. Lacrimal sac lymphoma: a case series and literature review.International journal of ophthalmology · 2022
    Article
  12. Article
  13. [Masquerade lacrimal duct stenosis: prevalence of lacrimal sac tumors].Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Clinical analysis of 90 cases of malignant lacrimal sac tumor.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2018
    Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 1 institution in 1 country.

L D SjöEye Pathology Institute, University of Copenhagen, Denmark.
E Ralfkiaer
B R Juhl
J U Prause
T Kivelä
C Auw-Haedrich
F Bacin
M Carrera
S E Coupland
B Delbosc
N Ducrey
B Kantelip
J L Kemeny
P Meyer
N C Sjö
S Heegaard
European Organization for Research and Treatment of Cancer
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo define the clinical and histopathological characteristics of primary lacrimal sac lymphoma in a predominantly white population.

methodsSpecimens of lacrimal sac lymphoma and follow up data were solicited from members of the Ophthalmic Oncology Task Force of the European Organization for Research and Treatment of Cancer (EORTC) and the European Ophthalmic Pathology Society (EOPS). Specimens were stained with haematoxylin and eosin and an immunohistochemical panel against leucocyte antigens was applied. Diagnosis was reached by consensus of five experienced pathologists according to the World Health Organization classification system. The histopathological findings were correlated with the clinical data.

resultsOf 15 primary lacrimal sac lymphomas, five (33%) were diffuse large B cell lymphoma (DLBCL), five (33%) were extranodal marginal zone B cell lymphoma of mucosa associated lymphoid tissue (MALT lymphoma), three were classified as "transitional MALT lymphoma," being in transition from MALT lymphoma to DLBCL, and two were unclassified B cell lymphomas. Nine of the patients were female, and the median age at the time of diagnosis was 71 years (range 45-95 years). The most frequent presenting symptoms were epiphora (85%), swelling in the region of the lacrimal sac (79%), and dacryocystitis (21%). All but one patient presented in stage I. Systemic spread occurred in three of nine patients (33%). The 5 year overall survival was 65%.

conclusionsDLBCL and MALT lymphoma are equally common in the lacrimal sac in contrast with the remaining periorbital and/or orbital region where MALT lymphoma predominates.

Indexed as

AgedAged, 80 and overAntigens, CDAntigens, NeoplasmFemaleHumansLacrimal Apparatus DiseasesLymphoma, B-CellLymphoma, B-Cell, Marginal ZoneLymphoma, Large B-Cell, DiffuseMaleMiddle AgedRetrospective StudiesAntigens, CDAntigens, Neoplasm

Identifiers

PMID16672329
PMCPMC1857190
OpenAlexW2133164282

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.