Evidence map›Paper›PMID 32789566›Full record

ArticleInternational journal of hematology2020

Lymphoplasmacytic lymphoma in a patient with Birt-Hogg-Dubé syndrome.

Keiji Kurata, Hisayuki Matsumoto, Naoe Jimbo, Kimikazu Yakushijin, Katsuya Yamamoto, Mitsuhiro Ito, Yuji Nakamachi, Hiroshi Matsuoka, Jun Saegusa, Kuniaki Seyama and 2 more

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Multiple Myeloma in a Patient with Birt-Hogg-Dubé Syndrome.Internal medicine (Tokyo, Japan) · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Keiji KurataDepartment of Medical Oncology and Hematology, Kobe University Hospital, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan. kkurata@med.kobe-u.ac.jp.ORCID http://orcid.org/0000-0003-1060-9218
Hisayuki MatsumotoDepartment of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
Naoe JimboDepartment of Diagnostic Pathology, Kobe University Hospital, Kobe, Japan.
Kimikazu YakushijinDepartment of Medical Oncology and Hematology, Kobe University Hospital, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Katsuya YamamotoDepartment of Medical Oncology and Hematology, Kobe University Hospital, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Mitsuhiro ItoDepartment of Medical Oncology and Hematology, Kobe University Hospital, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Yuji NakamachiDepartment of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
Hiroshi MatsuokaDepartment of Medical Oncology and Hematology, Kobe University Hospital, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Jun SaegusaDepartment of Clinical Laboratory, Kobe University Hospital, Kobe, Japan.
Kuniaki SeyamaDivisions of Respiratory Medicine, Faculty of Medicine, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Tomoo ItohDepartment of Diagnostic Pathology, Kobe University Hospital, Kobe, Japan.
Hironobu MinamiDepartment of Medical Oncology and Hematology, Kobe University Hospital, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.
Kobe University Hospital · JPJuntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Birt-Hogg-Dubé (BHD) syndrome is an autosomal dominant disease characterized by benign skin hamartomas, pulmonary cysts leading to spontaneous pneumothorax, and an increased risk of renal cancer. BHD syndrome is caused by germline mutations in the folliculin (FLCN) gene, a putative tumor suppressor, which result in loss of function of the folliculin protein and may cause cancer predisposition. In a 45-year-old woman with anemia, lymphadenopathy, and a history of recurrent spontaneous pneumothorax,

Indexed as

Antigens, CD20Biomarkers, TumorBirt-Hogg-Dube SyndromeExonsFemaleGenetic Predisposition to DiseaseGerm-Line MutationHumansMiddle AgedMyeloid Differentiation Factor 88Positron Emission Tomography Computed TomographyProto-Oncogene ProteinsSyndecan-1Tumor Suppressor ProteinsWaldenstrom MacroglobulinemiaAntigens, CD20Biomarkers, TumorFLCN protein, humanMYD88 protein, humanMyeloid Differentiation Factor 88Proto-Oncogene ProteinsSyndecan-1Tumor Suppressor ProteinsBirt–Hogg–Dubé syndromeFolliculinGene mutationHereditary tumor syndromeLymphoplasmacytic lymphoma

Identifiers

PMID32789566
OpenAlexW3048569012

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.