Evidence map›Paper›PMID 36575002›Full record

ArticleJournal of clinical and experimental hematopathology : JCEH2022

Combined use of pathological and genomic alteration analyses for the diagnosis of gray zone lymphoma.

Komei Nishimura, Kana Miyazaki, Kazutaka Suzuki, Kensuke Hachiya, Yasutaka Tono, Satoshi Tamaru, Hiroshi Imai, Hiroaki Miyoshi, Koichi Ohshima, Yoshinaga Okugawa and 2 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of clinical and experimental hematopathology : JCEH, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 76% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 4 institutions in 1 country.

Komei NishimuraDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.
Kana MiyazakiDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.
Kazutaka SuzukiDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.
Kensuke HachiyaDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.
Yasutaka TonoDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.
Satoshi TamaruDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.
Hiroshi ImaiPathology Division, Mie University Hospital, Tsu, Japan.
Hiroaki MiyoshiDepartment of Pathology, Kurume University School of Medicine, Kurume, Japan.
Koichi OhshimaDepartment of Pathology, Kurume University School of Medicine, Kurume, Japan.
Yoshinaga OkugawaDepartment of Genomic Medicine, Mie University Hospital, Tsu, Japan.
Isao TawaraDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.
Motoko YamaguchiDepartment of Hematological Malignancies, Mie University Graduate School of Medicine, Tsu, Japan.
Mie University · JPKurume University · JPMie University Hospital · JPChugoku Central Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histiocytic sarcoma (HS) is a rare malignancy showing morphologic and immunophenotypic features of histiocytes. HS has morphologic overlap with many other diseases, including various kinds of lymphomas. Gray zone lymphoma (GZL) is a rare B-cell lymphoma subtype characterized by overlapping features between diffuse large B-cell lymphoma and classic Hodgkin lymphoma. The histologic overlap with other diverse diseases of HS and the pathological diversity of GZL make it difficult to render a diagnosis. A 44-year-old woman who was initially diagnosed with HS was diagnosed with GZL after reexamination, including a genetic alteration test. After 6 cycles of brentuximab vedotin, doxorubicin, vinblastine, and dacarbazine, she achieved a complete response. Genomic alteration assessment may be useful for the accurate diagnosis of malignant lymphomas, which are difficult to diagnose, such as GZL.

Indexed as

Hodgkin DiseaseLymphoma, Large B-Cell, DiffuseAdultAntineoplastic Combined Chemotherapy ProtocolsDacarbazineDoxorubicinFemaleGenomicsHumansDacarbazineDoxorubicingenomic alteration testgray zone lymphomahistiocytic sarcoma

Identifiers

PMID36575002
PMCPMC9898712
OpenAlexW4312900063

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.