Evidence map›Paper›PMID 28824063›Full record

ArticleInternal medicine (Tokyo, Japan)2017

Recurrent Subcutaneous Sweet's Disease in a Myelofibrosis Patient Treated with Ruxolitinib before Allogeneic Stem Cell Transplantation.

Teppei Sakoda, Yoko Kanamitsu, Yasuo Mori, Kensuke Sasaki, Etsuko Yonemitsu, Konosuke Nagae, Goichi Yoshimoto, Kenjiro Kamezaki, Koji Kato, Katsuto Takenaka and 4 more

Abstract readCase Reports
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
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

14 authors.

Teppei SakodaMedicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Japan.
Yoko KanamitsuMedicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Japan.
Yasuo MoriMedicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Japan.
Kensuke SasakiMedicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Japan.
Etsuko YonemitsuDepartment of Dermatology, Kyushu University Graduate School of Medical Sciences, Japan.
Konosuke NagaeDepartment of Dermatology, Kyushu University Graduate School of Medical Sciences, Japan.
Goichi YoshimotoMedicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Japan.
Kenjiro KamezakiCenter for Cellular and Molecular Medicine, Kyushu University Hospital, Japan.
Koji KatoMedicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Japan.
Katsuto TakenakaCenter for Cellular and Molecular Medicine, Kyushu University Hospital, Japan.
Toshihiro MiyamotoMedicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Japan.
Masutaka FurueDepartment of Dermatology, Kyushu University Graduate School of Medical Sciences, Japan.
Hiromi IwasakiCenter for Cellular and Molecular Medicine, Kyushu University Hospital, Japan.
Koichi AkashiMedicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-SCT) has a curative potential for myelofibrosis (MF) patients; however, its association with a high therapy-related mortality (TRM) remains a big obstacle that needs to be overcome. Ruxolitinib (RUXO), a novel JAK1/2 inhibitor, can be used as a bridging therapy until allo-SCT can be performed to reduce TRM. We herein report a RUXO-treated MF patient who developed recurrent subcutaneous Sweet's disease (SSD) that was successfully treated by the administration of systemic glucocorticoids. We performed allo-SCT as previously scheduled, resulting in a good clinical course without deterioration of SSD. RUXO administration, as well as MF itself, might therefore sometimes cause this rare non-infectious event.

Indexed as

AgedChronic DiseaseGlucocorticoidsHematopoietic Stem Cell TransplantationHumansMaleNitrilesPrimary MyelofibrosisPyrazolesPyrimidinesSweet SyndromeGlucocorticoidsNitrilesPyrazolesPyrimidinesruxolitinibmyelofibrosisruxolitinibstem cell transplantationsubcutaneousSweet's disease

Identifiers

PMID28824063
PMCPMC5643178

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.