Evidence map›Paper›PMID 42029883›Full record

ArticleInternational journal of hematology2026

Splenic rupture secondary to pegfilgrastim in a healthy allogeneic peripheral blood hematopoietic stem cell donor.

Ryo Takahashi, Koichi Oya, Yuki Ishizawa, Yusuke Nagano, Ryo Sato, Masashi Hosokawa, Akane Yamada, Takuma Suzuki, Keiko Aizawa, Satoshi Ito and 3 more

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In one paragraph

Article in International journal of hematology, 2026. 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
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.

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

13 authors.

Ryo TakahashiDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Koichi OyaDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Yuki IshizawaDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Yusuke NaganoDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Ryo SatoDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Masashi HosokawaDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Akane YamadaDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Takuma SuzukiDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Keiko AizawaDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Satoshi ItoDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Daniel PeltierDivision of Hematology/Oncology and Stem Cell Transplantation, Department of Pediatrics, Wells Center for Pediatric Research, Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN, USA.
Hisayuki YokoyamaDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan.
Tomomi ToubaiDivision of Hematology and Cell Therapy, Department of Internal Medicine III , Yamagata University Faculty of Medicine, Yamagata, Japan. toubai@med.id.yamagata-u.ac.jp.ORCID http://orcid.org/0000-0001-6658-7543

Funding

Japan Society for the Promotion of Science JP23K07850
6 · The paper itself

Abstract

Granulocyte-colony stimulating factor (G-CSF) is widely used to mobilize peripheral blood stem cells (PBSCs) for hematopoietic cell transplantation (HCT). G-CSF is generally well-tolerated but can cause life-threatening complications such as splenic rupture in rare cases. Long-acting pegfilgrastim (Peg-G) is increasingly used for PBSC mobilization, but its risk for splenic rupture is less well characterized. Here, we report a case of splenic rupture secondary to Peg-G administered for PBSC mobilization in a healthy 25-year-old male haploidentical donor. He presented with left upper quadrant abdominal pain shortly after PBSC harvest 5 days following administration of Peg-G. Computed tomography (CT) revealed splenomegaly with rupture, and small bloody peri-splenic and pelvic ascites. He was managed conservatively, but the next evening his symptoms temporarily worsened, prompting a repeat CT scan, which showed no change. Thereafter, the pain did not recur, and the patient was discharged on day 8. One month later, a follow-up CT demonstrated complete resolution. To our knowledge, this is the first case of splenic rupture secondary to Peg-G for PBSC mobilization in a healthy allogeneic donor and highlights the importance of vigilance for this rare complication when G-CSF or Peg-G is used for mobilization.

Indexed as

FilgrastimGranulocyte Colony-Stimulating FactorHematopoietic Stem Cell MobilizationPeripheral Blood Stem Cell TransplantationPolyethylene GlycolsSplenic RuptureAdultHumansMaleTomography, X-Ray ComputedTransplantation, HomologousFilgrastimGranulocyte Colony-Stimulating FactorpegfilgrastimPolyethylene GlycolsMobilizationPegfilgrastimPeripheral blood hematopoietic stem cellsSplenic rupture

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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.