Evidence map›Paper›PMID 40128507›Full record

ArticleDiscover oncology2025

Histiocyte-rich rhabdomyoblastic tumor easily misdiagnosed as rhabdomyosarcoma: a case report.

Ting Xu, Shuai Luo

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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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

1 citing paper in PubMed.

  1. 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

2 authors.

Ting XuDepartment of Pathology, Zhejiang Provincial People's Hospital Bijie Hospital, Bijie, Guizhou, People's Republic of China.
Shuai LuoDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, People's Republic of China. 1421227850@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHistiocyte-rich rhabdomyoblastic tumor (HRRMT) is an extremely rare tumor of uncertain origin. Morphologically, it closely resembles inflammatory leiomyosarcoma (ILMS) without smooth muscle differentiation, making clinical diagnosis particularly challenging. Due to its rarity, HRRMT is often misdiagnosed as rhabdomyosarcoma, leading to unnecessary aggressive treatment. CASE PRESENTATION: A 62-year-old male was admitted to the hospital after an incidental discovery of a mass on his right thigh, first noticed seven days prior. Clinical examination revealed a well-circumscribed, painless mass measuring approximately 5 × 6 cm. Ultrasound and magnetic resonance imaging (MRI) suggested rhabdomyosarcoma in the distal sartorius muscle. However, histopathological analysis following surgical resection confirmed HRRMT. The patient did not undergo postoperative radiotherapy or chemotherapy, and no recurrence was observed during six months of follow-up.

conclusionsHRRMT is a rare tumor with favorable biological behavior. Given its morphological overlap with ILMS and rhabdomyosarcoma, early and accurate diagnosis is essential to prevent overtreatment. Extensive surgical resection remains an effective therapeutic approach. We report a case of HRRMT that is easily misdiagnosed as rhabdomyosarcoma, which will be a valuable case.

Indexed as

Differential diagnosisHistiocyte-rich rhabdomyoblastic tumorPathological diagnosisRhabdomyoblastic tumorTreatment

Identifiers

PMID40128507
PMCPMC11933611

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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.