Evidence map›Paper›PMID 40657459›Full record

ArticleSultan Qaboos University medical journal2025

Clinicopathological Spectrum of Myxoid Soft Tissue Tumours with Emphasis on Diagnostic Differentials.

Sanjana Ahuja, Nisha Modi, Amit Varma, Shivani Kapur, Kamal Malukani, Harshita Deep Sahu

Abstract read
In one paragraph

Article in Sultan Qaboos University medical journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sanjana AhujaDepartment of Pathology and Lab Medicine, Sri Aurobindo Medical College & Post Graduate Institute, Indore, India.
Nisha ModiDepartment of Pathology and Lab Medicine, Sri Aurobindo Medical College & Post Graduate Institute, Indore, India.
Amit VarmaDepartment of Pathology and Lab Medicine, Sri Aurobindo Medical College & Post Graduate Institute, Indore, India.
Shivani KapurDepartment of Pathology and Lab Medicine, Sri Aurobindo Medical College & Post Graduate Institute, Indore, India.
Kamal MalukaniDepartment of Pathology and Lab Medicine, Sri Aurobindo Medical College & Post Graduate Institute, Indore, India.
Harshita Deep SahuDepartment of Pathology and Lab Medicine, Sri Aurobindo Medical College & Post Graduate Institute, Indore, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Myxoid soft tissue tumours (MSTTs) represent a complex group of mesenchymal neoplasms characterised by the production of an extracellular myxoid matrix, which often poses diagnostic challenges. This study aimed to identify the relative frequency, distribution and morphological spectrum of MSTT as well as to illustrate commonly encountered diagnostic difficulties. Methods: This retrospective study of the clinicopathological profiles of MSTT cases at Sri Aurobindo Medical College & Post Graduate Institute, Indore, India, was conducted from January 2020 to December 2023. Results: A total of 110 MSTT cases were included in this study. These cases accounted for 7.3% of the soft tissue tumours (STTs), with a predominance of benign MSTT (n = 67, 60.9%). The fibroblastic/myofibroblastic family of STT constituted the majority (33.6%). The upper limb (34%) was the most frequently involved anatomical site for benign MSTT, with the 20-40 age range being the most common (46.3%). Tumour sizes were predominantly below 5 cm (57%), with 84% located superficially. In malignant MSTT, the lower limb (49%) was largely affected, with the 40-60 age group being predominant (46.5%), and the most common tumour size range was 5-10 cm (46.5%). Myxoid schwannoma (13.4%) was the most prevalent benign entity, while myxofibrosarcoma (20.9%) was the most frequent malignancy. A statistically significant correlation was observed between histological grade and tumour size ( Conclusions: This study presented a comprehensive array of clinical and morphological features of MSTT with variable clinical significance. It highlighted potential caveats to aid in accurate diagnosis for optimal treatment selection.

Indexed as

Soft Tissue NeoplasmsAdolescentAdultAgedChildDiagnosis, DifferentialFemaleHumansIndiaMaleMiddle AgedMyxomaRetrospective StudiesDifferential DiagnosisImmunohistochemistryIndiaMyxomaSarcomasSoft Tissue Neoplasms

Identifiers

PMID40657459
PMCPMC12255337

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