Evidence map›Paper›PMID 36128863›Full record

ArticleJournal of pathology and translational medicine2022

Special AT-rich sequence-binding protein 2 (SATB2) in the differential diagnosis of osteogenic and non-osteogenic bone and soft tissue tumors.

Sharon Milton, Anne Jennifer Prabhu, V T K Titus, Rikki John, Selvamani Backianathan, Vrisha Madhuri

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Article in Journal of pathology and translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 · Its place in the literature

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3 citing papers in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Sharon MiltonDepartments of Pathology, Christian Medical College Vellore, Tamil Nadu, India.
Anne Jennifer PrabhuDepartments of Pathology, Christian Medical College Vellore, Tamil Nadu, India.
V T K TitusDepartments of Orthopaedics, Christian Medical College Vellore, Tamil Nadu, India.
Rikki JohnDepartments of Paediatric Oncology and Haematology, Christian Medical College Vellore, Tamil Nadu, India.
Selvamani BackianathanDepartments of Radiotherapy, Christian Medical College Vellore, Tamil Nadu, India.
Vrisha MadhuriDepartments of Paediatric Orthopaedics, Christian Medical College Vellore, Tamil Nadu, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe diagnosis of osteosarcoma (OSA) depends on clinicopathological and radiological correlation. A biopsy is considered the gold standard for OSA diagnosis. However, since OSA is a great histological mimicker, diagnostic challenges exist. Immunohistochemistry (IHC) can serve as an adjunct for the histological diagnosis of OSA. Special AT-rich sequence-binding protein 2 (SATB2) was recently described as a reliable adjunct immunohistochemical marker for the diagnosis of OSA.

methodsWe investigated the IHC expression of SATB2 in 95 OSA and 100 non-osteogenic bone and soft tissue tumors using a monoclonal antibody (clone EPNCIR30A). The diagnostic utility of SATB2 and correlation with clinicopathological parameters were analyzed.

resultsSATB2 IHC was positive in 88 out of 95 cases (92.6%) of OSA and 50 out of 100 cases (50.0%) of primary non-osteogenic bone and soft tissue tumors. Of the 59 bone tumors, 37 cases (62.7%) were positive for SATB2, and of the 41 soft tissue tumors, 13 cases (31.7%) were positive for SATB2. The sensitivity of SATB2 as a diagnostic test was 92.6%, specificity 50%, positive predictive value 63.8%, and negative predictive value 87.7%.

conclusionsAlthough SATB2 is a useful diagnostic marker for OSA, other clinical, histological and immunohistochemical features should be considered for the interpretation of SATB2.

Indexed as

ImmunohistochemistryNon-osteogenicOsteoidOsteosarcomaSATB2 protein

Identifiers

PMID36128863
PMCPMC9510043

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