PRAME immunohistochemistry in soft tissue tumors and mimics: a study of 350 cases highlighting its imperfect specificity but potentially useful diagnostic applications
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
PubMed
37477762
DOI
10.1007/s00428-023-03606-6
PII: 10.1007/s00428-023-03606-6
Knihovny.cz E-zdroje
- Klíčová slova
- Differential diagnosis, Immunohistochemistry, Immunotherapy, Melanoma, PRAME, Sarcoma, Soft tissue,
- MeSH
- antigeny nádorové MeSH
- diferenciální diagnóza MeSH
- DNA-helikasy MeSH
- dospělí MeSH
- Ewingův sarkom * diagnóza MeSH
- fibrosarkom * diagnóza MeSH
- imunohistochemie MeSH
- jaderné proteiny MeSH
- lidé MeSH
- melanom * patologie MeSH
- nádorové biomarkery metabolismus MeSH
- nádory kůže * patologie MeSH
- nádory měkkých tkání * diagnóza patologie MeSH
- sarkom * diagnóza patologie MeSH
- transkripční faktory MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antigeny nádorové MeSH
- DNA-helikasy MeSH
- jaderné proteiny MeSH
- nádorové biomarkery MeSH
- PRAME protein, human MeSH Prohlížeč
- SMARCA4 protein, human MeSH Prohlížeč
- transkripční faktory MeSH
Preferentially expressed antigen in melanoma (PRAME) immunohistochemistry is currently used in pathology for the assessment of melanocytic neoplasms; however, knowledge of its expression patterns in soft tissue tumors is limited. PRAME immunohistochemistry (clone QR005) was assessed on whole tissue sections of 350 soft-tissue tumors and mimics (> 50 histotypes). PRAME immunoreactivity was evaluated as follows: 0 "negative" (0% positive cells); 1+ (1-25% positive cells); 2+ (26-50% positive cells); 3+ (51-75% positive cells), and 4+ "diffuse" (> 75% positive cells). PRAME was expressed in 111 lesions (0 benign, 6 intermediate malignancy, and 105 malignant), including fibrosarcomatous dermatofibrosarcoma protuberans (2/4, 0 diffuse), NTRK-rearranged spindle cell neoplasm (2/4, 0 diffuse), atypical fibroxanthoma (1/7, 0 diffuse), Kaposi sarcoma (1/5, 0 diffuse), myxoid liposarcoma (11/11, 9 diffuse), synovial sarcoma (11/11, 6 diffuse), intimal sarcoma (7/7, 5 diffuse), biphenotypic sinonasal sarcoma (3/3, 1 diffuse), angiosarcoma (10/15, 6 diffuse), malignant peripheral nerve sheath tumor (9/12, 4 diffuse), pleomorphic rhabdomyosarcoma (2/3, 2 diffuse), alveolar rhabdomyosarcoma (2/6, 0 diffuse), embryonal rhabdomyosarcoma (7/7, 4 diffuse), undifferentiated pleomorphic sarcoma (2/12, 1 diffuse), leiomyosarcoma (2/15, 1 diffuse), clear cell sarcoma of soft tissue (1/10, 0 diffuse), low-grade fibromyxoid sarcoma (1/5, 0 diffuse), Ewing sarcoma (2/10, 1 diffuse), CIC-rearranged sarcoma (8/8, 4 diffuse), BCOR-sarcoma (2/5, 1 diffuse), melanoma (20/20, 14 diffuse), and thoracic SMARCA4-deficient undifferentiated tumor (5/5, all diffuse). All tested cases of spindle cell lipoma, dedifferentiated/pleomorphic liposarcoma, dermatofibrosarcoma protuberans, solitary fibrous tumor, inflammatory myofibroblastic tumor, myxoinflammatory fibroblastic sarcoma, nodular fasciitis, myxofibrosarcoma, epithelioid hemangioendothelioma, atypical vascular lesion, hemangioma, lymphangioma, vascular malformation, papillary endothelial hyperplasia, GIST, gastrointestinal clear-cell sarcoma, malignant melanotic nerve sheath tumor, neurofibroma, schwannoma, granular cell tumor, alveolar soft part sarcoma, epithelioid sarcoma, extraskeletal myxoid chondrosarcoma, myoepithelioma, ossifying fibromyxoid tumor, angiomatoid fibrous histiocytoma, PEComa, dermatofibroma, pleomorphic dermal sarcoma, and chordoma were negative. PRAME shows imperfect specificity in soft-tissue pathology but may serve as a diagnostic adjunct in selected differential diagnoses that show contrasting expression patterns.
Bioptical Laboratory Ltd Plzen Czech Republic
Department of Biopathology Institut Bergonié Bordeaux France
Department of Pathology Bordeaux University Hospital UMR 1312 Inserm Bordeaux France
Department of Pathology Faculty of Medicine in Plzen Charles University Pilsen Czech Republic
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