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Nodular fasciitis is a benign, pseudoneoplastic condition often misdiagnosed as sarcoma due to its rapid growth, high cellularity, and mitotic activity. Herein is reported a case of a 7-year-old patient with a painless, enlarging nodule in the left superolateral orbit. Ultrasound revealed a 7.5 mm cystic mass, which was excised via an upper eyelid crease anterior orbitotomy. Histopathologic studies showed benign spindle cells, and molecular testing identified a UBC::USP6 fusion, confirming the diagnosis of nodular fasciitis. Nodular fasciitis is most common in the limbs, trunk, and head or neck region, with fewer than 1% of cases occurring in the orbit. Molecular testing is critical in differentiating this condition from malignancies. Complete surgical excision is the preferred treatment, with a low recurrence rate of 1% to 2%. This is the first reported pediatric case of orbital nodular fasciitis with a UBC::USP6 fusion mutation.
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http://dx.doi.org/10.1097/IOP.0000000000002981 | DOI Listing |
Int J Surg Pathol
August 2025
Department of Pathology and Laboratory Medicine, Aga Khan University Hospital, Karachi, Pakistan.
Nodular fasciitis is a benign, self-limiting, and rapidly proliferating fibroblastic/myofibroblastic lesion. Nodular fasciitis, in the head and neck region, in particular, poses significant diagnostic challenges due to its rapid growth and resemblance to malignant neoplasms. In this single-center observational study, we report on 50 patients who presented with nodular fasciitis in the head and neck region, with a male-to-female patient ratio of 1.
View Article and Find Full Text PDFJ Clin Pathol
August 2025
Department of Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Aims: To investigate immunohistochemical expression of the E26 transformation-specific factors (ETS)-related gene () in a large number of soft tissue neoplasms using a tissue microarray technique.
Methods: 489 cases of soft tissue neoplasms, including benign and malignant entities, were collected from the files of the respective institutions and constructed into tissue microarrays. Tissue microarrays were stained for ERG immunohistochemistry using two antibodies, EP111 and EPR3864.
Childs Nerv Syst
August 2025
Department of Radiology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Purpose: Cranial fasciitis (CF) is a rare benign myofibroblastic proliferation predominantly affecting the pediatric skull, often mimicking malignant processes radiologically. While CF is well described pathologically, its imaging characteristics remain underreported, especially in orbital involvement.
Methods: We retrospectively reviewed the literature through PubMed and Scopus using the search terms "cranial fasciitis" and "nodular fasciitis AND orbit.
Pathol Oncol Res
July 2025
Department of Cellular and Molecular Pathology, Royal National Orthopaedic Hospital, Stanmore, United Kingdom.
Many subtypes of bone and soft tissue tumours harbour specific chromosome translocations leading to chimeric fusion genes. The identification of these specific fusion genes is the basis of molecular diagnoses in such tumours. Break-apart FISH is a robust method that is commonly used to identify these translocations and provide diagnostic support to histological interpretations.
View Article and Find Full Text PDFBMC Musculoskelet Disord
July 2025
Department of Ultrasound, Shandong Provincial Hospital, No.324, Jingwu Road, Jinan, 250021, Shandong, China.
Background: Although nodular fasciimmon and can occur in various anatomical locations, its occurrence within a nerve is extremely rare. Nodular fasciitis usually resolves spontaneously after partial resection. However, it often presents diagnostic challenges due to its resemblance to malignant diseases, resulting in excessive treatments such as extended nerve excision and nerve transplantation.
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