Oct 2026· Khirurgiia· Vol 10, pp.
117-123
· 0 citations· 16 references
Medicine
Abstract
The authors describe epithelioid soft tissue sarcoma in a child with emphasis on diagnostic difficulties associated with morphological verification and differential diagnosis, as well as evaluate the effectiveness of complex treatment, including radical surgery and adjuvant radiotherapy. An 11-year-old boy was diagnosed with epithelioid sarcoma of soft tissues of the right shoulder. Anamnesis, clinical examination, ultrasound, MRI, CT of the chest and abdominal cavity, scintigraphy and PET-CT were used to make the diagnosis. Additionally, bone marrow puncture was performed to exclude systemic spread. Treatment included total excision of tumor with defect closure and subsequent adjuvant radiotherapy. Assessment of effectiveness was based on clinical data and follow-up survey. The diagnosis was confirmed only after repeated morphological revisions and expanded immunohistochemical analysis. The patient underwent total resection of tumor and defect closure with subsequent radiotherapy. There were no major complications. The authors achieved local control of disease and good quality of life in their patient. This case illustrates the difficulties of early diagnosis of epithelioid sarcoma in childhood. This example complements available clinical base and has practical value for improving approaches to management of children with rare soft tissue tumors.
This case highlights the diagnostic value of characteristic imaging findings and the therapeutic importance of complete resection followed by adjuvant chemotherapy in children withUndifferentiated embryonal sarcoma of the liver.
Hyung Jun Kwon, Jinyoung Park· Advances in Pediatric Surger...· 0 citations
Introduction. Ameloblastoma is a rare, aggressive odontogenic tumor characterized by a high risk of recurrence. Although radical surgical resection remains the primary treatment modality, surgical intervention may become unfeasible in cases of multiple recurrences and tumor infiltration into vital structures. In such i...
G. Jonaitis, L. Zaleckas· Lietuvos chirurgija· 0 citations
Leiomyosarcoma (LMS) is a rare, smooth-muscle malignancy and an uncommon sinonasal tumor, often diagnosed at a late stage due to non-specific symptoms and complex anatomy. We report an 82-year-old man with a two-month history of facial pain, epistaxis, and right-sided hearing loss. Imaging and endoscopic evaluation sho...
Timothy Morley, Sarah E. Ridge, Jared Bunevich et al.· Cureus· 0 citations
Advanced cutaneous malignancies with basaloid morphology can present diagnostic and therapeutic challenges, particularly when pathological interpretations differ and disease progresses during systemic treatment. We describe the clinical course of a 53-year-old woman with an extensive, unresectable cutaneous tumor invol...
I. Bivolarski, Tanio Stefanov, Martin Dimitrov et al.· Cureus· 0 citations
This article examines the interpretation and clinical significance of resection margins in soft tissue sarcomas of the head and neck in children, particularly in rhabdomyosarcoma, which is the most common type of tumor in this group in pediatric practice. It examines the current understanding of soft tissue sarcomas as...
S. S. Baranov, I. N. Vorozhtsov, I. Kazantsev et al.· Head and neck. Russian Journ...· 0 citations
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