Neuromuscular Choristoma of the Brachial Plexus Presenting as a Supraclavicular Mass in a Pediatric Patient: A Case Report.
Autor: | DeFoor MT; Department of Orthopaedics, San Antonio Military Medical Center, Fort Sam Houston, Texas., Gaviria M; Department of Orthopaedics, San Antonio Military Medical Center, Fort Sam Houston, Texas., Lopuch A; Uniformed Services University of the Health Sciences School of Medicine, Bethesda, Maryland., Kao E; Department of Pathology, San Antonio Military Medical Center, Fort Sam Houston, Texas., Sabbag CM; Department of Orthopaedics, San Antonio Military Medical Center, Fort Sam Houston, Texas. |
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Jazyk: | angličtina |
Zdroj: | JBJS case connector [JBJS Case Connect] 2024 Sep 06; Vol. 14 (3). Date of Electronic Publication: 2024 Sep 06 (Print Publication: 2024). |
DOI: | e24.00230 |
Abstrakt: | Case: This case demonstrates a 2-year-old boy with a rare benign supraclavicular mass diagnosed as neuromuscular choristoma through open biopsy. Postoperatively, he underwent semiannual surveillance with ultrasound without development of neurological complaints, limb deformity, or recurrence at 2-year follow-up. Conclusion: Neuromuscular choristoma involving the brachial plexus is a rare tumor that should be in the differential diagnosis of pediatric peripheral nerve-based tumors. The intimate association with neural elements limits complete resection. Therefore, open biopsy with partial resection is recommended. While postoperative fibromatosis may occur, open biopsy remains the gold standard for definitive diagnosis. Ultrasound can be used to monitor recurrence. Competing Interests: Disclosure: The Disclosure of Potential Conflicts of Interest forms are provided with the online version of the article (http://links.lww.com/JBJSCC/C432). (Copyright © 2024 by The Journal of Bone and Joint Surgery, Incorporated.) |
Databáze: | MEDLINE |
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