Year :
2025
| Month :
November
| Volume :
19
| Issue :
11
| Page :
PD01 - PD04
Full Version
An Unusual Acral Swelling: Histopathological Confirmation of Superficial Acral Fibromyxoma
Published: November 1, 2025 | DOI: https://doi.org/10.7860/JCDR/2025/81426.21935
Chaitanya Mahajan, Varun Shetty, Iqbal M Ali
1. Resident, Department of General Surgery, Dr. D. Y. Patil Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth, Pimpri, Pune, Maharashtra, India.
2. Assistant Professor, Department of General Surgery, Dr. D. Y. Patil Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth, Pimpri, Pune, Maharashtra, India.
3. Professor, Department of General Surgery, Dr. D. Y. Patil Hospital and Research Centre, Pimpri, Pune. Dr. D. Y. Patil Vidyapeeth, Pimpri, Pune, Maharashtra, India.
Correspondence Address :
Varun Shetty,
Swarganga Society, B1/704, 7th Floor, Vallabh Nagar, Pimpri, Pune, Maharashtra, India.
E-mail: shettyvarun03@gmail.com
Abstract
Superficial Acral Fibromyxoma (SAF) is an uncommon, benign mesenchymal neoplasm that predominantly involves the subungual and periungual soft tissues of the digits. Its indolent growth, painless nature, and non specific clinical features often lead to misdiagnosis, resulting in delayed treatment or inappropriate management. The present case described a 36-year-old male who presented with a decade-long history of a gradually enlarging, painless mass on the distal phalanx of the right ring finger, followed by a recent phase of accelerated growth over two months. Magnetic Resonance Imaging (MRI) demonstrated a well-circumscribed, T2-hyperintense lesion without underlying osseous involvement. Complete surgical excision was performed. Histopathological evaluation revealed a proliferation of bland spindle and stellate fibroblastic cells embedded in a fibromyxoid stroma, without evidence of cytologic atypia or mitotic activity. Immunohistochemical analysis showed diffuse positivity for CD34 and vimentin, with negative staining for S-100 and Epithelial Membrane Antigen (EMA), supporting the diagnosis of SAF. The postoperative course was uneventful, and there has been no evidence of recurrence to date. Given the potential for local recurrence, especially in incompletely excised lesions, accurate diagnosis through histopathology and Immunohistochemistry (IHC) is essential. Awareness of SAF's distinguishing features among clinicians, radiologists, and pathologists can aid in timely diagnosis, reduce the risk of misclassification, and facilitate appropriate surgical management, ultimately improving patient outcomes.
Keywords
Benign, Immunohistochemistry, Soft-tissue neoplasms, Subungual
DOI: 10.7860/JCDR/2025/81426.21935
Date of Submission: Jun 21, 2025
Date of Peer Review: Jul 11, 2025
Date of Acceptance: Jul 28, 2025
Date of Publishing: Nov 01, 2025
AUTHOR DECLARATION:
• Financial or Other Competing Interests: None
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. Yes
PLAGIARISM CHECKING METHODS:
• Plagiarism X-checker: Jul 02, 2025
• Manual Googling: Jul 24, 2025
• iThenticate Software: Jul 26, 2025 (5%)
ETYMOLOGY: Author Origin
EMENDATIONS: 5
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