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Management of Fibrous Hamartoma of Infancy: A Contemporary Series.
Smith, Savannah R; Dantes, Goeto; Oliver, Hannah; Dutrueil, Valerie; Alemayehu, Hanna.
Affiliation
  • Smith SR; Department of Surgery, Emory University, Atlanta, GA, USA. Electronic address: savannah.reid.smith@emory.edu.
  • Dantes G; Department of Surgery, Emory University, Atlanta, GA, USA.
  • Oliver H; Department of Neuroscience, Georgia Institute of Technology, Atlanta, GA, USA.
  • Dutrueil V; Pediatric Biostatistics Core, Department of Pediatrics, Emory University, Atlanta, GA, USA.
  • Alemayehu H; Division of Pediatric Surgery, Department of Surgery, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, GA, USA.
J Pediatr Surg ; 59(10): 161535, 2024 Oct.
Article in En | MEDLINE | ID: mdl-38631996
ABSTRACT

BACKGROUND:

Fibrous hamartoma of infancy (FHI) is a rare, benign, soft tissue mass that may be locally infiltrative. Primary excision is the mainstay of treatment; however, given the infiltrative nature, margin negativity can be difficult to achieve. The management of residual disease in the setting of positive margins after primary excision is not well described.

METHODS:

All patients undergoing FHI excision from 2012 to 2022 were included. Demographics, operative data, margin status, recurrence, and post-operative follow-up data were obtained via retrospective chart review.

RESULTS:

Nine patients were identified who underwent FHI excision. The median age at time of excision was 9 months (IQR 16). Seven (78%) were male, and the majority (78%) were white. Seven (78%) underwent preoperative imaging via ultrasound or MRI, and 4 (44%) had a preoperative biopsy to confirm diagnosis. Common locations included upper extremity (n = 4, 44%) and lower extremity/inguinal region (n = 4, 44%). Six patients (67%) had positive margins on pathology - 3 (33%) on the upper extremity, 2 (22%) on the lower extremity/inguinal region, and one (11%) on the flank. One patient (11%) had a local recurrence which did not undergo re-excision.

CONCLUSIONS:

FHI remains a rare diagnosis. There is a high margin positivity rate; however, local clinically significant mass recurrence remains uncommon. With low rates of clinically significant mass development coupled with the benign nature of disease, a "watch and wait" approach may be appropriate for patients with positive histologic margins after complete gross excision to avoid reoperation and need for complex reconstructions. LEVEL OF EVIDENCE Level 4.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hamartoma Limits: Female / Humans / Infant / Male Language: En Journal: J Pediatr Surg / J. pediatr. surg / Journal of pediatric surgery Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hamartoma Limits: Female / Humans / Infant / Male Language: En Journal: J Pediatr Surg / J. pediatr. surg / Journal of pediatric surgery Year: 2024 Document type: Article Country of publication: