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10-Year Clinical Follow-Up after Decompression of Lipofibromatous Hamartoma of the Median Nerve in a 3-Year-Old Patient: Case Report and Review of the Literature.

Seung Jin YooDae Hwan KimSeong Hyun ChoKyung Ryeol LeeKyu Bum Seo
Published in: Children (Basel, Switzerland) (2023)
Lipofibromatous hamartoma, first reported in 1953, is a rare, slowly progressive soft tissue tumor, the characteristics of which include the enlargement of the affected nerve via the epineurial and perineurial proliferation of adipose and fibrous tissues. Out of 200 previously reported cases of lipofibromatous hamartoma of the median nerve, there have been approximately 25 pediatric cases under the age of 18. Herein, we report a case of lipofibromatous hamatoma of the median nerve in a 3-year-old female patient who was surgically decompressed via carpal tunnel release and epineurolysis. The patient was followed-up on an outpatient clinic basis annually with sonographic evaluations, and the postoperative 10th-year follow-up did not show recurrence or any deficits in motor and sensory functions.
Keyphrases
  • case report
  • peripheral nerve
  • soft tissue
  • patients undergoing
  • multiple sclerosis
  • gene expression
  • primary care
  • signaling pathway
  • adipose tissue
  • minimally invasive
  • type diabetes
  • young adults
  • childhood cancer