• 제목/요약/키워드: Macrodactyly

검색결과 6건 처리시간 0.018초

성인 족부의 거대지 치료 (1예 보고) (Treatment of Macrodactyly in the Adult Foot - A case report -)

  • 안재훈;김병성;강종원;김동훈;최원식
    • 대한족부족관절학회지
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    • 제7권1호
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    • pp.126-130
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    • 2003
  • Macrodactyly is a rare congenital anomaly characterized by the overgrowth of some or all tissue elements of a digit or digits in the hand or foot. We report of a case of macrodactyly in a foot of an adult female, which was treated successfully with the staged foot narrowing operations.

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발가락 거대지 환자에게 7년에 걸쳐 시행한 단계적 수술: 증례 보고 (Two-Stage Operation Over a Period of 7 Years for a Patient with Macrodactyly: A Case Report)

  • 권용욱;서영채;전가원;이효영
    • 대한족부족관절학회지
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    • 제27권1호
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    • pp.24-29
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    • 2023
  • Macrodactyly of the toe is a rare congenital anomaly characterized by the overgrowth of a digit/digits in the foot and is one of the most difficult conditions to treat. Since the condition alters functionality and appearance, the treatment goal is to restore function and cosmetically enhance the appearance. Various surgical techniques are used for toe macrodactyly, including amputation, debulking, and epiphysiodesis. Herein, we present a case of a six-year-old patient with a second toe macrodactyly who was successfully treated with a two-stage operation over a seven-year period. We initially performed an ostectomy of the middle phalanx with a fusion of the proximal and distal phalanges and then performed a soft tissue debulking procedure.

선천성 족지 기형의 치료 (Treatment of Congenital toe Anomalies)

  • 차성무;서진수
    • 대한족부족관절학회지
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    • 제16권3호
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    • pp.148-155
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    • 2012
  • There are many different type of congenital toe anomalies such as syndactyly, polydactyly which are more common, and less frequently macrodactyly and curly toe. Congenital anomaly of hand can decrease the hand function and easy to be visualized, so the early treatment of anomaly is natural and recommended. On the other hand, Congenital anomaly of foot rarely decrease the foot function and was hidden in the shoe, so treatment of anomaly was delayed frequently. However, the surgery can be needed, as the foot getting grown-up, discomfort of shoe fitting or intractable plantar keratosis due to secondary deformation of foot can occur. A distinct feature and surgical consideration was compared with congenital anomaly of hand and it should be taken into account in the treatment of adult toe anomalies.

족부에 발생한 지방종 거대증(1예 보고) (Macrodystrophia Lipomatosa of the Foot (A Case Report))

  • 노경환;남기영;유재철;이준영
    • 대한족부족관절학회지
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    • 제13권1호
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    • pp.103-105
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    • 2009
  • Macrodystrophia lipomatosa is a congenital macrodactyly characterized by progressive overgrowth of all the mesenchymal elements of a digit or digits with a disproportionate increase in the fibroadipose tissue. We reported a case of macrodystrophia lipomatosa of the foot, which is a rare case, and reviewed the literatures.

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지방섬유성 과오종 : 증례보고 (Two Cases of Lipofibromatous Hamartoma)

  • 김남중;박은수;최환준;신호성;정성균;이영만
    • Archives of Plastic Surgery
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    • 제36권3호
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    • pp.356-360
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    • 2009
  • Purpose: Lipofibromatous Hamartoma(LFH) of nerve is a tumor - like lipomatous process principally involving the young persons. This is rare disease characterized by a soft slowly growing mass surrounding and infiltrating major nerves and their branches of the palm and digits. LFH of nerve usually affects the median nerve, with the most common sites of presentation being the distal forearm and hand in the wrist or palm. It may cause symptoms of compression neuropathy and is associated with macrodactyly. Recently, MRI plays a major role in confirming the diagnosis of LFH. Therefore, we present two cases of LFH in the hand with MRI features and surgical management. Methods: One is 6 - years - old female who presented with macrodactyly involving both the soft tissue and bony parts of the second, third and forth digits of her right hand. The other one is 16 - years - old man who presented involving the soft tissue of the second and third digits of his right hand, with pain and numbness, along with motor and sensory deficits in the median nerve distribution. To evaluation about LFH, we enforced preoperative MRI and physical examination. After confirming the diagnosis of LFH, we proposed decompression of all compromised peripheral nerve to help alleviate pain and paresthesia to reduce the likelihood of permanent motor and sensory sequelae. Results: A characteristic feature on MRI is the appearance of serpentiform nerve fascicle surrounded by fibro - fatty tissue within the expended nerve sheet. Distribution of fat between fascicles is asymmetric. Two cases were treated by limited debulking of the redundant tumor tissue and excision of epineurial fatty tissue. These cases were performed with relief of symptom. Conclusion: MRI not only confirms the diagnosis, it also provides a detailed assessment of nerve involvement preoperatively. Especially, on coronal images, the nerve has a spagetti - like appearance that is pathognomonic of LFH. Recommendations for early treatment include decompression of the carpal tunnel, debulking of the fibro - fatty sheath, microsurgical dissection of the neural elements and excision of involve nerve with or without grafting.