• Title/Summary/Keyword: Lipomatosa

Search Result 4, Processing Time 0.019 seconds

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

  • Noh, Kyung-Hwan;Nam, Ki-Young;Yoo, Jae-Chol;Lee, Jun-Young
    • Journal of Korean Foot and Ankle Society
    • /
    • v.13 no.1
    • /
    • pp.103-105
    • /
    • 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.

  • PDF

Recurred Macrodystrophia Lipomatosa of the Foot: A Case Report (족부에 재발한 지방종 거대증: 증례 보고)

  • Lee, Myoung Jin;Kim, Dong Ryul
    • Journal of Korean Foot and Ankle Society
    • /
    • v.20 no.1
    • /
    • pp.32-35
    • /
    • 2016
  • We reported on a rare case of recurred macrodystrophia lipomatosa of the foot, and reviewed the literature. A 62-year-old male patient presented with right foot second toe pain; preoperative magnetic resonance imaging and radiograph examination was performed. After surgery the biopsy confirmed the diagnosis. American Orthopaedic Foot and Ankle Society score was checked before and after surgery. Wide excision of the affected area including ray amputation is an effective way to prevent recurrence and relieve the pain after surgery. The 2nd toe ray amputation was performed in the treatment of recurred macrodystrophia lipomatosa of the foot, and is thought to be an effective way to relieve pain and prevent recurrence. After minimally invasive surgery with complete excision surgery, additional data on recurrence and pain relief rate are needed.

A Review of Macrodystrophia Lipomatosa: Revisitation

  • Prasetyono, Theddeus OH;Hanafi, Enjeline;Astriana, Windi
    • Archives of Plastic Surgery
    • /
    • v.42 no.4
    • /
    • pp.391-406
    • /
    • 2015
  • Macrodystrophia lipomatosa (MDL) is a rare congenital non-hereditary disorder that has significant impact on patient morbidity. This study provides a comprehensive review of the natural history, diagnosis, management, and outcomes of the disorder. A literature search in PubMed was conducted to identify cases of MDL from January 1950 to 14 February 2014. After ruling out articles without information related to the management of the disorder, a summary of 32 studies was performed. An additional three cases from the authors are also presented. Based on 57 journal articles and three additional cases from the authors, around 108 cases of MDL were reviewed. Most patients were males who were admitted to a treatment clinic in the first four years of life. The lower extremities were more frequently affected, with unilateral presentation being most common. They commonly underwent a single-staged surgical procedure with follow-up periods ranging from more than one year up to 21 years. Out of 43 cases that underwent surgical procedures, 13 reported no complications, and there were seven cases of esthetic satisfaction and 15 cases of significant functional improvement. Depending on the severity of a patient's condition, the use of non-invasive diagnostic tools should be carefully considered. Surgery might be a better choice of management than observation, taking into account possible future complications in the absence of surgery and the beneficial outcomes of surgical procedures.