2016
DOI: 10.14260/jemds/2016/871
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Macrodactyly of Lower Limbs-an Update

Abstract: Congenital macrodactyly is a rare congenital malformation characterized by progressive enlargement of all mesenchymal elements of a digit. The most characteristic finding noted was excessive overgrowth of fibrofatty tissue with unusually large fatty lobules fixed by a mesh of dense fibrous tissue. Hypertrophy and tortuosity of the digital nerve, a striking feature in macrodactyly of the hand was notably absent in cases affecting the foot. Most of the cases are reported as isolated anomalies. In macrodactyly of… Show more

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Cited by 5 publications
(11 citation statements)
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“…Pedal macrodactyly mostly involved the progressive type in other studies (Table 1 ); however, static type preponderance in this study might be on account of our large cohort of cases which revealed the natural growth feature of the entities. Another reason was that disproportionate progressive overgrowth of toes frequently started from the age of 2 years onward [ 15 ] or early childhood [ 2 , 16 ], but patients under 2 years old in the static type group accounted for 45% ( n = 48) cases. Therefore, it is likely that a few “real” progressive type cases may not have presented in a timely manner.…”
Section: Discussionmentioning
confidence: 99%
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“…Pedal macrodactyly mostly involved the progressive type in other studies (Table 1 ); however, static type preponderance in this study might be on account of our large cohort of cases which revealed the natural growth feature of the entities. Another reason was that disproportionate progressive overgrowth of toes frequently started from the age of 2 years onward [ 15 ] or early childhood [ 2 , 16 ], but patients under 2 years old in the static type group accounted for 45% ( n = 48) cases. Therefore, it is likely that a few “real” progressive type cases may not have presented in a timely manner.…”
Section: Discussionmentioning
confidence: 99%
“…A total of 107 patients with macrodactyly of the foot underwent surgical treatment at our hospital between March 2011 and May 2020. Patients with diagnoses of other known overgrowth syndromes or otherwise uncharacterized syndromic presentations of lower extremity enlargement were excluded, such as Klippel–Trenaunay syndrome, Proteus syndrome, CLOVES syndrome, Ollier’s disease, Maffucci syndrome, Milroy’s disease, neurofibromatosis, and vascular anomalies [ 2 ]. Therefore, 93 patients with isolated macrodactyly of the foot were included in this study.…”
Section: Methodsmentioning
confidence: 99%
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“…Few surgical principles must be followed when planning a soft tissue debulking procedure: mid-lateral incision along the digits are preferred, when crossing creases extend as zigzag incisions onto the glabrous skin (to avoid scar contracture), nerve excision can be done as it limits nerve tissue-induced overgrowth, always debulk one side of a digit at a time with proper visualization and preservation of the digital artery, wait for at least three months to debulk the opposite half of the same digit, epiphysiodesis is recommended once the digit approaches the size of the same digit in the parent of the same sex, perform corrective osteotomy for angular deformity at the time of epiphysiodesis, and downsizing of the nail plate and bed is important to achieve a better cosmetic outcome [4][5][6][7][8].…”
Section: Discussionmentioning
confidence: 99%
“…Complications reported after surgery include wound dehiscence, infection, prolonged edema, ischemia of wound margins, sensory disturbances, recurrence/regrowth, scar contracture, joint stiffness, and keloid formation. Tolerton et al have recommended methotrexate therapy to suppress keloid formation and to control recurrence after surgical revision for keloid [ 4 , 8 , 11 ].…”
Section: Discussionmentioning
confidence: 99%