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Congenital fibrolipomatous hamartoma of the calcaneusD 17.2
Synonym(s)
OMIM 609808; Precalcaneal congenital fibrolipomatous hamartoma
HistoryThis section has been translated automatically.
Larralde de Luna M et al.(1990)
DefinitionThis section has been translated automatically.
Rare mostly sporadic malformation (autosomal-dominant inheritance is discussed) with formation of unilateral or bilateral, skin-colored, painless, plate-shaped or nodular, soft bulges in the medial area of the calcaneus and/or the ankle. The lesions are congenital and grow slowly during the first years of life.
HistologyThis section has been translated automatically.
Formation of normal fatty tissue.
TherapyThis section has been translated automatically.
Excision only in case of mechanically disturbing situation.
The changes usually already exist at birth and grow with the affected person. The prognosis is good, they are regressed by puberty at the latest. They do not cause pain and do not interfere with walking. Excisions are therefore strongly discouraged.
LiteratureThis section has been translated automatically.
- Hafez D et al (2018) Precalcaneal congenital fibrolipomatous hamartoma. Dermatol Online J 24.
- Kumar R et al (2018) Congenital Fibrolipomatous Hamartoma and Congenital Nevus of Infancy: A Syndromic or Chance Association. J Indian Assoc Pediatr Surgery 23:219-221.
- Larralde de Luna M et al (1990) Pedal papules in newborn infants. Med Cutan Ibero Lat On 18:9-12.
- Tella E et al (2017) Precalcaneal congenital fibrolipomatous hamartoma. Arch Pediatr 24:499-500.
- Yang JH et al (2011) Precalcaneal congenital fibrolipomatous hamartoma. Ann Dermatol 23:92-94.