Congenital fibrolipomatous hamartoma of the calcaneus D 17.2

Author: Prof. Dr. med. Peter Altmeyer

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Last updated on: 29.04.2023

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Synonym(s)

OMIM 609808; Precalcaneal congenital fibrolipomatous hamartoma

History
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Larralde de Luna M et al.(1990)

Definition
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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.

Histology
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Formation of normal fatty tissue.

Therapy
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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.

Literature
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  1. Hafez D et al (2018) Precalcaneal congenital fibrolipomatous hamartoma. Dermatol Online J 24.
  2. 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.
  3. Larralde de Luna M et al (1990) Pedal papules in newborn infants. Med Cutan Ibero Lat On 18:9-12.
  4. Tella E et al (2017) Precalcaneal congenital fibrolipomatous hamartoma. Arch Pediatr 24:499-500.
  5. Yang JH et al (2011) Precalcaneal congenital fibrolipomatous hamartoma. Ann Dermatol 23:92-94.

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Please ask your physician for a reliable diagnosis. This website is only meant as a reference.

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Last updated on: 29.04.2023