Literature DB >> 16799319

An unusual congenital facial anomaly: erectile proboscis-like structure.

Mehmet Mutaf1, Dağhan Isik, Berker Büyükgüral.   

Abstract

We report a 3-week-old male infant with an unusual congenital facial anomaly, which is characterized by a proboscis-like erectile structure arising from the right malar region. Although it is a tubular structure resembling the proboscis lateralis, this case was more likely to be a new congenital anomaly because of the following reasons: (1) in contrast with the proboscis lateralis, which originates from the medial portion of the orbital roof, the structure was located at the right malar region in our case; (2) although it was soft and freely dangling on the face, this proboscis-like structure was strongly erectile, with contraction of the orbicularis oculi muscle when the infant cried; (3) histopathological examination revealed that the structure was composed by normal fibroadipose tissue and striated muscle covered with a healthy skin and subcutaneous tissue. In contrast with histopathological characteristics of a proboscis lateralis, there was neither osteocartilaginous tissue nor mucosa in the structure. Although it is a typical finding for a proboscis lateralis, no lumen was found in the presented anomaly. Because of these unique characteristics, which remarkably differ from previously reported facial anomalies, we thought this case worth reporting. A literature review revealed that no similar case has been reported in the literature.

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Year:  2006        PMID: 16799319     DOI: 10.1097/01.sap.0000205773.52107.22

Source DB:  PubMed          Journal:  Ann Plast Surg        ISSN: 0148-7043            Impact factor:   1.539


  2 in total

Review 1.  Proboscis lateralis.

Authors:  S Martin; E Hogan; E P Sorenson; A A Cohen-Gadol; R S Tubbs; M Loukas
Journal:  Childs Nerv Syst       Date:  2013-01-25       Impact factor: 1.475

2.  Proboscis Lateralis : A Rare Bilateral Case in Association with Holoprosencephaly.

Authors:  Vasavi Kolluru; Sendhil Coumary
Journal:  J Clin Diagn Res       Date:  2015-08-01
  2 in total

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