Proboscis Lateral: A Case Report

Introduction: The lateral proboscis is a rudimentary nasal structure located off the vertical midline of the face. This malformation is often accompanied by other anomalies, most commonly ophthalmic conditions such as anophthalmia, microphthalmia, and colobomas, as well as facial anomalies like maxillary hypoplasia or facial clefts, and cranio-cerebral anomalies including encephalocele and holoprosencephaly. Methods: This report presents a case of a newborn with a lateral proboscis identified at birth. The pregnancy was poorly monitored, and the anomaly was discovered immediately after delivery. Results: The newborn exhibited a lateral proboscis with a rudimentary nasal structure extending from the right side of the face, along with associated ophthalmic anomalies including microphthalmia. No additional facial clefts or cranio-cerebral abnormalities were noted. The infant was managed with early reconstruction plans and supportive care. Discussion: Early reconstruction is recommended, starting at a young age. Cartilaginous or bony support may be considered by the end of adolescence to achieve a satisfactory aesthetic result. This case highlights the importance of early diagnosis and intervention for optimizing outcomes in such rare malformations. Conclusion The presented case of lateral proboscis demonstrates a favorable outcome despite the challenges associated with this rare condition. Early surgical intervention and proper management are crucial for achieving positive results and improving the patient's quality of life.

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Publication Details

Published
2024-12-12
DOI
https://doi.org/10.37191/mapsci-jgcorm-2(1)-013
Primary Topic
Congenital Ear and Nasal Anomalies
Type
article
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article

Proboscis Lateral: A Case Report

Montacer Hafsi
Congenital Ear and Nasal Anomalies
article

Proboscis Lateral: A Case Report

Montacer Hafsi
article en

Abstract

Introduction: The lateral proboscis is a rudimentary nasal structure located off the vertical midline of the face. This malformation is often accompanied by other anomalies, most commonly ophthalmic conditions such as anophthalmia, microphthalmia, and colobomas, as well as facial anomalies like maxillary hypoplasia or facial clefts, and cranio-cerebral anomalies including encephalocele and holoprosencephaly. Methods: This report presents a case of a newborn with a lateral proboscis identified at birth. The pregnancy was poorly monitored, and the anomaly was discovered immediately after delivery. Results: The newborn exhibited a lateral proboscis with a rudimentary nasal structure extending from the right side of the face, along with associated ophthalmic anomalies including microphthalmia. No additional facial clefts or cranio-cerebral abnormalities were noted. The infant was managed with early reconstruction plans and supportive care. Discussion: Early reconstruction is recommended, starting at a young age. Cartilaginous or bony support may be considered by the end of adolescence to achieve a satisfactory aesthetic result. This case highlights the importance of early diagnosis and intervention for optimizing outcomes in such rare malformations. Conclusion The presented case of lateral proboscis demonstrates a favorable outcome despite the challenges associated with this rare condition. Early surgical intervention and proper management are crucial for achieving positive results and improving the patient's quality of life.

Openalex Percentile: Top 54%
Congenital Ear and Nasal Anomalies
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