Proboscis lateralis of type IV has not yet been reported from the Indian subcontinent. The authors gives a report on a case of this type and describes the technique of reconstruction not described before. A case of a right-sided proboscis lateralis associated with ipsilateral hemi-nasal aplasia and contralateral nostril and alar defect, a contralateral cleft lip and alveolus, hypertelorism and mild hydrocephalus is presented and documented on a boy coming from the Indian subcontinent.
Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
Duplication of the Lacrimal Sac With Three Canaliculi.
Ophthalmic Plast Reconstr Surg
September 2024
Govindram Seksaria Institute of Dacryology, L.V. Prasad Eye Institute, Hyderabad-34, India.
Article Synopsis
- * Duplication of body structures is rare and has been documented in several organs, but duplication of the lacrimal sac is not previously reported.
- * This case highlights a specific instance of nasolacrimal duct obstruction accompanied by duplication of the lacrimal sac and the presence of three canaliculi.
Prenatal diagnosis of proboscis lateralis.
Arch Gynecol Obstet
August 2024
Department of Obstetrics and Gynaecology, University of Tuebingen, Calwerstrasse 7, 72076, Tuebingen, Germany.
A case report of proboscis lateralis: emphasis on the reconstruction of the lacrimal drainage system.
Transl Pediatr
May 2024
Department of Otorhinolaryngology, Head and Neck Surgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing Key Laboratory for Pediatric Diseases of Otolaryngology Head and Neck Surgery, Beijing, China.
Article Synopsis
- Proboscis lateralis (PL) is a rare craniofacial congenital malformation, with a classification system developed in 1985 that highlights its associated anomalies, notably sinonasal deformities and ocular issues.
- A case study of a 20-month-old girl with PL revealed complications after initial surgery, leading to the need for a second procedure to reconstruct the lacrimal drainage system, which was successfully performed with a multidisciplinary team.
- This case emphasizes the importance of comprehensive treatment plans for PL that take into account associated ocular anomalies and ensure proper lacrimal drainage reconstruction.
Proboscis Lateralis With Choanal Atresia.
J Craniofac Surg
February 2024
School of Medicine, Pontifical Javeriana University, Bogota, Colombia.
The case of a female patient who was born with proboscis lateralis, choanal atresia, and telecanthus is submitted. A report is made on the initial management of this patient, the clinical follow-up that has been carried out so far, and a review of the literature is conducted, taking into account the limited information found in this specific pathology, in order to contribute to its diagnostic orientation and treatment from a plastic and craniofacial surgery point of view.
View Article and Find Full Text PDFCoexistence of proboscis lateralis and multiple craniofacial, neurological, cardiac and spinal deformities: a one-of-a-kind case report.
BMC Pediatr
February 2023
President, Associazione Naso Sano, Perugia, Italy.
Article Synopsis
- Proboscis lateralis (PL) is a rare congenital facial deformity characterized by a tubular structure protruding from the inner corner of the eye, often linked to other craniofacial deformities.
- A reported case involved a full-term female newborn with PL alongside several serious health issues, including brain and heart anomalies.
- The findings suggest the need for comprehensive assessments of additional organ system defects in individuals diagnosed with PL due to its association with various complications.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!