A Curious Case of Multimorbidity in a Patient With Goldenhar Syndrome Presenting With Vomiting

Division

West Florida

Hospital

Oak Hill Hospital

Document Type

Case Report

Publication Date

10-29-2024

Keywords

anatomical variability, gallstone pancreatitis, goldenhar syndrome surgery, hepatitis c (hcv) infection, primary biliary cirrhosis (pbc)

Disciplines

Congenital, Hereditary, and Neonatal Diseases and Abnormalities | Internal Medicine | Medicine and Health Sciences | Musculoskeletal Diseases

Abstract

Goldenhar syndrome, also known as oculo-auriculo-vertebral dysplasia or hemifacial microsomia, is a rare congenital anomaly involving the first and second branchial arches. In this case report, we present a distinctive instance of a 43-year-old male with Goldenhar syndrome who presented with nausea and recurrent bilious vomiting. Initial diagnostic imaging raised concerns about pancreatitis, leading to a comprehensive evaluation that revealed gallstone pancreatitis as the cause of his symptoms. Despite the seemingly straightforward diagnosis, the case was complicated by anatomical abnormalities that required multiple interventions and led to additional complications related to the patient's underlying condition. The complexities of this case highlight the potential challenges in managing what may initially appear to be uncomplicated presentations in patients with Goldenhar syndrome, emphasizing the critical importance of a multidisciplinary approach. This report underscores the need for timely, well-reasoned clinical strategies to ensure optimal care and prevent adverse outcomes in such patients.

Publisher or Conference

Cureus

Link to Full Text

Share

COinS