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Published on: February 28, 2025
Complicated oesophageal duplication cyst in a 55-year-old man: a rare case from Pakistan
Arham Amir Khawaja1, Arif Javaid1, Haseeb Mehmood Qadri2
1Department of General Surgery and Surgical Oncology, Shaikh Zayed Medical Complex, Lahore, Pakistan.
Insights
Oesophageal duplication cysts (ODCs) are rare congenital anomalies, particularly in adults. This case highlights surgical management for a large ODC presenting with significant symptoms.
Area of Science:
- Gastroenterology
- Surgical Oncology
- Developmental Biology
Background:
- Duplication cysts are congenital anomalies found along the gastrointestinal tract.
- Oesophageal duplication cysts (ODCs) are rare, especially in adults, often presenting with non-specific symptoms.
Observation:
- A 55-year-old male presented with haematemesis, dysphagia, and weight loss.
- Computed tomography confirmed a large Oesophageal Duplication Cyst.
- Surgical management involved subtotal oesophagectomy with gastric pull-up.
Findings:
- Histopathology confirmed a foregut duplication cyst.
- The patient experienced post-operative atelectasis but recovered fully.
- Adult ODC requires exclusion of malignancy and other mediastinal lesions.
Implications:
- Complete surgical excision is the optimal treatment for symptomatic or large ODCs.
- Early diagnosis and management are crucial to prevent complications.
- This case underscores the importance of considering ODC in adult patients with relevant symptoms.
Abstract:
Duplication cysts are congenital anomalies that arise during early embryonic development. They occur in the small intestine, oesophagus, stomach, and colon. Oesophageal duplication cyst (ODC) is rare among newborns, but even rarer in adults. We report the case of a 55-year-old male with the presenting complaints of haematemesis, dysphagia, and significant weight loss for the past eight months. Clinical examination was unremarkable, except that the patient had pallor. Computed tomography scan confirmed the presence of ODC. Subtotal oesophagectomy with gastric pull-up and sub-aortic oesophagogastrostomy was completed. Histopathology was consistent with foregut duplication cyst. Post-operative period was complicated by left basal atelectasis, and the patient was discharged without long-term sequelae. Adult ODC can be regarded as a diagnosis of exclusion after ruling out oesophageal malignancy, high-grade oesophageal varices, mediastinal masses, and submucosal lesions. Complete surgical excision with restoration of gut continuity is optimal management in complicated, large (>5cm) ODC.
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