Exophthalmos, characterized by protrusion of the eyeballs, can be a sign of serious underlying conditions, including multiple myeloma. In this context, it may indicate a relapse of the disease, often associated with extramedullary infiltration of plasma cells into orbital tissues...
Open access
Research Article10.9734/ajcrs/2025/v8i2654
A cholecystogastric fistula is among the rarest and most serious complications of peptic ulcer disease. It can present with non-specific symptoms and resemble other conditions, such as perforation peritonitis. This makes it preoperative diagnosis challenging. This case report des...
Open access
Research Article10.9734/ajcrs/2025/v8i2652
Gastrointestinal stromal tumours (GISTs) are rare connective tissue tumours, accounting for only 1% of malignant tumours of the digestive tract, with a preferential location in the stomach (60%) and the small intestine (30%). Anorectal location is very rare and infrequently repor...
Open access
Research Article10.9734/ajcrs/2025/v8i1651
Tijani Nissrine, Bouali Mounir, Ettaoussi Abdelhak, Majd Abdessamad, Kamal Khadija, El Bakuri Abdelilah & El hattabi Khalid·Asian Journal of Case Reports in Surgery·2025
Pancreatic cancer represents a significant challenge in digestive oncology, a cancer with a poor prognosis, with an increasing incidence (Kpossou et al., 2021), without clearly identified risk factors allowing screening or diagnosis at an early stage. Surgery remains the only cur...
Open access
Research Article10.9734/ajcrs/2025/v8i1650
Tijani Nissrine, Bouali Mounir, Ettaoussi Abdelhak, Majd Abdessamad, Kamal Khadija, El Bakuri Abdelilah & El hattabi Khalid·Asian Journal of Case Reports in Surgery·2025
Non-traumatic splenic rupture a rare condition in which establishing a positive diagnosis is often difficult, and delayed diagnosis can be life-threatening. The etiologies are multiple and the symptoms are not specific. It is often ultrasound or CT scan that confirms the diagnosi...
Open access
Research Article10.9734/ajcrs/2025/v8i1649
Small bowel perforation due to blunt abdominal trauma is an uncommon but serious condition that can result in peritonitis and sepsis if not promptly treated. The most frequent causes include motor vehicle accidents, bicycle handlebar injuries, and, in rare instances—particularly...
Open access
Research Article10.9734/ajcrs/2025/v8i1648
Katyayni Singh, Sudipta Saha, Manoj Andley, Ranvir Singh, Sabah Fatima, Sumanthareddy B H, Rishav Pacheria, Shashank Mishra & Himanshu Anand·Asian Journal of Case Reports in Surgery·2025
Introduction: Mucoepidermoid Carcinoma (MEC) is a rare variety of esophageal primary cancers with a global incidence of merely 1%. The clinical presentation of this cancer is indistinguishable from the common varieties of esophageal cancers, without any characteristic features of...
Open access
Research Article10.9734/ajcrs/2025/v8i1647
Introduction: Primary mammary tuberculosis is a rare form of extrapulmonary TB, typically spreading to the breast from nearby lymph nodes, ribs, or pleura. It's uncommonly the initial infection site and is predominantly found in multiparous women during their reproductive or lact...
Open access
Research Article10.9734/ajcrs/2025/v8i1646
BOUFELOUSSEN Mohammed, El Azzaoui Imad, EL MESSAOUDI Imane, Dabbagh Mahmoud, Bouzroud Mohamed, Najih Mohamed, Elkaoui Hakim, Bouchentouf Sidi Mohammed & Mountassir Moujahid·Asian Journal of Case Reports in Surgery·2025
Hydatid disease is a parasitosis considered benign and slow to develop, it can affect both sexes and at all ages. The hydatid cyst of pouch of Douglas is an exceptional form of the disease. It is either primary and isolated, or secondary to another location. We report a case of a...
Open access
Research Article10.9734/ajcrs/2025/v8i1644
Mediastinal teratoma is rare congenital neoplasm which is usually discovered in the late second or third decade of life. A 24 year old young female with no past significant history came to a private hospital with complaints of central chest pain for 6 months. On examination her v...
Open access
Research Article10.9734/ajcrs/2025/v8i1643