Primary gastric yolk tumours are extremely rare. We report a 52-year-old male who presented to the Sultan Qaboos University Hospital, Muscat, Oman, in 2017 after having undergone a gastrectomy abroad due to a suspected poorly-differentiated adenocarcinoma. The patient subsequently returned to Oman to receive chemotherapy. However, while undergoing chemotherapy, an abdominal computed tomography scan revealed a lobulated mesenteric mass. Microscopic examination of the resected lesion confirmed a diagnosis of a yolk sac tumour. The mass was diffusely positive for α-fetoprotein (AFP) and a gastric carcinoma stain was negative. Gastrectomy slides from the patient’s previous surgery were examined retrospectively. The morphology was typical for a ...
Objectives: Cerebral venous thrombosis (CVT) can have varied and life-threatening manifestations. Th...
A congenital pulmonary airway malformation (CPAM) is a rare cystic anomaly that may occur during dev...
β-thalassaemia major is an autosomal recessive form of haemoglobinopathy that is characterised by co...
The coexistence of cystic fibrosis (CF) and sarcoidosis is rare. We report a 22-year-old male cystic...
Septic arthritis is a surgical emergency requiring prompt drainage of the accumulation of pus in the...
Amyloidosis is a disorder characterised by the extracellular deposition of amyloid, a fibrillary pro...
ABSTRACT: Pulmonary hyalinising granuloma (PHG) is a rare fibrosclerosing inflammatory lung conditio...
Conidiobolomycosis is a rare fungal infection that affects adults in tropical regions. We report a 4...
Choosing the best anticoagulant therapy for a pregnant patient with a mechanical prosthetic valve is...
Tuberous sclerosis complex (TSC) is a multisystem neurocutaneous disorder inherited in an autosomal ...
Paediatric hypercalcaemia is a rare condition which can be easily overlooked or misdiagnosed. We rep...
ABSTRACT: Cardiac blood cysts are rare benign neoplasms, usually involving the cardiac valves and ar...
A ruptured sinus of Valsalva aneurysm (RSVA) is a rare cardiac anomaly. Traditionally, RSVAs were re...
Dermatofibrosarcoma protuberans (DFSP) is a rare, slow-growing mesenchymal neoplasm of the dermis an...
Primary extradural meningiomas are rare tumours and calvarial meningiomas with extensive bony change...
Objectives: Cerebral venous thrombosis (CVT) can have varied and life-threatening manifestations. Th...
A congenital pulmonary airway malformation (CPAM) is a rare cystic anomaly that may occur during dev...
β-thalassaemia major is an autosomal recessive form of haemoglobinopathy that is characterised by co...
The coexistence of cystic fibrosis (CF) and sarcoidosis is rare. We report a 22-year-old male cystic...
Septic arthritis is a surgical emergency requiring prompt drainage of the accumulation of pus in the...
Amyloidosis is a disorder characterised by the extracellular deposition of amyloid, a fibrillary pro...
ABSTRACT: Pulmonary hyalinising granuloma (PHG) is a rare fibrosclerosing inflammatory lung conditio...
Conidiobolomycosis is a rare fungal infection that affects adults in tropical regions. We report a 4...
Choosing the best anticoagulant therapy for a pregnant patient with a mechanical prosthetic valve is...
Tuberous sclerosis complex (TSC) is a multisystem neurocutaneous disorder inherited in an autosomal ...
Paediatric hypercalcaemia is a rare condition which can be easily overlooked or misdiagnosed. We rep...
ABSTRACT: Cardiac blood cysts are rare benign neoplasms, usually involving the cardiac valves and ar...
A ruptured sinus of Valsalva aneurysm (RSVA) is a rare cardiac anomaly. Traditionally, RSVAs were re...
Dermatofibrosarcoma protuberans (DFSP) is a rare, slow-growing mesenchymal neoplasm of the dermis an...
Primary extradural meningiomas are rare tumours and calvarial meningiomas with extensive bony change...
Objectives: Cerebral venous thrombosis (CVT) can have varied and life-threatening manifestations. Th...
A congenital pulmonary airway malformation (CPAM) is a rare cystic anomaly that may occur during dev...
β-thalassaemia major is an autosomal recessive form of haemoglobinopathy that is characterised by co...