A congenital pulmonary airway malformation (CPAM) is a rare cystic anomaly that may occur during development of the fetal airways. The vast majority of CPAMs are detected in neonates; as such, it is unusual for diagnosis to occur in adulthood. We report a 21-year-old male patient who presented to the emergency department of the Hospital Ampang, Kuala Lumpur, Malaysia, in 2015 with chest pain, breathlessness and tachypnoea. Based on an initial chest X-ray, the patient was misdiagnosed with pneumothorax and underwent urgent chest tube insertion; however, his condition deteriorated over the course of the next three days. Further imaging was suggestive of infected bullae or an undiagnosed CPAM. The patient therefore underwent video-assisted tho...
Background: Removal of spherical object like beads from tracheobronchial tree is very difficult...
ABSTRACT: Objectives: Little is known about nurses’ and patients’ perceptions of learning needs foll...
Tuberous sclerosis complex (TSC) is a multisystem neurocutaneous disorder inherited in an autosomal ...
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...
Conidiobolomycosis is a rare fungal infection that affects adults in tropical regions. We report a 4...
The coexistence of cystic fibrosis (CF) and sarcoidosis is rare. We report a 22-year-old male cystic...
The use of ultrasonography in acute and critical care medicine is becoming increasingly common. Howe...
Large diaphragmatic defects can be repaired with latissimus dorsi and serratus anterior muscle flaps...
Primary gastric yolk tumours are extremely rare. We report a 52-year-old male who presented to the S...
In recent years, tattoos have become more commonplace. However, this can result in various inflammat...
Paediatric hypercalcaemia is a rare condition which can be easily overlooked or misdiagnosed. We rep...
Opium users may present with central or peripheral nervous system-related symptoms, gastrointestinal...
ABSTRACT: Pulmonary hyalinising granuloma (PHG) is a rare fibrosclerosing inflammatory lung conditio...
β-thalassaemia major is an autosomal recessive form of haemoglobinopathy that is characterised by co...
Background: Removal of spherical object like beads from tracheobronchial tree is very difficult...
ABSTRACT: Objectives: Little is known about nurses’ and patients’ perceptions of learning needs foll...
Tuberous sclerosis complex (TSC) is a multisystem neurocutaneous disorder inherited in an autosomal ...
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...
Conidiobolomycosis is a rare fungal infection that affects adults in tropical regions. We report a 4...
The coexistence of cystic fibrosis (CF) and sarcoidosis is rare. We report a 22-year-old male cystic...
The use of ultrasonography in acute and critical care medicine is becoming increasingly common. Howe...
Large diaphragmatic defects can be repaired with latissimus dorsi and serratus anterior muscle flaps...
Primary gastric yolk tumours are extremely rare. We report a 52-year-old male who presented to the S...
In recent years, tattoos have become more commonplace. However, this can result in various inflammat...
Paediatric hypercalcaemia is a rare condition which can be easily overlooked or misdiagnosed. We rep...
Opium users may present with central or peripheral nervous system-related symptoms, gastrointestinal...
ABSTRACT: Pulmonary hyalinising granuloma (PHG) is a rare fibrosclerosing inflammatory lung conditio...
β-thalassaemia major is an autosomal recessive form of haemoglobinopathy that is characterised by co...
Background: Removal of spherical object like beads from tracheobronchial tree is very difficult...
ABSTRACT: Objectives: Little is known about nurses’ and patients’ perceptions of learning needs foll...
Tuberous sclerosis complex (TSC) is a multisystem neurocutaneous disorder inherited in an autosomal ...