A Rare Case of Osteogenesis Imperfecta Type V Osteogenesis imperfecta (OI) is a hereditary bone condition characterised by fragile bones to be more susceptible to fracture. We reported a rare case of a 6-year-old girl with OI Type V and hyperplastic callus formation. She presented with recurrent fractures since birth with no family history of a similar condition. Clinically, her height and weight were lower than the 5th percentile for her age. She had deformities with limitation of movement of elbows, kyphoscoliosis, a more extensive right thigh, and anterior bowing of both legs. Radiographic examination revealed interosseous membrane of forearm ossification, dislocation of the right radial head and hyper-callosity of both femurs during fracture healing. She was treated with intravenous pamidronate and had posterior instrumentation and fusion for scoliosis and intramedullary rodding for her femur fracture. On a recent follow-up at the age of 16 years, she was ambulating well with no progression of the spinal deformity.

Sporotrichosis is a mycosis caused by a saprophytic dimorphic fungus named Sporothrix schenckii. Infections occur following traumatic inoculation of fungus from plants and infected cat bites and scratches. We report a case of a farmer who presented with a solitary subcutaneous nodule initially diagnosed as a soft tissue tumour. A history of agricultural activity and feline contact should draw the clinician's attention to sporotrichosis, as the diagnosis can be easily missed in atypical cases. The diagnosis, microbiology and management of the case are discussed.
Biopsy, Needle ; Diagnosis, Differential ; Soft Tissue Neoplasms/*diagnosis ; Sporothrix/isolation & purification ; Sporotrichosis/*diagnosis ; Sporotrichosis/microbiology ; Sporotrichosis/surgery