Bizarre parosteal osteochondromatous proliferation
| Bizarre parosteal osteochondromatous proliferation | |
|---|---|
| Synonyms | Nora's lesion |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Pain, swelling, palpable mass |
| Complications | Recurrence after surgical removal |
| Onset | Typically in young adults |
| Duration | Chronic |
| Types | N/A |
| Causes | Unknown |
| Risks | Unknown |
| Diagnosis | X-ray, MRI, Histopathology |
| Differential diagnosis | Osteochondroma, Parosteal osteosarcoma, Myositis ossificans |
| Prevention | N/A |
| Treatment | Surgical excision |
| Medication | N/A |
| Prognosis | Generally good, but recurrence is possible |
| Frequency | Rare |
| Deaths | N/A |
Other Names: BPOP; Nora lesion; Nora’s Lesion
Bizarre Parosteal Osteochondromatous Proliferation (BPOP), also known as Nora’s lesion, is an uncommon, benign bone tumor that grows on the surface of the bone.
In some cases, BPOP does not cause symptoms. However, at other times, it can be painful and lead to bone deformity. It is more commonly located on the hands and feet, but can also affect the long bones or bones of the skull and face.
A biopsy of the affected bone is important, as BPOP may resemble malignant bone tumors, especially chondrosarcoma or parosteal osteosarcoma.
The cause is still unknown though injuries or bone defects may trigger the condition in some cases.
Treatment involves surgery to remove the tumor. There is a 20%-50% chance that the condition may reappear after surgery.
NIH genetic and rare disease info[edit]
Bizarre parosteal osteochondromatous proliferation is a rare disease.
| Rare and genetic diseases | ||||||
|---|---|---|---|---|---|---|
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Rare diseases - Bizarre parosteal osteochondromatous proliferation
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