• The Journal of the Korean bone and joint tumor society
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• v.5 no.3
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• pp.178-182
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• 1999

We report a case of bizarre parosteal osteochondromatous proliferation of the right femur in an 18-year-old man. Roentgenograms showed a calcific mass attached to the underlying cortex with a broad base. Histologically, the lesion showed hypercellular cartilaginous tissue with maturation into trabecular bone, which contained spindle cells and lymphocytes in the intertrabecular spaces. Bizarre parosteal osteochondromatous proliferations are a form of heterotopic ossification and should not be mistaken for osteosarcoma or chondrosarcoma.

• Journal of Korean Foot and Ankle Society
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• v.17 no.1
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• pp.68-73
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• 2013

Bizarre parosteal osteochondromatous proliferation (BPOP) is an rare benign tumor which involve mostly tubular bones of feet and hand. BPOP has clinical, radiographic, and histologic similarities with osteochondroma.Radiologically, BPOP has not central continuity with underlying osseous medulla. Histologically, the lesion has marked proliferative activity, and enlarged, bizzare, and binucleated chondrocytes.Despite the high risk of recurrence, treatment of choice is surgical resection. This report presents two cases of BPOP of the big toe with reviews of clinical, radiographic, and histological characteristics.

• Journal of Korean Foot and Ankle Society
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• v.2 no.1
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• pp.48-51
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• 1998

Bizarre parosteal osteochondromatous proliferation of bone (BPOP) was first described in 1983 by Nora et. al., who reported 35 cases of a bizarre proliferative lesion involving the small bones of the hands and less often the feet. These lesions simulate osteochondromas and conlain cartilage cap exhibiting atypical chondrocytes often undergoing ossification. Radiologically, they differ from osteochondromas. The lesion recurs in a significant number of cases after local excision, and the disturbing cytologic features may lead to a mistaken diagnosis of malignancy. The purpose of this report is to describe a case of bizarre parosleal osteochondromatous proliferation of the foot in a patient without traumatic history.

• The Journal of the Korean bone and joint tumor society
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• v.20 no.2
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• pp.104-108
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• 2014

Bizarre parosteal osteochondromatous proliferation (Nora's lesion) is a rare benign tumor and known to be primarily occur in the small tubular bone of the hands and feet. However, it is very unusual to be reported that it occurs in metatarsal bone in Korea. Thus, we report this tumor of metatarsal bone including the literature review because we have experienced this example.

• The Journal of the Korean bone and joint tumor society
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• v.17 no.2
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• pp.91-94
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• 2011

Bizarre parosteal osteochondromatous proliferation (BPOP) otherwise known as Nora's lesion, is a benign surface tumor of the small tubular bone of the hands and feet with high probability of local recurrence. The report of BPOP in the foot is very rare in our country. We report a case of BPOP of proximal phalanx of right $3^{rd}$ toe in 44-year-old female, successfully managed by en-bloc marginal excision with a review of the literatures.

• Journal of Korean Foot and Ankle Society
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• v.25 no.4
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• pp.195-198
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• 2021

Nora et al. first reported a bizarre parostealosteochondromatous proliferation (BPOP) as a small size bone malformation mainly in the foot and hand in April 1983 that was called Nora's lesion or Nora's disease. Nora's disease is known for its low incidence and is characterized as a benign lesion, without a malignancy or metastasis with different histological, radiological, and clinical features from other common lesions. Several cases of Nora's disease on the hand, foot, and long bone have been reported in Korea. This paper reports a case of BPOP of the proximal phalanx of the great toe.