Bizarre parosteal osteochondromatous proliferation
| Bizarre parosteal osteochondromatous proliferation | |
|---|---|
| Other names | Nora lesion or Nora disease[1][2] |
| Specialty | Orthopedics |
| Symptoms | Painless lump in finger or toe[1] |
| Risk factors | Possibly trauma in a minority[1] |
| Diagnostic method | Medical imaging[1] |
| Differential diagnosis | Mainly subungal exostosis[1] |
| Treatment | Surgical excision.[1] |
| Prognosis | Up to 50% recur after surgery[1] |
| Frequency | Rare,[2] <5% of cartilage tumors,[3] M=F[1] |
Bizarre parosteal osteochondromatous proliferation (BPOP), also known as Nora's lesion,[4] is a type of non-cancerous bone tumor belonging to the group of cartilage tumors.[1][2][5] It is generally seen in the tubular bones of the hands and feet,[6] where it presents with a rapidly enlarging painless lump in a finger or toe.[1]
It is composed of bone, cartilage and spindle cells.[1] Some people report previous trauma.[1]
Diagnosis is by medical imaging.[1] Treatment is by surgical excision.[1] Up to 50% recur after surgery.[1]
It is rare,[2] and occurs more often in the 20s and 30s.[1] Combined with subungal exostosis, it accounts for less than 5% of cartilage tumors.[3] Males and females are affected equally.[1] The condition was first described by Frederick E. Nora in 1983.[6][7]
Signs and symptoms[edit]
BPOP generally presents with a 1–3 cm painless lump in a finger or more frequently a toe.[1] Growth can be rapid.[2]
Mechanism[edit]
It is composed of bone, cartilage and spindle cells.[1] A small number of people have reported previous trauma.[1]
Diagnosis[edit]
Medical imaging usually shows a well-defined wide-based bony growth on the surface of bone.[6]
Differential diagnosis[edit]
BPOP is distinct from subungal exostosis.[1][6] Conditions that may appear similar to BPOP include: myositis ossficans, ostechondroma, surface osteosarcoma and granulomatous infection.[2]
Treatment[edit]
Treatment is by surgical excision.[1]
Outcomes[edit]
Up to 50% recur after surgery.[1][2]
Epidemiology[edit]
BPOP is rare.[2] It is most often seen in people in their 20s and 30s.[1] Combined with subungal exostosis, it accounts for less than 5% of cartilage tumors.[3] Males and females are affected equally.[1][6]
History[edit]
Bizarre parosteal osteochondromatous proliferation was first described by Frederick E. Nora in 1983.[6][7] Generally in the US, it has been thought of as a mouthful and hence it is sometimes referred to as Nora's lesion.[4]
Other animals[edit]
In 1998 a report of a similar lesion to BPOP was reported in a wallaby.[8]
References[edit]
- ^ a b c d e f g h i j k l m n o p q r s t u v w x y WHO Classification of Tumours Editorial Board, ed. (2020). "Bizarre parosteal osteochondromatous proliferation". Soft Tissue and Bone Tumours: WHO Classification of Tumours. Vol. 3 (5th ed.). Lyon (France): International Agency for Research on Cancer. pp. 348–350. ISBN 978-92-832-4503-2.
- ^ a b c d e f g h Bocklage, Therese J.; Quinn, Robert; Verschraegen, Claire; Schmit, Berndt (2014). "16. Cartilaginous tumours of bones and joints". Bone and Soft Tissue Tumors: A Multidisciplinary Review with Case Presentations. London: JP Medical Ltd. p. 379. ISBN 978-1-907816-22-2.
- ^ a b c Engel, Hannes; Herget, Georg W.; Füllgraf, Hannah; Sutter, Reto; Benndorf, Matthias; Bamberg, Fabian; Jungmann, Pia M. (March 2021). "Chondrogenic Bone Tumors: The Importance of Imaging Characteristics". RöFo: Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin. 193 (3): 262–275. doi:10.1055/a-1288-1209. ISSN 1438-9010. PMID 33152784.
- ^ a b Davies, A. Mark; Sundaram, Murali; James, Steven J. (2009). Imaging of Bone Tumors and Tumor-Like Lesions: Techniques and Applications. Springer Science & Business Media. p. 684. ISBN 978-3-540-77982-7.
- ^ "ICD-11 - ICD-11 for Mortality and Morbidity Statistics". icd.who.int. Retrieved 6 July 2021.
- ^ a b c d e f Mahajan, Sumit; Chandra, Rajesh; Mohan Lal, Yash (December 2012). ""Nora lesion" – Bizarre parosteal osteochondromatous proliferation". Journal of Clinical Orthopaedics and Trauma. 3 (2): 119–121. doi:10.1016/j.jcot.2012.07.001. ISSN 0976-5662. PMC 3872810. PMID 26403451.
- ^ a b Nora, F. E.; Dahlin, D. C.; Beabout, J. W. (April 1983). "Bizarre parosteal osteochondromatous proliferations of the hands and feet". The American Journal of Surgical Pathology. 7 (3): 245–250. doi:10.1097/00000478-198304000-00003. ISSN 0147-5185. PMID 6837834. S2CID 36384395.
- ^ Rungsipipat, A.; Yamaguchi, R.; Naganobu, K.; Iwamoto, K.; Uchida, K.; Tateyama, S.; Kurogi, T.; Katayama, N. (1998). "A bone tumour resembling bizarre parosteal osteochondromatous proliferation in a wallaby". Australian Veterinary Journal. 76 (8): 561–564. doi:10.1111/j.1751-0813.1998.tb10218.x. ISSN 1751-0813. PMID 9741726.