| Osteoma cutis | |
|---|---|
| Other names | POH |
 | |
| Perforating osteoma cutis, skin of the foot | |
| Specialty | Oncology, dermatology  |
Osteoma cutis is a cutaneous condition characterized by the presence of bone within the skin in the absence of a preexisting or associated lesion.[1]: 529 Osteoma cutis often manifests as solid, varying-sized, skin-colored subcutaneous nodules.[2]
Signs and symptoms[edit]
Osteoma cutis can present clinically as a single, asymptomatic lesion or as many lesions, depending on the circumstances.[3] Their sizes vary from 0.1 to 5.0 cm.[4] These lesions might show up as miliary lesions, papules, plaques, or nodules.[3] They feel firm to the touch and might occasionally be the cause of yellowish or white spots on the skin.[5] Bony spicules may occasionally be released from an ulcerated layer of skin above the epidermis.[6]
Causes[edit]
There are two types of osteoma cutis: primary and secondary. When an osteoma cutis does not have an underlying lesion, it is categorized as primary. Primary osteoma cutis can arise alone or in combination with metabolic syndrome.[7] When osteoma cutis is linked to neoplasia, dysembryoplasia, scarring, or inflammatory processes, it is considered secondary.[3]
Authors have discovered a link between persistent acne and osteoma cutis.[8] Prolonged acne is the cause of about 85% of cases of osteoma cutis.[3]
GNAS1 gene mutations, a crucial regulatory gene in Albright hereditary osteodystrophy and progressive osseous heteroplasia, have been linked to osteoma cutis.[9]
Mechanism[edit]
The exact process underlying the development of osteoma cutis is still unknown. There are numerous possibilities that range from nevoid tumors to hamartomas.[4] The most widely accepted theory is that of fibroblast metaplasia.[3]
One idea suggests that the development of osteoma cutis may be caused by the metaplasia of fibroblasts into osteoblasts as a result of changes to the genes that control the formation of new bone.[10]
According to an alternative theory, primordial mesenchymal cells often transform into osteoblasts but move to an ectopic site.[11]
Certain authors claim that gene mutations may also cause skin ossification.[3]
Diagnosis[edit]
Histologically, extensive eosinophilic deposits in the dermis and subcutaneous tissue are indicative of osteoma cutis. There are calcified and conspicuous cement lines and bone spicules. Occasionally, transepidermal removal of bony spicules might result in epidermal perforation. Since membrane ossification is the primary mechanism for bone development, there is no corresponding cartilage formation. Osteocytes, osteoblasts, and osteoclasts can all be seen in osteoma cutis. Haversian systems are seen in huge deposits. Bone marrow components are rarely seen.[3]
Treatment[edit]
Osteoma cutis treatment options vary depending on the condition's severity, extent, location, and cause.[12]
Applying tretinoin cream is one non-invasive therapeutic approach, yet its effectiveness is limited, especially for small and superficial lesions.[12][13]
Combinations of dermabrasion and punch biopsy, YAG laser, scalpel incisions, curettage, and CO2 laser are examples of invasive treatment techniques.[3]
See also[edit]
References[edit]
- ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
- ^ Niebel, Dennis; Poortinga, Sietske; Wenzel, rg (2020-09-22). "Osteoma Cutis and Calcinosis Cutis: "Similar but Different"". The Journal of Clinical and Aesthetic Dermatology. 13 (11). Matrix Medical Communications: 28–31. PMC 7716738. PMID 33282099.
- ^ a b c d e f g h Limaiem, Faten; Sergent, Shane R. (2023-05-23). "Osteoma Cutis". StatPearls Publishing. PMID 32644642. Retrieved 2024-02-28.
- ^ a b Alhazmi, Daniah; Badr, Fatma; Jadu, Fatima; Jan, Ahmed M.; Abdulsalam, Zainab (2017). "Osteoma Cutis of the Face in CBCT Images". Case Reports in Dentistry. 2017. Hindawi Limited: 1–4. doi:10.1155/2017/8468965. ISSN 2090-6447. PMC 5468557. PMID 28638666.
- ^ Bouraoui, Saadia; Mlika, Mona; Kort, Rim; Cherif, Fayka; Lahmar, Ahlem; Sabeh, Mzabi (2011-12-12). "Miliary osteoma cutis of the face". Journal of Dermatological Case Reports. 5 (4). Specjalisci Dermatolodzy: 77–81. doi:10.3315/jdcr.2011.1082. ISSN 1898-7249. PMC 3241951. PMID 22408708.
- ^ Cohen, Philip R (2018). "Perforating osteoma cutis: case report and literature review of patients with a solitary perforating osteoma cutis lesion". Dermatology Online Journal. 24 (3). doi:10.5070/D3243038608. ISSN 1087-2108. PMID 29634878.
- ^ Ward, Susannah; Sugo, Ella; Verge, Charles F.; Wargon, Orli (2011-01-12). "Three cases of osteoma cutis occurring in infancy. A brief overview of osteoma cutis and its association with pseudo-pseudohypoparathyroidism". Australasian Journal of Dermatology. 52 (2). Wiley: 127–131. doi:10.1111/j.1440-0960.2010.00722.x. ISSN 0004-8380. PMID 21605097. S2CID 205454453.
- ^ Thielen, AM; Stucki, L; Braun, RP; Masouyé, I; Germanier, L; Harms, M; Salomon, D; Borradori, L (2006-01-27). "Multiple cutaneous osteomas of the face associated with chronic inflammatory acne". Journal of the European Academy of Dermatology and Venereology. 20 (3). Wiley: 321–326. doi:10.1111/j.1468-3083.2006.01425.x. ISSN 0926-9959. PMID 16503897. S2CID 23216763.
- ^ Elli, F.M.; Barbieri, A.M.; Bordogna, P.; Ferrari, P.; Bufo, R.; Ferrante, E.; Giardino, E.; Beck-Peccoz, P.; Spada, A.; Mantovani, G. (2013). "Screening for GNAS genetic and epigenetic alterations in progressive osseous heteroplasia: First Italian series". Bone. 56 (2). Elsevier BV: 276–280. doi:10.1016/j.bone.2013.06.015. hdl:2434/226706. ISSN 8756-3282. PMID 23796510.
- ^ Mahy, P R; Urist, M R (December 1988). "Experimental heterotopic bone formation induced by bone morphogenetic protein and recombinant human interleukin-1B". Clinical Orthopaedics and Related Research. 237 (237): 236–244. doi:10.1097/00003086-198812000-00035. PMID 3263906.
- ^ Myllylä, R.M.; Haapasaari, K.M.; Palatsi, R.; Germain-Lee, E.L.; Hägg, P.M.; Ignatius, J.; Tuukkanen, J. (2011). "Multiple miliary osteoma cutis is a distinct disease entity: four case reports and review of the literature". British Journal of Dermatology. 164 (3). Oxford University Press (OUP): 544–552. doi:10.1111/j.1365-2133.2010.10121.x. ISSN 0007-0963. PMID 21062265.
- ^ a b D Cohen, T Chetov, E Cagnano, S Naimer, D A Vardy, A (2001-01-01). "Treatment of multiple miliary osteoma cutis of the face with local application of tretinoin (all- trans retinoic acid): a case report and review of the literature". Journal of Dermatological Treatment. 12 (3). Informa UK Limited: 171–173. doi:10.1080/09546630152607925. ISSN 0954-6634. PMID 12243710. S2CID 218896657.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ FULTON, JAMES E. (1987). "Dermabrasion-Loo-Punch-Excision Technique for the Treatment of Acne-Induced Osteoma Cutis". The Journal of Dermatologic Surgery and Oncology. 13 (6). Wiley: 655–659. doi:10.1111/j.1524-4725.1987.tb00532.x. ISSN 0148-0812. PMID 2953769.
Further reading[edit]
- Barolet, Augustin C.; Litvinov, Ivan V.; Barolet, Daniel (2020). "Multiple miliary osteoma cutis treatment response to Q-switched Nd:YAG laser: A case report". SAGE Open Medical Case Reports. 8. SAGE Publications: 2050313X2091056. doi:10.1177/2050313x20910562. ISSN 2050-313X. PMC 7057398. PMID 32180982.
- Delaleu, J.; Cordoliani, F.; Bagot, M.; Bouaziz, J.-D.; Vignon-Pennamen, M.-D.; Lepelletier, C. (2020). "Osteoma cutis miliaire de la face". Annales de Dermatologie et de Vénéréologie (in French). 147 (4). Elsevier BV: 313–315. doi:10.1016/j.annder.2020.01.008. ISSN 0151-9638. PMID 32081454.