| dc.contributor.author | Yarikkaya, Enver | |
| dc.contributor.author | Erdogan-Durmus, Senay | |
| dc.contributor.author | Erzurumluoglu, Nurhan | |
| dc.contributor.author | Ozekinci, Selver | |
| dc.date.accessioned | 2021-03-02T20:45:20Z | |
| dc.date.available | 2021-03-02T20:45:20Z | |
| dc.date.issued | 2018 | |
| dc.identifier.citation | Erdogan-Durmus S., Ozekinci S., Yarikkaya E., Erzurumluoglu N., "Acral angioosteoma cutis: A rare case", INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY, cilt.84, sa.6, ss.685-686, 2018 | |
| dc.identifier.issn | 0378-6323 | |
| dc.identifier.other | av_037ac854-1112-47b0-b0a4-6bf3b1d48ae2 | |
| dc.identifier.other | vv_1032021 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12627/8284 | |
| dc.identifier.uri | https://doi.org/10.4103/ijdvl.ijdvl_117_17 | |
| dc.description.abstract | Acral angioosteoma cutis is a rare and benign cutaneous lesion clinically characterized by an exophytic growth resembling pyogenic granuloma on the acral skin; first described in 2006. Its pathogenesis is still unclear while well-formed capillaries, pale stoma, bland fibroblast-like cells, and multiple tiny spicules of woven bone constitute the histological hallmarks. Here, we present a case of acral angioosteoma cutis in a 34-year-old man to increase awareness regarding this rare condition. | |
| dc.language.iso | eng | |
| dc.subject | Dermatoloji | |
| dc.subject | Dahili Tıp Bilimleri | |
| dc.subject | Sağlık Bilimleri | |
| dc.subject | Tıp | |
| dc.subject | Klinik Tıp (MED) | |
| dc.subject | Klinik Tıp | |
| dc.subject | DERMATOLOJİ | |
| dc.title | Acral angioosteoma cutis: A rare case | |
| dc.type | Makale | |
| dc.relation.journal | INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY | |
| dc.contributor.department | Istanbul Okmeydani Training & Research Hospital , , | |
| dc.identifier.volume | 84 | |
| dc.identifier.issue | 6 | |
| dc.identifier.startpage | 685 | |
| dc.identifier.endpage | 686 | |
| dc.contributor.firstauthorID | 355907 | |
