Background: An odontogenic keratocyst is a lesion characterized by aggressive and infiltrative growth. The lesion is characterized by the existence of satellite microcysts (microtumours) and frequent recurrence (up to 30%). Ehlers–Danlos syndrome is a condition in which collagen production or its post-translational modifications are affected. Defects in connective tissues cause symptoms, which range from mild joint hypermobility to life-threatening complications. Case presentation: We present an extremely rare case of an 11-year old girl with Ehlers–Danlos syndrome and coexistence of multiple odontogenic keratocysts. Conclusions: This case shows mainly atypical or rare association between multiple odontogenic keratocysts and Ehlers–Danlos syndrome.
Multiple odontogenic keratocysts in Ehlers–Danlos syndrome: a rare case report / A. Starzynska, P. Adamska, L. Adamski, A. Sejda, P. Wychowanski, M. Studniarek, B.A. Jereczek-Fossa. - In: BMC ORAL HEALTH. - ISSN 1472-6831. - 21:1(2021 Mar 09), pp. 107.1-107.7. [10.1186/s12903-021-01472-9]
Multiple odontogenic keratocysts in Ehlers–Danlos syndrome: a rare case report
B.A. Jereczek-FossaUltimo
2021
Abstract
Background: An odontogenic keratocyst is a lesion characterized by aggressive and infiltrative growth. The lesion is characterized by the existence of satellite microcysts (microtumours) and frequent recurrence (up to 30%). Ehlers–Danlos syndrome is a condition in which collagen production or its post-translational modifications are affected. Defects in connective tissues cause symptoms, which range from mild joint hypermobility to life-threatening complications. Case presentation: We present an extremely rare case of an 11-year old girl with Ehlers–Danlos syndrome and coexistence of multiple odontogenic keratocysts. Conclusions: This case shows mainly atypical or rare association between multiple odontogenic keratocysts and Ehlers–Danlos syndrome.File | Dimensione | Formato | |
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