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  1. Article: Exploring a rare case of juvenile psammomatoid ossifying fibroma in the ethmoid: a case study and review.

    Aaboudech, Taha Yassine / El Ouazzani, Hafsa / Kadiri, Habiba / Essakalli, Leila / Bouteyine, Ayoub / Benadbdenbi, Hanae / Rguieg, Naji / Cherradi, Nadia

    Journal of surgical case reports

    2024  Volume 2024, Issue 4, Page(s) rjae242

    Abstract: Juvenile ossifying fibroma (JOF) and its variants, including juvenile psammomatoid ossifying fibroma (JPOF), represent rare yet clinically significant benign fibro-osseous lesions that primarily occur in children and young adolescents. They can be found ... ...

    Abstract Juvenile ossifying fibroma (JOF) and its variants, including juvenile psammomatoid ossifying fibroma (JPOF), represent rare yet clinically significant benign fibro-osseous lesions that primarily occur in children and young adolescents. They can be found in diverse anatomical sites such as the jaw, nasal cavity, paranasal sinuses, and orbit. JOF exhibits an aggressive nature, necessitating early radiological detection and surgical intervention. Similarly, JPOF, with a locally malignant potential, requires surgical removal, typically conducted through endoscopic approaches. We report a case of a 5-year-old girl with JPOF arising in the ethmoid, revealed by recurrent epistaxis and proptosis. The text emphasizes the importance of early diagnosis through histopathology as a diagnostic tool and underscores the need for appropriate management.
    Language English
    Publishing date 2024-04-20
    Publishing country England
    Document type Case Reports
    ZDB-ID 2580919-2
    ISSN 2042-8812
    ISSN 2042-8812
    DOI 10.1093/jscr/rjae242
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Retroperitoneal lymphatic malformations: A case report.

    Zebbakh, Hajar / Imrani, Kaoutar / Lemrabet, Abir / Aaboudech, Taha Yassine / Bernoussi, Zakia / MoatassimBillah, Nabil / Nassar, Ittimade

    Radiology case reports

    2023  Volume 18, Issue 9, Page(s) 3175–3178

    Abstract: Retroperitoneal lymphatic malformation is a rare benign vascular malformation, of various locations, which can reveal itself at any age in its abdominal localizations. The retroperitoneal localization of this malformation is extremely rare. The clinical ... ...

    Abstract Retroperitoneal lymphatic malformation is a rare benign vascular malformation, of various locations, which can reveal itself at any age in its abdominal localizations. The retroperitoneal localization of this malformation is extremely rare. The clinical symptomatology is polymorphic depending on the lesion volume and the presence or absence of complications. The diagnosis is evoked by the liquid character of the retroperitoneal mass on ultrasound, CT scan and abdomino-pelvic MRI, brought during surgery and confirmed by the histological study of the surgical specimen. The treatment of choice is complete surgical removal of the mass.
    Language English
    Publishing date 2023-06-27
    Publishing country Netherlands
    Document type Case Reports
    ZDB-ID 2406300-9
    ISSN 1930-0433
    ISSN 1930-0433
    DOI 10.1016/j.radcr.2023.05.078
    Database MEDical Literature Analysis and Retrieval System OnLINE

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