Intraosseous hibernoma: clinicopathologic and imaging analysis of 18 cases.

Autor: Gangahar, Chiraag N¹ (AUTHOR), Dehner, Carina A¹ (AUTHOR), Wang, David P² (AUTHOR), Amini, Behrang³ (AUTHOR), Hillen, Travis⁴ (AUTHOR), O'Conor, Christopher⁵ (AUTHOR), Jennings, Sydney N⁶ (AUTHOR), Byrnes, Kathleen¹ (AUTHOR), Montgomery, Elizabeth A⁷ (AUTHOR), Czerniak, Bogdan A² (AUTHOR), Bridge, Julia A^8,9 (AUTHOR), Schroeder, Molly C¹ (AUTHOR), Jennings, Jack W⁴ (AUTHOR), Wang, Wei‐Lien² (AUTHOR), Chrisinger, John S A¹ (AUTHOR) jschrisi@wustl.edu

Publikováno v: Histopathology. Jul2023, Vol. 83 Issue 1, p40-48. 9p.

Keratocystoma: A Distinctive Salivary Gland Neoplasm Characterized by RUNX2 Rearrangements.

Autor: Bishop, Justin A., Nakaguro, Masato, Urano, Makoto, Yamamoto, Yoshinari, Utsumi, Yoshitaka, Li, Rong, Weinreb, Ilan, Nagashima, Yoji, Gangahar, Chiraag, Yamashiro, Katsushige, Hashimoto, Kimio, Rooper, Lisa M., Carlile, Brian, Wang, Richard C., Gagan, Jeffrey, Nagao, Toshitaka

Publikováno v: American Journal of Surgical Pathology; Mar2024, Vol. 48 Issue 3, p317-328, 12p

15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies

Autor: Zhou, Hui-Fang, O’Conor, Christopher J., Gangahar, Chiraag, Dehner, Louis P.

Publikováno v: Case Reports in Pediatrics.

Background. Omphalocele is a rare congenital abdominal wall defect. It is frequently associated with genetic abnormality and other congenital anomalies, although isolated omphalocele cases do exist. Data have shown that omphalocele with co-occurring

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=hindawi_publ::f17aa79b44eaafefdc4a6a11a5635279

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