Oncogenic osteomalacia caused by an occult paranasal sinus tumor

2015 ◽  
Vol 42 (2) ◽  
pp. 167-169 ◽  
Author(s):  
Tomofumi Okamiya ◽  
Katsumasa Takahashi ◽  
Hideo Kamada ◽  
Junko Hirato ◽  
Toru Motoi ◽  
...  
Medicine ◽  
2018 ◽  
Vol 97 (30) ◽  
pp. e11650 ◽  
Author(s):  
Yu-Min Chang ◽  
Yun-Hsiang Chang ◽  
Ke-Hung Chien ◽  
Chang-Min Liang ◽  
Ming-Cheng Tai ◽  
...  

Head & Neck ◽  
2008 ◽  
Vol 30 (6) ◽  
pp. 815-820 ◽  
Author(s):  
Akitoshi Nagasaki ◽  
Takashi Miyagi ◽  
Tamiko Taira ◽  
Akihiko Shinhama ◽  
Shizuo Kojya ◽  
...  

ORL ◽  
2001 ◽  
Vol 63 (6) ◽  
pp. 366-371 ◽  
Author(s):  
Uta M. Kühn ◽  
Wolf J. Mann ◽  
Ronald G. Amedee

2011 ◽  
Vol 4 (2) ◽  
pp. 119-121
Author(s):  
Jagveer Singh Yadav ◽  
Mahendra Chouhan ◽  
Jaimanti Bakshi ◽  
Uma Nahar Saikia

ABSTRACT Paranasal sinuses are normally lined by respiratory mucosa which is pseudostratified ciliated columnar epithelium. Cholesteatoma of paranasal sinus is a condition where respiratory mucosa is either partially or totally replaced by hyperkeratotic squamous epithelium which lead to formation of lamellar sheet of keratin and this condition is known as cholesteatoma. We report one such rare occurrence of maxillary sinus cholesteatoma managed endoscopically.


2017 ◽  
Vol 78 (01) ◽  
pp. e9-e11 ◽  
Author(s):  
Malia Gresham ◽  
Steven Shen ◽  
Yi Zhang ◽  
Kelly Gallagher

AbstractOncogenic osteomalacia (OO) is an uncommon but treatable cause of osteomalacia related to tumor production of FGF23, usually caused by benign mesenchymal neoplasms. Paranasal sinus glomangiomas are a rare cause of OO, with only one previously reported case. Here we describe a second case (first reported in English) of paranasal sinus glomangioma-induced osteomalacia in a 42-year-old man. He presented with weakness and multiple spontaneous fractures, and was found to have an ethmoid sinus glomangioma with intracranial extension. The tumor was removed via endoscopic endonasal approach to the anterior skull base, which resulted in complete resolution of symptoms and no further evidence of disease 1 year postoperatively.


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