scholarly journals Case Report: Temporal Bone Lesion Extending Into Infratemporal Fossa

2020 ◽  
Vol 78 (4) ◽  
pp. e17-e20
Author(s):  
Ashley Lazar ◽  
Carolyn Brookes
1995 ◽  
Vol 109 (6) ◽  
pp. 565-568 ◽  
Author(s):  
Ahmad Khashaba ◽  
Giuseppe De Donato ◽  
Gabriele Vassallo ◽  
Mauro Landolfi ◽  
Alessandra Russo ◽  
...  

AbstractOsteoblastoma is a benign bone lesion that mainly affects the long bones and rarely the temporal bones. Very few cases have been reported in the literature. This paper reviews the literature, discusses the differential diagnosis, clinical presentation, and CT scan findings of such a condition and details our experience with a young patient who had a temporal bone (mastoid process) osteoblastoma.


2010 ◽  
Vol 120 (S4) ◽  
pp. S180-S180 ◽  
Author(s):  
Daniel S. Roberts ◽  
William C. Faquin ◽  
Daniel G. Deschler

2007 ◽  
Vol 86 (10) ◽  
pp. 614-616 ◽  
Author(s):  
Joo Hyung Lee ◽  
Min Kyo Jung ◽  
Chang Eun Song ◽  
Sang Won Yeo ◽  
Hye Kyung Lee ◽  
...  

Inflammatory pseudotumors are histologically benign but locally destructive lesions that are usually found in the lung, although some cases of temporal bone involvement have been reported. To the best of our knowledge, no case of simultaneous involvement of the temporal bone and the lung has been previously reported in the literature. We describe such a case in a 39-year-old man. The temporal bone lesion was removed in its entirety, and the lung lesion was treated with steroid therapy. At the 2-month follow-up, the size of the lung mass on chest x-ray was significantly reduced, and at 1 year, the patient was asymptomatic.


2021 ◽  
Vol 9 (6) ◽  
Author(s):  
Nicolau Moreira Abrahão ◽  
Guilherme Correa Guimarães ◽  
Arthur Menino Castilho ◽  
Vagner Antônio Rodrigues da Silva

2003 ◽  
Vol 82 (12) ◽  
pp. 926-937 ◽  
Author(s):  
Carsten Christof Boedeker ◽  
Gian Kayser ◽  
Gerd Jürgen Ridder ◽  
Wolfgang Maier ◽  
Jörg Schipper

2019 ◽  
Vol 5 (1) ◽  
pp. 20180029
Author(s):  
Yaotse Elikplim Nordjoe ◽  
Ouidad Azdad ◽  
Mohamed Lahkim ◽  
Laila Jroundi ◽  
Fatima Zahrae Laamrani

Facial nerve aplasia is an extremely rare condition that is usually syndromic, namely, in Moebius syndrome. The occurrence of isolated agenesis of facial nerve is even rarer, with only few cases reported in the literature. We report a case of congenital facial paralysis due to facial nerve aplasia diagnosed on MRI, while no noticeable abnormality was detected on the temporal bone CT.


Neurosurgery ◽  
2001 ◽  
Vol 48 (4) ◽  
pp. 945-948
Author(s):  
Renatta J. Osterdock ◽  
Sandea Greene ◽  
Christopher R. Mascott ◽  
Ronald Amedee ◽  
Byron E. Crawford
Keyword(s):  

1989 ◽  
Vol 82 (10) ◽  
pp. 1377-1381 ◽  
Author(s):  
Toshio Suzuki ◽  
Kazutoyo Kobayashi ◽  
Akikatsu Kataura

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