Endolymphatic sac carcinoma of the right petrous bone in Von Hippel–Lindau disease

2006 ◽  
Vol 13 (4) ◽  
pp. 471-474 ◽  
Author(s):  
D.P. Muzumdar ◽  
A. Goel ◽  
S. Fattepurkar ◽  
N. Goel
2003 ◽  
Vol 117 (8) ◽  
pp. 666-669 ◽  
Author(s):  
P. S. Richards ◽  
A. G. Clifton

We present a case of a papillary tumour of the petrous bone. The established terminology for this rare neoplasm is endolymphatic sac tumour (ELST) but the true origin remains controversial. ELSTs are associated with von Hippel-Lindau disease. They are locally invasive, highly vascular and often require endovascular embolization prior to surgery. Both radiologically and histologically ELSTs are easily mistaken for other more common tumours such as paragangliomas and renal or papillary thyroid carcinoma metastases. This is important because local excision is curative.


2008 ◽  
Vol 108 (4) ◽  
pp. 751-756 ◽  
Author(s):  
Russell R. Lonser ◽  
Martin Baggenstos ◽  
H. Jeffrey Kim ◽  
John A. Butman ◽  
Alexander O. Vortmeyer

Object Although endolymphatic sac tumors (ELSTs) frequently destroy the posterior petrous bone and cause hearing loss, the anatomical origin of these neoplasms is unknown. To determine the precise topographic origin of ELSTs, the authors analyzed the imaging, operative, and pathological findings in patients with von Hippel–Lindau disease (VHL) and ELSTs. Methods Consecutive VHL patients with small (≤ 1.5 cm) ELSTs who underwent resection at the National Institutes of Health were included. Clinical, imaging, operative, and pathological findings were analyzed. Results Ten consecutive VHL patients (6 male and 4 female) with 10 small ELSTs (≤ 1.5 cm; 9 left, 1 right) were included. Serial imaging captured the development of 6 ELSTs and revealed that they originated within the intraosseous (vestibular aqueduct) portion of the endolymphatic duct/sac system. Imaging just before surgery demonstrated that the epicenters of 9 ELSTs (1 ELST was not visible on preoperative imaging) were in the vestibular aqueduct. Inspection during surgery established that all 10 ELSTs were limited to the intraosseous endolymphatic duct/sac and the immediately surrounding region. Histological analysis confirmed tumor within the intraosseous portion (vestibular aqueduct) of the endolymphatic duct/sac in all 10 patients. Conclusions ELSTs originate from endolymphatic epithelium within the vestibular aqueduct. High-resolution imaging through the region of the vestibular aqueduct is essential for diagnosis. Surgical exploration of the endolymphatic duct and sac is required for complete resection.


2000 ◽  
Vol 175 (3) ◽  
pp. 925-926 ◽  
Author(s):  
K. Ayadi ◽  
Kh. Ben Mahfoudh ◽  
M. Khannous ◽  
J. Mnif

Neurology ◽  
1999 ◽  
Vol 53 (1) ◽  
pp. 208-208 ◽  
Author(s):  
N. Kawahara ◽  
H. Kume ◽  
K. Ueki ◽  
K. Mishima ◽  
T. Sasaki ◽  
...  

2012 ◽  
Vol 122 (10) ◽  
pp. 2300-2303 ◽  
Author(s):  
Clemens Honeder ◽  
Wolfgang Gstoettner ◽  
Christian Matula ◽  
Christian Czerny ◽  
Andreas Gruber ◽  
...  

1997 ◽  
Vol 87 (3) ◽  
pp. 445-449 ◽  
Author(s):  
Jean-Christophe Ouallet ◽  
Kathlyn Marsot-Dupuch ◽  
Remy Van Effenterre ◽  
Michele Kujas ◽  
Jean-Michel Tubiana

✓ This report describes a patient with von Hippel—Lindau disease who presented with an 8-year history of a slow-growing, locally invasive vascularized lesion of the temporal bone involving the cerebellopontine angle. The mass, studied by computerized tomography scanning and magnetic resonance imaging techniques, was partly cystic in appearance. After removal of the mass, pathological studies confirmed a papillary cystic tumor with characteristics that have been described in tumors with an endolymphatic sac origin. These rare neoplasms constitute a distinct pathological entity and deserve wider recognition.


2011 ◽  
Vol 13 (12) ◽  
pp. 1032-1041 ◽  
Author(s):  
Marie Louise Mølgaard Poulsen ◽  
Steen Gimsing ◽  
Michael Kosteljanetz ◽  
Hans Ulrik Møller ◽  
Carsten Alfred Brandt ◽  
...  

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