Temporal Bone Tumor

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J M Tubiana - One of the best experts on this subject based on the ideXlab platform.

  • papillary adenoma of endolymphatic sac origin a Temporal Bone Tumor in von hippel lindau disease case report
    Journal of Neurosurgery, 1997
    Co-Authors: J C Ouallet, K Marsotdupuch, R Van Effenterre, M Kujas, J M Tubiana
    Abstract:

    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.

Tina C Huang - One of the best experts on this subject based on the ideXlab platform.

  • Progressive Facial Paralysis Secondary to a Rare Temporal Bone Tumor
    2017
    Co-Authors: Noah P Parker, Tina C Huang
    Abstract:

    Paragangliomas are slow-growing benign neoplasms arising from foci of neural crest– derived chemoreceptor tissue, paraganglia. Paragangliomas are most often discovered based on mass effect on nearby structures and are rarely functional outside of the adrenal gland. In the head and neck, paraganglia most commonly reside at the carotid bifurcation, the inferior ganglion region or cervical portion of the vagus nerve, the jugular bulb, and the middle ear cavity; thus, most are discovered in these locations. 1 In the skull base, paraganglia in the area of the jugular bulb and along the cochlear promontory make glomus tympanicum and glomus jugulare the most frequently encountered paragangliomas. Although these 2 Tumors are relatively common in the Temporal Bone, a primary paraganglioma of the fallopian canal, or glomus faciale, is rare. In fact, to our knowledge, only 8 reports exist. 1-8 We describe the presentation, workup, and treatment of the ninth report in the literature.

  • progressive facial paralysis secondary to a rare Temporal Bone Tumor glomus faciale
    Archives of Otolaryngology-head & Neck Surgery, 2011
    Co-Authors: Noah P Parker, Tina C Huang
    Abstract:

    P aragangliomas are slow-growing benign neoplasms arising from foci of neural crest– derived chemoreceptor tissue, paraganglia. Paragangliomas are most often discovered based on mass effect on nearby structures and are rarely functional outside of the adrenal gland. In the head and neck, paraganglia most commonly reside at the carotid bifurcation, the inferior ganglion region or cervical portion of the vagus nerve, the jugular bulb, and the middle ear cavity; thus, most are discovered in these locations. In the skull base, paraganglia in the area of the jugular bulb and along the cochlear promontory make glomus tympanicum and glomus jugulare the most frequently encountered paragangliomas. Although these 2 Tumors are relatively common in the Temporal Bone, a primary paraganglioma of the fallopian canal, or glomus faciale, is rare. In fact, to our knowledge, only 8 reports exist. We describe the presentation, workup, and treatment of the ninth report in the literature.

J C Ouallet - One of the best experts on this subject based on the ideXlab platform.

  • papillary adenoma of endolymphatic sac origin a Temporal Bone Tumor in von hippel lindau disease case report
    Journal of Neurosurgery, 1997
    Co-Authors: J C Ouallet, K Marsotdupuch, R Van Effenterre, M Kujas, J M Tubiana
    Abstract:

    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.

Noah P Parker - One of the best experts on this subject based on the ideXlab platform.

  • Progressive Facial Paralysis Secondary to a Rare Temporal Bone Tumor
    2017
    Co-Authors: Noah P Parker, Tina C Huang
    Abstract:

    Paragangliomas are slow-growing benign neoplasms arising from foci of neural crest– derived chemoreceptor tissue, paraganglia. Paragangliomas are most often discovered based on mass effect on nearby structures and are rarely functional outside of the adrenal gland. In the head and neck, paraganglia most commonly reside at the carotid bifurcation, the inferior ganglion region or cervical portion of the vagus nerve, the jugular bulb, and the middle ear cavity; thus, most are discovered in these locations. 1 In the skull base, paraganglia in the area of the jugular bulb and along the cochlear promontory make glomus tympanicum and glomus jugulare the most frequently encountered paragangliomas. Although these 2 Tumors are relatively common in the Temporal Bone, a primary paraganglioma of the fallopian canal, or glomus faciale, is rare. In fact, to our knowledge, only 8 reports exist. 1-8 We describe the presentation, workup, and treatment of the ninth report in the literature.

  • progressive facial paralysis secondary to a rare Temporal Bone Tumor glomus faciale
    Archives of Otolaryngology-head & Neck Surgery, 2011
    Co-Authors: Noah P Parker, Tina C Huang
    Abstract:

    P aragangliomas are slow-growing benign neoplasms arising from foci of neural crest– derived chemoreceptor tissue, paraganglia. Paragangliomas are most often discovered based on mass effect on nearby structures and are rarely functional outside of the adrenal gland. In the head and neck, paraganglia most commonly reside at the carotid bifurcation, the inferior ganglion region or cervical portion of the vagus nerve, the jugular bulb, and the middle ear cavity; thus, most are discovered in these locations. In the skull base, paraganglia in the area of the jugular bulb and along the cochlear promontory make glomus tympanicum and glomus jugulare the most frequently encountered paragangliomas. Although these 2 Tumors are relatively common in the Temporal Bone, a primary paraganglioma of the fallopian canal, or glomus faciale, is rare. In fact, to our knowledge, only 8 reports exist. We describe the presentation, workup, and treatment of the ninth report in the literature.

K Marsotdupuch - One of the best experts on this subject based on the ideXlab platform.

  • papillary adenoma of endolymphatic sac origin a Temporal Bone Tumor in von hippel lindau disease case report
    Journal of Neurosurgery, 1997
    Co-Authors: J C Ouallet, K Marsotdupuch, R Van Effenterre, M Kujas, J M Tubiana
    Abstract:

    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.