6533b86cfe1ef96bd12c8cd6

RESEARCH PRODUCT

Amyloidoma of the gasserian ganglion as a cause of symptomatic neuralgia of the trigeminal nerve: report of three cases.

Jürgen BohlStephan StörkelAntje BornemannHans-hilmar GoebelWibke Müller-forellO. HeyGamm HAxel Perneczky

subject

AdultPathologymedicine.medical_specialtySchwannomaDiagnosis DifferentialTrigeminal ganglionTrigeminal neuralgiamedicineHumansCranial Nerve NeoplasmsTrigeminal nerveAmyloidomaStaining and Labelingbusiness.industryAmyloidosisCongo RedAmyloidosisMiddle AgedTrigeminal Neuralgiamedicine.diseaseCranial Nerve DiseasesGanglionMicroscopy Electronmedicine.anatomical_structureNeurologyTrigeminal GanglionNeuralgiaFemaleNeurology (clinical)businessNeurilemmoma

description

Three cases of symptomatic neuralgia of the trigeminal nerve due to an amyloidoma in the gasserian ganglion are described. The correct diagnosis was not made prior to histological examination of the surgical biopsy specimens. Medical history and clinical observation led to the diagnosis of a malignant process of the nasal cavities in the first patient; of an inflammatory dental focus in the second patient; and of multiple sclerosis in the third patient. CT findings were normal in cases 1 and 2; in case 3, a schwannoma was suspected from the CT appearances. In case 1, MRI had not been performed; in cases 2 and 3, MRI revealed a tumour mass which was also considered to be a schwannoma. Histologically, the tumours consisted of masses of amyloid deposits which had largely replaced the pre-existing ganglionic cells and satellite cells. Electron microscopy confirmed the fibrillar structure of the deposits. Immunohistochemistry and immunocytochemistry revealed the amyloid to belong to the AL-lambda subtype.

10.1007/bf00870665https://pubmed.ncbi.nlm.nih.gov/7511158