propylthiouracil and Hearing-Loss--Sensorineural

propylthiouracil has been researched along with Hearing-Loss--Sensorineural* in 3 studies

Other Studies

3 other study(ies) available for propylthiouracil and Hearing-Loss--Sensorineural

ArticleYear
Progressive bilateral sensorineural hearing loss induced by an antithyroid drug.
    ORL; journal for oto-rhino-laryngology and its related specialties, 2004, Volume: 66, Issue:5

    We report a patient with antithyroid drug-induced progressive bilateral sensorineural hearing loss associated with myeloperoxidase-antineutrophil cytoplasmic antibodies (MPO-ANCA). While antithyroid drugs have been linked to MPO-ANCA-associated small-vessel vasculitis, sensorineural hearing loss rarely was noted. A 36-year-old man treated for hyperthyroidism with propylthiouracil (PTU) developed progressive bilateral sensorineural hearing loss accompanied by fever and arthritis. MPO-ANCA were demonstrated in serum. Distortion product otoacoustic emissions test results suggested dysfunction of outer hair cells of the organ of Corti. Inner ear blood flow impairment from ANCA-associated small-vessel vasculitis presumably caused cochlear dysfunction. PTU withdrawal and high-dose methylprednisolone administration greatly improved hearing on both sides.

    Topics: Adult; Antibodies, Antineutrophil Cytoplasmic; Antithyroid Agents; Graves Disease; Hearing Loss, Bilateral; Hearing Loss, Sensorineural; Humans; Male; Peroxidase; Propylthiouracil

2004
Sudden sensorineural hearing loss: a case report supporting the immunologic theory.
    Arquivos de neuro-psiquiatria, 2003, Volume: 61, Issue:4

    Sudden sensorineural hearing loss (SSNHL) is one of the autoimmune diseases of the inner ear (AIED), which is characterized by a hearing loss of above 30 decibels in at least three contiguous audiometric frequencies over a time course of 72 hours or shorter. Its cause can be found in only 10% to 15% of patients. Histopathologic findings have reported retrograde neuronal degeneration and atrophy of Corti's organ and of the vascular stria. This paper describes a case of a middle-aged female patient undergoing a treatment for hyperthyroidism who developed bilateral SSNHL. The patient was treated with methylprednisone (1 mg/kg/day) for three days with considerable hearing improvement. This treatment was followed by lung and kidney tuberculosis. The immune mechanism of this entity and the possibility of interconnected participation of the antigen type, of an autoimmune disease and of bacterial infection are discussed.

    Topics: Anti-Inflammatory Agents; Antithyroid Agents; Autoimmune Diseases; Cross Reactions; Female; Hearing Loss, Sensorineural; Humans; Hyperthyroidism; Methylprednisolone; Middle Aged; Propylthiouracil

2003
Propylthiouracil hypersensitivity with circumstantial evidence for drug-induced reversible sensorineural deafness: a case report.
    Hormone research, 1991, Volume: 35, Issue:3-4

    Severe adverse reactions to propylthiouracil occur in 1-5% of patients. Three major side effects, namely agranulocytosis, hepatotoxicity and drug-induced hypersensitivity, have been described though these syndromes are not distinct entities and there can be overlaps in the clinical manifestations. The drug-induced hypersensitivity may be an immune-mediated reaction with multiorgan involvement in which a combination of polyarthritis, cutaneous vasculitis and fever is common. We report a patient with propylthiouracil-induced hypersensitivity with an unusual combination of high spiking fever, migratory polyarthritis, reversible sensorineural deafness, normochromic normocytic anaemia, leucocytosis and hepatotoxicity associated with polyclonal activation of multiple autoantibodies. This case illustrates the highly variable clinical manifestations of the syndrome. The prompt recovery upon withdrawal of the drug indicates the importance of early diagnosis.

    Topics: Adult; Arthritis; Carbimazole; Drug Hypersensitivity; Female; Graves Disease; Hearing Loss, Sensorineural; Humans; Propranolol; Propylthiouracil; Thyroxine

1991