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dysphonia/kanama

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Sayfa 1 itibaren 97 Sonuçlar

Dysphonia and vocal fold telangiectasia in hereditary hemorrhagic telangiectasia.

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OBJECTIVE This case report is the first documentation of dysphonia and vocal fold telangiectasia as a complication of hereditary hemorrhagic telangiectasia (HHT). METHODS Case report of a 40-year-old man with HHT presenting with 2 years of worsening hoarseness. RESULTS Hoarseness corresponded with a

Acute dysphonia secondary to vocal fold hemorrhage after vardenafil use.

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Owing to their vasodilatory effects, the phosphodiesterase-5 inhibitors have become widely used for the treatment of erectile dysfunction. Among the reported adverse events of these agents are epistaxis, variceal bleeding, intracranial hemorrhage, and hemorrhoidal bleeding. We report a case of vocal

Sudden dysphonia due to spontaneous bleeding in secondary parathyroid hyperplasia.

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Subtle submucosal hemorrhage causing dysphonia.

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Acute vocal fold hemorrhage with minimal dysphonia.

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[Bleeding into vocal cords in hyperkinetic dysphonia and its consequences].

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Perioperative complications and safety of type II thyroplasty (TPII) for adductor spasmodic dysphonia.

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Type II thyroplasty (TPII) is one of the surgical options offered in the management of adductor spasmodic dysphonia (AdSD); however, there have been no detailed reports of its safety and associated complications during the perioperative period. Our aim was to assess the complications and safety of

Asymptomatic parathyroid adenoma manifested by intratumoral hemorrhage.

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A 48-year-old woman whose past history was unrevealing presented with sudden swelling of the neck with pain and dysphonia. Neck ultrasonography suggested the possibility of hemorrhage in a parathyroid adenoma. Surgical exploration revealed a hemorrhagic parathyroid adenoma of the chief cell type.

Dysphonia associated with lingual thyroid gland and hypothyroidism: improvement after lingual thyroidectomy.

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We present a unique and medically complex case of improved voice after lingual thyroidectomy. A 10-year-old boy with multifactorial dysphonia presented with bilateral vocal fold lesions and sulci in the context of hypothyroidism as a result of a congenital lingual thyroid gland. Despite hormone

Rivaroxaban and retropharyngeal haemorrhage.

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Haemorrhage is a well-known and accepted complication of anticoagulation. A retropharyngeal haemorrhage (RH) is a rare condition that without prompt recognition and management may result in fatal complications. We report a case of RH in a 67-year-old man anticoagulated with rivaroxaban for atrial

Spontaneous supraglottic haemorrhage in a patient receiving warfarin sodium treatment.

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A case of spontaneous, isolated supraglottic haemorrhage in a patient recently started with warfarin sodium treatment is described. The symptoms of sore throat, dysphonia, stridor, dysphagia or a neck swelling in a patient taking anticoagulants should alert the clinician to the possibility of this

Lingual thyroid causing dysphonia: evaluation and management. Case report.

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BACKGROUND Lingual thyroid gland is a rare clinical entity that is caused by the failure of the thyroid gland to descend to a normal cervical location during embryogenesis. The occurrence of an ectopic thyroid gland located at the base of the tongue may cause problems for the patient, with symptoms

Thyroid Gland Hemorrhage in a Patient with Past Medical History of Renal Clear Cell Carcinoma: Report of a Very Rare Case.

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BACKGROUND The incidence of metastasis to the thyroid gland is extremely rare, with hemorrhage being a particularly uncommon manifestation of metastatic thyroid disease. CASE REPORT A 68-year-old man who underwent a right nephrectomy for RCC 8 years ago was referred to the Emergency Department (ED)

Dysphonia in performers: toward a clinical definition of laryngology of the performing voice.

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OBJECTIVE To identify causes of dysphonia in performers and compare causes and aspects of treatment of dysphonia in performers and nonperformers. METHODS Case-control study. METHODS A chart review of all new patients presenting with a chief complaint of dysphonia over a 1-year period was performed.
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