ABSTRACT
Woakes' syndrome is a group of disease which include recurrent nasal polyps resulting in the broadening of the nasal pyramid, the onset of hypoplasia of frontal sinus and bronchiectasis, as well as the production of mucous discharge. Children and young adults are mostly susceptible to Woakes' syndrome due to the plasticity of the bone. Even though the exact etiology is unknown, genetic factor is thought to be influential because it is often diagnosed in siblings. Otolaryngologically, the mainstream method of removing nasal polyp by endoscopic sinus surgery as well as topical or systemic treatment can be helpful. We report two siblings who visited our clinic both complaining of nasal obstruction. The patients presented with recurrent nasal polyps and showed signs of bronchiectasis, which led to the diagnosis of Woakes' syndrome. These rare cases are presented here with a review of related literature.
ABSTRACT
Woakes' syndrome is a group of disease which include recurrent nasal polyps resulting in the broadening of the nasal pyramid, the onset of hypoplasia of frontal sinus and bronchiectasis, as well as the production of mucous discharge. Children and young adults are mostly susceptible to Woakes' syndrome due to the plasticity of the bone. Even though the exact etiology is unknown, genetic factor is thought to be influential because it is often diagnosed in siblings. Otolaryngologically, the mainstream method of removing nasal polyp by endoscopic sinus surgery as well as topical or systemic treatment can be helpful. We report two siblings who visited our clinic both complaining of nasal obstruction. The patients presented with recurrent nasal polyps and showed signs of bronchiectasis, which led to the diagnosis of Woakes' syndrome. These rare cases are presented here with a review of related literature.
Subject(s)
Child , Humans , Young Adult , Bronchiectasis , Diagnosis , Fibrinogen , Frontal Sinus , Methods , Nasal Obstruction , Nasal Polyps , Plastics , SiblingsABSTRACT
Lymphoepithelioma-like carcinoma exhibits immunohistochemically similar features to lymphoepithelioma and commonly occurs in the skin, salivary gland, breast, lung, gastrointestinal tract, liver, urinary tract, prostate, vulva and vagina. Lymphoepithelioma-like carcinoma from the thyroid gland is extremely rare. We recently experienced a case of lymphoepithelioma-like carcinoma of thyroid gland in a 28-year-old female, who presented a thyroid nodule that was suspicious of papillary carcinoma. We report this unusual case of lymphoepithelioma-like carcinoma of thyroid gland with a brief review of literature.
Subject(s)
Adult , Female , Humans , Breast , Carcinoma , Carcinoma, Papillary , Gastrointestinal Tract , Liver , Lung , Prostate , Salivary Glands , Skin , Thyroid Gland , Thyroid Nodule , Thyroidectomy , Urinary Tract , Vagina , VulvaABSTRACT
Pleomorphic adenoma is the most common benign neoplasm of the parotid gland and it accounts for approximately 80% of all reported tumor from parotid. Recurrence rate was noted as 20–45% and high risk factors related to recurrence were the following: over 40 years of age, women, over 30 mm mass size, below 10 mm safety margin, tumor puncture and tumor spillage during surgery, relation to the facial nerve, tumor site, surgical procedure. We experienced a 45-year-old woman who presented a huge left parotid mass. She had a huge parotid pleomorphic adenoma that was removed 18 years ago but had recurred 8 years ago. We removed the mass and obtained good postoperative results.