An Isolated case of Laryngeal Amyloidosis
Journal Title: Scholars Journal of Medical Case Reports - Year 2015, Vol 3, Issue 8
Abstract
Abstract: A variety of benign and malignant lesions involve larynx. Though rare, amyloidosis can involve paraglottic region of larynx, false cords and true cords. An isolated case of laryngeal amyloidosis has been treated with Microlaryngoscopy and excision. The main stay of confirmation was by hisytopathological examinartion with special staining with congo red. A three year follow up of the patient showed no residual or recurrent disease. Systemic examination did not reveal any involvement of other organs. Keywords: malignant lesions , larynx , amyloidosis, Microlaryngoscopy.
Authors and Affiliations
Jagannatha Prasad, Kalyana Chakravarthi, Subba Rao M. V, Rama Krishna Tirumala Bukkapatnam
Giant Fibromatosis of the Chest Wall: A Rare Entity
Fibromatosis also termed as desmoids is a rare benign but locally aggressive neoplasm characterized by mass like or infiltrative growth of fibrous tissue. It usually arises from the abdominal wall or the extremities, rar...
Non Traumatic Arteriovenous Fistula of the Superficial Temporal Artery
Spontaneous arteriovenous fistula (AVF) of superficial temporal artery (STA) is a very rare condition. The pathogenesis is poorly understood. The treatment may be surgical by excision or endovascular by embolization. A m...
Lethal Urosepsis Due to Occlusion of an Indwelling Bladder Catheter
An 87-year-old woman, who had had hypertension and neurological bladder with an indwelling bladder catheter, complained of lower abdominal pain, appetite loss and a poor physical condition. However, her family selected t...
Tuberculous liver abscess- An unusual presentation
Hepatic tuberculosis is one of the rarest forms of extra-pulmonary tuberculosis. The focal or nodular form presenting as tuberculoma or abscess is uncommon.The diagnosis is most often delayed or missed because of nonspec...
A case of misdiagnosis of classical galactosemia - Role of genetic analysis in making correct diagnosis
Abstract: Galactosemia is an autosomal recessive disorder caused by deficient or absent activities of one of the three enzymes involved in the galactose metabolic pathway. The predominant form is classic type galactosemi...