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Rhabdomyoma larynx

Márcia Monteiro Pinho, Jair de Carvalho E Castro, Rosana Grandelle Ramos
Introduction Rhabdomyoma is a rare benign tumor derived from skeletal muscles. Laryngeal rhabdomyomas are even rarer, with only approximately 40 reported cases in world literature. Laryngeal rhabdomyomas usually are seen as masses covered by mucosa. They are often solitary asymptomatic tumors, but symptoms such as hoarseness can occur. The radiologic features are usually those typical of benign neoplasms, showing well-delineated borders. The differential diagnoses for laryngeal masses include cysts, laryngoceles, and benign and malignant neoplasms...
October 2013: International Archives of Otorhinolaryngology
Rachel B Cain, Sharon H Gnagi, Dawn E Jaroszewski, David G Lott
No abstract text is available yet for this article.
March 2014: Otolaryngology—Head and Neck Surgery
Lorraine A de Trey, Stephan Schmid, Gerhard F Huber
Background. Adult rhabdomyoma is a rare benign tumour with the differentiation of striated muscle tissue, which mainly occurs in the head and neck region. Twenty-six cases of multifocal adult rhabdomyoma are documented in the literature. Method. We report a 55-year-old male with simultaneous diagnosis of 7 adult rhabdomyomas and review the literature of multifocal adult rhabdomyoma. Result. Review of the literature revealed 26 cases of multifocal adult rhabdomyoma, of which only 7 presented with more than 2 lesions...
2013: Case Reports in Otolaryngology
Shachi J Sharma, Melanie Kreisel, Tobias Kroll, Stefan Gattenloehner, Jens P Klussmann, Claus Wittekindt
The extracardiac juvenile rhabdomyoma is extremely rare in the field of Otorhinolaryngology. The tumour usually arises from the soft tissue of the face or from mucosal sites, especially the oropharynx and the oral cavity but only sporadic endolaryngeal cases have been described in literature so far with predominance of young males. Here, we describe the very rare case of endolaryngeal extracardiac juvenile rhabdomyoma in a 42-year-old male. Clinical examination showed a mass of the right vocal cord, resembling a cystic lesion...
February 2013: European Archives of Oto-rhino-laryngology
Mark D Dunbar, Pamela Ginn, Matthew Winter, Karri Barabas Miller, William Craft
A 3-year-old, female spayed Australian Shepherd dog was presented to Veterinary Healthcare Associates in Winter Haven, FL with a history of respiratory stridor, difficulty swallowing, and a change in bark for approximately 3 months. Radiographs revealed a soft tissue mass caudal to the epiglottis. Oral and computerized tomographic (CT) examinations were performed under general anesthesia and revealed a small firm mass in the caudal larynx on the right side. Cytologic evaluation of a fine-needle aspirate of the mass revealed cells consistent with a rhabdomyoma, oncocytoma, or granular cell tumor...
December 2012: Veterinary Clinical Pathology
Nancy Elawabdeh, Steve Sobol, Angela C Blount, Bahig M Shehata
Tuberous sclerosis (TSC) is an autosomal-dominant genetic disease characterized by a spectrum of pathologic manifestations involving skin, brain, kidney, and heart. These manifestations include neuroectodermal, mesodermal, and skin lesions as well as a variety of associated tumors and hamartomas. We report an 11-year-old male with previously diagnosed TSC who presented with a laryngeal mass shown on histology to be fetal cellular rhabdomyoma. Cardiac rhabdomyomas are common in TSC patients, but to our knowledge, the association between TSC and extracardiac rhabdomyomas has not been previously reported...
February 2013: Fetal and Pediatric Pathology
George Papaspyrou, Jochen A Werner, Marion Roessler, Kenneth O Devaney, Alessandra Rinaldo, Alfio Ferlito
Rhabdomyomas are rare benign mesenchymal tumors with skeletal muscle differentiation. They are less commonly encountered than are their malignant counterparts, rhabdomyosarcomas. Rhabdomyomas fall into 2 general categories: cardiac and extracardiac types. Extracardiac rhabdomyomas are among the rarest tumors in humans and can be subclassified as fetal, juvenile, and adult types depending on the individual tumor's degree of differentiation by light microscopy. Adult extracardiac rhabdomyoma has a strong predilection for occurrence in the head and neck, mainly in the area of larynx and pharynx...
May 2011: American Journal of Otolaryngology
A Farboud, R Pratap, H Helquist, P Montgomery
INTRODUCTION: Rhabdomyoma of the larynx is a rare condition, with less than 40 cases recorded worldwide. CLINICAL RECORD: A 76-year-old man was referred to our clinic with progressive, severe hoarseness and dysphagia. He had been diagnosed with obstructive sleep apnoea by the respiratory physicians and commenced on nocturnal continuous positive airway pressure ventilation. Transnasal laryngoscopy revealed bilaterally enlarged tissue in the region of the arytenoids; biopsies revealed the (previously unreported) diagnosis of bilateral, synchronous rhabdomyoma of the arytenoids...
November 2009: Journal of Laryngology and Otology
Barbara Pichi, Valentina Manciocco, Paolo Marchesi, Raul Pellini, Paolo Ruscito, Antonello Vidiri, Renato Covello, Giusepe Spriano
Rhabdomyoma is an exceedingly rare soft tissue benign tumor of skeletal muscle origin classified into cardiac and extracardiac types based on location. Extracardiac rhabdomyoma is further classified into adult, genital, and fetal type depending on the degree of differentiation. Adult rhabdomyomas are rare, but morphologically characteristic, benign mesenchymal tumors with mature skeletal muscle differentiation that in 90% of cases arise in the head and neck region, mainly in the mucosa of the oropharynx, nasopharynx, and larynx, from the branchial musculature of third and fourth branchial arches...
June 2008: Dysphagia
Agata K Brys, Osamu Sakai, Jaimie DeRosa, Stanley M Shapshay
We describe a case involving a 79-year-old man with symptoms of slowly progressive hoarseness resulting from a rhabdomyoma originating deep to the right true and false vocal folds. We also review the pathology and radiologic findings of rhabdomyoma.
July 2005: Ear, Nose, & Throat Journal
Kevin Jensen, Keith Swartz
Rhabdomyomas are benign tumors of skeletal muscle derivation. Rhabdomyomas of the head and neck are unusual, and laryngeal rhabdomyomas of the adult type are rare. When they do occur, patients may present with symptoms that have progressed slowly over several years. In extraordinary cases, stridor and airway obstruction manifest. We report a case of adult rhabdomyoma of the larynx that features some of its typical and atypical presenting characteristics. This case also exemplifies the favorable prognosis that results following complete yet conservative surgical excision...
February 2006: Ear, Nose, & Throat Journal
No abstract text is available yet for this article.
April 1963: Archives of Otolaryngology
No abstract text is available yet for this article.
December 1959: Laryngoscope
A J O'Hara, M McConnell, K Wyatt, C Huxtable
A 4-year-old spayed female Golden Retriever was presented for investigation of progressive loss of bark, continuous panting and increased upper respiratory noise. Examination of the larynx and pharynx under general anaesthesia identified a spherical 5 x 3 cm mass involving the right arytenoid cartilage. Cytological examination of fine needle aspirates from the mass suggested the tumour was a carcinoma, however histological examination in association with immunoperoxidase and histochemical staining identified the mass as a laryngeal rhabdomyoma...
December 2001: Australian Veterinary Journal
J M Orrit, C Romero, C Mallofré, J Traserra
Rhabdomyomas of the larynx are extremely rare benign tumors. Only 25 have been well documented until now. These tumors display a low growing pattern. Diagnosis is based on immunocytochemical studies and electron microscopy. Three histological types are distinguished: adult, fetal and fetal myxoidal or genital. Surgery is the treatment of choice. A new case, adult type, is presented and the literature reviewed.
October 2000: Acta Otorrinolaringológica Española
F Roberts, A J Kirk, I A More, J Butler, R P Reid
Extracardiac rhabdomyomas are rare benign tumours showing striated muscle differentiation. Seventy percent of these lesions occur in the head and neck region. The most common sites for these lesions are the larynx, pharynx, and the floor of the mouth. There has been only one previous report of a rhabdomyoma of the oesophagus; two further cases are described.
July 2000: Journal of Clinical Pathology
J LaBagnara, E Hitchcock, T Spitzer
Rhabdomyomas of the larynx are exceedingly rare. The incidence, sites of occurrence in the larynx, and treatment of these benign striated muscle tumors are reviewed. A case of rhabdomyoma involving the vocalis muscle is presented with magnetic resonance imaging and video-stroboscopic documentation.
June 1999: Journal of Voice: Official Journal of the Voice Foundation
C Clercx, D Desmecht, L Michiels, K McEntee, N Hardy, M Henroteaux
A three-year-old male golden retriever had had progressive dyspnoea, exercise intolerance, stridor, and a modified bark for five months. A mass 2 cm in diameter was present dorsal to the right side of the larynx. Histological examination revealed cross-striations in some elongated cells, consistent with a diagnosis of rhabdomyoma, a diagnosis which was confirmed by positive immunohistochemical staining for myoglobin and desmin. The mass could not be removed without total laryngectomy and a permanent tracheostomy and the dog was euthanased...
August 15, 1998: Veterinary Record
A Rinaldo, G M Mannarà, C Fisher, A Ferlito
Hamartoma of the larynx is an extremely rare lesion, and the number of well-documented and acceptable cases is limited. The world literature is critically reviewed in order to develop a more accurate clinicopathological profile of this tumorlike malformation, which has to be differentiated from choristoma, teratoma, and rhabdomyoma, among others. Management consists of local excision, and the prognosis is good.
March 1998: Annals of Otology, Rhinology, and Laryngology
P Zbären, H Läng, M Becker
Two rare benign tumors of the larynx are presented. The first case is a recurrent multifocal rhabdomyoma, the second a lipoma of the larynx. Both tumors were growing beneath a normal-looking mucosa; deep biopsies were necessary to obtain a histologic diagnosis. Lipomas can be diagnosed by CT or MRI. A review of the literature of these two rare benign tumors is also presented.
November 1995: ORL; Journal for Oto-rhino-laryngology and its related Specialties
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