Rhabdomyoma is a benign tumor that comes from skeletal tissue, it classified as cardiac and extracardiac according to the location. Extracardiac rhabdomyomas most frequently originate in head neck at larynx pharynx, being parapharyngeal space an exceptional We present clinical case of 86-year-old man asymptomatic patient with laterocervical mass years evolution, has increased its size progressi...

Cardiac rhabdomyoma can be subclinical or have a fatal presentation according to the onset age and involved site, size, and degree of invasion. Although most cardiac rhabdomyomas become smaller with time, emergency intervention is indicated when severe obstruction has occurred. In this report, we describe the spontaneous regression of a large cardiac rhabdomyoma (20.5 × 15.6 mm) presenting as s...

Fetal rhabdomyoma is not generally considered part of nevoid basal cell carcinoma syndrome. However, a review of the literature revealed five patients with this syndrome who also had fetal rhabdomyomas in various locations. We report the first patient with nevoid basal cell carcinoma syndrome and a fetal rhabdomyoma of the tongue. We recommend that embryonal rhabdomyosarcoma be ruled out to avo...

Rhabdomyoma is a rare benign tumour, majority arising from the cardiac muscle. Seventy to 90 percent of extra cardiac rhabdomyomas are found in the head and neck region, usually within the upper aero digestive tract. We report a case of rhabdomyoma of anterior neck in a neonate. Although rhabdomyomas of posterior neck have been reported, those reported in anterior triangle are infrequent. The l...

Rhabdomyoma is an uncommon benign mesenchymal tumor with skeletal muscle differentiation that may occur either in the heart or in extracardiac sites. Even though the head and neck region is the most common area of extracardiac rhabdomyoma, the larynx is rarely involved. We present the case of an 85-year-old woman who reported a 10-day history of breathing difficulties, dysphagia, and dysphonia....

The accidental finding of a giant left ventricular rhabdomyoma in a female infant with no tuberous sclerosis is described herein. This is the first report of a huge cardiac rhabdomyoma occluding the left ventricular cavity, which was not associated with tuberous sclerosis. The clinical management of the baby and the difficult therapeutical choices involved both pediatricians and pediatric cardi...

Fetal rhabdomyoma is a rare neoplasm composed of immature striated muscle cells that resemble rhabdomesenchymal cells during weeks 6-10 of embryogenesis. This tumor, though well-described in many anatomic locations, is most commonly found in the head and neck region. We report a case which highlights the difficulty in diagnosing a fetal rhabdomyoma in the lacrimal gland of a 56 year old woman. ...

Cardiac tumors are rare in neonates, most are rhabdomyomas. Because of large size, they may cause homodynamic instability and even death in neonatal period. In 50% cases, rhabdomyoma is associated with tuberous sclerosis [1]. About 100 cases have been reported in literature [1, 3]. We are reporting a case of term neonate, with antenatally diagnosed cardiac masses, who expired at 36 h of life an...

Cardiac tumours occur very rarely in infancy. When present, the commonest of these are rhabdomyomata.1 Until now, only a few cases of rhabdomyoma have been diagnosed echocardiographically.2-4 Affected infants with severe involvement usually die as a result of obstruction to blood flow, and thus operation may be undertaken in an attempt at palliation. Tuberous sclerosis is often associated with ...