2006
DOI: 10.1002/hed.20358
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Adult extracardiac rhabdomyoma: Light and immunohistochemical studies of two cases in the parapharyngeal space

Abstract: The head and neck area harbors 90% of adult rhabdomyomas and should be considered in a differential diagnosis in this region. Immunohistochemistry confirms that the tumors are almost totally mature neoplasms of clonal origin.

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Cited by 14 publications
(4 citation statements)
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“…Adult rhabdomyoma is a rare benign tumor of striated muscle and most commonly (90%) occurring in the head and neck region. 5 However, it has also been reported in other locations such as esophagus and extremities. 6,7 It is usually more often diagnosed in adult male over 40-yearold with a median age of 60-year-old.…”
Section: Discussionmentioning
confidence: 98%
“…Adult rhabdomyoma is a rare benign tumor of striated muscle and most commonly (90%) occurring in the head and neck region. 5 However, it has also been reported in other locations such as esophagus and extremities. 6,7 It is usually more often diagnosed in adult male over 40-yearold with a median age of 60-year-old.…”
Section: Discussionmentioning
confidence: 98%
“…Adult rhabdomyomas are rare, benign mesenchymal tumors of skeletal muscle origin which usually present as a solitary mass in the head and neck region. To date, there are very few case reports of rhabdomyoma diagnosed based on cytology (Table ) . In a review of the literature, the most common location is the oropharyngeal area with only 1 case located in the parapharyngeal region .…”
Section: Discussionmentioning
confidence: 99%
“…Rarely, rhabdomyomas have been found to be located in the extremities, esophagus, stomach, mediastinum, orbit, prostate, and heart [11]. Symptoms, which are nonspecific, depend on the localization and the size of the tumor [2]. Occasionally, when lesions involve the oral cavity and oral pharynx, a mass in the throat may be observed.…”
Section: Discussionmentioning
confidence: 99%
“…Histologically the AR presents polygonal cells, eosinophilic granular cytoplasm, cross-striations, and spider cells; the expression of desmin, muscle-specific actin, myoglobin, and myogenin can be immunohistochemically demonstrated [1]. The most important differential diagnoses are granular cell tumors, hibernomas, oncocytomas, and paragangliomas, but all these tumors do not histologically present cross-striation and do not content glycogen [2]. FR is rarer than AR; it is histologically characterized by small eosinophilic cells, sometimes with cross-striations, rare nucleoli, and the same immunohistochemical features of AR [1].…”
Section: Introductionmentioning
confidence: 99%