2014
DOI: 10.1017/s002221511400293x
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A rare case of subglottic embryonal rhabdomyosarcoma: managed with the aim of organ preservation

Abstract: While surgery has been successfully used to treat this neoplasm, combination therapy, as described in our study, also seems effective and has the added advantage of preserving laryngeal function.

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Cited by 11 publications
(4 citation statements)
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“…Rhabdomyosarcomas are rarely found in the larynx, in which most of the cases of head and neck rhabdomyosarcomas occur in the orbit, nasopharynx, and nose [2,3]. A particular study undertaken over a period of 20 years reported that children presenting with head and neck rhabdomyosarcomas have a mean age of 5.3 years and a median age of four years.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Rhabdomyosarcomas are rarely found in the larynx, in which most of the cases of head and neck rhabdomyosarcomas occur in the orbit, nasopharynx, and nose [2,3]. A particular study undertaken over a period of 20 years reported that children presenting with head and neck rhabdomyosarcomas have a mean age of 5.3 years and a median age of four years.…”
Section: Discussionmentioning
confidence: 99%
“…The tumor often resembles the muscle cells found in 7to 10-day-old embryos. The four principal histological variants of rhabdomyosarcoma consist of embryonal, alveolar, pleomorphic, and botryoid, whereby, in general, the embryonal and pleomorphic subtypes occur in the younger and older population, respectively [1,2]. Their clinical presentation may be distinguished from other laryngeal malignancies, in which some may present with subtle clinical signs.…”
Section: Introductionmentioning
confidence: 99%
“…They represent less than 1% of all laryngeal tumors. A variety of uncommon sarcoma subtypes arising from the submucosal connective tissue have been described in the larynx, mainly as case reports or small series including synovial sarcoma [54][55][56], well-differentiated and dedifferentiated liposarcoma [57][58][59], alveolar soft part sarcoma [60], low-grade fibro-myxoid sarcoma [61], embryonal rhabdomyosarcoma [62][63][64][65][66], Kaposi sarcoma [67], and undifferentiated sarcoma [68][69][70] (Figures 2 and 3). Synovial sarcoma represents an aggressive soft tissue tumor classically arising from mesenchymal tissue.…”
Section: Soft Tissue Sarcomasmentioning
confidence: 99%
“…Als seltene maligne Tumorentitäten, die primär in der Subglottis entspringen, können z. B. das Rhabdomyosarkom [76], das Neurofibrosarkom [77], ein lymphoepitheliales Karzinom [78], ein kleinzelliges Karzinom der Subglottis mit schlechter Prognose aufgrund einer raschen Fernmetastasierung [79] sowie primäre Schleimhautmelanome angeführt werden [80]. Metastatische Tumorabsiedlungen in den Larynx sind eine Rarität.…”
Section: Sonstige Tumoreunclassified