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Imaging findings in noncraniofacial childhood rhabdomyosarcoma.

Van Rijn RR, Wilde JC, Bras J, Oldenburger F, McHugh KM, Merks JH - Pediatr Radiol (2008)

Bottom Line: Rhabdomyosarcoma (RMS) is the most common soft-tissue sarcoma of childhood.This paper is focuses on imaging for diagnosis, staging, and follow-up of noncraniofacial RMS.

View Article: PubMed Central - PubMed

Affiliation: Department of Radiology, Academic Medical Centre Amsterdam, Suite G1-224, Meibergdreef 9, 1105 AZ, Amsterdam Zuid-Oost, The Netherlands. r.r.vanrijn@amc.uva.nl

ABSTRACT
Rhabdomyosarcoma (RMS) is the most common soft-tissue sarcoma of childhood. This paper is focuses on imaging for diagnosis, staging, and follow-up of noncraniofacial RMS.

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Related in: MedlinePlus

Sclerosing RMS: small cells, primitive spindle-shaped cells and eosinophilic rhabdomyoblasts in a background of hyaline sclerosis (H&E, original magnification 10×20)
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Fig4: Sclerosing RMS: small cells, primitive spindle-shaped cells and eosinophilic rhabdomyoblasts in a background of hyaline sclerosis (H&E, original magnification 10×20)

Mentions: Both embryonal and alveolar RMS may show rhabdoid tumour-like features and anaplasia (focal or diffuse) [9, 10]. More recently, under the heading sclerosing RMS, a variant with hyalin sclerosis has been described (Fig. 4) [11]. It is unclear whether this is a distinct subtype.Fig. 4


Imaging findings in noncraniofacial childhood rhabdomyosarcoma.

Van Rijn RR, Wilde JC, Bras J, Oldenburger F, McHugh KM, Merks JH - Pediatr Radiol (2008)

Sclerosing RMS: small cells, primitive spindle-shaped cells and eosinophilic rhabdomyoblasts in a background of hyaline sclerosis (H&E, original magnification 10×20)
© Copyright Policy
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC2367394&req=5

Fig4: Sclerosing RMS: small cells, primitive spindle-shaped cells and eosinophilic rhabdomyoblasts in a background of hyaline sclerosis (H&E, original magnification 10×20)
Mentions: Both embryonal and alveolar RMS may show rhabdoid tumour-like features and anaplasia (focal or diffuse) [9, 10]. More recently, under the heading sclerosing RMS, a variant with hyalin sclerosis has been described (Fig. 4) [11]. It is unclear whether this is a distinct subtype.Fig. 4

Bottom Line: Rhabdomyosarcoma (RMS) is the most common soft-tissue sarcoma of childhood.This paper is focuses on imaging for diagnosis, staging, and follow-up of noncraniofacial RMS.

View Article: PubMed Central - PubMed

Affiliation: Department of Radiology, Academic Medical Centre Amsterdam, Suite G1-224, Meibergdreef 9, 1105 AZ, Amsterdam Zuid-Oost, The Netherlands. r.r.vanrijn@amc.uva.nl

ABSTRACT
Rhabdomyosarcoma (RMS) is the most common soft-tissue sarcoma of childhood. This paper is focuses on imaging for diagnosis, staging, and follow-up of noncraniofacial RMS.

Show MeSH
Related in: MedlinePlus