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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease soft tissue sarcoma
Comorbidity C0035412|rhabdomyosarcoma
Sentences 9
PubMedID- 21853140 While rhabdomyosarcoma (rsc) represent 50% of all soft tissue sarcomas and ∼10% of all malignant solid tumors in children [1], adult pleomorphic rscs are relatively rare.
PubMedID- 22288325 Bckground: rhabdomyosarcoma is one of the most frequent soft tissue sarcomas in children.
PubMedID- 21707915 Recent findings have shown that caveolins are also expressed in rhabdomyosarcoma, a group of heterogeneous childhood soft-tissue sarcomas in which the cancer cells seem to derive from progenitors that resemble myogenic cells.
PubMedID- 22197543 rhabdomyosarcoma (rms) is one of the most frequent soft tissue sarcomas in children.
PubMedID- 23584957 sarcomas, including rhabdomyosarcoma (rms), are rarely encountered in effusion specimens; therefore, difficulties in the accurate diagnosis of metastatic sarcomas in effusions can occasionally arise.
PubMedID- 25949226 Background: rhabdomyosarcoma (rms) is one of the most common soft tissue sarcomas among children.
PubMedID- 26075135 Although a variety of sarcomas, including rhabdomyosarcoma, fibrosarcoma, leiomyosarcoma, and stromal sarcoma, have been described in the prostate, ss is a rare occurrence, with only seven previously reported cases [1–6].
PubMedID- 21772793 Pathologic review confirmed a high-grade sarcoma consistent with rhabdomyosarcoma (figure 2).
PubMedID- 26153023 rhabdomyosarcoma represents about 50% of soft-tissue sarcomas and 10% of malignant solid tumors in childhood.

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