2001
DOI: 10.1046/j.1365-2559.2001.1301e.x
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Gastric carcinosarcoma, coexistence of adenosquamous carcinoma and rhabdomyosarcoma: a case report

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Cited by 36 publications
(29 citation statements)
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“…At least 45 cases of gastric carcinosarcoma have been reported around the world [1][2][3][4][5][6][8][9][10][11][12][13][14][18][19][20][21][22][23][24][25][26][27], with the majority from Japan [13] (Table 2). As gastric carcinosarcoma is very rare, the effects of chemotherapy or radiotherapy have not yet been reported.…”
Section: Discussionmentioning
confidence: 99%
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“…At least 45 cases of gastric carcinosarcoma have been reported around the world [1][2][3][4][5][6][8][9][10][11][12][13][14][18][19][20][21][22][23][24][25][26][27], with the majority from Japan [13] (Table 2). As gastric carcinosarcoma is very rare, the effects of chemotherapy or radiotherapy have not yet been reported.…”
Section: Discussionmentioning
confidence: 99%
“…Histological identifi cation of the coexistence of carcinomatous and sarcomatous components in the tumor is indispensable for diagnosis. In all reported cases this coexistence has been confi rmed by using conventional hematoxylin and eosin (H&E) staining, with the additional use of immunohistochemical analyses in some cases [10,[12][13][14].…”
Section: Introductionmentioning
confidence: 96%
“…Due to this tumor detecting at advance stage and its rapid growth, most of SCSs are associated with a poor clinical outcome. Sato et al reported a mean survival of 10 months in patients with SCS [140]. The current standard therapy for SCS is partial or total gastrectomy with regional lymph node dissection.…”
Section: Sarcomatoid Carcinomamentioning
confidence: 99%
“…SCS usually occurs in the antral or pyloric region and infiltrates the gastric wall frequently. Macroscopically, it is a polypoid, exophytic, or endophytic mass with ulceration ( Fig.14) [139,140,[142][143][144][145][146]. Histologically, SCS exhibits an adenocarcinoma component with variable differentiation and a high-grade sarcomatous component composed of spindle cells with high cellularity, frequent mitotic counts with atypical forms and pleomorphism (Fig.15).…”
Section: Sarcomatoid Carcinomamentioning
confidence: 99%
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