Zobrazeno 1 - 10
of 162
pro vyhledávání: '"Lin Xu-Yong"'
Publikováno v:
Diagnostic Pathology, Vol 8, Iss 1, p 18 (2013)
Abstract Sclerosing rhabdomyosarcoma (SRMS) is exceedingly rare, and may cause a great diagnostic confusion. Histologically, it is characterized by abundant extracellular hyalinized matrix mimicking primitive chondroid or osteoid tissue. So, it may b
Externí odkaz:
https://doaj.org/article/84689c5308284a6ab7fb4deb2d3d4129
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 172 (2012)
Abstract Enteropathy-associated T-cell lymphoma (EATL) is a rare peripheral T-cell lymphoma which was classified into 2 types based on histology. EATL is often, but not always, associated with celiac disease. EATL type I is a large cell lymphoma whic
Externí odkaz:
https://doaj.org/article/fdd4281ee62f4f8c84c0d964ecc62c29
Autor:
Lin Xu-Yong, Wang Yan, Fan Chui-Feng, Liu Yang, Yu Juan-Han, Dai Shun-Dong, Wang Liang, Wang En-Hua
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 174 (2012)
Abstract Pulmonary sclerosing hemangioma (PSH) is an uncommon pulmonary tumor. Histologically, PSH typically consists of two types of cells, surface cuboidal cells and polygonal cells, four architectural patterns including papillary, sclerotic, solid
Externí odkaz:
https://doaj.org/article/5abc7cc781d34a17b0cdf2e08e2ce384
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 155 (2012)
Abstract Pleomorphic lipoma is a relatively uncommon entity, and is considered as a variant of spindle cell lipoma. Histologically, spindle cell lipoma/pleomorphic lipoma consists of varying quantity of mature fat, bland spindle cells and ropey colla
Externí odkaz:
https://doaj.org/article/35b3d7c270c64b03a403bb90575a1d4b
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 137 (2012)
Abstract Mucoepidermoid carcinoma is a common malignant epithelial tumor of salivary glands, but relatively rare in lung. The histological features of mucoepidermoid carcinoma of the lung are similar to its counterpart arising from the salivary gland
Externí odkaz:
https://doaj.org/article/1f10f3551bcd4865ab6fef1b7b60a2b9
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 122 (2012)
Abstract Angiomyolipoma (AML) is a rare mesenchymal neoplasm of the tumor, composed of a varying heterogeneous mixture of three tissue components: blood vessels, smooth muscle and adipose cells. Hepatic AML may demonstrate a marked histological diver
Externí odkaz:
https://doaj.org/article/900743859a94498981e90d4a36e973f2
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 118 (2012)
Abstract Summary Epithelioid angiosarcoma of the parotid gland is rare, and may pose a great diagnostic challenge. We report a case of primary epithelioid angiosarcoma in a 64-year-old male without history of radiation. The histopathological findings
Externí odkaz:
https://doaj.org/article/1da9e9c8ef5f4058ae2cdfa6df753a72
Autor:
Han Yang, Qiu Xue-shan, Li Qing-chang, Han Yu-chen, Lin Xu-yong, Zhang Qing-fu, Wang Jian, Wang En-hua, Li Ze-liang
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 47 (2012)
Abstract Genital rhabdomyoma is very rare tumor that usually occurs in the vulvar of young women. Epididymis rhabdomyoma in a young man is extremely uncommon and has rarely been reported. Here, we report a case of epididymis rhabdomyoma of a 17-year-
Externí odkaz:
https://doaj.org/article/e3115ea62e1749f28fa1f5cf384fa5cc
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Publikováno v:
OncoTargets and therapy
Deep benign fibrous histiocytoma (FH) is an uncommon and poorly recognized tumor that arises in subcutaneous or deep soft tissue. Deep benign FH of the trachea is even more rare. Deep benign FH recurs in approximately 20% of cases, so surgical resect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e11c0ae99ca72c9a3e8d06d00de5e084
http://europepmc.org/articles/PMC6628974
http://europepmc.org/articles/PMC6628974