Titlebook: Rare Malignant Skin Tumors; Franco Rongioletti,Irina Margaritescu,Bruce R Smol Book 2015 Springer Science+Business Media New York 2015 cut

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書目名稱Rare Malignant Skin Tumors影響因子(影響力)




書目名稱Rare Malignant Skin Tumors影響因子(影響力)學(xué)科排名




書目名稱Rare Malignant Skin Tumors網(wǎng)絡(luò)公開度




書目名稱Rare Malignant Skin Tumors網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Rare Malignant Skin Tumors被引頻次




書目名稱Rare Malignant Skin Tumors被引頻次學(xué)科排名




書目名稱Rare Malignant Skin Tumors年度引用




書目名稱Rare Malignant Skin Tumors年度引用學(xué)科排名




書目名稱Rare Malignant Skin Tumors讀者反饋




書目名稱Rare Malignant Skin Tumors讀者反饋學(xué)科排名

粘土

Lymphoepithelioma-Like CarcinomaLymphoepithelioma-like carcinoma of the skin (LELCS) is a rare neoplasm of unknown etiology and low malignant potential, microscopically similar to undifferentiated nasopharyngeal carcinoma, first described by Swanson et al. in 1988.

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Basal Cell Carcinoma with Matrical DifferentiationBasal cell carcinoma (BCC) is the most common type of skin cancer. Many variants are acknowledged, but the presence of matrical differentiation (recapitulating the follicular hair matrix) is exceedingly rare. Description of the entity is limited to single case reports or small case series.

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Trichilemmal CarcinomaTrichilemmal carcinoma (TC) is a rare cutaneous adnexal neoplasm that occurs on the sun-exposed areas of elderly people. The neoplasm was originally described as a clinical entity by Headington in 1976. The pathogenesis seems to be related to actinic damage, long-term low-dose irradiation, and malignant transformation of trichilemmoma.

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Primary Cutaneous Apocrine AdenocarcinomaPrimary cutaneous apocrine adenocarcinoma first described by Horn in 1944 represents a very rare tumor with less than 100 cases reported in the literature.

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Franco Rongioletti,Irina Margaritescu,Bruce R SmolProvides a bedside clinical reference.Richly illustrated with photomicrographs depicting histologic changes.Written by experts in their fields.Includes supplementary material:

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Fibroepithelioma of Pinkusa rare variant of BCC with an indolent behavior which usually develops as a soft, polypoid, or nodular tumor on the lower back with a characteristic unique histology of thin anastomosing strands of basaloid or squamous cells surrounded by abundant stroma. Some authors consider FEP a fenestrated variant of trichoblastoma.

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