Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Elizabeth K, Satter"'
Publikováno v:
Journal of Cutaneous Pathology. 43:809-814
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b221951c64109ae77d0e1018a1d0cae5
https://doi.org/10.1111/cup.12763
https://doi.org/10.1111/cup.12763
Publikováno v:
International Journal of Pediatric Otorhinolaryngology Extra. 9:166-169
Even though the overall prevalence of pediatric melanoma is low, the incidence continues to rise. Spitzoid melanocytic lesions have been the subject of controversy for over a decade, resulting in a confounding nosological classification. Despite the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::218ef85566a20b804cd55840631133ae
https://doi.org/10.1016/j.pedex.2014.10.001
https://doi.org/10.1016/j.pedex.2014.10.001
Rapidly fatal metastatic cutaneous angiosarcoma initially mimicking a furuncle in a middle-aged male
Publikováno v:
Cantor, Aaron S; Satter, Elizabeth; & Douglas, Mark. (2017). Rapidly fatal metastatic cutaneous angiosarcoma initially mimicking a furuncle in a middle-aged male. Dermatology Online Journal, 23(10). Retrieved from: http://www.escholarship.org/uc/item/0053z21b
Cutaneous angiosarcomas are rare but typically occur in three distinct clinical settings and are most commonly found on the scalp or face of elderly men. Positive prognostic factors include tumor size less than 5 cm, primary tumor location below the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79e1c9e8159684d2fdfa7c8c8958178b
http://www.escholarship.org/uc/item/0053z21b
http://www.escholarship.org/uc/item/0053z21b
Autor:
Elizabeth K. Satter
Publikováno v:
The American Journal of Dermatopathology. 37:505-507
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1318db84a04235ff5fcc3139d2b764e4
https://doi.org/10.1097/dad.0000000000000143
https://doi.org/10.1097/dad.0000000000000143
Autor:
Julia M. Kwan, Elizabeth K. Satter
Publikováno v:
Journal of the American Academy of Dermatology. 72:924-926
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95c82cf95c4e07c040a91e0ecdca169a
https://doi.org/10.1016/j.jaad.2012.06.032
https://doi.org/10.1016/j.jaad.2012.06.032
Publikováno v:
The American Journal of Dermatopathology. 37:246-248
Intradermal nodular fasciitis is a rare but not extraordinary pathological finding with approximately 100 cases reported since originally described in 1990. Intradermal proliferative fasciitis, however, has only been reported twice and both arose in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c93ee36448fffe24dabc850e3524b458
https://doi.org/10.1097/dad.0b013e3182987465
https://doi.org/10.1097/dad.0b013e3182987465
Publikováno v:
Pediatric Dermatology. 29:507-510
We describe two full-term infants who presented with congenital cutaneous candidiasis (CCC) and compare their clinical presentation and outcome with that of neonatal candidiasis and chronic mucocutaneous candidiasis. Although candidal vulvovaginitis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6de8175af92f890c7ebbd95587ee533
https://doi.org/10.1111/j.1525-1470.2011.01468.x
https://doi.org/10.1111/j.1525-1470.2011.01468.x
Publikováno v:
Pediatric Dermatology. 27:364-367
Although yaws is rare in developed countries, as worldwide travel has become commonplace, it is essential to recognize this condition when evaluating patients who traveled from endemic regions. Herein, we discuss a case of secondary yaws presenting a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::375f4ee03790a783f330d757911cba9d
https://doi.org/10.1111/j.1525-1470.2010.01184.x
https://doi.org/10.1111/j.1525-1470.2010.01184.x
Autor:
Elizabeth K. Satter
Publikováno v:
Journal of Cutaneous Pathology. 36:56-59
Superficial angiomyxoma (SA) is a distinct soft tissue tumor characterized by a circumscribed collection of spindled and stellate fibroblasts that are admixed with thin-walled blood vessels and embedded in a mucinous stroma. Because of its relative i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f82d19cb359b64733164951eb5182be4
https://doi.org/10.1111/j.1600-0560.2008.01216.x
https://doi.org/10.1111/j.1600-0560.2008.01216.x
Publikováno v:
Pediatric Dermatology. 25:291-295
Langerhans cell histiocytosis is a rare proliferative disorder where pathologic Langerhans cells accumulate in a variety of organs. Historically, the nomenclature regarding this entity has been confusing because the disease had been subcategorized si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2f4645675ce4e6c2c85d6583a04cdc5
https://doi.org/10.1111/j.1525-1470.2008.00669.x
https://doi.org/10.1111/j.1525-1470.2008.00669.x