Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Michael C. Royer"'
Autor:
Shane P Sweeney, Michael C. Royer
Publikováno v:
The American Journal of dermatopathology. 42(8)
Melanoma with cartilaginous differentiation is a rare histologic subtype that has been reported in the literature. It often presents clinically different than conventional melanomas and can be diagnostically challenging. Molecular alterations in prev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38da39e66f28246ee4d66f8de7290449
https://pubmed.ncbi.nlm.nih.gov/32701697
https://pubmed.ncbi.nlm.nih.gov/32701697
Autor:
Shaw T, Locke, William C, Schaffenburg, Jennifer P, Breedlove, Daniel W, Davis Ii, Lynden P, Bowden Iii, Michael C, Royer
Publikováno v:
Cutis. 103(4)
Nevus sebaceus (NS), also known as an organoid nevus, is a congenital skin hamartoma involving the pilosebaceous unit, epidermis, and adnexa, frequently occurring in the scalp area. During childhood, the lesion remains unchanged but may subsequently
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::07b36ca1a9cbaa15dd4ea08115aabb41
https://pubmed.ncbi.nlm.nih.gov/31116824
https://pubmed.ncbi.nlm.nih.gov/31116824
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 7, Pp 33-36 (2015)
Indian Dermatology Online Journal
Indian Dermatology Online Journal
We describe a case of Mevalonate Kinase Deficiency (MKD) also known as Hyperimmunoglobulinemia D Syndrome (HIDS) presenting as a Sweet-like syndrome in a 5-week-old with multiple erythematous plaques, fever, aseptic meningitis, and bronchiolitis. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5604af4750b3e4a08e6e46f28bbdb49d
http://www.idoj.in/article.asp?issn=2229-5178
http://www.idoj.in/article.asp?issn=2229-5178
Autor:
Michael C. Royer, Mark S. Lincoln
Publikováno v:
The American Journal of Dermatopathology. 38:e122-e124
Spindle cell/pleomorphic lipoma is an uncommonly encountered benign neoplasm that is usually found in the subcutaneous tissues. Rare cases reported in the literature have an intradermal location. This lesion usually presents as a subcutaneous nodule
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c66f54429c560e0146cc4e03912d14
https://doi.org/10.1097/dad.0000000000000546
https://doi.org/10.1097/dad.0000000000000546
Publikováno v:
Case Reports in Dermatological Medicine
Case Reports in Dermatological Medicine, Vol 2017 (2017)
Case Reports in Dermatological Medicine, Vol 2017 (2017)
Sweet’s Syndrome is a rare neutrophilic dermatosis thought to be a result of immune dysregulation occurring in the setting of drug exposure, recent infection, pregnancy, and underlying malignancy or idiopathic with specific and widely accepted diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b68576b4d47582ef1916106210d9b70
http://europepmc.org/articles/PMC5664242
http://europepmc.org/articles/PMC5664242
Publikováno v:
The American Journal of dermatopathology. 39(1)
The congenital melanocytic nevus is a pigmented melanocytic lesion that presents at birth or shortly thereafter. It is commonly described on the skin, usually on the trunk and extremities. Only five intraoral cases of congenital melanocytic nevi have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23c46dd86bf11d832718754a25e23bcc
https://pubmed.ncbi.nlm.nih.gov/28045755
https://pubmed.ncbi.nlm.nih.gov/28045755
Publikováno v:
The American Journal of Dermatopathology. 36:e121-e124
Granular cell basal cell carcinoma (BCC), characterized by large cells with abundant eosinophilic cytoplasm and conspicuous granularity, is an extremely rare variant of BCC with only 14 cases reported in the literature to date. A case of an 82-year-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3ce320fbc6775d39337598b5784f7ec
https://doi.org/10.1097/dad.0000000000000020
https://doi.org/10.1097/dad.0000000000000020
Publikováno v:
The American Journal of dermatopathology. 38(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a610b7528b2631ee6c31c77061e6db6
https://pubmed.ncbi.nlm.nih.gov/27442047
https://pubmed.ncbi.nlm.nih.gov/27442047
Publikováno v:
The American Journal of dermatopathology. 38(4)
Deep penetrating fibrous histiocytoma (DPFH) is a rare variant of fibrous histiocytoma that can arise in the subcutis and deep soft tissues with different clinical implications from dermatofibromas. Dermatofibromas are mainly cosmetic annoyances and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6b6f9c6e6cb3e01b7d0ae5bb8feb5df
https://pubmed.ncbi.nlm.nih.gov/26999346
https://pubmed.ncbi.nlm.nih.gov/26999346
Publikováno v:
The American Journal of Dermatopathology. 34:305-309
Apocrine nevus is a rare tumor composed of increased mature apocrine glands and ductal structures within a fibrous stroma, located predominantly in the reticular dermis. They have been reported in association with apocrine carcinoma, extramammary Pag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0370d41f40ef532b0c36fcfc51ef6bb4
https://doi.org/10.1097/dad.0b013e31823adf0e
https://doi.org/10.1097/dad.0b013e31823adf0e