Zobrazeno 1 - 10
of 302
pro vyhledávání: '"Timothy H, McCalmont"'
Autor:
Jose L. Cortez, MD, MS, Sally Y. Tan, MD, MPH, Rebecca Abelman, MD, Peter Chin-Hong, MD, Timothy H. McCalmont, MD, Lindy Fox, MD, Anna Haemel, MD
Publikováno v:
JAAD Case Reports, Vol 27, Iss , Pp 32-34 (2022)
Externí odkaz:
https://doaj.org/article/d7eb1b02218e4879aa02ad4235cbcaa8
Autor:
Andrew S McNeal, Rachel L Belote, Hanlin Zeng, Marcus Urquijo, Kendra Barker, Rodrigo Torres, Meghan Curtin, A Hunter Shain, Robert HI Andtbacka, Sheri Holmen, David H Lum, Timothy H McCalmont, Matt W VanBrocklin, Douglas Grossman, Maria L Wei, Ursula E Lang, Robert L Judson-Torres
Publikováno v:
eLife, Vol 10 (2021)
Benign melanocytic nevi frequently emerge when an acquired BRAFV600E mutation triggers unchecked proliferation and subsequent arrest in melanocytes. Recent observations have challenged the role of oncogene-induced senescence in melanocytic nevus form
Externí odkaz:
https://doaj.org/article/53ad9d885af34b1391f8b61352342926
Autor:
Ayushi Gautam, Zhengda Sun, Ethan Winkler, Hua Su, Timothy H. McCalmont, Helen Kim, Tarik Tihan, William Y. Hoffman, Chris F. Dowd, Ilona J. Frieden, Daniel L. Cooke
Publikováno v:
Interdisciplinary Neurosurgery, Vol 20, Iss , Pp - (2020)
Background: We report a rare case of a 19-year-old female progressively affected by a peripheral arteriovenous malformation (pAVM), a midline cerebellar astrocytoma, and a brain arteriovenous malformation (bAVM). Case description: She presented with
Externí odkaz:
https://doaj.org/article/dc15d3e763d6465690df72ef19353b9b
Publikováno v:
International Journal of Women's Dermatology, Vol 5, Iss 5, Pp 384-386 (2019)
Cutaneous endometriosis is a disorder that primarily affects women of reproductive age. The disorder is most commonly associated with cyclical pain during menses, but it can be difficult to diagnose in the absence of these symptoms and requires biops
Externí odkaz:
https://doaj.org/article/db8a39f20c2b4ef7b206fc2c55b7e082
Publikováno v:
The American Journal of Dermatopathology. 44:943-947
The seminal case report of plexiform melanocytic schwannoma, published a decade ago, indicated that this is a rare variant of schwannoma demonstrating immunohistochemical expression of melanocytic markers, electron microscopic evidence of melanosome
Autor:
Iwei Yeh, Ursula E. Lang, Emeline Durieux, Meng Kian Tee, Aparna Jorapur, A. Hunter Shain, Veronique Haddad, Daniel Pissaloux, Xu Chen, Lorenzo Cerroni, Robert L. Judson, Philip E. LeBoit, Timothy H. McCalmont, Boris C. Bastian, Arnaud de la Fouchardière
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Deep penetrating nevi (DPN) are unusual melanocytic neoplasms with unknown genetic drivers. Here the authors show that majority of DPN harbor activating mutations in the β-catenin and the MAP-kinase pathways; this characteristic can help in the clas
Externí odkaz:
https://doaj.org/article/fbd6a7307720476793d06dd7588353f5
Autor:
Laura B. Pincus, Ziba Rahbar, Philip E. LeBoit, Timothy G. Berger, M. Kari Connolly, Jarish N. Cohen, Timothy H. McCalmont
Publikováno v:
Journal of Cutaneous Pathology. 49:408-411
A 72-year-old male presented with scarring alopecia on the scalp vertex, multiple crusted plaques on the hairline, and a history of vesicular eruption on the face. The scalp showed crusted plaques with loss of follicular ostia. No follicular pustules
Autor:
Lucinda L. Kohn, Mitchell Braun, Kelly M. Cordoro, Timothy H. McCalmont, Sonal D. Shah, Ilona J. Frieden, Anubhav N. Mathur
Publikováno v:
Pediatric Dermatology. 39:84-90
To characterize the skin and mucosal findings of NEMO syndrome.Retrospective review of clinical characteristics from a cohort of two families with mutations in IKBKG (the NEMO-encoding gene). A literature review identified 86 studies describing 192 p
Publikováno v:
The American Journal of Dermatopathology. 43:788-793
Pseudocarcinomatous desmoplastic trichoepithelioma (PDTE) features verrucous squamous epidermal hyperplasia with a jagged undersurface overlying cords of follicular germinative cells in a fibrotic stroma. To date, only 5 cases have been reported. We
Autor:
Tracy Funk, Morna J. Dorsey, Timothy H. McCalmont, Belen Rubio-Gonzalez, Ilona J. Frieden, Laura B. Pincus
Publikováno v:
Pediatric Dermatology. 38:229-232
DOCK8 immunodeficiency syndrome (DIDS) represents a rare primary immunodeficiency associated with cutaneous viral infections, allergy, and increased risk of malignancy. We report a case of folliculotropic mycosis fungoides with spontaneous resolution