Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Dario Batolo"'
Publikováno v:
Pediatric Dermatology. 15:125-128
We report a 9-year-old boy affected by LEOPARD syndrome, who also had ichthyosis, axillary freckling, two cafe au lait spots, and one neurofibroma. The diagnosis of LEOPARD syndrome has been made on clinical grounds, whereas the ichthyosis and neurof
Autor:
Raffaele Gianotti, M. Pippione, Dario Batolo, Sergio Chimenti, Daniele Innocenzi, Carlo Tomasini, Alfredo Rebora, Carmelo Urso, R Filotico, P. A. Fanti, Maria Lentini, Franco Rongioletti
Publikováno v:
Journal of Cutaneous Pathology. 31:137-140
Background: Melanocytic nevi in the genital, acral, and flexural sites often display clinical and histologic features that may simulate melanoma. We verified whether this is the case also for nevi of the breast. Methods: Eleven dermatopathologists, f
Publikováno v:
Scopus-Elsevier
We describe two boys affected by Down syndrome (DS), who showed milia-like idiopathic calcinosis cutis (MICC). The clinical diagnosis was confirmed by histological examination. All reported cases are reviewed and compared. Syringeal structures play a
Autor:
Tamotsu Kanzaki, Makoto Kuroda, Kayoko Suzuki, Chee-Ching Sun, D. Bessis, Dario Batolo, Albert-Adrien Ramelet, Yasuko Yamanaka, Hiroshi Shimizu, R. Dedrick, J.-L. Lévêque, H. Apak, Laurent Misery, D. Jullien, Vincenzo Bettoli, Dirk Schneider, Hirohiko Akamatsu, Gottfried Weidinger, N. Valenzuela, T. Celkan, Peter Altmeyer, Hsuan-Hsiang Chen, Mei-Ping Tseng, Yoshikazu Mizoguchi, Masanori Ban, Akiko Yagami, Gisela Albrecht, Alessandro Borghi, Gérald Pierard, R. Lurie, S. Ozdil, Antonio Chuh, L. de Andres, E. Goubanova, X. Matias-Guiu, Maddalena Siragusa, Annarosa Virgili, Kei Kuroda, S. Kuruoglu, Toshiro Kikuchi, Z. Laron, Jacques Clèdes, Mu-Hyoung Lee, Matthias Braeutigam, I. Caro, D. Ben-Amitai, Stefania Pizzigoni, B. Guillot, Masako Mizoguchi, Masashi Akiyama, W. Dummer, R. Curell, O. Dereure, Kenjiro Terasaki, A. Joshi, Carmelo Schepis, Seok-Beom Hong, Kazuo Hara, Yoshiro Ichiki, Yasuo Kitajima, E.H. Aydemir, Jean-Luc Leveque, A. Alomar, Thomas Vogt, M.A. Barnadas, P. Natta, Yvonne Gaber, Kayoko Matsunaga, R.G.B. Langley, Manigé Fartasch, Michael Meurer, Thomas Ruzicka, Emmanuelle Legroux-Crespel, A. Özkan, N. Jumez, Maria Lentini, I. Yildiz, Akihiko Shibaki, Vincenzo De Sanctis, Margitta Worm, J.C. Prinz
Publikováno v:
Dermatology. 208:377-379
Publikováno v:
Journal of cutaneous pathology. 33(11)
Background: Tenascin is an extracellular matrix protein frequently expressed around neoplastic and non-neoplastic lesions of the skin. Actinic keratoses (AKs) are intraepidermal neoplastic lesions of the sun-exposed skin. They are classified accordin
Autor:
M. Pippione, Sergio Chimenti, Raffaele Gianotti, Alfredo Rebora, Carmelo Urso, Franco Rongioletti, Dario Batolo, Calogero Saieva, R Filotico, Daniele Innocenzi, Carlo Tomasini, Maria Lentini
AIMS: The histological features used in the diagnosis of melanoma may be present in benign naevi, but quantitative data are not available. The aim of this study was to establish the real prevalence of such features in naevi. METHODS: Ten dermatopatho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddbd3eac9be387173bb3091eb7581087
https://europepmc.org/articles/PMC1770759/
https://europepmc.org/articles/PMC1770759/
Publikováno v:
Pediatric Dermatology. 11:258-260
An 11-year-old girl with Down syndrome had whitish, milia-like lesions on the acral areas of the limbs, and periorbital syringomas. Calcium deposits were the histologic counterparts of the milia-like lesions. This is the first European report of this
Publikováno v:
The American Journal of dermatopathology. 23(5)
To assess if the quantity of silver-stained nucleolar organizer region (AgNOR) proteins predicts the behavior of actinic keratosis (AK), we performed a standardized AgNOR analysis on 51 cases of AK; in addition, 10 cases of squamous cell (SCC) and 10
Publikováno v:
Pediatric dermatology. 18(1)
We describe an 8-year-old boy with Rubinstein-Taybi syndrome, a multiple congenital anomaly/mental retardation syndrome characterized by broad thumbs and great toes, peculiar facies, and mental retardation caused by mutations in the transcriptional c