Results 81 to 90 of about 72,671 (182)

An update on oculodermal melanocytosis and rare associated conditions

, 2017
Oculodermal melanocytosis (ODM) is a rare disease, which is characterized by hyperpigmentation of facial skin and several parts of the eye, such as the sclera, conjunctiva, cornea, iris, ciliary body, and choroid.
SCAVELLA, VITTORIO LUIGI, PLATEROTI, Rocco, Abdolrahimzadeh, Barmak, Rahimi, Siavash, PLATEROTI, ANDREA MARIA   +4 more
core   +1 more source

Beyond an Extensive Dermal Melanocytosis: A Case of Phacomatosis Pigmentovascularis of Cesioflammea Type

Portuguese Journal of Pediatrics, 2023
Bárbara Aguiar, Inês Vidreiro, Margarida Valente, Hugo Cavaco   +3 more
doaj   +1 more source

Imatinib Mesylate-Induced Acquired Dermal Melanocytosis and Acquired Bilateral Nevus of Ota-Like Macules. [PDF]

Ann Dermatol, 2021
Jang JW, Song CH, Jung YJ, Cheon DU, Koh WS, Ro YS, Ko JY.   +6 more
europepmc   +1 more source

MELANOSIS (PIGMENTED MELANOCYTOSIS) OF THE PROSTATE GLAND.

, 1989
A case of stromal melanosis of the prostate gland is reported. Ultrastructurally, dendritic processes and melanosomes, but no basal lamina were observed in melanin-containing cells.
DI GREGORIO C, LOSI, Lorena, BOTTICELLI AR, MANENTI A., FANO RA, A.R. Botticelli, C. Di Gregorio, L. Losi, R.A. Fano, A. Manenti   +9 more
core   +1 more source

Nevus of Ota Associated with Nevus of Ito : A Rare Case Report

JK Science
Except for the difference in distribution, Nevus of Ito and Nevus of Ota are very similar. In this report, we present the rare simultaneous occurrence of Nevus of Ota and Nevus of Ito in a21-year-old female patient.
Noel Sam Thomas, Neha Mariam Joseph
doaj  

Halolike Phenomenon Around a Café au Lait Spot Superimposed on a Mongolian Spot

, 2017
An 8-month-old Caucasian infant with neurofibromatosis type 1 presented with a congenital plexiform neurofibroma and multiple café au lait spots. A pale area surrounded one of the café au lait spots located on the left gluteus in the area of dermal ...
TENGATTINI, VERA, Annalisa Patrizi, NERI, IRIA, Beatrice Rivalta, RIVALTA, BEATRICE, Iria Neri, PATRIZI, ANNALISA, LAMBERTINI, MARTINA, Martina Lambertini, Vera Tengattini   +9 more
core   +1 more source

Iridociliary melanoma associated with ocular melanocytosis in a 6-year-old boy

, 2008
A previously healthy 6-year-old boy presented to the ophthalmologist and was found to have congenital ocular melanocytosis associated with uveal melanoma.
Augsburger, James J., Rahman, Amina Malik, Correa, Zelia M.   +2 more
core   +1 more source

Gene discovery in extensive dermal melanocytosis reveals multiple mosaic causes.

BACKGROUND: Extensive and/or atypical dermal melanocytosis (EDM) is abnormal macular blue/black skin pigmentation which can be associated with other congenital abnormalities and an increased risk of melanoma. It is likely underdiagnosed due to phenotypic
Nicole Knöpfel (18009232), Thomas Cullup (4281352), Fereshteh Izadi (19684040), Debra Lomas (20900819), Daniela Dyankova-Peeva (23218882), Robert A Henderson (20203296), Davide Zecchin (9027344), Sara Barberan Martin (8123174), Satyamaanasa Polubothu (11505751), Aimie Sauvadet (11921615), Veronica Kinsler (7561352), Ignacio Del Valle Torres (20420342), Frances Macrae (23780637), Claire O'Neil (23780634), Rezwanuzzaman Laskar (23780631), Dale Bryant (7914443)   +15 more
core   +1 more source

Cases of primary malignant melanoma and melanocytosis of the esophagus observed by magnifying endoscopy : Application to differential diagnosis : case series [PDF]

, 2017
Rationale: Primary malignant melanoma of the esophagus (PMME) is a rare disease with an extremely poor prognosis. In contrast, melanocytosis is a benign condition defined as melanocytic proliferation with melanin deposition.
Ishikawa, Kazuma, Sato, Yasushi, サトウ, ヤスシ, オオヌマ, ヒロユキ, ミヤニシ, コウジ, Hirakawa, Masahiro, Ohnuma, Hiroyuki, カトウ, ジュンジ, Kato, Junji, キクチ, ショウヘイ, Kikuchi, Shohei, 852, Miyanishi, Koji, ヒラカワ, マサヒロ, 321662/profile-ja.html, 佐藤, 康史, イシカワ, カズマ   +16 more
core  

Primary Leptomeningeal Melanocytosis in a 10-Year-Old Girl

, 2011
Primary leptomeningeal melanocytosis is rarely encountered in the pediatric population. Despite being considered a nonmalignant condition, it uniformly carries a poor prognosis given the ineluctable progression of meningeal infiltration.
Raoul de Haller, Marie Zenobi, El Hassani, Yassine, Benedict Rilliet, Yassine El Hassani, Marc Ansari, De Haller, Raoul Michel, Fluss, Joel Victor, Brunsvig, Kirsten, Ansari Djaberi, Marc Georges, Hanquinet, Sylviane, Johannes A. Lobrinus, Kirsten L. Brunsvig, Lobrinus, Johannes Alexander, Zenobi, Marie, Joel Fluss, Sylviane Hanquinet, Rilliet, Bénédict, Brunsvig KL, Ansari M, Lobrinus JA, Rilliet B, de Haller R, El Hassani Y, Hanquinet S, Zenobi M, Fluss J   +26 more
core   +1 more source