BAP1 – Inactivated Melanocytoma. Description of the Case and Overview of the Issue
Authors:
Z. Szép 1,2; N. Majtánová 3; J. Majtán 4,5
Authors place of work:
Katedra dermatovenerológie LF SZU a výučbové centrá Onkologický ústav sv. Alžbety s. r. o., Bratislava, a Dermatovenerologická klinika LF SZU a FNsP Trnava, vedúci katedry a prednosta kliniky doc. MUDr. Zoltán Szép, PhD., MPH
1; Unilabs Slovensko, s. r. o., Diagnostické centrum patológie, Bratislava, vedúca oddelenia prim. MUDr. Iveta Mečiarová, PhD.
2; Očná klinika LF SZU a UNB – pracovisko Nemocnica sv. Cyrila a Metoda, Bratislava, prednosta prof. MUDr. Petr Kolář, PhD.
3; Ústav molekulárnej biológie SAV, v. v. i., Bratislava, riaditeľka Ing. Eva Kutejová, DrSc.
4; Ústav mikrobiológie LF SZU, Bratislava, prednostka prof. RNDr. Shubhada Bopegamage, CSc.
5
Published in the journal:
Čes-slov Derm, 99, 2024, No. 3, p. 126-131
Category:
Case Reports
Summary
BAP1-inactivated melanocytoma is a rare melanocytic lesion that was first described by Thomas Wiesner in 2011. It belongs to the group of so-called melanocytomas, which represent a group of intermediate melanocytic lesions. It occurs mostly sporadically, but rarely it can be part of the so-called hereditary BAP1 tumor predisposition syndrome. We present the case of a 33-year-old woman with a solitary BAP1-inactivated melanocytoma.
Keywords:
melanocytoma – BAP1 – hereditary BAP1 tumor predisposition syndrome
Zdroje
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Do redakce došlo dne 6. 11. 2023.
Adresa pro korespondenci:
doc. MUDr. Zoltán Szép, PhD, MPH
Onkologický ústav sv. Alžbety
Heydukova 10
812 50 Bratislava
Slovenská republika
e-mail: zoltan.szep@ousa.sk
Štítky
Dermatology & STDs Paediatric dermatology & STDsČlánok vyšiel v časopise
Czech-Slovak Dermatology
2024 Číslo 3
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