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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 & STDs
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