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Syringocystadenoma papilliferum

Zuletzt geändert von Thomas Brinkmeier am 2025/04/25 21:37

Syringocystadenoma papilliferum

Engl: Syringocystadenoma papilliferum

Histr: Erstbeschreibung durch Elliot im Jahre 1893

Def: Zysten des dermalen Ausführungsganges apokriner Schweißdrüsen mit warzenartiger Oberfläche durch in das Lumen hineinragende Proliferationen

Man: meist kongenital, sonst Manifestation in den ersten Lj.

KL: kleine solitäre, ggf. leicht verruköse oder linear angeordnete Papeln

Lok: Prädilektionsstelle: Kopfbereich, Intertrigines

Hi: von der Epidermis ausgehender Tumor mit erweitertem Gangsystem und zylindrischem Drüsenepithel

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IHC: Cytokeratin-7- und Cytokeratin-19-Expression im Bereich der luminalen Säulenzellen

Kopl: - Vergrößerung während der Pubertät

- selten: Entstehung eines Basalzellkarzinoms bzw. maligne Entartung (Syringocystadenokarzinom)

Lit: -  

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- Case Rep Dermatol. 2022 May 30;14(2):127-131. http://doi.org/10.1159/000524821

Ass: - Naevus sebaceus (30%)

- verruköses Karzinom der Haut

Vork: selten

Lit: J Cutan Pathol. 2019 Aug 26. http://doi.org/10.1111/cup.13572

Lit: -  

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- Case Rep Dermatol Med. 2022 Feb 3;2022:8076649. http://doi.org/10.1155/2022/8076649

- Dermatol Pract Concept. 2023 Oct 1;13(4):e2023239. http://doi.org/10.5826/dpc.1304a239

- Indian J Dermatol Venereol Leprol. 2024 Jul 3:1-4. http://doi.org/10.25259/IJDVL_659_2023

Th: Exzision

  
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