PIK3CA mutation status in apocrine carcinoma arising in apocrine gland hyperplasia/apocrine nevus: A study of four cases.

Goto, Keisuke; Kiniwa, Yukiko; Hishima, Tsunekazu; Honma, Keiichiro; Matsushita, Shigeto; Aoki, Megumi; Nishihara, Katsuhiko; Hiraki, Tsubasa

Goto, Keisuke; Kiniwa, Yukiko; Hishima, Tsunekazu; Honma, Keiichiro; Matsushita, Shigeto; Aoki, Megumi; Nishihara, Katsuhiko; Hiraki, Tsubasa.

Affiliation

Goto K; Department of Diagnostic Pathology, Shizuoka Cancer Center Hospital, Sunto, Japan.
Kiniwa Y; Department of Pathology, Tokyo Metropolitan Cancer and Infectious Disease Center Komagome Hospital, Tokyo, Japan.
Hishima T; Department of Diagnostic Pathology and Cytology, Osaka International Cancer Institute, Osaka, Japan.
Honma K; Department of Dermato-Oncology/Dermatology, National Hospital Organization Kagoshima Medical Center, Kagoshima, Japan.
Matsushita S; Department of Pathology, Itabashi Central Clinical Laboratory, Tokyo, Japan.
Aoki M; Department of Anatomic Pathology, Tokyo Medical University, Tokyo, Japan.
Nishihara K; Department of Diagnostic Pathology, Chutoen General Medical Center, Kakegawa, Japan.
Hiraki T; Department of Clinical Laboratory and Diagnostic Pathology, Osaka National Hospital, Osaka, Japan.

J Cutan Pathol ; 51(6): 399-402, 2024 Jun.

Article de En | MEDLINE | ID: mdl-38238254

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Glandes apocrines / Tumeurs des glandes sudoripares / Phosphatidylinositol 3-kinases de classe I / Hyperplasie Limites: Adult / Aged / Female / Humans / Male / Middle aged Langue: En Journal: J Cutan Pathol Année: 2024 Type de document: Article Pays d'affiliation: Japon

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