Low-grade endometrial stromal sarcoma with a novel MEAF6-SUZ12 fusion.


Journal

Virchows Archiv : an international journal of pathology
ISSN: 1432-2307
Titre abrégé: Virchows Arch
Pays: Germany
ID NLM: 9423843

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 19 03 2019
accepted: 07 05 2019
revised: 23 04 2019
pubmed: 19 5 2019
medline: 13 11 2019
entrez: 19 5 2019
Statut: ppublish

Résumé

Endometrial stromal sarcoma (ESS) is a rare mesenchymal neoplasm. Herein, we report a low-grade ESS with a novel MEAF6-SUZ12 fusion gene. A 40-year-old woman presented with a 9.0-cm abdominal wall mass juxtaposed to the postoperative scar of surgeries for uterine "leiomyomas" and cesarean section. Histologically, mostly hypocellular and myxoid nodules were comprised of uniform spindle cells and exhibited tongue-like infiltration. Immunohistochemically, the tumor cells were positive for CD10, estrogen receptor, and CD34 (focal). There were occasional h-caldesmon-positive cohesive nests. RNA sequencing along with reverse transcriptase-polymerase chain reaction and Sanger sequencing identified an in-frame fusion of MEAF6 (exon 4) and SUZ12 (exon 2). Upon review of the previous "leiomyomas," we revised their diagnoses as low-grade ESS. The patient is alive without disease 2 years after the surgery. In addition to expanding the molecular landscape of low-grade ESS, this case highlights the challenge of diagnosing low-grade ESS in an uncommon clinicopathological setting.

Identifiants

pubmed: 31101969
doi: 10.1007/s00428-019-02588-8
pii: 10.1007/s00428-019-02588-8
doi:

Substances chimiques

Neoplasm Proteins 0
Oncogene Proteins, Fusion 0
SUZ12 protein, human 0
Transcription Factors 0
Polycomb Repressive Complex 2 EC 2.1.1.43

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

527-531

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 18K15108
Organisme : Japan Society for the Promotion of Science
ID : 18K15110
Organisme : Japan Agency for Medical Research and Development
ID : 17ck0106168h0003
Organisme : National Cancer Center Research and Development Fund
ID : 29-A-2

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Auteurs

Naohiro Makise (N)

Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Department of Pathology, the University of Tokyo, Tokyo, Japan.

Masaya Sekimizu (M)

Department of Clinical Genomics, National Cancer Center Research Institute, Tokyo, Japan.

Eisuke Kobayashi (E)

Department of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.

Hiroshi Yoshida (H)

Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

Masashi Fukayama (M)

Department of Pathology, the University of Tokyo, Tokyo, Japan.

Tomoyasu Kato (T)

Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.
Department of Gynecologic Oncology, National Cancer Center Hospital, Tokyo, Japan.

Akira Kawai (A)

Department of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan.
Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.

Hitoshi Ichikawa (H)

Department of Clinical Genomics, National Cancer Center Research Institute, Tokyo, Japan.
Division of Translational Genomics, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Tokyo, Japan.

Akihiko Yoshida (A)

Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan. akyoshid@ncc.go.jp.
Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan. akyoshid@ncc.go.jp.

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Classifications MeSH