Metastatic gastrointestinal stromal tumor of the greater omentum. Case report

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Gastrointestinal stromal tumors (GIST) are the most common type of mesenchymal malignancies of the gastrointestinal (GI) tract. Almost 10% of them are originated outside of the GI tract (extra-GIST), while GIST of the greater omentum constitutes about 1% among stromal tumors. More than 80% of GIST have mutations in c-KIT and PDGFRA genes. Herein we demonstrate the case of successful treatment of patient with giant omental GIST with c-KIT exon 11 mutation. 64-years-old woman, was admitted to the Department of abdominal oncology with complaints of shortness of breath and abdominal enlargement in volume. CT-scan revealed a large tumor in the abdominal cavity with tumor size of 54×34×22 cm. The patient underwent left thoraco-abdominal approach. It was found that the tumor was originated from the greater omentum with several metastases located on the peritoneum of the left lateral channel. Resection of the large omentum, splenectomy, liver resection and was done. Postoperative immunohistochemical study showed the expression of CD117, CD34 in tumor cells. Ki-67 index was 12–15%. Genetic study revealed c-KIT exon 11 mutation. Treatment with imatinib 400 mg per day was started. Patient has been treated with imatinib for 12 years. On control examination we have found a metastasis in the anterior abdominal wall 3,5×3×2,5 cm in diameter. Afterwards we performed resection of anterior abdominal wall with metastasis on 9 November 2017. Immunohistochemical study confirmed metastasis of GIST. The index of tumor proliferation activity (Ki-67) was 45%. Patient prolonged imatinib treatment at the dose of 400 mg per day after operation. No signs of progression have been revealed on control examination 72 months after the operation. 12-year progression-free survival during imatinib treatment is unique in our practice. Moreover, in the case of further progression, we have second and third-line targeted therapy (sunitinib and regorafenib) and surgery treatment in local progression.

作者简介

Vladimir Yugay

Blokhin National Medical Research Center of Oncology

编辑信件的主要联系方式.
Email: yugay_vladimir@mail.ru
ORCID iD: 0000-0001-6169-2723
SPIN 代码: 2271-3639

oncologist

俄罗斯联邦, Moscow

Maxim Nikulin

Blokhin National Medical Research Center of Oncology; Yevdokimov Moscow State University of Medicine and Dentistry

Email: yugay_vladimir@mail.ru
ORCID iD: 0000-0002-9608-4696
SPIN 代码: 9455-5566

Cand. Sci. (Med.)

俄罗斯联邦, Moscow

Natalya Mazurenko

Blokhin National Medical Research Center of Oncology

Email: yugay_vladimir@mail.ru
ORCID iD: 0000-0003-4767-6983
SPIN 代码: 9169-8910

D. Sci. (Biol.), Prof.

俄罗斯联邦, Moscow

Valerija Mochal'nikova

Blokhin National Medical Research Center of Oncology

Email: yugay_vladimir@mail.ru
ORCID iD: 0000-0001-5275-7134
SPIN 代码: 7131-1273

pathologist

俄罗斯联邦, Moscow

Dar'ja Filonenko

Loginov Moscow Clinical Scientific Center

Email: yugay_vladimir@mail.ru
ORCID iD: 0000-0002-7224-3111

Cand. Sci. (Med.)

俄罗斯联邦, Moscow

Andrey Meshherjakov

Blokhin National Medical Research Center of Oncology

Email: yugay_vladimir@mail.ru
ORCID iD: 0000-0002-6009-653X
SPIN 代码: 3987-0910

D. Sci. (Med.)

俄罗斯联邦, Moscow

Vladislav Bugaev

Blokhin National Medical Research Center of Oncology

Email: yugay_vladimir@mail.ru
SPIN 代码: 7913-4919

Cand. Sci. (Med.)

俄罗斯联邦, Moscow

Petr Arhiri

Blokhin National Medical Research Center of Oncology; Russian Medical Academy of Continuous Professional Education

Email: yugay_vladimir@mail.ru
ORCID iD: 0000-0002-6791-2923
SPIN 代码: 6880-4902

Cand. Sci. (Med.)

俄罗斯联邦, Moscow

Anna Stroganova

Blokhin National Medical Research Center of Oncology

Email: yugay_vladimir@mail.ru
ORCID iD: 0000-0002-7297-5240
SPIN 代码: 5295-3338

Cand. Sci. (Med.)

俄罗斯联邦, Moscow

Ivan Stilidi

Blokhin National Medical Research Center of Oncology; Russian Medical Academy of Continuous Professional Education; Pirogov Russian National Research Medical University

Email: yugay_vladimir@mail.ru
ORCID iD: 0000-0002-0493-1166
SPIN 代码: 9622-7106

D. Sci. (Med.), Prof., Acad. RAS

俄罗斯联邦, Moscow

参考

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2. Fig. 1. Gastrointestinal stromal tumor of the large omentum. The loops of the intestine and the liver are shifted to the right.

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3. Fig. 2. Gastrointestinal stromal tumor of the large omentum. The tumor shifts the diaphragm upwards with compression of the left lung.

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4. Fig. 3. Removed gastrointestinal stromal tumor of the large omentum with a resected section of the left lobe of the liver and the spleen.

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5. Fig. 4. Primary EGIST. Spindle cells with hyperchromic nuclei with high mitotic rate. Cells form regular structures like "intertwining" bundles. Hematoxylin-eosin staining, ×100.

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6. Fig. 5. Primary EGIST. Immunohistochemical study. Expression of CD117, ×100.

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7. Fig. 6. Metastasis of a gastrointestinal stromal tumor of the large omentum in the anterior abdominal wall 12 years after surgery.

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8. Fig. 7. Metastatic EGIST. High mitotic index. Staining with hematoxylin-eosin, ×200.

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9. Fig. 8. Metastatic GIST. Immunohistochemical study. Ki67 proliferation index is 45%, ×100.

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