A rare case report of omental synovial sarcoma complicated hemoperitoneum and literature review.
Autor: | Van Manh N; Department of Gastrointestinal Surgery, 175 Military Hospital, Ho Chi Minh City, Vietnam. manhnguyen2388@gmail.com., Huy DT; Department of Gastrointestinal Surgery, 175 Military Hospital, Ho Chi Minh City, Vietnam., Tram Anh VT; Department of Palliative Care, Institute of Oncology and Nuclear Medicine, 175 Military Hospital, Ho Chi Minh City, Vietnam., Thanh NH; Deparment of Gastroenterology, Vinmec Times City International Hospital, Ha Noi City, Vietnam., Smith KM; Colorado Permanente Medical Group, Denver City, CO, USA. |
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Jazyk: | angličtina |
Zdroj: | World journal of surgical oncology [World J Surg Oncol] 2024 Nov 14; Vol. 22 (1), pp. 301. Date of Electronic Publication: 2024 Nov 14. |
DOI: | 10.1186/s12957-024-03559-3 |
Abstrakt: | Background: Synovial sarcoma is a rare malignant soft tissue tumor originating mainly in the extremities and usually related to the joint capsule, tendon sheath, or synovial capsule. Only a few cases of synovial sarcoma arising in the abdomen, particularly the omentum, have been reported. We presented a case of omental synovial sarcoma and reviewed 7 cases of this disease. Case Presentation: A 37-year-old man presented to the hospital with abdominal pain and distension for 2 months. A computed tomography scan revealed a massive heterogeneous low attenuation mass with amorphous solid components between the stomach and colon with suspected hemoperitoneum. The patient underwent surgery, and the pathological result demonstrated a greater omentum biphasic synovial sarcoma. Chemotherapy was administered with a good response. He has no signs of recurrence during 3 years of follow-up. Among 7 cases of omental synovial sarcoma, the mean age was 42, ranging from 16 to 66 years old with predominantly female (71.4%), tumor size from 9.5 cm to 20 cm. Biphasic synovial sarcoma accounted for 50%. The recurrence rate within one year is high (57.1%). Conclusions: Primary omental synovial sarcoma is uncommon and presents with nonspecific clinical symptoms, often leading to potential misdiagnosis with other conditions before surgery. They occur predominantly in females, mainly middle-aged, with a large mass size before presentation. Due to the high recurrence and mortality rate, it needs to be recognized at the early stage. Competing Interests: Declarations Ethics approval and consent to participate This is a case report that does not need ethics approval. Informed consent Written consent has been obtained from the patient. Competing interests The authors declare no competing interests. (© 2024. The Author(s).) |
Databáze: | MEDLINE |
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