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妊娠期间的腹部纤维黏液样肉瘤:早产和败血症的罕见病因

Abdominal Fibromyxoid Sarcoma in Pregnancy: An Unusual Cause of Preterm Labor and Sepsis.

作者信息

Barger Abigail, Vishnia Maya, Hanna Marie, Horgan Rebecca, Martins Juliana

机构信息

Department of Obstetrics and Gynecology, Eastern Virginia Medical School, Norfolk, Virginia.

出版信息

AJP Rep. 2024 Jun 10;14(2):e188-e192. doi: 10.1055/a-2332-6187. eCollection 2024 Apr.

Abstract

Cancer in pregnancy is rare, with incidence less than 1%, and the most common cancers being melanoma, breast, and cervical cancers. Fibromyxoid sarcoma is a soft tissue tumor involving deep soft tissues of the extremities and trunk, rarely located in the abdomen. A low-grade fibromyxoid sarcoma (LGFMS) falls in the family of fibrosarcoma. Only two cases of LGFMS in pregnancy have been reported. We report a case of abdominal LGFMS in pregnancy leading to preterm labor, sepsis, and an acute abdomen requiring surgery in the third trimester. A 19-year-old woman, gravida 1 at 32 weeks and 5 days presented to an outside hospital with preterm contractions and cervical effacement. She had a known abdominal mass, suspected to be accessory liver lobe, measuring 9.0 × 6.4 × 7.7 cm in the right upper quadrant. At 33 weeks of gestation, she developed fever and hypotension. Magnetic resonance imaging confirmed the presence of the mass, which was now on the left side of the abdomen and associated with a suspected abscess. She underwent cesarean delivery, and complete surgical resection of the mass along with a small bowel resection. Final pathology of the mass revealed a LGFMS. This case also highlights the need for a multidisciplinary approach to manage a rare presentation of sepsis and preterm labor in pregnancy.

摘要

妊娠期癌症较为罕见,发病率低于1%,最常见的癌症是黑色素瘤、乳腺癌和宫颈癌。纤维黏液样肉瘤是一种软组织肿瘤,累及四肢和躯干的深部软组织,很少位于腹部。低级别纤维黏液样肉瘤(LGFMS)属于纤维肉瘤家族。妊娠期LGFMS仅报道过两例。我们报告一例妊娠期腹部LGFMS病例,该病例导致早产、败血症以及在孕晚期出现需要手术治疗的急腹症。一名19岁女性,孕1产0,孕32周5天,因早产宫缩和宫颈管消退被送往一家外地医院。她已知有腹部肿块,怀疑是副肝叶,位于右上腹,大小为9.0×6.4×7.7cm。妊娠33周时,她出现发热和低血压。磁共振成像证实了肿块的存在,此时肿块位于腹部左侧,且伴有疑似脓肿。她接受了剖宫产,并对肿块进行了完整的手术切除,同时切除了一小段小肠。肿块的最终病理检查显示为LGFMS。该病例还凸显了采用多学科方法处理妊娠期罕见的败血症和早产情况的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dda/11164575/3d331f173416/10-1055-a-2332-6187-i24apr0017-1.jpg

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