Zhang Tao, Feng Run-Lin, Yin Si-Fan, Feng Wen-Bo, Yin Zhi-Yuan, Wang Hao, Ke Chang-Xing
Department of Urology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Department of Pathology, The Second Affiliated Hospital of Kunming Medical University, Kunming, China.
Front Oncol. 2022 Nov 23;12:1058700. doi: 10.3389/fonc.2022.1058700. eCollection 2022.
Endometrial stromal sarcoma is a relatively rare malignant tumor that derives from the malignant transformation of primitive uterine mesenchymal cells. It can lead to distant metastases. High-grade endometrial stromal sarcoma is extremely rare. The adrenal glands are an unreported site of metastasis.
A 71-year-old woman with a diagnosis of endometrial stromal sarcoma 30 months ago. After receiving treatment with radiotherapy and chemotherapy, the patient was kept asymptomatic during the follow-up until 2 years later, when she complained of dyspnea. Pulmonary and right adrenal gland metastases were detected by F-FDG PET/CT. The right upper lobe mass was diagnosed as a high-grade endometrial stromal sarcoma metastasis after postoperative pathology. Due to the patient's high risk of surgery, as she had many underlying diseases, we performed adequate preoperative preparation. The physical examination revealed that a hard mass was palpable in the right renal area. The right adrenal mass was resected in our hospital. Immunohistochemistry showed ER (-), PR (-), CD10 (+), P16 (+), Ki-67 (50%). The final diagnosis on pathological examination was a high-grade ESS metastatic to the right adrenal gland. The patient continued treatment in other hospitals after surgical resection. After four months of postoperative follow-up, metastasis was detected again during a PET/CT examination at an outside hospital.
Endometrial stromal sarcoma is rare, and the adrenal glands are an unreported site of metastasis. It has no specific clinical symptoms and mainly found for other reasons. The diagnosis still depends on pathology and immunohistochemistry. If there is no relevant past history, it is difficult to exclude a primary adrenal tumor.
子宫内膜间质肉瘤是一种相对罕见的恶性肿瘤,起源于原始子宫间充质细胞的恶性转化。它可导致远处转移。高级别子宫内膜间质肉瘤极为罕见。肾上腺是未被报道的转移部位。
一名71岁女性,30个月前被诊断为子宫内膜间质肉瘤。接受放疗和化疗后,患者在随访期间一直无症状,直到2年后出现呼吸困难。F-FDG PET/CT检查发现肺部和右肾上腺转移。术后病理诊断右上叶肿块为高级别子宫内膜间质肉瘤转移。由于患者手术风险高,存在多种基础疾病,我们进行了充分的术前准备。体格检查发现右肾区可触及一硬肿块。在我院切除了右肾上腺肿块。免疫组化显示ER(-)、PR(-)、CD10(+)、P16(+)、Ki-67(50%)。病理检查最终诊断为高级别子宫内膜间质肉瘤转移至右肾上腺。手术切除后患者在其他医院继续治疗。术后4个月随访时,在外院进行PET/CT检查时再次发现转移。
子宫内膜间质肉瘤罕见,肾上腺是未被报道的转移部位。它没有特异性临床症状,主要因其他原因发现。诊断仍依赖于病理和免疫组化。如果没有相关既往史,很难排除原发性肾上腺肿瘤。