Lee Yurimi, Na Kiyong, Woo Ha Young, Kim Hyun-Soo
Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.
Department of Pathology, Chungnam National University School of Medicine, Daejeon 35015, Korea.
Diagnostics (Basel). 2022 Apr 27;12(5):1102. doi: 10.3390/diagnostics12051102.
Alveolar soft part sarcoma (ASPS) is a rare malignant mesenchymal tumor mainly affecting adolescents and young adults, with a predilection for the deep soft tissues of extremities. ASPS arising in the female genital tract is extremely rare and poses a significant diagnostic challenge. We herein present two rare cases of ASPS, one occurring in the uterine corpus of a 27-year-old woman, and the other in the uterine cervix of a 10-year-old girl. We described the clinical, histological, immunophenotypical, and molecular characteristics of primary uterine ASPS. We performed immunostaining for transcription factor E3 (TFE3), human melanoma black 45 (HMB45), melan-A, desmin, pan-cytokeratin (CK), paired box 8 (PAX8), CD10, hormone receptors, and S100, and targeted RNA and DNA sequencing using commercially available cancer gene panel. In case 1, a 27-year-old woman was referred to our hospital after laparoscopic uterine myomectomy at an outside hospital. Imaging studies revealed a residual tumor in the uterine corpus. In case 2, a 10-year-old girl underwent surgical excision for the cervical mass and was diagnosed as having ASPS. She was then referred to our hospital for further management. Both patients received total hysterectomy. Histologically, they displayed characteristic histological features of ASPS. Strong nuclear TFE3 immunoreactivity, periodic acid-Schiff-positive, diastase-resistant intracytoplasmic rod-shaped crystalloids or granules, and the identification of - fusion confirmed the diagnosis of ASPS in both cases. Lack of immunoreactivity for HMB45, melan-A, desmin, pan-CK, PAX8, and S100 excluded the possibility of perivascular epithelioid cell tumor, clear cell sarcoma, metastatic renal cell carcinoma, granular cell tumor, and paraganglioma. Our observations can help pathologists make an accurate diagnosis of uterine ASPS and suggest that pathologists should include primary uterine ASPS in the differential diagnosis of uterine mesenchymal tumors.
肺泡软部肉瘤(ASPS)是一种罕见的恶性间叶性肿瘤,主要影响青少年和年轻成年人,好发于四肢深部软组织。发生于女性生殖道的ASPS极为罕见,对诊断构成重大挑战。我们在此报告两例罕见的ASPS病例,一例发生在一名27岁女性的子宫体,另一例发生在一名10岁女孩的子宫颈。我们描述了原发性子宫ASPS的临床、组织学、免疫表型和分子特征。我们进行了转录因子E3(TFE3)、人黑素瘤黑色45(HMB45)、黑素A、结蛋白、全细胞角蛋白(CK)、配对盒8(PAX8)、CD10、激素受体和S100的免疫染色,并使用市售癌症基因检测板进行靶向RNA和DNA测序。病例1,一名27岁女性在外部医院接受腹腔镜子宫肌瘤切除术后转诊至我院。影像学检查显示子宫体有残留肿瘤。病例2,一名10岁女孩因宫颈肿块接受手术切除,被诊断为ASPS。随后她转诊至我院进行进一步治疗。两名患者均接受了全子宫切除术。组织学上,它们表现出ASPS的特征性组织学特征。强烈的核TFE3免疫反应性、高碘酸-希夫阳性、淀粉酶抗性胞浆内棒状晶体或颗粒以及 - 融合的鉴定证实了两例均为ASPS。HMB45、黑素A、结蛋白、全CK、PAX8和S100缺乏免疫反应性排除了血管周上皮样细胞瘤、透明细胞肉瘤、转移性肾细胞癌、颗粒细胞瘤和副神经节瘤的可能性。我们的观察结果有助于病理学家准确诊断子宫ASPS,并表明病理学家在子宫间叶性肿瘤的鉴别诊断中应考虑原发性子宫ASPS。