Abrams J, Talcott J, Corson J M
Department of Pathology, Brigham and Women's Hospital, Boston, MA 02115.
Am J Surg Pathol. 1989 Feb;13(2):133-40. doi: 10.1097/00000478-198902000-00006.
Two cases of low-grade endometrial stromal sarcoma (ESS) presenting as cystic pulmonary metastases are reported. Both lung lesions were initially thought to represent examples of so-called mesenchymal cystic hamartoma. A diligent search of the past medical records in the first case revealed that a primary low-grade ESS of the uterus had been resected 27 years earlier. In the second case, a uterine tumor was seen by computed tomography scan and subsequent pathologic examination of the hysterectomy specimen established the presence of a low-grade ESS. Peritoneal metastases, present in both cases, also presented diagnostic problems until the uterine primaries were recognized. Immunoreactivity for desmin was detected in all primary and metastatic tumor sites examined. We conclude that ESS should be included among the desmin-positive spindle cell sarcomas and that metastatic ESS should be included in the differential diagnosis of "benign" mesenchymal cystic hamartoma of the lung.
报告了两例表现为肺部囊性转移的低级别子宫内膜间质肉瘤(ESS)。最初,两个肺部病变均被认为是所谓的间质性囊性错构瘤。对第一例患者过去的病历进行仔细查阅发现,27年前曾切除过子宫原发性低级别ESS。在第二例中,通过计算机断层扫描发现子宫肿瘤,随后对子宫切除标本进行病理检查确定存在低级别ESS。两例均存在腹膜转移,在识别出子宫原发性肿瘤之前,腹膜转移也带来了诊断难题。在所检查的所有原发性和转移性肿瘤部位均检测到结蛋白免疫反应性。我们得出结论,ESS应纳入结蛋白阳性梭形细胞肉瘤中,并且转移性ESS应纳入肺部“良性”间质性囊性错构瘤的鉴别诊断中。